How the Brain Works,
Coherently
Coherently
Abstract:
All neuroscience is based
on a modular brain, each component responsible for certain 'functions,' without
explanation of how they cooperate in coordinated responses.
This article offers a new theory of neuropsychology—how the brain works, coherently.
It provides an accumulation of authoritative evidence that the Reticular
Activating System (RAS), including its ‘sentinel,’ the Reticular Formation
(RF), with two-way communications with all of the brain and body, is the
perfect candidate for the ‘Command and Control System’ in all sentient beings,
the de facto manager and coordinator of all brain and body activities.
The RF, processing 100
million internal and environmental sensory impulses per second, selects
‘significant’ stimuli, resolving many biological imbalances ‘silently.’
Others are forwarded to thalamus and midbrain—the locus of RAS and
consciousness—thence to the cortex, the ‘hard-drive’ memory of data,
sensory and motor neurons, and sensory and motor sequences. RAS extracts
nine times more information from cortex to thalamus, providing cognition; and
registers relevant cortex memory response sequences in the prefrontal lobes for
resolution and implementation via the premotor cortex. The prefrontal
cortex is ‘RAM’ workspace, balancing responses until one predominates.
RF/RAS monitors and generates responses (or response-impulses) to any
disequilibria in 1) any biological/physiological function, 2) in the innate
Social-Animal Needs we share with our cousin, the chimpanzee, and 3) in the
hundreds of significant, self-adopted beliefs and affections—conscious and
subconscious—which constitute the unique ‘Love/Belief System’ wired
in each of our brains, between stimlus and cognition. These
two sets of programs mingle (one can love SA-Needs for food, sex, socializing,
etc), continually generating desires and fears representing the great majority
of RF ‘significant’ stimuli which engross consciousness.
We each see, hear, and read―experience―the world
through our Social-Animal Needs and the unique
set of elements, conscious
and sbubconscious,
of our particular
Love/Belief Systems.
The Reticular Activating
System can be
imputed to generate all
our emotions,
and all our
psychopathologies
RAS interprets the
world differently to each of us, and triggers our responses or
response-impulses. Those with unexamined, anarchic Love/Belief Systems
are, for the most part, on autopilot—not living, but being lived by the
Reticular Activating System, programmed by their Social Animal Needs, and by
the conscious and subconscious Elements which make up their
particular Love/Belief Systems, or what theologians know as our ‘hearts.’
Following is the diagram I will propose as
illustrative of all cognitive brain processing: a new theory
of neuropsychology.
This diagram is meant to illustrate the theory that all
neurological processes are
under the control and
management of the
Reticular Activating System.
Further, that all brain
processing is innervated
by the Reticular Formation
or by the superior “I”
The “I” at the top of the diagram represents the Agent responsible
for the needs and faculties we do not share with our ‘cousin,’ the chimpanzee,
and accounts for the superiority of our capabilities. The literature provides
us with a wide range of Agents from which to choose.
Although no neuroscientists seem to be represented, many renowned psychologists
and psychiatrists have found it necessary to postulate an Agent of our superior
capabilities. St. Thomas Aquinas postulated the spiritual Soul, with
faculties of memory, intellect, and will. Freud’s Agent was “I” (Gernan
‘ich,’ which was translated as ego), with the faculties of
perception, conscious thought, memory, learning, choice, judgment, and
action. Jung referred to a ‘self,’ or ‘God within us;’ Karen Horney to
our “real self, ... the central inner force,... which is the deep source of
growth, . . the spring of emotional forces, of constructive energies, of
directive and judiciary powers;” Roberto Assagioli to our ‘higher
self;’ Martin Buber to ‘I’ and ‘Thou;’ Arthur Deikman to the ‘Observing Self;’
Antonio Damasio to a ‘proto self;’ Ernest Becker (See his Pulitizer Prize
winning Denial of Death,) refers to our “proud, rich,
lively, infinitely transcendent, free, inner spirit;” And myriad
mystics, saints, and sages have claimed an ineffable realization of their ‘True
Inner Self.’ 

But, whichever ‘self’ you
choose, it seems that the failure of biologists to find any significant
differences between ourselves and the chimpanzee makes the hypothesis of a non-biologicalelement
in humans—a ‘self’ of some kind—mandatory.
For the first time to my
knowledge, I will identify specific
needs and faculties of a
transcendent Self, which, coupled
with those we share with
the chimpanzee, and this new
coherent brain theory,
will shed a beacon of light on all
motivation and behavior,
all psychopathologies, and a
resolution of the
mind/brain/behavior enigma.
(See end of article for
Adobe PDF® version)
How the Brain Works,
Coherently
Coherently
A multidisciplinary systems
analysis of mind/brain/behavior
Eugene B. Shea
analysis of mind/brain/behavior
Eugene B. Shea
While neurobiologists have been making great
strides in identifying brain diseases and genetic anomalies, enabling them to
develop wonderful biochemical products and gene therapy to treat them,
cognitive neuroscientists and neuropsychologists are having a much tougher time
of it. They are trying to understand the brain processes in
stimulus/response, in hopes of eventually arriving at an understanding of
the enigmatic relationships of mind/brain/behavior.
Many neurologists, biologists, physiologists—even some physicists and
mathematicians—are exercising their truly prodigious powers of imagination to
justify their conviction that consciousness, reasoning, decision-making, etc.―all
our ‘higher’ faculties―must be functions of some yet to be discovered
faculties of the cortex .

But since this article will take strong exception to the direction of the
research of cognitive neuroscience and neuropsychology, I must devote the
following portion to explaining why I believe the great majority are on the
wrong track. Then we'll take a look at how the brain most probably does
work―coherently.
First however, I want to clearly and largely exempt Bernard J. Baars, Ph.D.,
and Nicole M. Gage, Ph.D. from my criticism, based on their marvelously lucid
and carefully researched new textbook, Cognition, Brain, and
Consciousness: Introduction to Cognitive Neuroscience - Academic
Press, 2007.
Dedicated neuroscientists, they struggle bravely
with such things as metacognition, intentionality, volition, “making choices in the absence of inherently
correct solutions,” which they boldly admit “remains, at least for now, a uniquely human
territory,” (with the
implication that it’s only a matter of time till scientists get around to
explaining it in neuronal terms). They also find it necessary to ascribe
genie-like faculties to the frontal lobes, e.g., having a “coarse map
of the entire cortex,” so it can select
and retrieve memories relevant to its decision-making
processes. [page 354]
But I am deeply indebted
to them for the wealth of current neuroscience research which has been included
in and corroborates my theory, and the glaring gaps in their studies―and in all neuropsychology―e.g,, the neural processes between stimulus and
cognition/response, which this article will address, and offer a
cogent theory. I think every serious student of cognitive neuroscience
should have a copy of this excellent book.
The major problem facing cognitive neuroscientists is that the chimpanzee's DNA
is now known to be 99+% identical to ours, so most ‘scientismists’ thought this
proved we were only a branch of the chimp family, and that the <1%
difference could account for our vastly superior capabilities.
But now they have found that the remaining <1% difference is primarily
related to hair, skin, bones, blood, muscle, etc.―hardly differences which
could begin to account for our superiority.
Our DNA is not similar to that of the chimpanzee,
it is, to all intents and
purposes, identical.
Then how come we're so different? Never at
loss for figments, most scientists have concluded that our differences, our
higher faculties, must be found in the cortex, particularly in the prefrontal
cortex, both of which are much larger than that of the chimp, imagining that a
larger but physiologically and biologically identical brain, must
account for our superiori
So hundreds of researchers are expending millions of people-hours, centering
all their efforts to locate human faculties of consciousness, reasoning, intentionality, conviction, imagination,
volition, etc, in some as yet und
iscovered faculties of the
human cortex.
Professor Sebastian Grossman, Ph.D., late Emeritus Chair of Bio-Psychology,
University of Chicago, pointed out “... neuropsychologists’
proclivity to ‘localize’ higher faculties such as consciousness in that part of
the brain that has undergone the most obvious evolutionary change...
.” (in a letter to the author)
Note the good Professor's precise use of the word ‘proclivity,’ and quote
marks around the word localize. In other words, they
arbitrarily posit our higher faculties in the cortex, not on the basis of any
scientific evidence, but because that’s where they want them to be.
And, with all due respect to Dr. Grossman, we now know the larger brain is not
at all ‘evolutionary’ in the Darwinian sense, having appeared on the
planet in an instant of
geological time.
Nor is there any validity to the popular ‘triune’ nature of the brain, as
composed of evolutionary development from reptilian to mammalian to primate
brains. The so-called ‘reptilian brain’ is not a brain at all, since it
represents only a portion of the reptile brain, which is comprised, like ours,
of brainstem, midbrain, and cortex. Nor, for the same reason,
is the mammalian brain a brain. And as we shall see, their neglect of
these specious lizard and mammalian ‘brains’ in favor of the cortex has led
researchers to only a perfunctory analysis of their marvelous functions,
without which we would be vegetables a few minutes before our
demise.
And cognitive neuroscientists are admittedly struggling with a ‘binding
problem.’ The various visual characteristics of an object―color, shape,
size, motion―are registered and interpreted in different parts of the
brain. So, they wonder, if I see something red, round, tennis ball-size,
and in motion, where in the cortex—where they think consciousness must
reside―do all of those percepts come together to instantly alert me to the fact
that I’m going to get hit in the face with a tomato? The famous binding
problem.
My first computer 30 years
ago, was a Model III Radio Shack running on a Z-80 processor, with 64K of
internal memory and two 64K floppy disk drives. My current Pentium 4 HT
3GHz, 2.99GHz, with 2G of RAM, and a 150G hard drive, operates on exactly the
same principles as my old Model III. The only substantial difference is a
faster processor and more importantly, vastly more RAM and memory―data and
program storage and work space.
Now consider the lowly rat, whose peanut-size brain, consisting of a brainstem,
a minuscule mid-brain and cortex, can generate perhaps only thirty or forty
different responses. But those few responses have insured the
perpetuation of the species for thousands of years. Now looking at the
successive anatomical forms of the mammalian brain of the rat, cat, owl monkey,
rhesus monkey, and chimpanzee, isn’t it obvious that these are simply
sequentially larger versions of the rat’s marvelously efficient brain?
Enlargements which, coupled with a more versatile body and more RAM work space
and memory, enable the chimpanzee to generate scores of responses and, by
operant conditioning and social learning, to acquire scores more?
And, since our DNA is identical, isn't it also obvious that our brain is
simply a larger chimp’s brain, and must also operate with the same components
and on the same principles? Much of what we know about the human brain has been learned from
experiments on primates.
Years ago pioneers working on artificial intelligence realized that for a
computer to emulate the brain it must be equipped with many facts: children
can’t be as old or older than their parents, shirts are bought at a department
store, etc. They first estimated maybe as many as a million facts; but
realized almost at once that they were dealing with tens of millions of
facts. Where but in the cortex could the brain store all these
facts?
Further, can you imagine
the number of neural motor sequence memories─ routines, and subroutines─necessary for a
typist to hit 9 keys a second for minutes at a time, without realizing what he
has typed? For sighted words to appear on a page, while he thinks of
something else? Can you imagine the number of subroutines necessary to
drive my car through traffic while I’m thinking of something else, and alert me
instantly to anything requiring my attention? For our subconscious
morning ablutions? For a concert pianist to have thousands of musical
phrases wired to his fingers’, hands’, arms’, feet, and legs’ motor
neurons? Some of which can be executed continuously for twenty
minutes?
The number of sensory sequence memories to read and absorb
information at 400 words, including hundreds of phrases, a minute? To
know thousands of words which I can rattle off correctly in millions of
different phrases? To know the appearance and something about 1,000
people on hearing their names? To recognize 1,000 people on sight from
many angles? To recognize the voices of scores of people? To
recognize hundreds of songs on hearing one or two phrases? And on what
instrument they are played? For an idiot-savant to memorize an
encyclopedia?
Where could we possibly store tens of millions of facts, and all these sensory
and motor sequences―routines, subroutines, and sub-subroutines―all this memory?
Why, only in the vast association areas of the cortex of course! We don’t
need another operating system; but we humans do obviously need more
working space (prefrontal cortex RAM) and more memory, a larger hard drive,
provided by the mammoth human cortex.

Note that none of these memories have any use or
meaning to the chimpanzee, which does very nicely with a much smaller but
identical cortex.
Most importantly, neuroscientists using their fMRI and PET scans, have
unanimously limited themselves to a modular model of the
brain, examining each segment (normal, lesioned, or diseased) during different
mental activities, as though each is independently responsible for (or
independently participates in) one or more of the multiplicity of activities of
which the brain is capable.

For example, handicapped by this modular approach,
they consider central nervous system activities such as thought, voluntary
movement, reasoning, perception, emotions, etc., asfunctions of the
parts of the brain which ‘light up’ when those activities are operant, while
those mental or physiological activities are impaired when that part of the
brain is damaged or diseased.
But doesn’t my computer hard drive operate exactly
the same way―activate relevant sectors when certain programs are run, and fail
to run those programs when those sectors are damaged? Does that mean my
computer operations are functions of those segments of the
hard drive? Isn’t the hard drive just a passive memory of operational
sequences called forth and managed from somewhere else? As Baars &
Gage warn, we shouldn’t confuse correlative with causal.
Calling mental and physiological activities
‘functions’ of active brain segments is like saying that maintaining an
airplane in straight and level flight is a function of the ailerons, rudder,
and elevator, because they are active during flight corrections. But
maintaining flight stability is a function of the autopilot or the pilot.
(Incidentally, as we shall see, the airplane is a
perfect analogy of this theory: RF/RAS is the autopilot, the “I” is the pilot,
and can override RAS responses, and create its own ‘responses,’ but whose images
of intent [see below] are executed by and through the
autopilot, the RAS.)
By the same token, I will argue that the ‘function’ of all brain
components is to each act
in accordance with the current demands
of the Reticular
Activating System, which alone has all the efferent
inputs to appraise all
internal and external circummstances, and
the afferent and
efferent connections (for control and feedback)
to and from all brain and
body components to generate and
execute 'appropriate'
responses to those circumstances─
and as we will see below,
to implement our acts of will.
All brain components can’t each be immediately apprised of
existing internal
and environmental circumstances, instantly
appraise those circumstances, and each independently
play its own variable part
in a relevant response,
as all neuroscientists
seem to assume.
Further, believing that the cortex is home to all our higher powers,
researchers have concentrated their analyses on the one-way upward course of
information from the senses through the reticular formation and thalamus up to
the cortex, where they think consciousness, processing, analysis, and
decision-making must take place. But according to Erich Harth in The
Creative Loop - How the Brain Makes a Mind, they have “studiously
ignored” the instantaneous downward passage of ten
times as much information from the cortex to the thalamus! Baars &
Gage recognize this phenomenon, but say these “neurons are running the
wrong way (i.e, from V1 downward to the visual thalamus)!” (sic, pg. 66)
I will try to prove that a much more efficient brain processing, and
a binding problem solution, lie in considering consciousness, in both
animals and humans, to be centered in the thalamus, the brain's
Central Command and
Control Center, which then uses the cortex
to retrieve relevant
memories and identify and feed ‘appropriate’
motor response routines
and subroutines to prefrontal cortex RAM
for processing (as
explained below), until the intensity of a given
response reaches an ‘enact
level,’ and is forwarded to the premotor
cortex and relevant brain
components for implementation,
or the stimulus abates and
the PFC reverts to inactive RAM.
For example, when I am attending to the voice of
someone who says, “Marilyn Monroe” (O.K., I'm 91), I suggest that those words
pass in neural networks through the reticular formation to the thalamus/RAS―and non-cognitive consciousness―which forwards it up to
auditory cortex regions.
But 9-10 times as much information is returned
from the cortex to the thalamus, enough information to give me a picture of a
beautiful blonde in a white dress and high heels standing over a subway exhaust
grille trying to hold her skirt down―a picture which would require scores of
thousands of computer bytes. Isn't it obvious this picture was simply
retrieved to thalamic consciousness from the cortex?
Researchers who concentrate their efforts to
understand cognitive neurology while confining their search for our
higher powers to some mysterious, yet-to-be-discovered faculties of the cortex,
while ignoring our unique metafaculties (explained below), the
remarkable functions of the Reticular Activating System, and
the vast range of its influence on human cognition and behavior are, I believe,
heading down a one-way dead-end road.
Some neuroscientists agree, at least in part: “From modern
neuroanatomy, it is apparent that the entire neocortex of humans continues to
be regulated by the paralimbic regions from which it evolved.” [A
General Theory of Love, Lewis, et al., pg; 33]
As Dr. Grossman puts it, “. . . the
reticular formation has been sadly neglected by contemporary neuroscientists,
.” (in a letter to the author)
In view of the above, it
is a major thesis of this article
that although we use the brain differently, e.g., for
everything from language to putting men on the
moon, and therefore develop different capacities of
its components, the human brain, in and of itself,
has no inherent functional capabilities which
differentiate it from the brain of the chimpanzee.
that although we use the brain differently, e.g., for
everything from language to putting men on the
moon, and therefore develop different capacities of
its components, the human brain, in and of itself,
has no inherent functional capabilities which
differentiate it from the brain of the chimpanzee.
The rest of this article will be devoted to a new
paradigm of the human brain, one which can resolve the binding problem, explain
from a systems standpoint how the brain does work, and shed a beacon of light
on the neurology of human motivation and behavior—a unified theory of
psychology, cybernetics, and neuroscience, and a resolution of the
mind/brain/behavior enigma.
How the Brain Does Work:
Coherently!
|
To understand human behavior, and identify the
locus of consciousness, a multidisciplinary systems analysis of the brain may
prove to be a more fruitful approach.
Look at it this way: if beings from
another planet were smart enough to get to earth, and simply observe an
automobile for a day or two without raising the hood, but listening, examining
the gas, the exhaust, etc., they would undoubtedly be able to tell, without
a design of each part, exactly what components were at work inside the
car. They would know that there must be a fuel vaporizer, combustion
chambers, ignition devices, a transmission, etc., etc.
Now, with ever-increasing analytical skills
and data, we have been observing each other and ourselves for more than three
thousand years, and apparently no one seems to be trying to analyze the brain
from a systems standpoint―to postulate the components and their functions which
must be at work ‘under the hood,’ in order to explain all the rational and
irrational physical, mental, and emotional responses which biologists,
physiologists, neuroscientists, and particularly cognitive and
existential psychologists, know the brain can generate and/or
implement.
A multidisciplinary systems analysis. . .
|
Drawing on the disciplines of psychology,
cybernetics, and neurology, and painting with a broader brush in a systems
analysis, we can perhaps begin to develop a schematic of the human and
chimpanzee brain components and their functions in all mammalian behavior.

From a systems standpoint, we know that every
complex mechanism―and so too, every complex organism― made
up of multiple subsystems, a mechanism whose subsystems can operate in varying
combinations, and each to varying degrees, to accomplish a number of different
tasks―like a battleship for example―must have a command and control system which
manages and coordinates the functions of the subsystems.
To operate effectively, a command and control system must have:
1. Immediate access
to all available internal and
environmental circumstantial information,
2. A means of rapidly assimilating,
evaluating, and
prioritizing that information,
3. A means of selecting and implementing
appropriate responses to the information, and
4. Immediate two-way communications, for
control
and feedback, with all of
the subsystems.
Now of course the body is a complex mechanism with
many subsystems, capable of operating in a coordinated way. So it must
have a command and control center, which all agree is the brain. But the
brain itself is a very complex organism with many subsystems capable of
operating in a coordinated way.
It is inconceivable that
the human and animal brain,
with all of its components and subsystems―much more
complicated than a battleship―could possibly coordinate
each of their functions in effective management of the
thousands of complex physical, mental, emotional, and
biological activities of the body, providing as it does,
instantaneous, coordinated reactions to
with all of its components and subsystems―much more
complicated than a battleship―could possibly coordinate
each of their functions in effective management of the
thousands of complex physical, mental, emotional, and
biological activities of the body, providing as it does,
instantaneous, coordinated reactions to
considerations of
vital interest, without
a
central priority evaluator
and responder to
its internal and environmental stimuli―
i.e., a command and control system.
its internal and environmental stimuli―
i.e., a command and control system.
But then where is it? What is it?
The only viable candidate for the brain’s
‘command and control system’ is the
Reticular Activating System, centered, with consciousness, in the thalamus, which sends and receives signals to and from all parts of the brain and body. |
The only known system of
the brain which has access
to all incoming
information, is known to immediately
scan and prioritize
that information, then select and
implement some ‘appropriate’
responses, and
has two-way communications
with all of the
subsystems, is the Reticular
Activating System,
including its ‘sentinel,’ the Reticular Formation.
including its ‘sentinel,’ the Reticular Formation.
Although scientists have
known about some of the
properties of the Reticular Activating System/
Reticular Formation for over 50 years, none of them,
to my knowledge, has suggested they form a command
and control system for all operations of the brain.
properties of the Reticular Activating System/
Reticular Formation for over 50 years, none of them,
to my knowledge, has suggested they form a command
and control system for all operations of the brain.
The key to a cogent systems analysis of the brain
was provided many years ago by the renowned Jerome S. Bruner, one of the
fathers of cognitive psychology, when he observed,
“The human mind has an ‘inhibitory system’ which
routinely and automatically removes from perception, reason, and judgment over
99% of available fact.”

I propose the Reticular Formation (RF)―in
both humans and all sentient beings―as the perfect neurological candidate for
Bruner’s ‘inhibitory system.’ The RF is an
uncharted—unchartable?—amorphous mass of millions of neurons, whose responses
are uniquely unspecific,
located inside the brain stem, about the size and shape of one’s
little finger. In 1958, physiologist H. W. Magoun described some of its
functions in The Waking Brain. Together with its
millions of communication pathways to and from the brain and the body, it was
named the Reticular Activating System (RAS), because
stimulation of the RF caused sleeping subjects to awaken, while damage to the
RF resulted in coma.

But now, even after fifty-plus years, neurologists have identified only a few
of the RF purposes. It is so complex that research on it has practically
come to a halt.
Although its centralized location
and countless connections would seem to enable it to perform myriad functions,
it is impossible, using current research methods, to identify more than a few
of them.

What little is known
about the RF/RAS raises questions which no one in the neuroscience community
seems prepared to address. For example,
“Nature appears to have gone to great pains to
cause essentially all the incoming and outgoing communication channels of the
brain to pass through the reticular system.” 

“[The reticular formation] is well
placed to monitor all the nerves connecting brain and body. It
‘knows’ what is going on better than any other part of the brain.” 

“[The reticular formation] alerts the
brain to incoming information from the senses,and from the centers of
thought, memory and feeling. More than that, it
adjudicates the relative importance of that information. ... In a way the RAS
is like a vigilant secretary, sorting out the trivia from the incoming
messages.” 

“The reticular formation
is, in essence, the physical basis of consciousness, the brain's chief
watchguard. ... The reticular formation continuously sifts and selects,
forwarding only the essential, the unusual, the dangerous to the conscious
mind. ... The reticular formation can both send and receive messages. If
it suddenly spots one that merits attention, it shoots up an alert through
ascending RAS pathways to receiving areas in the cortex. Timed to arrive simultaneously with
the impulses sent directly from sensory receptors, [ ! ! ! ] the
RAS alerts the cortex to these impulses.”

“The RAS determines which
of the many bits of information are important enough - or novel enough - to
report to the higher portions of the brain. ... Normally, the information
relating to automatic actions, such as the heartbeat and digestion, is dealt with
directly by the RAS, which sends out regulating impulses when they are needed
without allowing any awareness of them to filter through to the conscious
brain.” 

“Researchers have a
relatively clear picture of the physical underpinnings of consciousness.
Information streaming in from nerve receptors in the skin, muscles, tendons,
joints, eyes, ears and mouth passes first through the thalamus and/or the
reticular formation - a group of nuclei in the brainstem. Thus, before
even reaching the cortex, impulses have passed through a series of processing
regions that behave somewhat like secretaries in an office who screen phone
calls, mail and visitors before passing them on to the boss.
“The reticular formation, sometimes called the
ruler of consciousness, stands at the critical junction — both in terms of
anatomy and function — of the senses and the higher brain. Vigilant day and
night, the neurons of the reticular formation sort all incoming impulses. By
some unknown means, they determine which deserve further attention, and
having done so, flag important impulses so that the cortex will take note of
them. At night, while the cortex is deep in sleep, the reticular
formation keeps tabs on the senses and in times of possible danger is first to
sound the alarm.”

“There is also direct
evidence that the RAS is able to produce the kinds of effects on the operation
of the muscles and glands that would accompany the role of a
response-selecting mechanism. It seems to be able to sensitize or
‘awaken’ selected nervous circuits and desensitize others. This is
sometimes accomplished by selective muscular activation: electric
signals sent over reticular nerve fibers down the spinal cord to terminate on the relay nerve cells whose
axons pass out to the muscles achieve a sort of ‘volume-control’ action that
increases or decreases the magnitude of the muscular response.” !
! 

“The reticular formation
monitors incoming stimuli and chooses those that should be passed on to the
brain and those that are irrelevant and may be ignored. ... In addition to
being a filter, the reticular formation controls respiration, cardiovascular
function, digestion, awareness levels, and patterns of sleep.
“In recent years, the reticular formation
has been discovered to be more significant than previously thought.
Scientists now believe it to be involved in higher mental processes, in
particular the focusing of attention, introspection, and reasoning.” 

Finally, since a picture is worth a thousand words. . .
I quote all these sources (with emphasis
added) to show the consensus of opinion that the RF isBruner’s inhibitory
system; that the RF, “like a vigilant secretary,” with the power to
inhibit, automatically makes it our very stimuli selector (and ipso
facto is responsible for all our repressions!); but that much more
than a secretary, its associated RAS also selects and implements responses
to those stimuli; that together they form the silent sovereign manager of all
human and animal vital functions; are also capable of “selective
muscular activation;” are now thought by some scientists “to
be involved in higher mental processes;” and lastly, to remark that,
remarkably, this is all they have to say about this mysterious element
in the brain. All of these authors then go on to discuss other parts
of the brain, with apparently no curiosity about how the RF is able to decide
what and what not to inhibit―how it decides which of the great multiplicity of
available sensory stimuli it will select for further
processing. 

From all the evidence, the human and chimpanzee RF/RAS
can only be characterized as a computer/servo-organism
which receives all incoming sensory data, scans and
prioritizes that data for further processing in accordance
with its ‘programs;’ and, through the Reticular Activating
System, generates and controls Responses or Response-
Impulses ‘appropriate’ to its iterations of the data.
It is a second major thesis of this article, representing a
new paradigm of the brain, that in all sentient beings, the
brain constitutes a coherent computer-servo organism
which, under the direction of the Reticular Activating
System, and at the instigation of the Reticular Formation,
uses the whole brain to try to maintain physiological and
biological homeostasis; in social beings to also try to
maintain stasis of bio-sociological needs; and in humans,
to also try to maintain stasis of our uniquely induced
psychological, emotional, and volitional states.
(Hereafter I will use the term ‘RAS’ to include
all the processes of the RF. Also, since the RAS can enact
responses, e.g., knee-jerk and 'silent' vital sign corrections, or only a
response-impulse, e.g. hunger pangs, the word ‘response’ will be used to
indicate response or response-impulse, or both, as the context requires).
What then, are the programs on which the RF/RAS is
operating? Well, as we have seen above, the RAS is known to control all
our vital functions, respiration, pulse, sleep/wake cycles, etc. But the
chimpanzee, without higher powers, also gets an immediate response to any
disequilibrium in any of its biological, physiological, and bio-sociological needs,
its Social-Animal Needs. Responses to these Needs must also
be generated by the RAS.
And since our DNA is 99+% identical to that of the
chimpanzee, we must assume that our basicRF/RAS programs are
the Social-Animal Needs (SA-Needs) we so obviously share with the
chimpanzee―Needs which are continually moving into operant and quiescent
states. Functioning as priority-interrupts, any Need can be
primary at any given time.
So it is the Reticular Activating System which
motivates children and chimps to imitate others, to seek belongingness,
which makes us sleepy when we are tired, and generates an instant mind/body
fight, flight, or freeze reaction to a threat, etc., etc. Of course, both
animals and humans learn from experience and improve their performance, so the
RAS must have access to all of the organism's Memories, in order to generate
the best, or most common precedent response for need gratification or fear
assuagement.
But we have some metaneeds and metafaculties absent
in our ‘cousin’ the chimpanzee. One of these is an insatiable
metaneed, our need to Know, and its corresponding metafaculty,Conviction, i.e,
knowing or believing. Unlike simple animal curiosity, we want
to know who, what, where, when, how, and why about everything. Aristotle
said, “We must know.”

Herein lies one of our major human problems: in our need to know, we readily
adopt―become convicted of―literally thousands of beliefs (some estimates
run in the hundreds of thousands!) based on our interpretation of our
experiences, or on inference, assumption, probabilities, deduction, induction,
syllogisms, the reports of others, and a host of generalizations.
This led Joseph Jastrow to conclude that “the mind is a belief-seeking
rather than a fact-seeking apparatus.” One needs only follow a
four-year old around for a few hours to confirm this idea. We humans have
an insatiable need to know, causing us to avidly adopt beliefs by the thousands
as we mature. Even things we know as facts act as beliefs, as do all
our doubts, disbeliefs, memories,
values, and our self-adopted ‘needs’
additional to the SA-Needs.

But the major things we need to know are “Who
am I? What am I? Why am I here? What is the meaning of
my life? I am a completely unique person―where do I belong?” In
answer to these fundamental questions, we do what everyone else is doing; we
look for things with which we can identify ourselves. We
start building a self image—we identify ourselves with
our body, our mind, our family, our friends, a significant other, and later,
our profession, possessions, religion, nationality, reputation, gender,
or a cause, etc.—a seemingly infinite number of things.
The beliefs and accompanying activities which make up our self-image thus serve
two purposes: they give us a sense of self identity: “I am an American, a boy
or girl, a Jones family member, a student, a group member, etc.” And they
are necessarily, per Assagioli (see below), accompanied by activities representative
of those self-identifications; activities in which we can temporarily ‘lose
ourselves,’ and, as long as we are so engaged, repress the nagging questions of“Who
am I? What am I? Why am I here?”
As Roberto Assagioli states in PsychoSynthesis, “We are dominated by
everything with which our self becomes identified.” Each
self-identification carries with it the responsibility of assuming all the
characteristics we believe are representative of, or
applicable to, that appellation. These self-identifications engender many
beliefs, including Karen Horney’s tyrannical ‘shoulds,’ which constitute
Freud's 'super-ego,' or
what we know as our conscience. Our self-image becomes perhaps the
most powerful element in our belief systems and beomes a very prolific
generator of beliefs.
As noted, we can simultaneously identify ourselves with a number of
things. Aldous Huxley describes it best:
. . . since the mind-body is capable of an
enormous variety of experiences, we are free to identify ourselves with an
almost infinite number of possible objects—with the pleasures of gluttony, for
example, or intemperance, or sensuality; with money, power, or fame; with our
family, regarded as a possession or actually an extension and projection of our
own selfness; with our artistic or scientific talents; with some favourite
branch of knowledge, some fascinating ‘special subject’; with our professions,
our political parties, our churches; with our pains and illnesses; with our
memories of success or misfortune, our hopes, fears and schemes for the future;
and finally with the eternal Reality within which and by which all the rest has
its being. And we are free, of course, to identify ourselves with more
than one of these things simultaneously. Thus a man can be at once the
craftiest of politicians and the dupe of his own verbiage, can have a passion
for brandy and money, and an equal passion for the poetry of George Meredith
and under-age girls and his mother, for horse-racing and detective stories and
the good of his country—the whole accompanied by a sneaking fear of hell-fire,
a hatred of Spinoza and an unblemished record for Sunday church-going.
So starting at birth (or possibly in the womb) we
each haphazardly develop a unique belief system in the brain. But since
most of our self-image beliefs and many others have an emotional or affective
component, I suggest it is better described as a Love/Belief System.
Eventually this System is comprised of scores of thousands of things we
believe, and an ever-changing group of purposes or people or ideas with which
we have allowed our Selves to become identified—all of them capable, as we
shall see, of giving rise to Desires and Fears.
Now most of us think we receive sights and
sounds in their pure form, which are then evaluated against relevant elements
of our Love/Belief Systems.
But our instantaneous,
involuntary reactions to
contradictions of
our beliefs or derogation of things with
which we are
identified, and positive reactions to their
support, are autonomic, and
those responses must
therefore have been
generated by the RF/RAS.
As William James wrote many years ago:
“It is clear that between what a man calls ‘me,’
and what he simply calls ‘mine,’ the line is difficult to draw. We feel
and act about certain things that are ours very much as we feel and act about
ourselves. Our fame, our children, the work of our hands, may be as dear to us
as our bodies are, and arouse the same acts of reprisal if attacked. ... In its
widest possible sense, however, a man’s Self is the sum total of all that he
can call his, not only his body, and his psychic powers, but his clothes and
his house, his wife and children, his ancestors and friends, his reputation and
his works, his land and horses and yacht and bank account. All these
things give him the same emotions. If they wax or prosper, he feels
triumphant, if they dwindle and die away, he feels cast down - not in the same
degree for each thing, but in much the same way for all.”
We humans uniquely respond autonomically to
hundreds of circumstances other than those related to the Social-Animal Needs,
but significantly related to our Loves and Beliefs, and must therefore
have been selected and interpreted by the RF/RAS prior to entering
consciousness.
So we have for example, the ‘cocktail party
phenomenon,’ the instantaneous, involuntary shift of our attention when a loved
one’s name is spoken, even in a babble of sounds. (The RAS instantly
reduces the volume of all other sounds!) Or when someone criticizes our
church, or our children, a feeling of resentment is instantly generated, and
one or more of our perceptual defenses are brought into
consciousness. We autonomically generate the same reaction we would
to a kick in the shins.
All our sights and sounds
come to us preselected,
preevaluated, and processed before they fully enter our
consciousness. Favorable stimuli are rushed intact to our
consciousness; but stimuli in conflict with elements of
our Love/Belief Systems are, failing complete repression,
modifed, justified, rationalized, etc., to make them
conformable to elements in our Love/Belief Systems.
We don’t see things as they are;
we see them as we are.
preevaluated, and processed before they fully enter our
consciousness. Favorable stimuli are rushed intact to our
consciousness; but stimuli in conflict with elements of
our Love/Belief Systems are, failing complete repression,
modifed, justified, rationalized, etc., to make them
conformable to elements in our Love/Belief Systems.
We don’t see things as they are;
we see them as we are.
ANAIS NIN
Further evidence of RF/RAS response-impulses: Haven't we all
heard snippets of words or glimpses of something which instantly registered as
‘important,’ without knowing what it was until the stimulus was replayed in our
consciousness for identification and cognition? And really bad news can
instantly cut off the supply of blood to the brain and cause us to faint before
it fully penetrates consciousness. RAS is our shock-absorber.
Can these responses also be a function of the RAS, or do they involve some
other brain function? Obviously the RAS autonomically selects and
implements responses to our vital functions: respiration, heart rate,
digestion, arousal, adrenalin level, etc. And if we share the
Social-Animal Needs, it's easy to understand how the RAS would generate an
instant response to a threat of pain or isolation or the taking of one’s
food. But although again, the RF/RAS is the only viable candidate,
how could it also pick out from the environment and generate instant responses
to the sound of a loved one’s name, or a diminution or enhancement of James’“reputation
and his works, his land and horses and yacht and bank account?”
The answer lies in the fact that Dr. Gary Lynch of the University of California
at Irvine has proved that “learning involves a physical change in the
circuitry of the brain.” When we learn something, new synapses are formed
in our brains, or existing connections are strengthened, sometimes in as little
as ten minutes. (Aside: perhaps in geniuses and idiot-savants, much
faster?) The brain is now known to be plastic.
The Plausible
Hypothesis:
|
Certainly it is not then an ‘astonishing
hypothesis’
to infer that if I love someone, that
person’s name becomes wired in or near my Reticular Formation, and the RAS
generates a response whenever that name is mentioned; or if I believe that
I am an honest, intelligent person, that belief becomes wired into my RF, and
any implication to the contrary triggers what is known as a ‘perceptual
defense.’ 


The point is that all of
our Loves and those Beliefs with
an emotional or affective component, are not additional
‘learnings’ to be stored in the brain as data. They must
somehow be processed differently, to be registered in or
near the Reticular Formation, where, with the Social
Animal Needs, they represent the principles or programs
an emotional or affective component, are not additional
‘learnings’ to be stored in the brain as data. They must
somehow be processed differently, to be registered in or
near the Reticular Formation, where, with the Social
Animal Needs, they represent the principles or programs
Therefore, until some ‘sensor’ and ‘response
generator’ of each of these brain actions is identified, what better candidate
than the Reticular Formation and Reticular Activating System? Why would
such a marvelous system be limited to sensing and issuing responses to
physiological, biological, and SA-Needs, and not include, as I
suggest in this article, our uniquely emotional, psychological, and volitional
states of disequilibrium?
The major thesis of this article is that in all sentient beings,
the RF/RAS manages the
entire brain, and through the brain,
all biological and
physiological functions, as the command
and control system of the
entire organism’s homeostasis.
In social animals, the
RF/RAS programs include the Social-Animal
Needs, Instincts, and Memories; in humans they are the SA-Needs,
Love/Belief System Elements, and Memories; and thereby include
stasis of our emotional, psychological, and volitional states.
Needs, Instincts, and Memories; in humans they are the SA-Needs,
Love/Belief System Elements, and Memories; and thereby include
stasis of our emotional, psychological, and volitional states.
In addition to all its
other functions, the RAS
works continuously to
bring us equanimity, i.e.,
Peace.
It seems the only plausible hypothesis is that the human Reticular Activating
System takes on an additional responsibility for the Love/Belief System, whose
programs consist of the myriad significant conscious and subconscious Loves and
Beliefs which we all adopt or with which we are introjected, since
infancy. This transformation of the RF, together with our uniquely
human metaneeds and metafaculties, makes of each of our brains what we have
always known as the mind.
So here is Bruner’s ‘inhibitory system,’ the centralized, indefatigable,
quintessential sentinel of the brain, and the Reticular Activating System―the
de facto manager of the brain―as it says in the illustration above, “deflecting
the trivial, letting the vital through to alert the mind.”
But ‘vital’ and ‘trivial’
are subjective terms, different for each individual. How does the RFknow what
is vital and what is trivial to each of us, if not in the way this article
describes? As noted earlier, I can find no serious literature which even
addresses the question.
Since the RAS is both our
stimuli and response-
selector, we are all seeing and hearing the
world―experiencing and responding to it―
through our Reticular Activating Systems.
selector, we are all seeing and hearing the
world―experiencing and responding to it―
through our Reticular Activating Systems.
Think about it. This means that we are all
wearing diffracting lenses over our eyes and earphones over our ears, which
select, evaluate and translate what we see, what we hear, what we
read. Our experiences all come to us selected and modified by the RAS before they
reach consciousness. In each of us our uniquely programmed RAS is interpreting
the world to us. Remember, the RF
not only selects important stimuli, it removes 99+% from our veryperception.
And this is why, as all psychologists know (but most seem to think only applies
to others):
The RF rushes favorable
sights and sounds unaltered
to consciousness; but if
unable to completely repress
unfavorable stimuli,
they reach us only after having
been colored, modified, or
rationalized to be
presented in their most
palatable form:
“The grapes were probably
sour anyway.”
The shocking conclusion we must draw is that the RAS operates exactly like the U. S. Government―a vast and
incredibly complex bureaucracy, comprised of scores of open
andsecret bureaus, departments, and branches, staffed by hundreds of
single-minded bureaucrats―whose responsibilities often overlap or conflict, and
with very imperfect commu<="" font="">nications
between them, each competing for our attention, each with some
priority-interrupt authority, each mindlessly trying to enact its own limited
agenda, and to justify and expand its authority by encouraging the acceptance
of data which validates its agenda and rejection of that which does not<=""
font="">―an appalling, but unfortunately, a compellingly exact
analogy. Can cognitive dissonance, and its associated existential
anxiety, be far behind?
We are living in a
post-hypnotic trance,
induced in early infancy.
―R. D. LAING
(Further, as we will see, our creative acts of
will must go back through the same system for afeasibility analysis before
they are enacted, where they are often displaced by
conflicting conscious and subconscious Loves and Beliefs.)
In addition to the metafaculty of conviction we also have the uniquely human
metafaculty ofcommitment. The animal is committed
by any RAS-generated response impulse strong enough to pass through the ‘action
gate’ in the frontal lobes to the premotor cortex. But we have the power
to commit ourselves to hundreds of things, not only unrelated to the SA-Needs,
but even opposed to them: celibacy, solitude, fasting, even suicide, etc.
Our metafaculty of ‘knowing’ includes the power
of metacognition. Baars and Gage recognize
metacognition as “the ability to know our own cognitive functions, and
to be able to use that knowledge; and point out that the prefrontal
cortex (where alternative responses are resolved) is necessary for
metacognition.
Cognitive psychologists, e.g., Merluzzi, et al., have long recognized the human
faculty of metacognition, which they say “refers to the
ability to monitor a wide variety of cognitive enterprises, ... to monitor
one's memory and comprehension, or knowing about knowing or an awareness ot
one's own cognitive machinery and the way it operates.

Both metacognition and commitment are manifest
in the well-known Benjamin Libet experiments, which clearly illustrate the
pre-conscious (i.e., subconscious) nature of RAS-generated
response-impulses, as well as the subject’s metacognizance and commitment
power over those impulses.
“Benjamin Libet of the University of California,
recorded electrical signals generated by the brains of his experimental
subjects and looked particularly at a signal called the ‘readiness potential’
that always appears just before a movement. Using special timing techniques,
he found that the readiness potential begins about half a second before a
subject begins to move a hand. This is expected, since brain activity
must begin before the brain issues a command to the muscles. What is
surprising, however, is that the subjects do not become aware of deciding to
move until only about two tenths of a second before the movement begins, some
three tenths of a second after the brain activity began.
“. . . to Libet [this] says that the intention to
act arises from brain activity that is not within our conscious awareness. . .
the brain initiates the impulse to act and the conscious self subsequently
becomes aware of it. Libet also finds that his subjects are able to veto
the impulse to act during the few tenths of a second after a subject becomes
aware of it. In this sense, consciousness becomes a gatekeeper for
intentions generated by the brain, letting through only those that somehow meet
an individual’s criteria.”

But what specifically are the ‘cognitive
functions’ of which metacognition makes us aware? I contend that these
are processes of the prefrontal cortex (PFC). Any sensory signal
interpreted by the RF as ‘significant,’ is brought to uncomprehending
consciousness in the thalamus and control of the RAS. The RAS
forwards the signal immediately on to the cortex for identification - what is
it? where is it? - and a search of the cortex for all relevant memories
and responses, which are forwarded to the frontal lobes for execution or
resolution.
Now in both human and chimpanzee, these responses, if unambiguous and
uninhibited by associated beliefs or memories (see ‘feasibiity
analysis’ below) are forwarded
through a ‘pass’ channel of the prefrontal cortex (PFC), premotor cortex, and
motor cortex, for initiation of the response. (The PFC doesn’t ‘light up’
for unambiguous, uninhibited, or habituated responses.)
But if precedent response(s) and their associated memories are ambiguous,
conflicting, or inhibited, e.g., a threat generating ‘fight, flight, or freeze’
responses, all responses from cortex memory in the form of their motor sequence
memories―each ‘weighted’ by memories of their associated results―are
registered by the RAS in the prefrontal cortex, where, accompanied by
continuous additional sensory stimuli directly from thalamus consciousness
regarding the significance and imminence of the threat, and additional
relevant memories retrieved by RAS from the cortex, the momentary urgency of
each response is adjusted until (in the animal) one response prevails and
immediately breaks through to the conveniently contiguous premotor cortex for
implementation, or the threat abates.
In other words, the vaunted prefrontal cortex (PFC) is simply RAM, random
access memory, which does not store memory, but provides current ‘work-space’
for ambiguous, conflicting, or inhibited response-impulses, their associated
memories, and sensory iterations from the thalamus, until, in the animal, one
response prevails and penetrates the gate to motor neurons to
enact a response. Naturally, if the threat disappears, the PFC is
restored to inactive RAM.
Neither animal nor human PFC’s decide which responses will be
executed, any more than a neuron, receiving both excitatory and inhibitory
impulses, decides when or when not to fire.
But this ‘simple’ PFC
function has led most
neuroscientists to ascribe our unique executive
powers of reasoning, analysis, and decision-making
to some mysterious, yet-to-be-discovered capabilities
of the PFC and cortex, simply because they are
larger than those of the chimpanzee.
neuroscientists to ascribe our unique executive
powers of reasoning, analysis, and decision-making
to some mysterious, yet-to-be-discovered capabilities
of the PFC and cortex, simply because they are
larger than those of the chimpanzee.

However, this weighting function of responses in
the PFC is not determinant in humans. As we have seen in the Libet
experiment, we have metacognizance of RAS-generated response-impulses, and
commitment power through direct thalamic channels to the PFC action gate―a
metapower executed by the commitment to a consciously generated response which
can override the RAS-generated response-impulses.
And we have another metafaculty, the faculty of Imagination,
the ability to create and manipulate words, images, ideas, and symbols in our
consciousness, and put them together in creative ways. Most all
philosophers and many scientists agree this is a uniquely human faculty, though
most scientismists disagree. I don't think the matter is debatable.
Baars & Gage take imagination for granted throughout their text.
So, except for knee-jerk responses, e.g., avoiding a flying object, if a RAS-
or self-generated response is even slightly ambiguous, conflicted, or
inhibited, we can either allow it to be executed, or we can
remember the effect of those responses, imagine alternative
responses, select a preferred response, and implement that response by committing ourselves
to its execution, just as a pilot can override the autopilot..
Unfortunately however, even in making a considered decision, our analysis of
alternative responses is limited to consideration only of our conscious memories
and SA-Need and Love/Belief elements, but is subject to strong
insidious influences from subconscious elements. Which is why we so often
have two reasons for what we do: a good reason, and the real
reason.
But it is not only ambiguous responses which
are resolved in the PFC. Rather, isn’t it obvious that every human
problem or problematic situation must be referred to the PFC RAM for
resolution? As Baars & Gage point out, “... the frontal
lobes are critical in a free-choice situation, when it is up to the subject
to decide how to interpret an ambiguous situation.” 

Don't we all live in a sea of ‘ambiguous situations’?
Aren't most of us, by virtue of our hundreds of significant Loves.
Beliefs, Values, Needs, etc., always operating on a dozen or two perpetual purposes?
Aren't we always concerned with longevity, good health, welfare of loved ones,
avoiding pain, danger, and disease, our love lives, work and family
responsibilities, our spiritual lives, financial security, our
reputations, projection and protection of our idealized self-image, observance
of our ‘shoulds,’ consistency of our Love/Belief systems, validity of our
religious and political persuasions, etc., etc.?
These are purposes to which either the environment or our imaginations continually
provide relevant stimuli, generating desires and fears, and to which, due to
their ultimately unresolveable nature, the RAS can only engender ambiguous,
conflicting, or inhibited responses. So most of us are ‘worrying’ our
poor PFC’S almost every waking moment. No wonder our PFC's occupy such a
large portion of our cortex! And why so many of us live ‘lives of
quiet desperation’ and ‘cognitive dissonance.’
In addition to choosing our responses, we can will
to generate acttions independently of RF/RAS impetus, even things we've never done before. How is this accomplished? How do we Will something to
happen?
Let’s suppose I decide to go to the grocery store.
First, I visualize, imagine myself at the grocery store, and of
course I must believe/know it can be accomplished (the brain automatically runs
each of our ‘images of intent’
through
a ‘feasibility analysis,’ and if it finds a problem, which it
often does, refers the conflict to the PFC and our consciousness, where it can
be resolved per above), then commit myself to going to the store: “I will be at the store.” This process authorizes the RAS to execute
the motor neuron programs which take me to the store, while I’m free to think
of something else if I wish. 


Creative Will is the
concurrent use of our
metafaculties of imagination, belief, and commitment.
metafaculties of imagination, belief, and commitment.
How does the brain do this? I submit that
when furnished with a clear picture of a result, a feasibility-check resulting
in belief in its attainability, and a commitment to achieve it, the RAS is
presented with a disequilibrium: “I’m here - I will be there.” In
response the RAS, holding that purpose until equilibrium is restored, takes it
to the cortex where it searches out relevant neuronal motor
sequence memories―routines―and forwards each in turn to the PFC where all
are given a subconscious pass to the premotor cortex and to the motor neurons
which, subject to continual subconscious subroutine adjustments―steering,
braking, accelerating, etc., based on thalamic sensory input―take me to the
store, leaving my consciousness free for daydreams.
This principle applies to long-range images of
intent: "I will be a doctor, lawyer, wife and mother, teacher,
millionaire, congressperson, missionary, etc. Any image of intent, firmly held,
creates a disequilibrium in the Reticular Activating System, and it constantly brings
to our attention from the deepest recesses of the memory and from the
environment the jig-saw-like pieces of the elements and opportunities which
will enable actualization of the intent.
Thus a black Elizabeth Train raised by a single
mother who told her she could do anything, and who as a young girl fell in love
with Don Ameche’s portrayal of an authoritative Naval Intelligence Officer,
rose to become a Rear Admiral, the highest ranking female Information Dominance
Corps officer, and the only female Intelligence Officer Admiral. Talk
about the power of the Soul! As Earl Nightingale states in his classic The
Strangest Secret, “We become what we think about.”
(Here's an interesting research project: Subjects have been equipped with
a beeper and asked tomake note of their
thoughts when it goes off. They've learned how often we think about
various subjects. But now they should add instructions that subjects
should also note what they were doing when the beeper sounded. I believe
this would clearly prove that during the majority of the day, our actions were
on RAS management while our thoughts were occupied elsewhere.
)

Unfortunately, as we mature, many of our RAS-generated responses―which must
include all our emotions―tend to become conditioned responses, and it’s usually
much easier to accede to these responses with the attitude, “That’s me;
that’s the way I am." Most of us become reconciled or
resigned to these specious synaptic selves, and allow our brains to
“become who we are.”
Conclusions
|
We need a new
paradigm of the human brain, as a brain which starts out physiologically and
functionally identical to that of the chimpanzee,
but is transformed into what can now be
defined as a ‘mind’ by virtue of our metafaculties of imagination, conviction, and
commitment, as well as by the thousands of self-adopted Loves and Beliefs and
their concomitant Desires and Fears which form a Love/Belief System, and become
wired into our brains.

We must also conclude that the thalamus and
mid-brain is home to consciousness of humans and all sentient beings,
constitutes the locus of the Command and Control Center of the
brain, and the RAS as the Governor, the de facto Manager of the brain.
The RF is its ‘sentinel.’ The inaptly named Reticular Activating
System should now be considered the brain’s Command and Control System; and,
until some limits to its jurisdiction are delineated, the RAS must be
seen to exercise its influence throughout the entire brain and body.
All other elements of the brain would then represent the subsystems or ‘tools’
of the RAS. Their functions―constantly contributing new sensory input and
feedback to the RAS processes, recovering memories, fleshing out the details of
percepts, generating emotions, physical and vocal reactions, etc.―are only
enacted when innervated by responses from the RAS/RF iterations, or
purposes enacted from thalamic consciousness through the RAS, but
originating in the person’s Will.
Sadly however, even our best intentions,
originating in our consciousness, must take a reverse path through the RAS and
Love/Belief System to reach the actions which will carry them out, often a
tortuous feasibility check, where they are very often displaced.
They just don't get done.
All the response-impulse
reactions of us ‘normal’
people, whether or not they are assented to, are
a perfect RAS reflection of our Social-Animal
Needs, and the Loves.Beliefs and concomitant
people, whether or not they are assented to, are
a perfect RAS reflection of our Social-Animal
Needs, and the Loves.Beliefs and concomitant
Desires and Fears arising
from our Love/Belief
Systems, or what
theologians know as our ‘hearts.’
To live in a different,
better world,
the mystics, saints, and
sages say:
“Nothing need change but our hearts.”
“Nothing need change but our hearts.”
If the doors of perception
were cleansed,
every thing would appear
to man as it is, infinite.
For man has closed himself
up, till he sees
all things thru' narrow
chinks of his cavern.
―WILLIAM BLAKE
And since our DNA has no
significant differences from that of the chimpanzee, and since DNA is known to
determine all the biological and physiological characteristics―all
the capabilities of the organism―and since we are putting
men on the moon and living in homes with all the accouterments of comfort and
safety, while chimpanzees are still living in trees, isn’t it also obvious that
in addition to a larger but biologically identical brain, we must be
uniquely endowed with a non-biological element, an
element whose metaneeds and metafaculties enable us to use, override, and
even reprogram the Reticular Activating System?―an element
which acts as Chief Executive Officer to a RAS Chief Operating Officer as it
were?―the element whose faculties enable us to generate an infinite variety of
responses?
If cognitive scientists are to understand the brain, they must suspend
their search for uniquely human faculties of the cortex, expand their studies
of the Reticular Activating System, including its ‘sentinel,’ the
Reticular Formation; and they must hypothesize an AGENT—call it ‘X’ if you
wilL—of the metafaculties of imagination, conviction, and
commitment.
Although neuron psychologists seem to be
conspicuously absent, many renowned students of human behavior have found it
necessary to postulate an ‘Agent’ of our superior capabilities. St.
Thomas Aquinas postulated the Soul, with faculties of memory, intellect, and
will. Freud’s Agent was “I” (Gernan “ich,” which was translated as ego), with
a plethora of faculties, including perception, conscious thought, memory,
learning, choice, judgment, and action. Jung referred to a ‘self,’ or
‘God within us;’ Karen Horney to our “real self, ...the central inner force,
...which is the deep source of growth, ...the spring of emotional forces, of
constructive energies, of directive and judiciary powers;” Roberto
Assagioli to our 'higher Self;’
Martin Buber to ‘I’ and ‘Thou;’ Arthur
Deikman to the ‘Observing Self;’ Antonio Damasio to a ‘proto self;’ Ernest
Becker (See his Pulitizer Prize winning Denial of Death,) refers to our “proud,
rich, lively, infinitely transcendent, free, inner spirit.” And myriad
mystics, saints, and sages have claimed an ineffable realization of their ‘True
spiritual Selves.’ 


Personally, I’m with Aquinas, Becker, Horney and
the saints: a spiritual “I”, or Soul, in the likeness of God; proud, rich,
lively, infinitely transcendent, free inner spirit. In my book The
Immortal “I” - A Unified Theory of Psychology, Neurology, and the Kingdom of
God, I have inferred a Soul with Needs to Exist, to Love, and to Know;
and Faculties of Imagination, Conviction, and Commitment. (See
theimmortali.com)
The Reticular Formation continuously monitors stimuli from the World, from the
Social Animal Needs, and from the Love/Belief System. Significant stimuli
are forwarded to RAS which retrieves all relevant stimulus/response memories
from the cortex. These responses are evaluated in relation to all Social
Animal Needs, Love/Belief System Elements, and other stimuli from the world.
The most ‘appropriate’ RAS responses are forwarded
with the stimulus to Consciousness, and the responses to the prefrontal cortex,
where, if not too strong or not requiring immediate implementation, or
if inhibited, ambiguous, or conflicted, on to “I” metacognizance and
control,which can select, alter, change, or veto any response―as indicated by
the black arrow. But if unopposed, the RAS-generated response is
enacted. In this way we become habituated to RAS generated
responses. The “I”, the Soul, becomes simply a Deikman 'Observing
Self,’ an idle bystander and atrophies; ‘our brains do become
who we are.’
The diagram also illustrates how “I” can initiate actions or purposes by “I”
Faculties of visualization, belief, and commitment (also indicated by the black
arrow); but commitments which must go back through the RAS for execution, where
they are often ‘displaced.’
These concepts enable us to understand, from a systems standpoint, how the
human brain workscoherently, and explains not only most human behavior
commonly considered ‘normal’―as well as our potential for enlightenment―but
also most psychopathologies including psychoses, neuroses, character disorders,
perceptual defense, denial, miscognition, obsessive-compulsion, cognitive
dissonance, displacement, repression, split personality, passive aggression,
the powers of the self-image, suggestion, hypnosis, positive and negative
thinking, etc., etc
All these effects can now be seen to be the result
of a Reticular Activating System operating flawlessly on our SA-Needs―many often magnified by becoming love objects―and myriad haphazardly adopted conscious and subconscious Loves and Beliefs, and their seething
concomitant Desires and Fears.
For example, all the mood-altering drugs, from crack to marijuana, act
primarily on what are called the mono-aminergic neurons, all of which
are located in a few discrete nuclei in the Reticular Formation.
The drugs must have the effect of
impairing RF functions. Since the RF is the “ruler of consciousness,”
anything can come through, from terrror to bliss or anything in between.
It can also release repressions which the RF/RAS functioning normally keeps
suppressed, and on occasion, some purification of the senses―Blake's “cleansing
of the doors of perception”―and rendering the experience enlightening.

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