Re: Pain-induced coma resulting from alteration of RAS. Real Science or Myth?Preface: I tried to post this msg with
the diagram ref-ed in it "attached".
Seems the post was 'blocked'. kpc
"John H." <j_hasenkam@yahoo,com .au> wrote in message
news:1171285815.783869.116640@s48g2000cws.googlegroups,com ...
> On Feb 8, 3:09 am, "Radium" <gluceg...@excite,com > wrote:
>> On Feb 7, 7:28 am, pboud <pboud_01NOSPA...@hotmail,com > wrote:
>> [...]
> I suspect that people are not responding to your questions because:
>
> No-one knows.
[The gist of what's in my lengthy
post, below: "motivation's" sub-
strate is distributed =throughout=
nervous systems.]
Thank you, John, for, once again,
presenting Opportunity for dis-
cussion.
Someone else has also written,
elsewhere, about folks "not knowing".
I tried to find that post, but didn't come-
across it. I experienced it as also pre-
senting-Opportunity for discussion.
So my Gratitude is to that Poster, too.
There is only a little-bit of 'Difficult'
stuff that 'must' be said, so I'll dis-
pense with that first.
The only 'reason' that "motivation"
has been 'presumed' to be "myst-
erious" derives in the ways that ex-
perimenters in Neuroscience have
been coerced, intergenerationally,
Professor to Student, into the 'pre-
sumption' that they 'must' seek to
explain "motivation" via Neuro-
chemical approaches.
As I've recently reiterated in another
thread stated by John H., be-cause
of the dynamics of "functional multi-
plexing", a Neurochemical 'approach'
is flat-out Impossible. The Neuro-
chemicals are as they are, not with
respect to systematic-functionality,
but with respect to actualizing sys-
tematic-functionality. The difference
is subtle but =Huge= be-cause
Neurochemistry is not locus-exclus-
ive.
So folks've been "barking up the wrong
tree", 'wondering' why they can't see
the 'squirrel' which is just not in 'where'
they've been looking.
[The 'Difficult' stuff, inherent, is that
Students have entered-into the a-
bove stuff, =Innocent=, only to be
coerced into 'having to' accept join-
ing-into "barking up the wrong tree".
It's a sorrow that, itself, reduces dir-
ectly to 'blindly'-automated TD E/I-
minimization, left-uncomprehended,
in which Educational Professionals
have acted as agents of 'the beast',
coercing their Students to accept
whatever it is that has merely been
formerly experienced as 'being-accept-
able'.
I'm =not= 'criticizing' Academicians,
because, after all, all Academicians
were once, themselves, =Innocent=
Students, coerced by their generation
of Professors.
The 'Difficult' stuff is always like this,
the only thing in-it being "construct-
ed" upon the nothingness of mere-
ly self-perpetuating TD E/I-minimiza-
tion.
There's Huge Sorrow in-it, though.
Folks literally being coerced into
abdicating their abilities to Think.
Always takes my breath away.
That's it for the 'Difficult' stuff.]
"Motivation" is distributed through-
out the global system [in AoK, the
"supersystem"; system-of-systems],
as is virtually every other functional
capability of nervous systems.
To see the substrate for "motivation",
one must work within the =entire=
Neuroanatomy, mapping "direction-
ality" in ways that simultaneously
cross-correlate it with behavior.
Everything that's necessary has
been in AoK, and the refs cited in
AoK, all along. I included refs to
super-Excellent experimental re-
sults in an effort to assist folks'
seeing. My favorite one of these
was cited in footnote #24 in the
paper version of AoK, Ap3. I in-
cluded a copy of the super-Ex-
cellent diagram in that version
[and I've decided that it's so Im-
portant that I 'have to' break NG-
posting 'rules' to attach a copy
of this super-Excellent diagram
to this post.]
Footnote #24 is the fifth-from-
the-last "jump-button in the elec-
tronic version of AoK, which, I'm
Sorry, I'm not running on my Inet
PC at this 'time', so I can't provide
the "jump" text.
Footnote #24 introduces, and
compactly sufficiently discusses,
"ramp architecture".
Here is the citation text, for the
ref I'm discussing here, as it
appears in the footnote:
"(For an excellent diagram of
one sort of 'ramp architecture'
that exists within the septal area,
see, 'The Septo-hippocampal
System: Significance of the Sub-
iculum", by R. B. Chronister, R.
W. Sikes, and L. E. White, Jr., in
=The Septal Nuclei=, Wayne State
University, 1974), (p. 123). It was
this diagram, and its associated
article, which precipitated the
development of the larger con-
cept of global 'ramp architecture'
and initiated my analysis of its in-
formation processing usefulness.
This article was alwo one which
drove home my understanding of
the way in which the CNS is =perm-
eated= by a rigorous 'columnar'
organization.)"
Although my discussion in this
post will focus upon "ramp arch-
itecture", I encourage folks who
have it to reread all of AoK, Ap3.
[All of it is necessary for a basic
comprehension of how and why
"motivation's" substrate is dis-
tributed throughout the global
system.
Please see the annotation I
added to the diagram.
Enough said?
Such stuff occurs =everywhere=
within nervous systems. The
task that faces a Neuroscientist
consists in 'walking' the gradients,
which =always= point directly to
TD E/I-minimization.
Understand?
I'll give an 'abstract' example. [It's
so much worthwhile at a chaulk-
board -- tracing the gradients, and
their pointing directly to TD E/I-min-
imization, with colored chaulk :-]
You find yourself at the center of
a 'maze' that, rather than having
well-defined [if deliberately-'con-
founding'] "paths", is comprised
of a densely-packed 'forrest' of
"rubber-branched" 'trees'. In this
'maze' there's no way of using
vision to find your way out of the
'maze' because the "rubber
branches" are so densely-packed
that they block all visual inform-
ation [other than that which en-
ables 'the' nervous system to
avoid injuries to the eyes from
"springing "rubber branches".]
But the 'maze'-designer included
all of the "instructions" that typ-
ically exist in a maze having well-
defined "paths", doing so by
tuning the flexibilities of the "rub-
ber branches" -- so the task that
faces the person at the center of
this densely-packed rubber-tree
'maze' is to use somatosensation
and proprioception to "feel" 'the'
path out of the 'maze'.
In this circumstance, as one in-
teracts with the "rubber trees",
one will "feel" less 'pressure'
in a direction and, because one
does, one will turn-into that dir-
ection, and move in that direction.
Whew! [It's 'hard' to do with just
words :-]
Can you see it?
Within nervous systems, neural
activation always occurs in an-
alogous ways, the "less-pressure"
condition =always= correlating to
'instantaneous' TD E/I(down).
Another reason that nervous sys-
tems are so tightly-integrated is
be-cause such instances of 'in-
stantaneous' TD E/I(down) can
occur in infinite ways -- and the
only way in which such infinities
can be 'appropriately' resolved
is by global-internal-cross-cor-
relation in which =overall= TD
E/I-minimization is the 'determin-
ing' thing, not the myriad small-
scale 'instantaneous' TD E/I(ups
& downs) that occur in-parallel.
In order to instantiate such over-
all TD E/I-minimization, it's nec-
essary that everything, all the way
'down' to infinitely-small scale,
be organized in ways that do, in
fact, constructively contribute to
convergence upon overall TD E/I-
minimization.
This sounds 'tautalogical', but,
returning to finding our ways out
of the "rubber-tree" 'maze', allows
us to see all that makes converg-
ence upon overall TD E/I-minimiz-
ation [with respect to the Infinities
that're =always= involved!] so
'easily' achievable.
So "move your arm" against the
rubber-tree branches to one 'side',
while doing the same on the other
'side', while turning-in-place.
"ZZZzzzzzzwww iiippp"
Out of all the somatosensory and
proprioceptive data that's flowing
into your nervous system as you
so "orient", up to the amygdalar
activation threshold [AoK, Ap5]
'one' resultant 'instantaneous' TD
E/I(up) is grater than all the others,
and, because of "ramp architecture"
like that which is depicted in the
attached diagram, that 'one' 'in-
stantaneous' TD E/I(up), via the
'normal' neural dynamics of individual
neurons, literally survives-within-the-
ramps better than relatively-smaller
instances of TD E/I that are 'simult-
neously' occurring.
Such neural-conduction-"survival"
occurs simply be-cause of sub-
amygdalar-activation-threshold
"power" [energy-flow], which, as
I've recently reiterated in another
thread, activates "inverting reward",
and, just like the grazing antelope,
you "orient" so as to maximize in-
verting reward -- which is 'just'
built-into the neural ramifictions of
=all= "ramp architecture". [Folks've
looked for it in terms of "specific
neurotransmitters", etc., but it can-
not be observed in terms of "spec-
ific neurotransmitters", etc., be-cause
the Neurochemistry is =always=
"functionally-multiplexed", in one
instance using one neurochemical,
and in another, a 'different' neuro-
chemical, and so forth, with all of
the various neurochemicals in-
stantiating the "ramp architecture",
not 'neurochemical subsystems'.]
So "inverting reward" is mediated
by this neurochemical "here", and
that neurochemical "there", but it's
=all= "inverting reward".
So, be-cause of the actuality of func-
tional multiplexing, one has recourse
to 'only' the Neuroanatomy, in which
everything is mapped from sensory
receptor-internally and internally-to
effectors.
Don't see the 'chemical soup'.
See the mapping that's right-there
to see in the Neuroanatomy.
Like in the diagram that I've attached
to this post.
=EVERYTHING= that's discussed in
AoK is =NECESSARY= for the min-
imal description of all that's involved
in "motivation".
So, as 'you' orient within the "rubber-
tree" 'maze', 'you' are able to 'read'
the 'maze'-designer's intent by liter-
ally =feeling= relative TD E/I, and
'moving' in the environmentally-
correlated direction, internal dir-
ections directly reflecting external
directions, but in an on-the-inside-
looking-out way which, at its most-
fundamental 'level', is functionally-
instantiated by the phenomenon of
decussation. It is decussation [our
"crosses"-within] that enables this
internal-external-directionality cross-
correlation -- and everything else that
happens 'within' nervous systems.
When one just looks at it [as is typ-
ically the case in graduate 'neuro-
anatomy' courses], decussation's
"map" seems 'nonsensically-hard'
to 'follow' -- talk about your "highway
interchange" :-]
But when one knows that everything
within nervous systems is ordered
to enable the doing of only one thing --
TD E/I-minimization -- decussation's
'difficulty' just 'goes away', and one
sees, in-it, the most-awesomely-
simple-possible-stuff.
That's why it's necessary to know
about TD E/I-minimization before
one can see the Neuroanatomy
[which is why "the Terrible Times"
were "Terrible" -- all those twists
and turns, 'disconnected' be-
cause understanding TD E/I-min-
imization is a necessary 'prerequ-
isite of seeing the Neuroanatomy
of-a-piece -- it was litterally a =Ter-
rible= struggle in which I had to
study everything, at first, not knowing
what I was even looking for. But
these things like the "ramp archi-
tecture" that's depicted in the dia-
gram, and a g'zillion other such
things =all= exhibit geometrical
'biases'. And I could see, in that
always-there-ness that there was
a general ordering-principle cor-
related to that always-right-there,
plain-as-day, geometrical 'bias'.
So I hopped around a lot, between
various disciplines [Physics, Psych-
ology, Sociology, Maths, Computer
Science, etc. and, of course, the
Neuroscience experimental results --
studying =everything= -- and slowly,
bit-by-bit, knitting it together in an
"abstract conceptual" perspective in
which there was only one 'rule' --
"there are no 'rules' [which is what
rendered me 'incompatable' with
grad school because, in grad school,
the progression of coerced 'rules' is
'sacrosanct' -- and, while so working,
I realized that the geometrical 'biases'
all conformed to stuff like inclined
planes [including some "pretty-fancy"
ones that loop-back-upon themselves,
forming the substrate for "inversion",
etc.], upon which stuff "slides" under
the force of 'gravity'.
So I knew that I was looking for
a generalized energy-flow dyn-
amic, and, after nine 'years' of
hammerin' on the problem, I
Verified that the generalized
energy-flow is TD E/I-minimiz-
ation.
Nervous system function literally
slides within the "ramp architect-
ure, always 'moving toward' TD
E/I-minimization. Within nervous
systems, energy always flows
[overall] in =that= direction.
Work on 'walking' through the
"rubber-tree" 'maze' until 'you'
can see TD E/I-minimization
happening within [at first] only
the mappings of the phenomen-
on of decussation.
Yeah, external-environmental
directions and directedness
are infinitely-variable, but, in-
ternally, there's 'just' energy-flow-
ing the =one= direction -- which
is what enables nervous systems
to ='climb'= the one-way flow of en-
ergy, from order to disorder, that
is what's =described= by 2nd
Thermo [WDB2T], thereby 'mov-
ing toward' increased 'order'.
So stay 'in' the "rubber-tree"
'maze' until 'you' get-it -- feel
'your' way through the 'pres-
sure'-density variations that
the maze's designer built-
into it [don't 'read' any 'hid-
den messages' -- I'm just
discussing the "rubber-tree"
'maze', wanting to help 'you'
understand TD E/I-minimiz-
ation.]
Don't 'fret' when your nervous
system becomes "quieted"
when you realize that after
following a 'promising' low-
"rubber-branch" 'path'. That's
'just' 'your' nervous system
Loving 'you' [AoK, Ap8.]
Learn from such and "look
elsewhere" for longer "low-
pressure" paths.
In this way, it's Certain that
'you' will find your way out of
the 'maze'.
[For folks who have been
reading over the 'years',
all I did in this post was to
reiterate my former "Truth's
One Map", discussions, try-
ing to give folks something
'tactile' to 'experience'.]
Neuroanatomy Texts, and
their contents', same-old,
same-old :-]
You know -- 'feel the wind'
with your own good 'weather
vanes', and 'move' accordingly.
k. p. collins [ken]