Neurologists
like to assume that all your memories are stored in your brain. But
there are actually quite a few reasons for doubting this unproven
assumption, including the research of scientists such as Karl Lashley
and John Lorber. Their research showed that minds can be astonishing
functional even when large parts of the brain are destroyed, either
through disease or deliberate surgical removal. Lorber documented
600 cases of people with heavy brain damage (mostly due to
hydraencephaly), and found that half of them had above average
intelligence. Some children with brain problems sometimes undergo an
operation called a hemispherectomy, in which half of their brain is
removed. An article in Scientific American tells
us, “Unbelievably, the surgery has no apparent effect on
personality or memory.”
Given
such very astonishing anomalies, we should give serious consideration
to all arguments against the claim that your brain is storing all
your memories. I will now discuss such an argument. The
argument can be summarized as follows: there is no plausible
mechanism by which the human brain could store very long-term
memories such as 50-year-old memories. Every neurological memory
theory that we have cannot explain any memories that have persisted
for more than a year.
The
Fact That Humans Can Remember Things for 50 Years
First,
let's look at the basic fact of extreme long-term memory storage. It
is a fact that humans can recall memories from 50 years ago. Some
people have tried to suggest that perhaps human memory doesn't work
for such a long time, and that remembering very old memories can be
explained by the idea of what is called “rehearsal.” The idea is
that perhaps a 60-year-old remembering is really just remembering
previous recollections that he had at an earlier age. So perhaps,
this idea goes, when you are 60 you are just remembering what you
remembered from your childhood at 50, and that at 50 you were just
remembered what you remembered from your childhood at age 40, and so
forth.
But
such an idea has been disproved by experiments. A scientific study
by Harry Bahrick was entitled “Semantic memory content in
permastore: Fifty years of memory for Spanish learned in school.” It
showed that “large portions of the originally acquired information
remain accessible for over 50 years in spite of the fact the
information is not used or rehearsed.” The same researcher tested a
large number of subjects to find out how well they could recall the
faces of high school classmates, and found very substantial recall
even with a group that had graduated 47 years ago. Bahrick reported
the following:
Subjects
are able to identify about 90% of the names and faces of the names of
their classes at graduation. The visual information is retained
virtually unimpaired for at least 35 years...Free-recall probability
does not diminish over 50 yr for names of classmates assigned to one
or more of the Relationship Categories A through F.
I
know for a fact that memories can persist for 50 years, without
rehearsal. Recently I was trying to recall all kinds of details from
my childhood, and recalled the names of persons I hadn't thought
about for decades, as well as a Christmas incident I hadn't thought
of for 50 years (I confirmed my recollection by asking my older
brother about it). Digging through my memories, I was able to recall
the colors (gold and purple) of a gym uniform I wore, something I
haven't thought about (nor seen in a photograph) for some 47 years.
Upon looking through a list of old children shows from the 1960's, I
saw the title “Lippy the Lion and Hardy Har Har,” which ran from
1962 to 1963 (and was not syndicated in repeats, to the best of my
knowledge). I then immediately sung part of the melody of the very
catchy theme song, which I hadn't heard in 53 years. I then looked up
a clip on a youtube.com, and verified that my recall was exactly
correct. I also recently recalled "The Patty Duke Show" from the 1960's, a show I haven't seen in 50 years, and recalled that in the opening title sequence we saw Patty walking down some stairs. I looked up the title sequence on www.youtube.com, and verified that my 50-year-old memory was correct. This proves that a 53-year-old memory can be instantly
recalled.
So
in trying to explain human memory, we need to have a theory that can
explain human memories that persist for 50 years. Very confusingly,
scientists use the term “long-term memory” for any memory lasting
longer than an hour, which is very unfortunate because almost every
thing you will find on the internet (seaching for “long term
memory”) does not actually explain very long-term memory such as
memories lasting for 50 years.
Why
LTP and Synapse Plasticity Cannot Explain Very Long-Term Memory
Now
let's look at neuroscientists' theories of memories. Quora.com is a
“expert answer” website which claims to give “the best answer
to any question.” One
of its web pages asks the question, “How are memories stored
and retrieved in the human brain?” The top answer (the one with
most upvotes) is by Paul King, a computational neuroscientist. King
very dogmatically gives us the following answer:
At
the most basic level, memories are stored as microscopic chemical
changes at the connection points between neurons in the brain..As
information flows through the neural circuits and networks of the
brain, the activity of the neurons causes the connection points to
become stronger or weaker in response. The strengthening and
weakening of the synapses (synaptic plasticity) is how the brain
stores information. This mechanism behind this is called "long-term
potentiation" or "LTP."
But there is
actually no proof that any information is being stored when synapses
are strengthened. From the mere fact that synapses may be
strengthened when learning occurs, we are not entitled to deduce that
information is being stored in synapses, for we also see blood
vessels in the leg strengthen after repeated exercise, and that does
not involve information storage. In order to actually prove that a
synapse is storing information, you would need to do an experiment
such as having one scientist store a symbol in an animal's brain (by
training), and then have another scientist (unaware of what symbol
had been stored) read that symbol from some synapses in the animal's
brain, correctly identifying the symbol. No such experiment has ever
been done.
The idea that a
memory forms after repeating strengthening of synapses is
inconsistent with the fact people very commonly remember things they
experienced only one time. Almost every time someone tells you about
a TV show they saw last night, or a conversation they recently had
with a friend, they are remembering something they only were saw or
heard one time, not through repeated experiences.
The
evidence does not even clearly indicate that LTP correlates with
memory, as one scientist's summary
of experimental results indicates (a summary utterly inconsistent
with the claim LTP is a general mechanism to explain memory).
What
this means is that LTP and memory have been dissociated from each
other in almost every conceivable fashion. LTP can be decreased and
memory enhanced. Hippocampus-dependent memory deficits can occur with
no discernable effect on LTP...There
will be no direct quantitative or even qualitative relationship
between LTP measured experimentally and memory measured
experimentally—that is already abundantly clear from the available
literature...The most damning observations probably are those
examples where LTP is completely lost and there is no effect on
hippocampus-dependent memory formation.
A
scientific paper
states this about LTP:
Based
on the data reviewed here, it does not appear that the
induction of LTP is a necessary or sufficient condition for the
storage of new memories.
Why
is it so difficult to see learning-associated synaptic changes?And
does their absence in numerous experiments favor the null hypothesis?
What
is misleadingly called “long-term potentiation” or LTP is a
not-very-long-lasting effect by which certain types of high-frequency
stimulation (such as stimulation by electrodes) produces an increase
in synaptic strength. Synapses are gaps between nerve cells, gaps
which neurotransmitters can jump over. The evidence that LTP even
occurs when people remember things is not very strong, and in 1999 a
scientist stated
(after decades of research on LTP) the following:
[Scientists] have
never been able to see it and actually correlate it with learning and
memory. In other words, they've never been able to train an animal,
look inside the brain, and see evidence that LTP occurred.
Since
then a few studies have claimed to find evidence that LTP occurred
during learning. But there is actually an insuperable problem in the
idea that long-term potentiation could explain very long-term
memories. The problem is that so-called long-term potentiation is
actually a very short-term
phenomenon. Speaking of long-term potentiation (LTP), and using the
term “decays to baseline levels” (which means “disappears”),
a scientific paper
says the following:
Potentiation
almost always decays to baseline levels within a week. These results
suggest that while LTP is long-lasting, it does not correspond to the
time course of a typical long-term memory. It is recognized that many
memories do not last a life-time, but taking this point into
consideration, we would then have to propose that LTP is only
involved in the storage of short-term to intermediate memories.
Again, we would be at a loss for a brain mechanism for the storage of
a long-term memory.
A
more recent scientific paper
(published in 2013) says something similar, although it tells us even
more strongly that so-called long-term potentiation (LTP) is really a
very
short-term
affair. For it tells us that “in general LTP decays back to
baseline within a few hours.” “Decays back to baseline” means
the same as “vanishes.”
Another
2013 paper
agrees that so-called long-term potentiation is really very
short-lived:
LTP
always decays and usually does so rapidly. Its rate of
decay is measured in hours or days (for review, see Abraham 2003).
Even with extended “training,” a decay to baseline levels is
observed within days to a week.
Scientists distinguish between two types of LTP: an E-LTP that can be produced by a single electrical stimulus, but only lasts one to three hours, and an L-LTP that requires multiple electrical stimulations, and can last about 8 hours or a little longer. But this fails to correspond to what we know about human memory, which is that humans can form a memory lasting decades after a single sensory experience.
Scientists distinguish between two types of LTP: an E-LTP that can be produced by a single electrical stimulus, but only lasts one to three hours, and an L-LTP that requires multiple electrical stimulations, and can last about 8 hours or a little longer. But this fails to correspond to what we know about human memory, which is that humans can form a memory lasting decades after a single sensory experience.
So evidently
long-term potentiation cannot be any foundation or mechanism for
long-term memories. This is the conclusion reached by the previous
paper when it makes this conclusion about long-term potentiation
(LTP):
In
summary, if synaptic LTP is the mechanism of associative learning—and
more generally, of memory—then it is disappointing that its
properties explain neither the basic properties of associative
learning nor the essential property of a memory mechanism. This dual
failure contrasts instructively with the success of the hypothesis
that DNA is the physical realization
of the gene.
The book "Neuronal Mechanisms of Memory Formation" hints on page 451 that LTP may be a poor candidate for such a thing. It says this:
The book "Neuronal Mechanisms of Memory Formation" hints on page 451 that LTP may be a poor candidate for such a thing. It says this:
Definitive
empirical support for synaptic plasticity modeled by LTP being a
mechanism of memory processing is still lacking. For each piece of
evidence that lends some support to the theory, there is likely to be
equally strong evidence to suggest the contrary. The field of
research reached a veritable stalemate some years ago when so-called
cornerstones of research that supported the hypothesis were unable to
be replicated...and the outcome was an increasing skepticism about
whether LTP can be considered a neural substrate for learning and
memory.
Referring to this scientific paper, another paper suggests that "LTP as a memory mechanism" may be more of a dogma than something well established by observations:
Shors and Matzel,,.concluded that LTP did not meet the criteria for providing a causal mechanism of memory. To make a long argument very short, they documented instances where changes in memory occur without LTP and where LTP occurs without changes in memory.....They report that between 1974 and 1997, more than 1300 articles occurred with “LTP” in the title. Of these, fewer than 80 described any behavioral manipulation relevant to assessing changes in memory. Furthermore, the articles that contained behavioral manipulations tended to provide evidence against the hypothesis that LTP is a memory mechanism. Thus, the claim that LTP is a molecular mechanism for learning and memory may be more of a dogma of neuroscientific memory research than a hypothesis that is being rigorously tested.
A 2014 book stated, "Although LTP is considered to be the primary model for how learning and memory storage occur at the synapse level, the evidence supporting this claim is still inconclusive and speculative." A 1995 scientific paper found. "There is a striking negative correlation of spatial learning ability with LTP." This is the exact opposite of what we should expect if LTP was some type of memory mechanism.
Referring to this scientific paper, another paper suggests that "LTP as a memory mechanism" may be more of a dogma than something well established by observations:
Shors and Matzel,,.concluded that LTP did not meet the criteria for providing a causal mechanism of memory. To make a long argument very short, they documented instances where changes in memory occur without LTP and where LTP occurs without changes in memory.....They report that between 1974 and 1997, more than 1300 articles occurred with “LTP” in the title. Of these, fewer than 80 described any behavioral manipulation relevant to assessing changes in memory. Furthermore, the articles that contained behavioral manipulations tended to provide evidence against the hypothesis that LTP is a memory mechanism. Thus, the claim that LTP is a molecular mechanism for learning and memory may be more of a dogma of neuroscientific memory research than a hypothesis that is being rigorously tested.
A 2014 book stated, "Although LTP is considered to be the primary model for how learning and memory storage occur at the synapse level, the evidence supporting this claim is still inconclusive and speculative." A 1995 scientific paper found. "There is a striking negative correlation of spatial learning ability with LTP." This is the exact opposite of what we should expect if LTP was some type of memory mechanism.
But what about
syntaptic plasticity, previously mentioned in my quote from the
neurologist King ? Since he claimed that LTP is the mechanism behind
synaptic plasticity, and LTP cannot explain any memory lasting longer
than a year, then synaptic plasticity will not work to explain very
long-term memories.
To study LTP, scientists typically perform something artificial called tetanic stimulation, using a frequency of 100 hertz. A normal brain does not transmit signals at a frequency so high. Of the common brain waves (alpha, beta, and gamma), only gamma waves have a frequency of greater than 30 hertz, and such gamma waves generally do not have a frequency higher than 50 hertz. LTP can be induced using a lower frequency, but only by prolonged stimulation such as stimulation lasting minutes. That type of sluggish low-frequency stimulation cannot explain human memories that can form instantly.
Why
Synapses Cannot Explain Very Long-Term Memory
Long-term
memory cannot be stored in synapses, because synapses don't last long
enough. Below is a quote from a scientific paper:
A
quantitative value has been attached to the synaptic turnover rate by
Stettler et al (2006), who examined the appearance and disappearance
of axonal boutons in the intact visual cortex in monkeys.. and found
the turnover rate to be 7% per week which would give the average
synapse a lifetime of a little over 3 months.
You can read Stettler's paper here.
You
can google for “synaptic turnover rate” for more information. We
cannot believe that synapses can store-long memories for 50 years if
synapses only have an average lifetime of about 3 months. The paper here says the half-life of synapses is "from days to months."
Synapses often protrude out of bump-like structures on dendrites called dendritic spines. But those spines have lifetimes of less than 2 years. Dendritic spines last no more than about a month in the hippocampus, and less than two years in the cortex. This study found that dendritic spines in the hippocampus last for only about 30 days. This study found that dendritic spines in the hippocampus have a turnover of about 40% each 4 days. This 2002 study found that a subgroup of dendritic spines in the cortex of mice brains (the more long-lasting subgroup) have a half-life of only 120 days. A paper on dendritic spines in the neocortex says, "Spines that appear and persist are rare." While a 2009 paper tried to insinuate a link between dendritic spines and memory, its data showed how unstable dendritic spines are. Speaking of dendritic spines in the cortex, the paper found that "most daily formed spines have an average lifetime of ~1.5 days and a small fraction have an average lifetime of ~1–2 months," and told us that the fraction of dendritic spines lasting for more than a year was less than 1 percent. A 2018 paper has a graph showing a 5-day "survival fraction" of only about 30% for dendritic spines in the cortex. A 2014 paper found that only 3% of new spines in the cortex persist for more than 22 days. Speaking of dendritic spines, a 2007 paper says, "Most spines that appear in adult animals are transient, and the addition of stable spines and synapses is rare." A 2016 paper found a dendritic spine turnover rate in the neocortex of 4% every 2 days. A 2018 paper found only about 30% of new and existing dendritic spines in the cortex remaining after 16 days (Figure 4 in the paper).
Furthermore, it is known that the proteins existing between the two knobs of the synapse (the very proteins involved in synapse strengthening) are very short-lived, having average lifetimes of no more than a few days. A graduate student studying memory states it like this:
Synapses often protrude out of bump-like structures on dendrites called dendritic spines. But those spines have lifetimes of less than 2 years. Dendritic spines last no more than about a month in the hippocampus, and less than two years in the cortex. This study found that dendritic spines in the hippocampus last for only about 30 days. This study found that dendritic spines in the hippocampus have a turnover of about 40% each 4 days. This 2002 study found that a subgroup of dendritic spines in the cortex of mice brains (the more long-lasting subgroup) have a half-life of only 120 days. A paper on dendritic spines in the neocortex says, "Spines that appear and persist are rare." While a 2009 paper tried to insinuate a link between dendritic spines and memory, its data showed how unstable dendritic spines are. Speaking of dendritic spines in the cortex, the paper found that "most daily formed spines have an average lifetime of ~1.5 days and a small fraction have an average lifetime of ~1–2 months," and told us that the fraction of dendritic spines lasting for more than a year was less than 1 percent. A 2018 paper has a graph showing a 5-day "survival fraction" of only about 30% for dendritic spines in the cortex. A 2014 paper found that only 3% of new spines in the cortex persist for more than 22 days. Speaking of dendritic spines, a 2007 paper says, "Most spines that appear in adult animals are transient, and the addition of stable spines and synapses is rare." A 2016 paper found a dendritic spine turnover rate in the neocortex of 4% every 2 days. A 2018 paper found only about 30% of new and existing dendritic spines in the cortex remaining after 16 days (Figure 4 in the paper).
Furthermore, it is known that the proteins existing between the two knobs of the synapse (the very proteins involved in synapse strengthening) are very short-lived, having average lifetimes of no more than a few days. A graduate student studying memory states it like this:
It’s
long been thought that memories are maintained by the strengthening
of synapses, but we know that the proteins involved in that
strengthening are very unstable. They turn over on the scale of hours
to, at most, a few days.
A
scientific paper
states the same thing:
Experience-dependent
behavioral memories can last a lifetime, whereas even a long-lived
protein or mRNA molecule has a half-life of around 24 hrs. Thus, the
constituent molecules that subserve the maintenance of a memory will
have completely turned over, i.e. have been broken down and
resynthesized, over the course of about 1 week.
The paper cited
above also states this (page 6):
The
mutually opposing effects of LTP and LTD further add to the eventual
disappearance of the memory maintained in the form of synaptic
strengths. Successive events of LTP and LTD, occurring in diverse and
unrelated contexts, counteract and overwrite each other and will, as
time goes by, tend to obliterate old patterns of synaptic weights,
covering them with layers of new ones. Once again, we are led to the
conclusion that the pattern of synaptic strengths cannot be relied
upon to preserve, for instance, childhood memories.
The latest and
greatest research on the lifetime of synapse proteins is the June
2018 paper “Local and global influences on protein turnover in
neurons and glia.” The paper starts out by noting that one earlier
2010 study found that the average half-life of brain proteins was
about 9 days, and that a 2013 study found that the average half-life
of brain proteins was about 5 days. The study then notes in Figure 3
that the average half-life of a synapse protein is only about 5 days,
and that all of the main types of brain proteins (such as nucleus,
mitochondrion, etc.) have half-lives of 15 days or less. The 2018 study here precisely measured the lifetimes of more than 3000 brain proteins from all over the brain, and found not a single one with a lifetime of more than 75 days (figure 2 shows the average protein lifetime was only 11 days).
The paper here states, "Experiments indicate in absence of activity average life times ranging from minutes for immature synapses to two months for mature ones with large weights."
When
you think about synapses, visualize the edge of a seashore. Just as
writing in the sand is a completely unstable way to store
information, long-term information cannot be held in synapses. The
proteins in between the synapses are turning over very rapidly
(lasting no longer than about a week), and the entire synapse is
replaced every few months.
In
November 2014 UCLA professor David Glanzman and his colleagues
published a scientific paper
publishing research results. The authors said, “These results
challenge the idea that stable synapses store long-term memories."
Scientific American published an article
on this research, an article entitled, “Memories May Not Live in
Neuron's Synapses.” Glanzman
stated,
“Long-term memory is not stored at the synapse,” thereby
contradicting decades of statements by neuroscientists who have
dogmatically made unwarranted claims that long-term memory is stored
in synapses.
Why
Very Long-Term Memories Cannot Be Stored in the Cell Nucleus
His
research has led Glanzman to a radical new idea: that memories are
not stored in synapses, but in the nerve cell nucleus. In fact, in
this
TED talk Glanzman dogmatically declares this doctrine. At 15:34 in
the talk, Glanzman says, “memories are stored in the cell nucleus –
it is stored as changes in chromatin.” This is not at all what
neurologists have been telling us for the past 20 years, and few
other neuroscientists have supported such an idea.
We should be extremely suspicious and skeptical whenever scientists suddenly start giving some new answer to a fundamental answer, an answer completely different from the answer they have been dogmatically declaring for years. For example, if scientists were to suddenly start telling us that galaxies are not hold together by gravity (as they've been telling us for decades), but by, say, “dark energy pulsations,” we should be extremely skeptical that the new explanation is correct. In this case, there are very good reasons why Glanzman's recently-hatched answer to where long-term memories are stored cannot be right.
Chromatin
is a term meaning DNA and surrounding histone protein molecules.
Histone molecules are not suitable for storing very long-term
memories because they are too short-lived. A scientific paper
tells us that the half-life of histones in the brain is only about
223 days, meaning that every 223 days half of the histone molecules
will be replaced.
So histone molecules
are not a stable platform for storing very long-term memories. But
what about DNA? The DNA molecule is stable. But there are several
reasons why your DNA molecules cannot be storing your memories. The
first reason is that your DNA molecules are already used for another
purpose – the storing of genetic information used in making
proteins. DNA molecules are like a book that already has its pages
printed, not a book with empty pages that you can fill. The second
reason is that DNA molecules use a bare bones “amino acid”
language quite unsuitable for writing all the different types of
human memories. The idea that somewhere your DNA has memory of your
childhood summer vacations (expressed in an amino-acid language) is
laughable.
The third reason is
that the DNA of humans has been exhaustively analyzed by various
multi-year projects such as the Human Genome Project and the ENCODE
project, as well as various companies that specialize in personal
analysis of the DNA of individual humans. Despite all of this huge
investigation and analysis, no one has found any trace whatsoever of
any type of real human memory (long-term or short-term) being stored
in DNA. If you do a Google search for “can DNA store memories,”
you will see various articles (most of them loosely-worded,
speculative and exaggerating) that discuss various genetic effects
(such as gene expression) that are not the same as an actual storage
of a human memory. Such articles are typically written by people
using the word “memories” in a very loose sense, not actually
referring to memories in the precise sense of a recollection.
The fourth reason is
that there is no known bodily mechanism by which lots of new
information can be written to the storage area inside a DNA molecule. The fifth reason is that the DNA we see in brain neurons is basically identical to the DNA we see in other parts of the body (such as the DNA from foot cells). If memories were stored in DNA, the DNA in brain neurons would be much different from that of the DNA in other body parts.
To completely defeat
the idea that your memories may be stored in your DNA, I will merely
remind the reader that DNA molecules are not read by brains – they
are read by cells. It takes about 1 minute for a cell to read only
the small part of the DNA needed to make a single protein (and DNA
has recipes for thousands of proteins). If your memories were stored
in DNA, it would take you hours to remember things that you can
actually recall instantly. Thinking that DNA can store memories is
like thinking that your refrigerator can cook a steak.
But
couldn't very-long term memories just be stored in some unknown part
of a neuron? No, because the proteins that make up neurons have short
lifetimes. A scientist explains
the timescales:
Protein
half-lives in the cell range from about 2 minutes to about 20 hours,
and half-lives of proteins typically are in the 2- to 4-hour time
range. Okay, you say, that's fine for proteins,
but what about "stable" things like the plasma membrane and
the cytoskeleton? Neuronal membrane phospholipids turn over with
half-lives in the minutes-to-hours range as well. The vast majority
of actin microfilaments in dendritic spines of hippocampal pyramidal
neurons turn over with astonishing rapidity—the average turnover
time for an actin microfilament in a dendritic spine is 44
seconds...As a first approximation, the entirety of the functional
components of your whole CNS [central nervous system] have been
broken down and resynthesized over a 2-month time span. This should
scare you. Your apparent stability as an individual is a perceptual
illusion.
It is occasionally speculated that long-term memories might be stored in microtubules in a cell. But such things do not last long enough to be a storage place for memories lasting decades. A scientific paper tells us how short-lived brain microtubules are:
Neurons possess more stable microtubules compared to other cell types (Okabe and Hirokawa, 1988; Seitz-Tutter et al., 1988; Stepanova et al., 2003). These stable microtubules have half-lives of several hours and co-exist with dynamic microtubules with half-lives of several minutes.
Why Long-Term Memories Cannot Be Stored in the DNA Methylome
Prior studies found no effects of zeb, a DNA methylation inhibitor (Zhou et al., 2002), on learning in A. mellifera (Lockett et al., 2010; Biergans et al., 2012). More recently, Biergans et al. (2016), conducted a meta-analysis of multiple honey bee studies with methylation inhibitors (zeb and RG108), but found no strong overall effect of inhibiting DNA methylation on honey bee learning.
It is occasionally speculated that long-term memories might be stored in microtubules in a cell. But such things do not last long enough to be a storage place for memories lasting decades. A scientific paper tells us how short-lived brain microtubules are:
Neurons possess more stable microtubules compared to other cell types (Okabe and Hirokawa, 1988; Seitz-Tutter et al., 1988; Stepanova et al., 2003). These stable microtubules have half-lives of several hours and co-exist with dynamic microtubules with half-lives of several minutes.
Why Long-Term Memories Cannot Be Stored in the DNA Methylome
DNA methylation occurs
when a very simple molecule becomes attached to part of a DNA
molecule. Such a simple methyl molecule can act like a kind of flag
that switches part of a gene on or off. The set of all of these
methyl molecules attached to DNA is known as the DNA methylome. It has been suggested by a few that maybe memories are stored in this DNA methylome.
The DNA methylome seems
like a fairly stable thing, and so you don't have the “low
stability” problem of very rapid protein molecule turnover that you
have with the theory that memories are stored in synapses. But there
are several reasons why it is not credible to maintain that human
memories are being stored in such a DNA methylome.
The first reason is that
we already know the function of this DNA methylome, that it is
something other than storing memories. The methyl molecules that make
up the methylome serve the purpose of genetic expression, a very
different task than storing memories. If you were to maintain that
the DNA methylome serves both
of these purposes, it would be kind of like the Saturday Night Live
comedic sketch
that described a product like “Miracle Whip.” It went like this:
Wife: New Shimmer
is a floor wax!
Husband: No, New Shimmer is a dessert topping!
Wife: It's a floor wax!
Husband: It's a dessert topping!
Wife: It's a floor wax, I'm telling you!
Husband: It's a dessert topping, you cow!
Spokesman: [ enters quickly ] Hey, hey, hey, calm down, you two. New Shimmer is both a floor wax and a dessert topping!
Husband: No, New Shimmer is a dessert topping!
Wife: It's a floor wax!
Husband: It's a dessert topping!
Wife: It's a floor wax, I'm telling you!
Husband: It's a dessert topping, you cow!
Spokesman: [ enters quickly ] Hey, hey, hey, calm down, you two. New Shimmer is both a floor wax and a dessert topping!
The
second reason for doubting that memories are stored in the DNA
methylome is that the DNA methylome couldn't be read with the speed
needed for memory recall that is very fast. The DNA methylome
consists of methyl molecules scattered across a DNA molecule. All
evidence suggests that reading DNA is relatively slow. DNA
transcription occurs at a rate of about 40 to 80 nucleotides per
second, and there are billions of such nucleotides. But think of how
fast people can recall memories. On the TV show Jeopardy we
see people recalling very obscure memories in only a few seconds.
When someone talks rapidly, he is retrieving language memories (such
as the memory of what a particular word means) in a fraction of a
second. That couldn't happen so fast if some relatively slow process
of reading DNA was being used.
The
third reason for doubting that memories are stored in the DNA
methylome is that the methylome does not grow in size as learning
occurs. As discussed here,
the DNA methylome is larger (percentage-wise) in a newborn baby than
in either a young adult or an old man.
The
fourth reason for doubting that memories are stored in the DNA
methylome
is that methylation suppression experiments do not affect memory very
dramatically. Scientists have ways of suppressing DNA methylation,
and they have tested the effects of such suppression on learning and
memory. A scientific paper
says that “inhibiting
DNA methylation alters olfactory extinction but not acquisition
learning.” Another scientific paper
says that when DNA methylation was inhibited, “long-term
memory strength itself was not affected.”
A scientific paper states the following:
These are not the type of
very dramatic effects on learning and memory that one would expect
from DNA methylation inhibition if memories were being stored in the
methylome. Other studies claiming a stronger effect of DNA methylation inhibition are typically unreliable studies using fewer than 15 animals per study group, and in such low-statistical-power studies there is a high chance of a false alarm or false positive.
There are actually two drugs for humans that work mainly by inhibiting DNA methlyation: azacitidine and decitabine. If DNA methlyation was a mechanism for memory storage, we would expect that the side effect lists for these drugs would make some mention of a possible effect on learning or memory. But these drugs do not produce such a side effect. It has been claimed by the few proponents of memory stored in the DNA methylation marks that such marks are a stable medium for writing information. But search for "DNA methylation turnover" and you will find contrary claims, such as a paper entitled "Rapid turnover of DNA methylation in human cells."
When It Comes to Explaining Very Long-Term Memory, Our Neuroscientists Are in Disarray
There are actually two drugs for humans that work mainly by inhibiting DNA methlyation: azacitidine and decitabine. If DNA methlyation was a mechanism for memory storage, we would expect that the side effect lists for these drugs would make some mention of a possible effect on learning or memory. But these drugs do not produce such a side effect. It has been claimed by the few proponents of memory stored in the DNA methylation marks that such marks are a stable medium for writing information. But search for "DNA methylation turnover" and you will find contrary claims, such as a paper entitled "Rapid turnover of DNA methylation in human cells."
When It Comes to Explaining Very Long-Term Memory, Our Neuroscientists Are in Disarray
So
how can we summarize the current state of scientific thought on how
long-term memory is stored? The word that comes to mind is: disarray.
In this matter our scientists are flailing about, wobbling this way
and that way; but they aren't getting anywhere in terms of presenting
a plausible answer as to how very long-term memory can be stored in
the brain. Our scientists have done nothing to plausibly solve the
permanence problem – the problem that very long-term memories
cannot be explained by evoking transient “shifting sands”
mechanisms such as LTP which last much less than a year (or in
neurons, which are rebuilt every two months due to protein turnover).
On this matter our scientists have merely presented explanatory
facades – theories that do not hold up to scrutiny, like some movie
studio building facade that you can see is a fake when you walk
around and look behind it, finding no rooms behind the front.
Another sign of this disarray is a 2013 scientific paper with the title, “"Very long-term memories may be stored in the pattern of holes in the perineuronal net." After basically explaining in its first paragraph why current theories of long-term memories do not work and are not plausible, the author goes on to suggest a wildly imaginative and absurdly ornate speculation that perhaps the brain is a kind of a giant 3D punchcard, storing information like data used to be stored on the old 2D punchcards used by IBM electronic machinery in the 1970's. The author provides no good evidence for this wacky speculation, mainly discussing imaginary experiments that would lend support to it. The very appearance of such a paper is another sign that currently scientists have no good explanation for very long-term memory. I may note that IBM punchcards only worked because they were read by IBM punchcard-reader machines. In order for the brain to work as giant 3D punchcard, we would have to imagine a brain-reader machine that is nowhere to be found in the human body. There has never existed such a thing as a punchcard that can read itself.
This scientific article quotes a neuroscientist speculating about memory storage. The article says:
Neuroscience has also been struggling to find where the brain stores its memories. “They may be ‘hiding’ in high-dimensional cavities,” Markram speculates.
High-dimensional cavities? Cavities are holes, not information storage media. I think the quote bolsters my claim that scientists do not have any plausible explanation of how brains can be storing memories for 50 years.
Often
the modern neuroscientist will engage in pretentious talk which makes
it sound as if there is some understanding of how very long-term
memory storage can occur. But just occasionally we will get a little
candor from our neuroscientists, such as when neuroscientist Sakina
Palida admitted
in 2015, “Up
to this point, we still don’t understand how we maintain memories
in our brains for up to our entire lifetimes.”
Concluding
Remarks on Long-Term Memory
For the reasons
given above, there is no plausible mechanism by which brains such as
ours could be storing memories lasting longer than a year. There are
only a few possible physical candidates for things that might store
very long-term memory in our brain, and as we have seen, none of them
are plausible candidates for a storage of very long-term memory.
The fact that our
neurologists claim to have theories as to how very long-term memories
could be stored does not mean that any such theory is tenable.
Imagine if you lived on a planet in which your consciousness and
long-term memory was due to a soul, and that the first time
scientists dissected a brain, they found that the brain was filled
with sawdust. No doubt such scientists would get busy inventing
clever theories purporting to explain how sawdust can generate
consciousness and long-term memories.
I
may note that memories stretching back 50 years are inexplicable not
merely from a neurological standpoint but also from a Darwinian
standpoint. As I will argue later, from the standpoint of survival of
the fittest and natural selection, there is no reason why any primate
organism should ever need to remember anything for longer than about
a year or two (it would work just fine to just keep remembering last
year's memories). I may note that according to an article
on wikipedia.com, the average life span in the Bronze Age was only 26
years old. There is no reason why natural selection (prior to the
Bronze Age) would have equipped us to remember things for a length of
time twice the average life span in the Bronze Age, and it is not
plausible that very long-term memories are a recent evolutionary
development.
In this post and
in other places on this site, when I use the term “memory” I am
referring to things such as episodic memories of life events, learned
vocabulary, learned facts, and learned visual information that we can
recall (such as identifying the name of an object, or recognizing a
face). I do not refer to muscular skills such as the skill of how to
ride a bike. Such skills are best referred to as “muscular skills”
rather than memory.
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