Dark Side: Neurotransmitters
There were cases where the murderer denied early
abuse, but many people will deny such abuse, only for it to be discovered later
that either they were too embarrassed to admit it, or they were protecting the abusing adult, typically a family member. It was also becoming known from many studies that
there was a high incidence of early childhood physical, emotional, or sexual
abuse in the prison population of psychopaths. A small survey of thirty-five
psychopathic offenders in youth detention facilities found that 70 percent
reported serious mistreatment throughout childhood. Given that the onset of
reliable memory for childhood events in adults may reach back to three to four
years of age, this implied that a higher percentage of adult criminal
psychopaths actually experienced significant abuse earlier than that. As such,
it was possible that more than 90 percent of them were abused at some point in
their early life. Add to this those psychopaths who protect their abusers, and
the percentage could approach 99 percent.
The environment can interact with
genes during development in a number of ways. One of those is through what’s
called a genotype-environment correlation. A child with genes predisposing him
to aggression may frequently misbehave, drawing hostility and abuse from his
caretaker. Or an aggressive parent may pass along genes for hostility and also
behave in a belligerent way toward his kids, and then both the genes and the
antisocial attitude continue down the line. Such a pattern could explain any murderous lines of ancestors. Even if genes for aggression washed out over the
generations, an expectation that families always act like this could have
remained.
Another form of gene-environment interaction is what’s known as epigenetic marking. Seemingly out of nowhere, your teenage daughter, who doesn’t have the svelte shape of you or even your mother, starts to put on weight and looks very much like your grandmother, her great-grandmother. To figure out why, you all decide to take standard DNA tests to determine your respective genetic codes. But it turns out that the DNA code controlling the appetite and obesity of your plumping daughter is more similar to the DNA code of yourself your lean mother than to that of your fleshy grandmother. So the genetics don’t seem to explain your daughter’s teenage-onset obesity. And she doesn’t eat much more than an average person. Something else unexpected must be going on. Perhaps her metabolism is malfunctioning. But how and why? Then your niece, who is studying genetics in her doctoral work, suggests something may have been passed down from great-grandmother to grandmother to you, and then to your daughter. That something is not the genetic code itself, but a small extra bit, or tag, of chemical information stuck on to several genes controlling obesity and metabolism.
The study called an epigenetic
tag, might have been added on to several of her great-grandmother’s genes while
she was a young child, enduring starvation during a decade-long famine in
Ireland, Poland, Bosnia, or the Bronx, nearly a century ago. Her
great-grandmother’s cellular response to the great stresses of that starvation
may have been to change her metabolic machinery to more efficiently use energy
and store fat, and to increase appetite once food was plentiful again. So your
daughter, her great-granddaughter, under other teenage stressors, and with a
plentiful food supply, responded by putting on weight to the point where she
now resembles the plump but hearty teenager her great-grandmother became when
the famine ended in her homeland eighty years ago. Some of these effects are
dependent on whether the ancestor was male or female, since certain genes are
“imprinted” on either the paternal or maternal side of the family.
The epigenetic tag is one of many
alterations to the genetic code that can be induced by environmental stressors.
This is one of the core mechanisms underlying the interaction of nature and
nurture. While there have been numerous recent studies on the role of
epigenetic interactions on metabolism, cancer, and susceptibility to infectious
and immune diseases, it is also a key to understanding some psychiatric
disorders, from schizophrenia to psychopathy.
The raw DNA base pair code in
this analogy is “thatthatisisthatthat,” and the way this raw sequence is laid
out directs the code to be transcribed into the sequence of words but not quite
a sentence. Normally the transcribed message from the DNA to the RNA would be
translated into the protein, here the mature and sensical sentences “That that
is, is. That that is not, is not. Is that it? It is.” But environmental
stressors can induce epigenetic tags to be added on to some of the original
genetic DNA, so that the punctuation, the spacing of the words, the text
formatting in general, can be altered to produce a slightly different meaning:
“That that is, is. That that is not, is not. Is that it? It is?” Same words,
same sequence, but a final question mark added changes the thrust of the message.
This slight “epigenetic” change to the sentence’s intended “genetic” meaning is
different from an actual mutation. In a mutation, the actual spelling of the
sentence is changed, either by inserting a letter (or more) or deleting an existing
letter. Such a change can, of course, radically alter the function of the sentence,
which may now become, “That that is, That that is not, is snot.
Another way of looking at the
epigenome function is to consider the new car you buy from the dealer. All that
original hardware is like your genome, while alterations you might make to soup
it up, give it some more pep, or, for your daughter, slow it down, are like the
epigenetic modifications. Epigenetic alterations are one of several reasons why
identical twins are not identical. Even with identical raw genetic codes,
differences in early environment, whether overly stressful or more positively
enriching, can change their behaviors down the line as teenagers and adults.
Identical twins can also have different numbers of the same genes inherited
from one parent or another, and this can also alter how the identical twins
look and behave. A third mechanism can involve a seemingly otherworldly
phenomenon caused by “retrotransposons.”
Retrotransposons are short bits
of DNA or RNA present in the nucleus of the cell surrounding the genes
themselves. Once thought to be junk DNA with no apparent purpose, these odd
snippets of information are not fixed in place but can move around, like grains
of rice in soup. They are capable of connecting widely separate genes, even on
different chromosomes, and they can alter cellular function. They can rearrange
the “sentences” our DNA types out, and in doing so can ultimately change,
usually subtly, human behavior, and account for not only differences in how
identical twins act, but also what makes schizophrenics psychotic and perhaps
why certain depressives become suicidal.
One of the most common ways the epigenome functions is when environmental stressors, especially early in life, wrap DNA filaments around spools of protein called histones. Stressors can also add or remove minuscule chemical side groups, called methyl and acetyl, to or from genes. These are just small groups of atoms that latch on to DNA strands. Such alterations can stop, slow down, or speed up a gene’s ability to be read and do its job. Changing a gene’s action alters the amount of proteins that are made, and therefore changes the balance of neurotransmitters in brain circuits, leading to changes in thoughts, emotions, and behaviors. These modifications are a big deal and have become a major focus in the understanding of the interaction of genes and environment, and are the key to understanding the nature-nurture problem. One of the main environmental stimuli that add these methyl and acetyl groups is stress, and these stimuli can include abuse, prenatal maternal anxiety, drugs, and even some foods. Stress releases the hormone cortisol, which transfers methyl and acetyl groups from donor molecules on to DNA.
Those several months following
birth are sometimes called the “fourth trimester,” and this extended period of
what should have been prenatal development means that early environment for a
human infant is particularly important. In fact, the most vulnerable time for a
human’s brain development in terms of environmental impact is from the period
of birth and for several months in this fourth trimester. It is in this time
that a human needs to avoid serious stressors, and it is when nurturing is so
critical.
Acknowledgements:
www.politie.nl and
a Chief Inspector – Mr. Henk van Essen© from 1th of March 2024 new Politiekorpschef
Janny Knol
www.aived.nl AIVD
– Mr. Erik Akerboom ©
Bibliography:
1. Criminal Investigations – Crime Scene Investigation.2000
2. Forensic Science.2006
3. Techniques of Crime Scene Investigation.2012
4. Forensics Pathology.2001
5. Pathology.2005
6. Forensic DNA Technology (Lewis Publishers,New York, 1991).
7. The Examination and Typing of Bloodstains in the Crime Laboratory (U.S. Department of Justice, Washington, D.C., 1971).
8. „A Short History of the Polymerase Chain Reaction". PCR Protocols. Methods in Molecular Biology.
9. Molecular Cloning: A Laboratory Manual (3rd ed.). Cold Spring Harbor,N.Y.: Cold Spring Harbor Laboratory Press.2001
10. "Antibodies as Thermolabile Switches: High Temperature Triggering for the Polymerase Chain Reaction". Bio/Technology.1994
11. Forensic Science Handbook, vol. III (Regents/Prentice Hall, Englewood Cliffs, NJ, 1993).
12. "Thermostable DNA Polymerases for a Wide Spectrum of Applications: Comparison of a Robust Hybrid TopoTaq to other enzymes". In Kieleczawa J. DNA Sequencing II: Optimizing Preparation and Cleanup. Jones and Bartlett. 2006
13. Nielsen B, et al., Acute and adaptive responses in humans to exercise in a warm, humid environment, Eur J Physiol 1997
14. Molnar GW, Survival of hypothermia by men immersed in the ocean. JAMA 1946
15. Paton BC, Accidental hypothermia. Pharmacol Ther 1983
16. Simpson K, Exposure to cold-starvation and neglect, in Simpson K (Ed): Modem Trends in Forensic Medicine. St Louis, MO, Mosby Co, 1953.
17. Fitzgerald FT, Hypoglycemia and accidental hypothermia in an alcoholic population. West J Med 1980
18. Stoner HB et al., Metabolic aspects of hypothermia in the elderly. Clin Sci 1980
19. MacGregor DC et al., The effects of ether, ethanol, propanol and butanol on tolerance to deep hypothermia. Dis Chest 1966
20. Cooper KE, Hunter AR, and Keatinge WR, Accidental hypothermia. Int Anesthesia Clin 1964
21. Keatinge WR. The effects of subcutaneous fat and of previous exposure to cold on the body temperature, peripheral blood flow and metabolic rate of men in cold water. J Physiol 1960
22. Sloan REG and Keatinge WR, Cooling rates of young people swimming in cold water. J Appl Physiol 1973
23. Keatinge WR, Role of cold and immersion accidents. In Adam JM (Ed) Hypothermia – Ashore and Afloat. 1981, Chapter 4, Aberdeen Univ. Press, GB.
24. Keatinge WR and Evans M, The respiratory and cardiovascular responses to immersion in cold and warm water. QJ Exp Physiol 1961
25. Keatinge WR and Nadel JA, Immediate respiratory response to sudden cooling of the skin. J Appl Physiol 1965
26. Golden F. St C. and Hurvey GR, The “After Drop” and death after rescue from immersion in cold water. In Adam JM (Ed). Hypothermia – Ashore and Afloat, Chapter 5, Aberdeen Univ. Press, GB 1981.
27. Burton AC and Bazett HC, Study of average temperature of tissue, of exchange of heat and vasomotor responses in man by means of bath coloremeter. Am J Physiol 1936
28. Adam JM, Cold Weather: Its characteristics, dangers and assessment, In Adam JM (Ed).Hypothermia – Ashore and Afloat, Aberdeen Univ. Press, GB1981.
29. Modell JH and Davis JH, Electrolyte changes in human drowning victims.Anesthesiology 1969
30. Bolte RG, et al., The use of extracorporeal rewarming in a child submerged for 66 minutes. JAMA 1988
31. Ornato JP, The resuscitation of near-drowning victims. JAMA 1986
32. Conn AW and Barker CA: Fresh water drowning and near-drowning — An update.1984;
33. Reh H, On the early postmortem course of “washerwoman’s skin at the fingertips.” Z Rechtsmed 1984;
34. Gonzales TA, Vance M, Helpern M, Legal Medicine and Toxicology. New York, Appleton-Century Co, 1937.
35. Peabody AJ, Diatoms and drowning – A review, Med Sci Law 1980
36. Foged N, Diatoms and drowning — Once more.Forens Sci Int 1983
37. "Microscale chaotic advection enables robust convective DNA replication.". Analytical Chemistry. 2013
38. Sourcebook in Forensic Serology, Immunology, and Biochemistry (U.S. Department of Justice, National Institute of Justice, Washington, D.C.,1983).
39. C. A. Villee et al., Biology (Saunders College Publishing, Philadelphia, 2nd ed.,1989).
40. Molecular Biology of the Gene (Benjamin/Cummings Publishing Company, Menlo Park, CA, 4th ed., 1987).
41. Molecular Evolutionary Genetics (Plenum Press, New York,1985).
42. Human Physiology. An Integrate. 2016
43. Dumas JL and Walker N, Bilateral scapular fractures secondary to electrical shock. Arch. Orthopaed & Trauma Surg, 1992; 111(5)
44. Stueland DT, et al., Bilateral humeral fractures from electrically induced muscular spasm. J. of Emerg. Med. 1989
45. Shaheen MA and Sabet NA, Bilateral simultaneous fracture of the femoral neck following electrical shock. Injury. 1984
46. Rajam KH, et al., Fracture of vertebral bodies caused by accidental electric shock. J. Indian Med Assoc. 1976
47. Wright RK, Broisz HG, and Shuman M, The investigation of electrical injuries and deaths. Presented at the meeting of the American Academy of Forensic Science, Reno, NV, February 2000.
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