Active areas of the brain when making decisions in stressful conditions

This 2013 human study was of decision making under stressful conditions.

Acute stress (ice water immersion) evoked habitual behavior rather than deliberative behavior. In my view, the subjects’ behaviors when under stress were driven more by their limbic system and lower brain areas than their cerebrum.

This finding wasn’t a big surprise. However, the researchers went on to state:

“Subjects with more executive resources to spare find themselves less susceptible to the behavioral changes brought about by stress response.”

I interpreted this statement to mean that when stressed, the more-capable subjects didn’t act out as much as the less-capable subjects acted out their respective feelings, instincts and impulses.

I felt that to understand this statement called for more investigation into the individual histories of the subjects:

  • What happened in their lives that enabled each person to acquire “more executive resources” or not?
  • What happened in their lives that made each person more or less sensitive to stress?
  • How are these two avenues of investigation related?

http://www.pnas.org/content/110/52/20941.full “Working-memory capacity protects model-based learning from stress”

When recognition memory is independent of hippocampal function

This 2014 human study provided additional details on the specialized brain circuits we have for recognizing faces.

Damage to the hippocampus didn’t impair recognition of new faces, “..but only at a short retention interval. Recognition memory for words, buildings, famous faces, and inverted faces was impaired.”

http://www.pnas.org/content/111/27/9935.full “When recognition memory is independent of hippocampal function”

Conserved epigenetic sensitivity to early life experience in the hippocampus

This 2012 human study was done by McGill University, whose researchers in Canada are at the forefront of epigenetic studies. The subject was epigenetic DNA methylation in the hippocampus of people who experienced abuse as children and who also committed suicide.

Comparisons were made with rats that were stressed in early life to identify genomic regions that are epigenetically changeable in response to a range of early life experiences.

http://www.pnas.org/content/109/Supplement_2/17266.full “Conserved epigenetic sensitivity to early life experience in the rat and human hippocampus”

Left–right dissociation of hippocampal memory processes in mice

This 2014 rodent study provided more details on the CA3 segment of the hippocampus:

“Silencing of either the left or right CA3 was sufficient to impair short-term memory…

Only left CA3 silencing impaired performance on an associative spatial long-term memory task, whereas right CA3 silencing had no effect.”

http://www.pnas.org/content/111/42/15238.full “Left–right dissociation of hippocampal memory processes in mice”

Hippocampal mechanisms involved in the enhancement of fear extinction caused by exposure to novelty

This 2014 Brazilian rodent study provided more information on the workings of the hippocampus. The researchers measured the effects of re-experiencing a fear within a specific context:

“Within a restricted time window, a brief exposure to a novel environment enhances the extinction of contextual fear.

The enhancement of extinction by the exposure to novelty depends on hippocampal gene expression..on hippocampal but not amygdalar processes.”

http://www.pnas.org/content/111/12/4572.full “Hippocampal molecular mechanisms involved in the enhancement of fear extinction caused by exposure to novelty”

Weakening memories by mispredicting their contexts

This 2014 human study showed that:

“Item memories are weakened when they are mispredicted by their context..weakening of the synapses that support the item’s representation in memory.

Note that our use of the term “pruning” is not meant to imply that traces are being deleted completely from memory.

Connecting the dots, two studies showed that our memories are formed within specific contexts and that our memories have contexts with specific places and times.

http://www.pnas.org/content/111/24/8997.full “Pruning of memories by context-based prediction error”

How painful long-lasting memories are stored and why they are so strong

This 2014 rodent study provided evidence for a portion of the neurophysiology that underlies how painful long-lasting memories are stored and why they are so strong. The amygdala was the brain area studied.

The researchers were misguided in news coverage by focusing on solutions such as external mechanisms to forget these memories. The researchers should think in terms of how their research can help people who can help themselves instead of having something externally done to them.

After all, we’re humans who can participate in therapy, not lab rats who need to be fixed.

http://www.pnas.org/content/111/51/E5584.full “Hebbian and neuromodulatory mechanisms interact to trigger associative memory formation”

Similarity in form and function of the hippocampus in rodents, monkeys, and humans

This 2013 study had something for the anti-evolutionists to chew on.

Is it anti-evolutionary for human brain and behavior researchers to not be informed by animal studies such as those that show prenatal hippocampal damage done to the fetus by the mother’s environment?

http://www.pnas.org/content/110/Supplement_2/10365.full “Similarity in form and function of the hippocampus in rodents, monkeys, and humans”

Metabolic costs and evolutionary implications of human brain development

This 2014 human study framed many of the other studies that relate to children’s brain development:

“The researchers found instead that the brain maxes out its glucose use at age 5. At age 4 the brain consumes glucose at a rate comparable to 66 percent of the body’s resting metabolic rate (43 percent of the body’s total energy expenditure).

To compensate for these heavy energy demands of our big brains, children grow more slowly and are less physically active during this age range.”

http://www.pnas.org/content/111/36/13010.full “Metabolic costs and evolutionary implications of human brain development”

Shorter telomere length in older men but not older women

This 2014 UK human study was the first on telomere length I’ve curated, so here’s some background information:

“Telomeres are..structures..that cap the ends of..chromosomes, protecting them from end-to-end fusion and degradation during cell division.

Human telomeric DNA naturally shortens with age during..cell divisions and as a result of oxidative attack.

At critical shortness, telomeres exhibit impaired function, leading to genomic instability, apoptosis, and cell senescence, often with altered transcriptional programming and mitochondrial dysfunction.

In humans, mutations that directly compromise telomere maintenance cause premature mortality and onset of a spectrum of diseases overlapping with the age-related diseases common in the population.

Shorter telomere length in white blood cells is linked and, in some cases, anticipates aging-related morbidity and mortality from conditions with immune system involvement, such as infectious diseases, cancer, and cardiovascular diseases, as well as risk factors, including hypertension, diabetes, obesity, and smoking.

A critical determinant of telomere length is the enzyme telomerase, which has the capacity to add..onto the..ends of telomeric DNA, extending telomere length and promoting genomic stability.

Acute mental stress appears to increase telomerase enzymatic activity at least transiently, and it has been suggested that high telomerase activity in conjunction with shorter telomere length may be indicative of a stressed system.”

The study put UK civil service men and women ages 54 through 76 through a series of stress tests. They found that men with longer telomeres had quicker recovery times than did men with shorter telomeres.

Men with shorter telomeres and low telomerase activity also had quicker recovery times than did men with shorter telomeres and high telomerase activity:

“In addition, we found that the (shorter telomeres and high telomerase activity men) had blunted reactivity to acute stress in diastolic blood pressure, heart rate, and cortisol.”

No telomere-based differences occurred with women:

“The explanation for the sex difference in response profiles in our study is not clear. Hormonal processes are unlikely to be directly responsible, because women in this study were postmenopausal.”

http://www.pnas.org/content/111/12/4519.full “Shorter telomeres with high telomerase activity are associated with raised allostatic load and impoverished psychosocial resources”