So, near the end of this post, I will propose some follow up research and/or experiments to do just that.
I will also suggest what those experiments and/or research efforts should show, so as to make it easier to test whether or not The Hypothesis is viable enough to pursue further.
But first, let's bring the history of The Hypothesis up to date.
Prions have been eliminated from The Hypothesis as a source for the toxins of power, thus we are left with either microbes or phages as originators of a toxin of power.
We have data that indicate a likely locus or focus point for this origin, which is the brain:
Microbial colonization of mammals is an evolution-driven process that modulate host physiology, many of which are associated with immunity and nutrient intake. Here, we report that colonization by gut microbiota impacts mammalian brain development and subsequent adult behavior ... our results suggest that the microbial colonization process initiates signaling mechanisms that affect neuronal circuits involved in motor control and anxiety behavior.(Hypothesis: Microbes Generate Toxins of Power, emphasis added). The full import of that research is that, following colonization, communication of various sorts takes place between and/or among human cells and microbes, which impacts the amygdala, and other limbic system areas:
We therefore studied the expression of these genes in the frontal cortex, striatum, amygdala, and hippocampus of GF and SPF mice, by means of in situ hybridization technique. In GF mice, NGFI-A mRNA expression was significantly lower in various subregions of the prefrontal cortex, including the orbital frontal cortex (Fig. 4 A and A′); as well as in the striatum (GF vs. SPF: 329 ± 33 vs. 586 ± 18, P < 0.0001), hippocampus (CA1 region, GF vs. SPF: 258 ± 15 vs. 499 ± 22, P < 0.0001; CA3 region, GF vs. SPF: 166 ± 13 vs. 236 ± 6, P < 0.001; dentate gyrus, GF vs. SPF: 76 ± 4 vs. 113 ± 5, P < 0.0001) and amygdala (GF vs. SPF: 126 ± 17 vs. 212 ± 19, P < 0.01) compared with SPF mice. Similarly, GF mice had significantly lower BDNF mRNA expression in the hippocampus, amygdala (Fig. 4 B and B′), and cingulate cortex (GF vs. SPF: 162 ± 6 vs. 193 ± 10, P < 0.05), which are key components of the neural circuitry underlying anxiety and fear ... Our results suggest that during evolution, the colonization of gut microbiota has become integrated into the programming of brain development, affecting motor control and anxiety-like behavior.(Hypothesis: Microbes Generate Toxins of Power - 2). The same method that was used to strengthen the appendix - microbe relationship hypothesis of Dr. Parker will work for testing The Hypothesis as well.
The team testing Dr. Parker's hypothesis used existing medical records, so I propose using that same method to test The Hypothesis, as follows:
1 - examine medical records of people who have been exposed to power (presidents, congress members, judges) covering a time when they behaved improperly in their official capacity;NOTE: the reason for analysis of medical records of those exposed to power, during times of improper official behavior, is because The Hypothesis contains a premise that certain good behaviors are anti-toxins to the toxins of power (See: Tables For The Toxins In Power).
2 - compare those to medical records of people who have not been exposed to power, at a time when those people were behaving properly;
3 - generate data about the differences in brain chemistry, structure, and brain function between the two groups, focusing on the limbic system, especially the amygdala.
If The Hypothesis is correct the NGFI-A mRNA, BDNF mRNA, chemicals, and other factors mentioned above (Hypothesis: Microbes Generate Toxins of Power - 2) should reveal data supportive of The Hypothesis.
The previous post in this series is here.