Gut microbiome balance and behavior
This week we focused on two examples of research highlighting
the effects of environmental differences on gut microbiota and its downstream effects
on brain function and behavior. Reber and colleagues (2016) used the chronic
subordinate stress to explore the effect of stress of gut microbiome and the protective
role m.vaccae immunization in those alteration. Results demonstrated that m.vaccae
had a protective effect to CSC induced changes in coping response, increased anxiety-like
behavior, reduced serotonin expression and reduced microglial density. M.vaccae
also prevented colitis resulting from stress. The protective effects of m.vaccae
in anxiety-like behavior and colitis were dependent on Treg. The CSC model is especially
relevant for disorders like PTSD, which are stress induced, and this research demonstrates
that m.vaccae immunization protects again some stress-induced changes in both
behavior and neural dynamics. The parallel is not as clear when it comes to the
compromised immunoregulation observed in high income regions; a germ-free line
would be a more adequate to explore if m.vaccae also has a protective role when
gut microbiome is compromised due to reduced exposure associated with high
income areas.
The article by Buffington et. al (2016) used a maternal high-fat
model to induce gut microbiome dysregulation. MHFD induced alterations in 8
different species of bacteria in offspring. These gut microbiome changes
induced social deficits, which were corrected with cohousing with control mice.
This rescue of symptoms was found to have a critical period, indicating that the
social deficit results from neurodevelopmental alterations resulting from gut
microbiome imbalance. L. reuteri was also used to rescue social-deficits and
that the effect was likely mediated by increased oxytocin signaling to the VTA.
Interestingly, other symptoms associated MHFD were not rescued (e.g. marble
burying, anxiety, repetitive behavior). This suggests that those deficits could
be associated with earlier stages of development or be mediated by other MHFD
induced changes on systems other than the gut microbiome. Together, these
articles highlight the reaching effects of gut microbiome disruption. I look
forward to seeing longitudinal studies in humans of probiotic use based on
articles like these.
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