Skip to main content

Post 5: Observation paradigms as a model of emotional stress and observational learning


In neuroscience and abnormal psychology today, the disregard of female animal models is considered one of the major oversights of research that has been otherwise foundational in understanding many neurological disorders. While reading Sial et al. (2015) and Allsop et al. (2018), this type of sex bias seemed especially evident and seemed to me an exemplar of studies that would be improved by the inclusion and analysis of female subjects. While all research aimed to apply to both sexes should include both sexes, the lack of female representation in these papers was especially concerning to me because they explicitly consider emotional stress and empathy. Past research has shown that male and female rodents have very different responses to stress, and I would posit that these responses are especially distinct for emotional stress (such as observational stress and learning seen here) compared to those due to pain or injury (such as shocks or injuries due to social defeat). Additionally, females tend to show more apparent empathy due to maternal behaviors. Sial et al. did call out the need for and utility of females in their research but had not yet created a similar paradigm that could include females. In the case that Sial et al. were able to adapt their paradigm for female mice to observe, I am curious whether the degree of stress and stress responses would be higher if a female mouse observed her offspring being socially defeated. Similarly, I would be interested in seeing the results of experiments similar to these in even more affiliative species and/or between mates, as they may have stronger stress responses to observing a conspecific experience trauma.

Another theme that has been uncovered during our class discussions that was evident in Sial et al. and Allsop et al. was the efficacy of behavioral measures of emotions and models of disorders. While Sial et al. did mention that the experiment can serve as a model for various stress-induced neuropsychiatric disorders, there was a distinct focus on PTSD, as witnessing traumatic events alone can cause PTSD in humans. However, the paradigm did not seem to specifically apply to PTSD, as emotional stressors are simply another type of stressor, and stressors are known to cause anxiety and depression-like behaviors in mice. Similarly, the use of freezing as a measure of fear in Allsop et al. brings up the recent debate of whether or not this behavior truly is indicative of fear. While we cannot perfectly model human psychological conditions in rodents, these papers take an important step toward modeling emotional stress and ethical behaviors. 

Comments

Popular posts from this blog

Week 2- Dopamine Modulation of Depressive-like Behaviors

The Chaudhury et al paper explored the neural circuit mechanisms involved in the dopamine modulation of certain symptoms of depression. In this study, the researchers looked at social interaction and sucrose preference as part of their social-defeat paradigm, which has been shown in the past to be indicative of depressive-like behaviors. Although I initially did not completely see the connection between the social-defeat stress model of depression and the tonic vs phasic firing of dopamine neurons, it seemed that susceptibility and resilience to stress played a role in the functional/behavioral effects of dopamine firing. It was interesting to see how chronic mild stress with phasic firing of VTA dopamine neurons converted even resilient mice into susceptible mice.  The Tye et al paper similarly looked at the dopamine modulation of depressive-like behaviors, focusing on motivation with the forced swim tests and open field tests, followed by measurement of anhedonia by quantifyi...

Sial & Allsop

Sial et al. derived a novel approach for studying what they deem vicarious defeat stress (VSDS) as a model for MDD, PTSD, and other mood-related disorders as an alternative to the classical CSDS paradigm. Using adult male mice, they demonstrate that their model induces a robust and measurable social avoidant phenotype as well as other stress and anxiety related behavioral outputs. Their subsequent rescue study with chronic fluoxetine treatment shows reversal of the behavioral phenotypes and emphasizes the predictive validity of the model. Allsop et al. found that BLA-projecting ACC neurons preferentially encode socially derived aversive cue information by encoding the demonstrator’s distress response during observational learning, hence enabling acquisition of negative valence of cue by BLA neurons and behavioral output. In order to test their hypothesis, Allsop et al. used an observational fear conditional paradigm to create association between a conditioned stimulu...

Buffington and Reber

Buffington et al. explore a mechanism by which maternal obesity can induce neuronal and subsequent behavioral disorders. Using a model of high-fat diet (MHFD)-induced obesity, the authors showcase the strong connection between the brain and the gut, and its impact on behavior. The findings are provocative; by exposing these offspring to the microbiome of control offspring, there was evidence of a rescued observed behavioral phenotype. Furthermore, a phylogenetic profiling of the gut microbiome revealed a decrease in L. reuteri within MHFD offspring, and introduction of live L. reuteri into the drinking water shows successful rescue of the behavioral issues in the MHFD offspring. L. reuteri-induced expression of oxytocin within the paraventricular nuclei of the hypothalamus provides a potential mechanistic explanation for the behavioral changes. I thought this paper provided robust support for the hypothesized interaction between the gut biome and the developing CNS, with tremendous po...