| Literature DB >> 29852242 |
Ann E Egan1, Abigail M K Thompson1, Dana Buesing1, Sarah M Fourman1, Amy E B Packard1, Tegesty Terefe1, Dan Li2, Xia Wang3, Seongho Song3, Matia B Solomon1, Yvonne M Ulrich-Lai4.
Abstract
Eating palatable foods can provide stress relief, but the mechanisms by which this occurs are unclear. We previously characterized a limited sucrose intake (LSI) paradigm in which twice-daily access to a small amount of 30% sucrose (vs. water as a control) reduces hypothalamic-pituitary-adrenocortical (HPA) axis responses to stress and alters neuronal activation in stress-regulatory brain regions in male rats. However, women may be more prone to 'comfort feeding' behaviors than men, and stress-related eating may vary across the menstrual cycle. This suggests that LSI effects may be sex- and estrous cycle-dependent. The present study therefore investigated the effects of LSI on HPA axis stress responsivity, as well as markers of neuronal activation/plasticity in stress- and reward-related neurocircuitry in female rats across the estrous cycle. We found that LSI reduced post-restraint stress plasma ACTH in female rats specifically during proestrus/estrus (P/E). LSI also increased basal (non-stress) FosB/deltaFosB- and pCREB-immunolabeling in the basolateral amygdala (BLA) and central amygdala specifically during P/E. Finally, Bayesian network modeling of the FosB/deltaFosB and pCREB expression data identified a neurocircuit that includes the BLA, nucleus accumbens, prefrontal cortex, and bed nucleus of the stria terminalis as likely being modified by LSI during P/E. When considered in the context of our prior results, the present findings suggest that palatable food reduces stress responses in female rats similar to males, but in an estrous cycle-dependent manner. Further, the BLA may contribute to the LSI effects in both sexes, whereas the involvement of other brain regions appears to be sex-dependent.Entities:
Keywords: ACTH; basolateral amygdala; corticosterone; nucleus accumbens; sex differences; sucrose
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Year: 2018 PMID: 29852242 PMCID: PMC6071329 DOI: 10.1016/j.neuroscience.2018.05.030
Source DB: PubMed Journal: Neuroscience ISSN: 0306-4522 Impact factor: 3.590