Palatable Food Affects HPA Axis Responsivity and Forebrain Neurocircuitry in an Estrous Cycle-specific Manner in Female Rats. (1st August 2018)
- Record Type:
- Journal Article
- Title:
- Palatable Food Affects HPA Axis Responsivity and Forebrain Neurocircuitry in an Estrous Cycle-specific Manner in Female Rats. (1st August 2018)
- Main Title:
- Palatable Food Affects HPA Axis Responsivity and Forebrain Neurocircuitry in an Estrous Cycle-specific Manner in Female Rats
- Authors:
- Egan, Ann E.
Thompson, Abigail M.K.
Buesing, Dana
Fourman, Sarah M.
Packard, Amy E.B.
Terefe, Tegesty
Li, Dan
Wang, Xia
Song, Seongho
Solomon, Matia B.
Ulrich-Lai, Yvonne M. - Abstract:
- Highlights: Limited sucrose intake (LSI) blunts the plasma ACTH response to restraint stress in female rats during proestrus/estrus. LSI does not blunt post-restraint plasma ACTH during the diestrus phase of the estrous cycle. Bayesian modeling is used with neuronal activation/plasticity markers to identify a brain network modified by LSI. The modeled network includes the BLA, NAc, PFC, and BST as likely being modified by LSI during proestrus/estrus. 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- andHighlights: Limited sucrose intake (LSI) blunts the plasma ACTH response to restraint stress in female rats during proestrus/estrus. LSI does not blunt post-restraint plasma ACTH during the diestrus phase of the estrous cycle. Bayesian modeling is used with neuronal activation/plasticity markers to identify a brain network modified by LSI. The modeled network includes the BLA, NAc, PFC, and BST as likely being modified by LSI during proestrus/estrus. 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. … (more)
- Is Part Of:
- Neuroscience. Volume 384(2018)
- Journal:
- Neuroscience
- Issue:
- Volume 384(2018)
- Issue Display:
- Volume 384, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 384
- Issue:
- 2018
- Issue Sort Value:
- 2018-0384-2018-0000
- Page Start:
- 224
- Page End:
- 240
- Publication Date:
- 2018-08-01
- Subjects:
- BLA basolateral amygdala -- CeA central amygdala -- HPA hypothalamic–pituitary–adrenocortical -- KPBS potassium phosphate-buffered saline -- LSI Limited sucrose intake -- NAc nucleus accumbens -- PBS phosphate-buffered saline -- pCREB phospho-cyclic AMP response element binding protein -- PFC prefrontal cortex -- PVN paraventricular nucleus of the hypothalamus -- RIA radioimmunoassay -- BSTad bed nucleus of the stria terminalis, anterodorsal division -- BSTpr bed nucleus of the stria terminalis, principal division -- ER estrogen receptor -- E estrus -- D1 diestrus 1 -- D2 diestrus 2 -- LP late proestrus -- MeApd posterodorsal subdivision of the medial amygdala -- P proestrus
sex differences -- sucrose -- ACTH -- corticosterone -- basolateral amygdala -- nucleus accumbens
Neurochemistry -- Periodicals
Neurophysiology -- Periodicals
Neurology -- Periodicals
Neurochimie -- Périodiques
Neurophysiologie -- Périodiques
Neurochemistry
Neurophysiology
Electronic journals
Periodicals
Electronic journals
612.8 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03064522 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/03064522 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/03064522 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuroscience.2018.05.030 ↗
- Languages:
- English
- ISSNs:
- 0306-4522
- Deposit Type:
- Legaldeposit
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