2013
DOI: 10.1016/j.neulet.2013.02.006
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Effects of intracerebroventricular ghrelin on food intake and Fos expression in the arcuate nucleus of the hypothalamus in female rats vary with estrous cycle phase

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Cited by 19 publications
(14 citation statements)
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“…This suggests that the interaction of fasting and E2 differentially regulates Ghsr in the ARC. While Ghsr expression does not change during the estrous cycle in female rats, ghrelin’s effects on food intake are only found during the diestrus cycle, when E2 levels are lower (Sakurazawa et al, 2013). The differential effect on ghrelin sensitivity and Ghsr expression may be due, in part, to changes in expression of downstream effectors of GHSR signaling (e.g., Cpt1c, Foxo1 ) as we have found in the ARC and in NPY pools.…”
Section: Discussionmentioning
confidence: 99%
“…This suggests that the interaction of fasting and E2 differentially regulates Ghsr in the ARC. While Ghsr expression does not change during the estrous cycle in female rats, ghrelin’s effects on food intake are only found during the diestrus cycle, when E2 levels are lower (Sakurazawa et al, 2013). The differential effect on ghrelin sensitivity and Ghsr expression may be due, in part, to changes in expression of downstream effectors of GHSR signaling (e.g., Cpt1c, Foxo1 ) as we have found in the ARC and in NPY pools.…”
Section: Discussionmentioning
confidence: 99%
“…Previous studies have demonstrated that feeding varies across differing stages of the oestrous cycle in rodents, nonhuman primates and humans . The feeding response to hunger‐related hormones (including ghrelin) and neurosteroids also varies throughout different stages of the oestrous cycle in female rats . It is recommended that future studies continue to investigate the extent to which oestrous cycle phase and fluctuations in ovarian hormones might influence the satiety response to oxytocin in female animal models.…”
Section: Resultsmentioning
confidence: 99%
“…What it is well described so far is that estrogens in the CNS increase the sensitivity to anorexigenic molecules such as leptin, released by adipocytes 4952 , cholecystokinin (CCK), produced by small intestine 53, 54 and insulin, synthesized by the pancreas 51, 52 and, at the same time, decrease the response to the orexigenic peptide ghrelin from the gastro-intestinal tract 55, 56 .…”
Section: Discussionmentioning
confidence: 99%