1993
DOI: 10.1016/0031-9384(93)90387-u
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Modulation of the satiety effect of cholecystokinin by estradiol

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Cited by 71 publications
(37 citation statements)
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“…Cumulative food intake was surprisingly similar among all amylin-treated animals, suggesting that amylin may somehow reset food intake to a particular value regardless of food access prior to and during treatment. The effects of other anorexigenic peptides, such as cholecystokinin (CCK), on food intake have been shown to be influenced by changes in endogenous estrogen (2,6). As the present studies did not control for the phase of the estrous cycle, the potential impact of estradiol levels on the efficacy of amylin therapy remains to be elucidated.…”
Section: Discussionmentioning
confidence: 84%
“…Cumulative food intake was surprisingly similar among all amylin-treated animals, suggesting that amylin may somehow reset food intake to a particular value regardless of food access prior to and during treatment. The effects of other anorexigenic peptides, such as cholecystokinin (CCK), on food intake have been shown to be influenced by changes in endogenous estrogen (2,6). As the present studies did not control for the phase of the estrous cycle, the potential impact of estradiol levels on the efficacy of amylin therapy remains to be elucidated.…”
Section: Discussionmentioning
confidence: 84%
“…Furthermore, with the onset of puberty, estrogen exerts physiological functions including affecting FI regulation and the action of intake regulatory hormones including ghrelin and cholecystokinin (CCK) (27). In rats, estradiol increases CCK's satiating effects (28,29) and attenuates ghrelin's orexigenic effects (30), leading to lower FI. Energy intake is decreased in the follicular compared with the luteal phase of the menstrual cycle because of higher levels of estrogen (31), which may have contributed to the greater reduction in FI in postpubertal girls after glucose.…”
Section: Discussionmentioning
confidence: 99%
“…Thus, MCH may be added to the growing list of orexigenic (e.g., ghrelin) and anorexigenic (e.g., cholecystokinin, glucagon, serotonin, leptin) compounds that are modulated by estradiol [39][40][41][42][43][44]. An important goal for future research is to determine the relative contribution of each of these compounds to the anorexigenic effect of estradiol.…”
Section: Discussionmentioning
confidence: 99%