GLUCOCORTICOIDS AND INSULIN - RECIPROCAL SIGNALS FOR ENERGY-BALANCE

被引:229
作者
STRACK, AM
SEBASTIAN, RJ
SCHWARTZ, MW
DALLMAN, MF
机构
[1] VET AFFAIRS MED CTR, DEPT MED, SEATTLE, WA 98108 USA
[2] UNIV WASHINGTON, SEATTLE, WA 98108 USA
关键词
FOOD INTAKE; NEUROPEPTIDE Y MESSENGER RIBONUCLEIC ACID; BODY WEIGHT GAIN; ADRENALECTOMY; STREPTOZOTOCIN DIABETES;
D O I
10.1152/ajpregu.1995.268.1.R142
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Signals that regulate long-term energy balance have been difficult to identify. Increasingly strong evidence indicates that insulin, acting on the central nervous system in part through its effect on neuropeptide Y (NPY), inhibits food intake. We hypothesized that corticosteroids and insulin might serve as interacting, reciprocal signals for energy balance, acting on energy acquisition, in part through their effects on hypothalamic NPY, as well as on energy stores. Because glucocorticoids also stimulate insulin secretion, their role is normally obscured. Glucocorticoids and insulin were clamped in adrenalectomized rats with steroid replacement and streptozotocin-induced diabetes. Glucocorticoids stimulated and insulin inhibited NPY mRNA and food intake. Glucocorticoids inhibited and insulin increased energy gain as determined by the change in body weight. When adrenalectomized diabetic rats were treated, corticosterone stimulated and insulin inhibited food intake, and, respectively, inhibited and increased overall energy gain. More than 50% of the variance was explained by regression analysis of the two hormones on food intake and body weight. Thus glucocorticoids and insulin are major, antagonistic, long-term regulators of energy balance. The effects of corticosterone and insulin on food intake may be mediated, in part, through regulation of hypothalamic NPY synthesis and secretion.
引用
收藏
页码:R142 / R149
页数:8
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