UNCHANGED HYPOTHALAMIC NEUROPEPTIDE-Y CONCENTRATIONS IN HYPERPHAGIC, HYPOGLYCEMIC RATS - EVIDENCE FOR SPECIFIC METABOLIC-REGULATION OF HYPOTHALAMIC NPY

被引:27
作者
CORRIN, SE [1 ]
MCCARTHY, HD [1 ]
MCKIBBIN, PE [1 ]
WILLIAMS, G [1 ]
机构
[1] UNIV LIVERPOOL,DEPT MED,POB 147,LIVERPOOL L69 3BX,ENGLAND
基金
英国医学研究理事会;
关键词
HYPOGLYCEMIA; HYPOTHALAMUS; NEUROPEPTIDE-Y; FOOD INTAKE; RATS;
D O I
10.1016/0196-9781(91)90080-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hypothalamic concentrations of neuropeptide Y (NPY), a potent central appetite stimulant, increase dramatically in food-restricted and insulin-deficient diabetic rats. This suggests that NPY may drive hyperphagia in these conditions, which are characterized by weight loss and insulin deficiency. To test the hypothesis that insulin deficiency and weight loss are specific stimuli to hypothalamic NPY, we measured NPY concentrations in individual hypothalamic regions in rats with hyperphagia caused by insulin-induced hypoglycemia. Groups of 8 male Wistar rats were injected with ultralente insulin (20-60 U/kg) to induce either acute hypoglycemia (7 h after a single injection) or chronic hypoglycemia (8 days with daily injections). In hypoglycemic rats, plasma insulin concentrations were increased 6- to 7-fold compared with saline-injected controls; food intake was significantly increased with acute and chronic hypoglycemia and weight gain was significantly increased in the chronically hypoglycemic group. NPY concentrations were measured by radioimmunoassay in 8 hypothalamic regions microdissected from fresh brain slices. NPY concentrations were not increased in any region in either acute or chronic hypoglycemia. NPY therefore seems unlikely to mediate hyperphagia in hyperinsulinemia-induced hypoglycemia, supporting the hypothesis that weight loss is a specific stimulus to hypothalamic NPY and that insulin deficiency may be the metabolic signal responsible.
引用
收藏
页码:425 / 430
页数:6
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