NEUROPEPTIDE-Y, THE HYPOTHALAMUS, AND DIABETES - INSIGHTS INTO THE CENTRAL CONTROL OF METABOLISM

被引:109
作者
FRANKISH, HM [1 ]
DRYDEN, S [1 ]
HOPKINS, D [1 ]
WANG, Q [1 ]
WILLIAMS, G [1 ]
机构
[1] UNIV LIVERPOOL, DEPT MED, DIABET & ENDOCRINOL RES GRP, LIVERPOOL L69 3BX, MERSEYSIDE, ENGLAND
基金
英国惠康基金;
关键词
NEUROPEPTIDE Y; INSULIN; HYPOTHALAMUS; DIABETES; OBESITY; RAT;
D O I
10.1016/0196-9781(94)00200-P
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
Neuropeptide Y (NPY), a major brain neurotransmitter, is expressed in neurons of the hypothalamic arcuate nucleus (ARC) that project mainly to the paraventricular nucleus (PVN), an important site of NPY release. NPY synthesis in the ARC is thought to be regulated by several factors, notably insulin, which may exert an inhibitory action. The effects of NPY injected into the PVN and other sites include hyperphagia, reduced energy expenditure and enhanced weight gain, insulin secretion, and stimulation of corticotropin and corticosterone release. The ARC-PVN projection appears to be overactive in insulin-deficient diabetic rats, and could contribute to the compensatory hyperphagia and reduced energy expenditure, and pituitary dysfunction found in these animals; overactivity of these NPY neurons may be due to reduction of insulin's normal inhibitory effect. The ARC PVN projection is also stimulated in rat models of obesity +/- non-insulin diabetes, possibly because the hypothalamus is resistant to inhibition by insulin; in these animals, enhanced activity of ARC NPY neurons could cause hyperphagia, reduced energy expenditure, and obesity, and perhaps contribute to hyperinsulinemia and altered pituitary secretion. Overall, these findings suggest that NPY released in the hypothalamuss, especially from the ARC-PVN projection, plays a key role in the hypothalamic regulation of energy balance and metabolism. NPY is also found in the human hypothalamus. Its roles (if any) in human homeostasis and glucoregulation remain enigmatic, but the animal studies have identified it as a potential target for new drugs to treat obesity and perhaps NIDDM.
引用
收藏
页码:757 / 771
页数:15
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