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下丘脑室旁核中的神经肽Y:协调能量代谢的中枢

Neuropeptide Y in hypothalamic paraventricular nucleus: a center coordinating energy metabolism.

作者信息

Billington C J, Briggs J E, Harker S, Grace M, Levine A S

机构信息

Department of Research, Minneapolis Department of Veterans Affairs Medical Center 55417.

出版信息

Am J Physiol. 1994 Jun;266(6 Pt 2):R1765-70. doi: 10.1152/ajpregu.1994.266.6.R1765.

Abstract

Intracerebroventricular injection of neuropeptide Y (NPY) has two effects on energy metabolism in addition to increased feeding: decreased brown fat thermogenesis and increased white fat lipoprotein lipase (LPL) enzymatic activity. We hypothesized that the paraventricular nucleus (PVN) of the hypothalamus is the controlling neural site for these responses. We further hypothesized that NPY stimulation at PVN would reduce gene expression for the critical brown fat thermogenic protein, uncoupling protein (UCP), and increase gene expression for the key white fat storage enzyme, LPL. In the first experiment, three groups of rats received injections every 6 h for 24 h (5 injections total) into the PVN:1) NPY (1 micrograms/1 microliters injection) and ad libitum food; 2) NPY (1 micrograms/1 microliters injection) and food restricted to control intake; 3) saline injection (1 microliter) and ad libitum food. Both NPY-treated groups showed significant reductions (P < 0.05) in brown fat UCP mRNA levels and marked stimulation of LPL mRNA levels relative to controls. In the second experiment, four groups of seven rats had NPY injected into the PVN:0 (vehicle control); 0.1 microgram; 0.5 microgram; and 1 microgram. Injections were made every 6 h for 24 h. There was a dose-related reduction in UCP mRNA produced by the NPY treatment. NPY treatment increased LPL mRNA, but a smooth dosing effect was not evident. The observation that NPY in the PVN can coordinate more than one component of energy metabolism is significant when considered with many reports of responsiveness of NPY activity in the arcuate nucleus-PVN neural circuit to perturbations of energy balance such as fasting and feeding, diabetes, and genetic obesity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

脑室内注射神经肽Y(NPY)除了增加摄食外,对能量代谢还有另外两种作用:降低棕色脂肪产热以及增加白色脂肪脂蛋白脂肪酶(LPL)的酶活性。我们推测下丘脑室旁核(PVN)是这些反应的神经控制部位。我们进一步推测,在PVN处刺激NPY会降低关键棕色脂肪产热蛋白解偶联蛋白(UCP)的基因表达,并增加关键白色脂肪储存酶LPL的基因表达。在第一个实验中,三组大鼠每6小时向PVN注射一次,共注射24小时(总共5次注射):1)NPY(每注射1微升含1微克)并自由摄食;2)NPY(每注射1微升含1微克)并限制食物摄入量以控制进食量;3)注射生理盐水(1微升)并自由摄食。相对于对照组,两个NPY处理组的棕色脂肪UCP mRNA水平均显著降低(P<0.05),且LPL mRNA水平受到明显刺激。在第二个实验中,四组每组7只大鼠向PVN注射NPY:0(溶剂对照);0.1微克;0.5微克;和1微克。每6小时注射一次,共注射24小时。NPY处理导致UCP mRNA呈剂量相关的降低。NPY处理增加了LPL mRNA,但未观察到明显的剂量效应。当考虑到弓状核 - PVN神经回路中NPY活性对能量平衡扰动(如禁食和进食、糖尿病和遗传性肥胖)的许多反应性报告时,PVN中的NPY能够协调能量代谢的多个组成部分这一观察结果具有重要意义。(摘要截短为250字)

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