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饥饿:早期信号、传感器及后遗症。

Starvation: early signals, sensors, and sequelae.

作者信息

Dallman M F, Akana S F, Bhatnagar S, Bell M E, Choi S, Chu A, Horsley C, Levin N, Meijer O, Soriano L R, Strack A M, Viau V

机构信息

Department of Physiology, University of California, San Francisco 94143-0444, USA.

出版信息

Endocrinology. 1999 Sep;140(9):4015-23. doi: 10.1210/endo.140.9.7001.

DOI:10.1210/endo.140.9.7001
PMID:10465271
Abstract

To identify the sequences of changes in putative signals, reception of these and responses to starvation, we sampled fed and starved rats at 2- to 6-h intervals after removal of food 2 h before dark. Metabolites, hormones, hypothalamic neuropeptide expression, fat depots, and leptin expression were measured. At 2 h, insulin decreased, and FFA and corticosterone (B) increased; by 4 h, leptin and glucose levels decreased. Neuropeptide Y messenger RNA (mRNA) increased 6 h after food removal and thereafter. Adrenal and plasma B did not follow ACTH and were elevated throughout, with a nadir at the dark-light transition. Leptin correlated inversely with adrenal B. Fat stores decreased during the last 12 h. Leptin mRNA in perirenal and sc fat peaked during the dark period, resembling plasma leptin in fed rats. We conclude that 1) within the first 4 h, hormonal and metabolic signals relay starvation-induced information to the hypothalamus; 2) hypothalamic neuropeptide synthesis responds rapidly to the altered metabolic signals; 3) catabolic activity quickly predominates, reinforced by elevated B, not driven by ACTH, but possibly to a minor extent by leptin, and more by adrenal neural activity; and 4) leptin secretion decreases before leptin mRNA or fat depot weight, showing synthesis-independent regulation.

摘要

为了确定假定信号、这些信号的接收以及对饥饿的反应中的变化序列,我们在天黑前2小时去除食物后,以2至6小时的间隔对喂食和饥饿的大鼠进行采样。测量了代谢物、激素、下丘脑神经肽表达、脂肪库和瘦素表达。2小时时,胰岛素下降,游离脂肪酸(FFA)和皮质酮(B)增加;4小时时,瘦素和葡萄糖水平下降。食物去除6小时后及之后,神经肽Y信使核糖核酸(mRNA)增加。肾上腺和血浆中的B不随促肾上腺皮质激素(ACTH)变化,且始终升高,在明暗交替时最低。瘦素与肾上腺B呈负相关。在最后12小时内脂肪储备减少。肾周和皮下脂肪中的瘦素mRNA在黑暗期达到峰值,类似于喂食大鼠的血浆瘦素。我们得出结论:1)在最初4小时内,激素和代谢信号将饥饿诱导的信息传递至下丘脑;2)下丘脑神经肽合成对改变的代谢信号迅速做出反应;3)分解代谢活动迅速占主导地位,B升高起到强化作用,并非由ACTH驱动,但可能在较小程度上由瘦素驱动,更多地由肾上腺神经活动驱动;4)瘦素分泌在瘦素mRNA或脂肪库重量下降之前就已减少,表明存在非合成依赖性调节。

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