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慢性去大脑大鼠的瘦素反应性

Leptin responsiveness in chronically decerebrate rats.

作者信息

Harris Ruth B S, Bartness Timothy J, Grill Harvey J

机构信息

Department of Foods and Nutrition, Dawson Hall, University of Georgia, Athens, GA 30602, USA.

出版信息

Endocrinology. 2007 Oct;148(10):4623-33. doi: 10.1210/en.2006-1565. Epub 2007 Jul 5.

Abstract

Peripheral infusions of physiological doses of leptin decrease body fat mass, but it is not known whether this results from direct effects on peripheral tissue or activation of central leptin receptors. In this study, we infused chronically decerebrate (CD) rats, in which the forebrain was surgically isolated from the caudal brainstem, with 60 microg leptin/d or PBS for 14 d from ip mini-osmotic pumps. The CD rats were tube fed an amount of food equivalent to the intake of ad libitum-fed intact controls or 75% of this amount to account for their reduced energy expenditure. Control rats fed ad libitum or tube fed 75, 100, or 125% of their ad libitum intake also were peripherally infused with leptin or PBS. CD rats had a lower serum testosterone, energy expenditure, and lean body mass compared with controls but had increased levels of adiponectin and leptin and were obese. Leptin increased body fat and decreased energy expenditure during the light period in 100%-fed CD rats, but not 75%-fed CD rats. Leptin decreased body fat of ad libitum- and 100%-fed but not 75%-fed or 125%-fed intact controls. Energy expenditure did not change in any control group. These results show that leptin can change body fat independent of a change in food intake or energy expenditure, that the forebrain normally prevents leptin from inhibiting energy expenditure through mechanisms initiated in the caudal brainstem or peripheral tissues, and that the leptin response in both intact and CD rats is determined by the energy status of the animal.

摘要

外周输注生理剂量的瘦素可降低体脂量,但尚不清楚这是直接作用于外周组织还是激活中枢瘦素受体的结果。在本研究中,我们通过腹腔内微型渗透泵,对慢性去大脑(CD)大鼠(其前脑通过手术与尾端脑干分离)连续14天输注60微克/天的瘦素或磷酸盐缓冲盐水(PBS)。给CD大鼠经口管饲相当于自由摄食的完整对照大鼠摄入量的食物量,或该量的75%,以考虑其能量消耗减少的情况。自由摄食或经口管饲自由摄入量的75%、100%或125%的对照大鼠也外周输注瘦素或PBS。与对照大鼠相比,CD大鼠的血清睾酮、能量消耗和去脂体重较低,但脂联素和瘦素水平升高,且肥胖。在光照期,瘦素使摄入100%食物量的CD大鼠体脂增加、能量消耗减少,但对摄入75%食物量的CD大鼠无此作用。瘦素使自由摄食和摄入100%食物量的完整对照大鼠体脂减少,但对摄入75%或125%食物量的对照大鼠无此作用。任何对照组的能量消耗均未改变。这些结果表明,瘦素可独立于食物摄入量或能量消耗的变化而改变体脂,前脑通常通过尾端脑干或外周组织启动的机制阻止瘦素抑制能量消耗,并且完整大鼠和CD大鼠的瘦素反应均由动物的能量状态决定。

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