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在饮食诱导的肥胖过程中,脂肪量增加并不会降低胃饥饿素的分泌。

Ghrelin secretion is not reduced by increased fat mass during diet-induced obesity.

作者信息

Qi Xiang, Reed Jason T, Wang Guiyun, Han Song, Englander Ella W, Greeley George H

机构信息

Department of Surgery, University of Texas Medical Branch, 301 Univ. Blvd., Galveston, TX 77555, USA.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2008 Aug;295(2):R429-35. doi: 10.1152/ajpregu.90329.2008. Epub 2008 May 21.

Abstract

Ghrelin is a stomach hormone that stimulates growth hormone (GH) secretion, adiposity, and food intake. Gastric ghrelin production and secretion are regulated by caloric intake; ghrelin secretion increases during fasting, decreases with refeeding, and is reduced by diet-induced obesity. The aim of the present study was to test the hypotheses that 1) an increase in body adiposity will play an inhibitory role in the reduction of gastric ghrelin synthesis and secretion during chronic ingestion of a high-fat (HF) diet and 2) chronic ingestion of an HF diet will suppress the rise in circulating ghrelin levels in response to acute fasting. Adult male Sprague-Dawley rats were fed a standard AIN-76A (approximately 5-12% of calories from fat) or an HF (approximately 45% of calories from fat) diet. The effect of increased adiposity on gastric ghrelin homeostasis was assessed by comparison of stomach ghrelin production and plasma ghrelin levels in obese and nonobese rats fed the HF diet. HF diet-fed, nonobese rats were generated by administration of triiodothyronine to lower body fat accumulation. Our findings indicate that an increased fat mass per se does not exert an inhibitory effect on ghrelin homeostasis during ingestion of the HF diet. Additionally, the magnitude of change in plasma ghrelin in response to fasting was not blunted, indicating that a presumed, endogenous signal for activation of ingestive behavior remains intact, despite excess stored calories in HF-fed rats.

摘要

胃饥饿素是一种胃激素,可刺激生长激素(GH)分泌、促进肥胖及增加食物摄入量。胃饥饿素的产生和分泌受热量摄入调节;禁食期间胃饥饿素分泌增加,重新进食时减少,且饮食诱导的肥胖会使其分泌减少。本研究的目的是检验以下假设:1)在长期摄入高脂(HF)饮食期间,身体肥胖程度增加将对胃饥饿素合成和分泌的减少起抑制作用;2)长期摄入HF饮食将抑制因急性禁食引起的循环胃饥饿素水平升高。成年雄性Sprague-Dawley大鼠分别喂食标准AIN-76A饮食(约5-12%的热量来自脂肪)或HF饮食(约45%的热量来自脂肪)。通过比较喂食HF饮食的肥胖和非肥胖大鼠的胃饥饿素产生情况及血浆胃饥饿素水平,评估肥胖程度增加对胃饥饿素稳态的影响。通过给予三碘甲状腺原氨酸以降低体脂积累,培育出喂食HF饮食的非肥胖大鼠。我们的研究结果表明,在摄入HF饮食期间,脂肪量增加本身对胃饥饿素稳态并无抑制作用。此外,禁食引起的血浆胃饥饿素变化幅度并未减弱,这表明尽管喂食HF饮食的大鼠体内储存了过多热量,但假定的激活摄食行为的内源性信号仍然完整。

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