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长期饮食限制影响大鼠血浆 ghrelin 和 GOAT mRNA 水平。

Long-term dietary restriction influences plasma ghrelin and GOAT mRNA level in rats.

机构信息

Faculty of Kinesiology, University of Calgary, Calgary, Alberta, Canada.

出版信息

Physiol Behav. 2010 Apr 19;99(5):605-10. doi: 10.1016/j.physbeh.2010.01.034. Epub 2010 Feb 9.

Abstract

The objective of this study was to examine the effect of chronic dietary restriction on the physical characteristics of the intestine and gut-derived satiety hormone production. Male Wistar rats (8 weeks) were randomized to ad libitum (AL) or 35% dietary restriction (DR) for 5 months. At the end of the study, physical measurements were made on the intestine and satiety hormone secretion and mRNA expression determined. A comparison group of young, growing AL rats (5 weeks) was also examined. The adult DR rats gained less weight over 5 months and had lower fat mass than adult AL rats (p<0.05). The weight of the small intestine as a percentage of total body weight was greater in adult DR compared to adult AL but lower than young AL rats. Compared to AL, DR down-regulated proglucagon and cholecystokinin mRNA in the duodenum and ghrelin mRNA in the stomach of adult rats but was not different from young AL. Ghrelin-O-acyltransferase (GOAT) mRNA in the stomach was up-regulated 21-fold in adult AL rats compared to young AL and 14-fold compared to adult DR rats. Total and des-acyl ghrelin was approximately 50% higher in adult DR and young AL rats compared to adult AL. Plasma leptin and insulin were lower in adult DR and young AL rats compared to adult AL. Our findings suggest that long-term energy deficits continue to drive up ghrelin levels which may have profound implications for practical implementation of DR as an anti-aging or anti-obesity strategy in humans.

摘要

本研究旨在探讨慢性饮食限制对肠道物理特性和肠道来源的饱腹感激素产生的影响。雄性 Wistar 大鼠(8 周龄)被随机分为自由进食(AL)或 35%饮食限制(DR)组,进行 5 个月的喂养。在研究结束时,对肠道进行物理测量,并测定饱腹感激素的分泌和 mRNA 表达。还检查了一组年轻、生长中的 AL 大鼠(5 周龄)作为比较组。成年 DR 大鼠在 5 个月内体重增加较少,体脂量低于成年 AL 大鼠(p<0.05)。与成年 AL 大鼠相比,成年 DR 大鼠的小肠重量占体重的百分比更大,但低于年轻 AL 大鼠。与 AL 相比,DR 下调了成年大鼠十二指肠中的前胰高血糖素和胆囊收缩素 mRNA 以及胃中的胃饥饿素 mRNA,但与年轻 AL 大鼠无差异。与年轻 AL 大鼠相比,成年 AL 大鼠胃中的 ghrelin-O-酰基转移酶(GOAT)mRNA 上调了 21 倍,与成年 DR 大鼠相比上调了 14 倍。与成年 AL 大鼠相比,成年 DR 和年轻 AL 大鼠的总和去酰基 ghrelin 约高 50%。与成年 AL 大鼠相比,成年 DR 和年轻 AL 大鼠的血浆瘦素和胰岛素水平较低。我们的研究结果表明,长期能量不足继续导致 ghrelin 水平升高,这可能对将 DR 作为人类抗衰老或抗肥胖策略的实际实施产生深远影响。

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