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反复间歇性束缚可延缓Zucker糖尿病脂肪大鼠进食和空腹时的高血糖,并在葡萄糖耐量试验期间改善血糖恢复至基线水平——食物摄入和皮质酮的作用

Recurrent intermittent restraint delays fed and fasting hyperglycemia and improves glucose return to baseline levels during glucose tolerance tests in the Zucker diabetic fatty rat--role of food intake and corticosterone.

作者信息

Bates Holly E, Kiraly Michael A, Yue Jessica T Y, Goche Montes Danitza, Elliott Melanie E, Riddell Michael C, Matthews Stephen G, Vranic Mladen

机构信息

Department of Physiology, University of Toronto, Toronto, Canada.

出版信息

Metabolism. 2007 Aug;56(8):1065-75. doi: 10.1016/j.metabol.2007.03.015.

Abstract

Short-term elevations of stress hormones cause an increase in glycemia. However, the effect of intermittent stress on development of type 2 diabetes mellitus is unclear. We hypothesized that recurrent intermittent restraint stress would deteriorate glycemia. Male, prediabetic Zucker diabetic fatty (ZDF) rats were restrained 1 hour per day, 5 days per week for 13 weeks and compared with unstressed, age-matched diabetic controls and lean nondiabetic rats. To differentiate the effects of recurrent restraint stress per se vs restraint-induced inhibition of food intake, a pair-fed group of rats was included. Surprisingly, recurrent restraint and pair feeding delayed fed and fasting hyperglycemia, such that they were lowered 50% by restraint and 30% by pair feeding after 13 weeks. Rats that were previously restrained or pair fed had lower glucose levels during a glucose tolerance test, but restraint further improved the return of glucose to baseline compared to pair feeding (P<.05). This was despite pair-fed rats having slightly lowered food intake and body weights compared with restrained rats. Restraint and pair feeding did not alter insulin responses to an intraperitoneal glucose tolerance test (IPGTT) or fasting insulin, and did not lower plasma lipids. Interestingly, restraint normalized basal corticosterone to one third that in control and pair-fed rats, prevented increases in pretreatment corticosterone seen with pair feeding, and led to habituation of restraint-induced corticosterone responses. After 13 weeks of treatment, multiple regression analysis showed that elevations in basal corticosterone could explain approximately 20% of the variance in fed glucose levels. In summary, intermittent restraint and its adaptations delayed hyperglycemia and improved glucose control in Zucker diabetic fatty rats. These benefits can be partially explained by restraint-induced lowering of food intake, but additional improvements compared to pair feeding may involve lower overall corticosterone exposure with repeated restraint. Paradoxically, these novel investigations suggest some types of occasional stress may limit development of diabetes.

摘要

应激激素的短期升高会导致血糖升高。然而,间歇性应激对2型糖尿病发生发展的影响尚不清楚。我们推测反复间歇性束缚应激会使血糖恶化。将雄性、糖尿病前期的Zucker糖尿病肥胖(ZDF)大鼠每天束缚1小时,每周5天,持续13周,并与未应激的、年龄匹配的糖尿病对照大鼠和瘦的非糖尿病大鼠进行比较。为了区分反复束缚应激本身的作用与束缚诱导的食物摄入抑制的作用,纳入了一组配对喂养的大鼠。令人惊讶的是,反复束缚和配对喂养延缓了喂食和空腹高血糖,13周后,束缚使其降低了50%,配对喂养使其降低了30%。先前接受束缚或配对喂养的大鼠在葡萄糖耐量试验期间血糖水平较低,但与配对喂养相比,束缚进一步改善了血糖恢复到基线的情况(P<0.05)。尽管配对喂养的大鼠与束缚大鼠相比食物摄入量和体重略有降低。束缚和配对喂养并未改变腹腔内葡萄糖耐量试验(IPGTT)的胰岛素反应或空腹胰岛素水平,也未降低血脂。有趣的是,束缚使基础皮质酮水平降至对照组和配对喂养大鼠的三分之一,防止了配对喂养时预处理皮质酮的升高,并导致束缚诱导的皮质酮反应产生适应性。治疗13周后,多元回归分析表明基础皮质酮的升高可解释喂食后血糖水平约20%的变化。总之,间歇性束缚及其适应性变化延缓了Zucker糖尿病肥胖大鼠的高血糖并改善了血糖控制。这些益处部分可通过束缚诱导的食物摄入量降低来解释,但与配对喂养相比的额外改善可能涉及反复束缚导致的总体皮质酮暴露降低。矛盾的是,这些新研究表明某些类型的偶尔应激可能会限制糖尿病的发展。

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