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在糖尿病的Zucker大鼠模型中,压痛先于2型疾病的发生。

Pressure pain precedes development of type 2 disease in Zucker rat model of diabetes.

作者信息

Romanovsky Dmitry, Walker James C, Dobretsov Maxim

机构信息

Department of Anesthesiology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.

出版信息

Neurosci Lett. 2008 Nov 21;445(3):220-3. doi: 10.1016/j.neulet.2008.08.087. Epub 2008 Sep 5.

Abstract

Decreased hind limb pressure pain threshold (PPT) is an early indicator of insulinopenia and neuropathy developing in STZ-rat models of type 1 diabetes and pre-diabetes. To test if pain on pressure is also a hallmark of compensated insulin resistance and type 2 diabetes in this work we measured PPT of Zucker lean (ZL), Zucker fatty (ZF) and Zucker fatty diabetic rats (ZDF; 8 animals per group). Using clinically accepted cut-off values for diagnosis of human diabetes and pre-diabetes, at 6th week of age (the study entry), all animals maintained random blood glucose within a normal range (< 7.9 mM). Over the following 4 weeks, the random glucose remained normal in lean and ZF rats; it however crossed 11 mM cut-off for the diagnosis of diabetes in all ZDF rats. With no detectable relation to blood glucose levels or changes throughout the study, lean, ZF and ZDF rats maintained respectively highest, intermediate and lowest PPT levels (83+/-1, 70+/-1 and 59+/-1 g; mean values for all tests per group). Thus in Zucker rat model, type 2 diabetes-associated impairment of nerve function precedes the development of hyperglycemia. Furthermore, since normoglycemic, but displaying decreased PPT, ZF rats were strongly hyperinsulinemic (plasma insulin concentration 30+/-4 ng/ml vs. 2.4+/-0.3 ng/ml in lean rats) these data suggest that hyperinsulinemia compensating for glucose metabolism might not restore compromised nerve function.

摘要

后肢压力疼痛阈值(PPT)降低是1型糖尿病和糖尿病前期的链脲佐菌素(STZ)大鼠模型中胰岛素缺乏和神经病变发展的早期指标。为了测试压力疼痛是否也是代偿性胰岛素抵抗和2型糖尿病的一个标志,在本研究中,我们测量了正常体重的 Zucker 大鼠(ZL)、肥胖 Zucker 大鼠(ZF)和肥胖 Zucker 糖尿病大鼠(ZDF;每组8只动物)的PPT。使用临床认可的人类糖尿病和糖尿病前期诊断临界值,在6周龄(研究开始时),所有动物的随机血糖维持在正常范围内(<7.9 mM)。在接下来的4周里,正常体重和ZF大鼠的随机血糖保持正常;然而,所有ZDF大鼠的随机血糖超过了糖尿病诊断的11 mM临界值。在整个研究过程中,PPT与血糖水平或变化没有可检测到的关系,正常体重、ZF和ZDF大鼠分别保持最高、中等和最低的PPT水平(83±1、70±1和59±1 g;每组所有测试的平均值)。因此,在Zucker大鼠模型中,2型糖尿病相关的神经功能损害先于高血糖的发展。此外,由于血糖正常但PPT降低的ZF大鼠胰岛素水平很高(血浆胰岛素浓度为30±4 ng/ml,而正常体重大鼠为2.4±0.3 ng/ml),这些数据表明,代偿葡萄糖代谢的高胰岛素血症可能无法恢复受损的神经功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ab/2585493/a055004478f4/nihms77591f1.jpg

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