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通过高脂喂养诱导β细胞功能异常大鼠的基础高血糖。非胰岛素依赖型糖尿病病因和发病机制的研究模型。

Inducement by fat feeding of basal hyperglycemia in rats with abnormal beta-cell function. Model for study of etiology and pathogenesis of NIDDM.

作者信息

Pascoe W S, Storlien L H

机构信息

Garvan Institute of Medical Research, St. Vincent's Hospital, Sydney, Australia.

出版信息

Diabetes. 1990 Feb;39(2):226-33. doi: 10.2337/diab.39.2.226.

Abstract

Non-insulin-dependent diabetes mellitus (NIDDM) is a heterogenous disorder characterized by defects in insulin action and secretion. This study was aimed at developing a rat model in which these pathogenic factors might be studied. Male Wistar rats were injected at 2 days of age with 45 or 30 mg/kg streptozocin (STZ) or vehicle (control). Fasting plasma glucose and insulin levels were not significantly different between the two groups between 5 and 8 wk of age. At 8 wk, half of each group was randomly assigned to isocaloric diets high in either fat (59% of calories) or starch (70% of calories). After 1 wk on the diets, 45-mg/kg-STZ-administered fat-fed animals displayed significant fasting hyperglycemia (8.6 +/- 0.2 mM; P less than 0.01), which was exacerbated by the stress of anesthesia and/or cannulation, whereas no changes were observed in any of the other groups before (STZ starch fed, 6.7 +/- 0.1 mM; control fat fed, 6.8 +/- 0.1 mM; control starch fed; 6.4 +/- 0.1 mM) or after anesthesia and/or cannulation. In the 30-mg/kg-STZ animals, fat feeding did not significantly elevate plasma glucose concentration, but a significant hyperglycemic response was seen with anesthesia and/or cannulation. In all STZ groups, substantial impairment of glucose-induced insulin secretion was observed, particularly early-phase insulin secretion. Further studies indicated that STZ animals on a diet conferring normal insulin sensitivity (starch) maintained basal normoglycemia and mildly impaired (i.v.) glucose tolerance despite this gross insulin secretory defect.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

非胰岛素依赖型糖尿病(NIDDM)是一种异质性疾病,其特征为胰岛素作用和分泌存在缺陷。本研究旨在建立一种可用于研究这些致病因素的大鼠模型。雄性Wistar大鼠在2日龄时注射45或30mg/kg链脲佐菌素(STZ)或赋形剂(对照组)。5至8周龄时,两组大鼠的空腹血糖和胰岛素水平无显著差异。8周时,每组中的一半大鼠被随机分配至高热量饮食组,其中一组饮食富含脂肪(占热量的59%),另一组富含淀粉(占热量的70%)。饮食1周后,给予45mg/kg STZ且喂食脂肪的动物出现显著的空腹高血糖(8.6±0.2mM;P<0.01),麻醉和/或插管应激会使其加重,而在麻醉和/或插管前后,其他任何组(STZ喂食淀粉组,6.7±0.1mM;对照组喂食脂肪组,6.8±0.1mM;对照组喂食淀粉组,6.4±0.1mM)均未观察到变化。在给予30mg/kg STZ的动物中,喂食脂肪并未显著提高血浆葡萄糖浓度,但麻醉和/或插管后出现了显著的高血糖反应。在所有STZ组中,均观察到葡萄糖诱导的胰岛素分泌严重受损,尤其是早期胰岛素分泌。进一步研究表明,尽管存在严重的胰岛素分泌缺陷,但给予正常胰岛素敏感性饮食(淀粉)的STZ动物仍维持基础血糖正常,且葡萄糖耐量轻度受损(静脉注射)。(摘要截断于250字)

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