Axen K V, Li X, Fung K, Sclafani A
Department of Health and Nutrition Sciences, Brooklyn College of City University of New York 11210.
Am J Physiol. 1994 Mar;266(3 Pt 2):R921-8. doi: 10.1152/ajpregu.1994.266.3.R921.
A model of non-insulin-dependent diabetes mellitus (NIDDM) has been developed in adult rats by combining bilateral electrolytic lesions of the ventromedial hypothalamus (VMH) and high fat-high sucrose diets. VMH-dietary obese rats showed fasting hyperinsulinemia (> or = 540 pM) and hypertriglyceridemia (> or = 180 mg/dl) generally within 3 wk on the protocol. Fasting hyperglycemia (> or = 10 mM) was observed in the majority of animals in seven consecutive experiments. Hyperglycemic animals showed impaired glucose tolerance despite high prevailing insulin levels. Pancreatic islets isolated from VMH-dietary obese rats showed a loss of insulin secretory response to glucose by week 5, before the onset of hyperglycemia. Islets from hyperglycemic rats no longer responded to an increase in glucose concentration and failed to suppress insulin release normally in response to 15 nM norepinephrine or to a decrease in glucose concentration. This model mimics the major characteristics of obesity-associated human NIDDM as well as several stages of its progression, rendering it useful for studying the etiology of the metabolic and secretory defects in the syndrome.
通过结合双侧腹内侧下丘脑(VMH)电解损伤和高脂肪高蔗糖饮食,在成年大鼠中建立了非胰岛素依赖型糖尿病(NIDDM)模型。VMH饮食诱导的肥胖大鼠在该方案下通常在3周内出现空腹高胰岛素血症(≥540 pM)和高甘油三酯血症(≥180 mg/dl)。在连续七次实验中,大多数动物出现空腹高血糖(≥10 mM)。尽管胰岛素水平普遍较高,但高血糖动物的葡萄糖耐量受损。从VMH饮食诱导的肥胖大鼠分离的胰岛在高血糖发作前的第5周显示对葡萄糖的胰岛素分泌反应丧失。高血糖大鼠的胰岛不再对葡萄糖浓度升高作出反应,并且在响应15 nM去甲肾上腺素或葡萄糖浓度降低时不能正常抑制胰岛素释放。该模型模拟了肥胖相关的人类NIDDM的主要特征及其进展的几个阶段,使其可用于研究该综合征中代谢和分泌缺陷的病因。