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遗传肥胖、膳食碳水化合物和年龄对雌性SHR/N-肥胖大鼠葡萄糖耐量参数以及肾脏和肾上腺组织学的影响。

Influence of genetic obesity, dietary carbohydrate and age on parameters of glucose tolerance and kidney and adrenal gland histology in female SHR/N-corpulent rats.

作者信息

Michaelis O E, Carswell N, Velasquez M T, Kimmel P L, Abraham A A, Canary J J, Hansen C T

机构信息

Beltsville Human Nutrition Research Center, United States Department of Agriculture, MD 20705.

出版信息

Int J Obes. 1990 Nov;14(11):973-85.

PMID:2177455
Abstract

Young female obese (cp/cp) and lean littermates (?/+) of the recently developed congenic strain, SHR/NIH-corpulent (SHR/N-cp), were fed for 6.5 months isocaloric diets containing 54 percent carbohydrate as either sucrose or starch. Glycemic, lipidemic and renal parameters were determined after 1, 3 and 6 months. Systolic blood pressure and plasma corticosterone levels were determined after 3 months. After 6.5 months rats were killed for histological examination. Obese rats were hyperglycemic following an oral glucose challenge (1 hour response greater than 11.1 mmol/l) (200 mg/dl), hyperinsulinemic, hypertriglyceridemic, and developed proteinuria and mild hypertension. Feeding sucrose, as compared to starch, further increased serum glucose, insulin and triglyceride levels and urinary protein excretion in obese rats and serum triglyceride levels in lean rats. An amelioration of glucose intolerance was observed in sucrose-fed obese rats by 6 months. In contrast to serum insulin levels, serum triglyceride levels increased with age in obese rats. Obese rats exhibited hypertrophy of the kidney and adrenal cortex with abnormal histology. The study demonstrates that obese female SHR/N-cp rats exhibit some of the metabolic and histopathological changes associated with NIDDM in humans and that feeding sucrose, as the source of dietary carbohydrate, further magnifies the expression of diabetes in this model.

摘要

对新培育的近交系SHR/NIH-肥胖(SHR/N-cp)品系的年轻雌性肥胖(cp/cp)大鼠及其瘦的同窝仔鼠(?/+),给予含54%碳水化合物(分别为蔗糖或淀粉)的等热量饮食,喂养6.5个月。在1、3和6个月后测定血糖、血脂和肾脏参数。在3个月后测定收缩压和血浆皮质酮水平。6.5个月后处死大鼠进行组织学检查。肥胖大鼠口服葡萄糖后出现高血糖(1小时反应大于11.1 mmol/l)(200 mg/dl)、高胰岛素血症、高甘油三酯血症,并出现蛋白尿和轻度高血压。与淀粉相比,喂食蔗糖进一步增加了肥胖大鼠的血清葡萄糖、胰岛素和甘油三酯水平以及尿蛋白排泄,以及瘦大鼠的血清甘油三酯水平。6个月时,喂食蔗糖的肥胖大鼠的葡萄糖耐量有所改善。与血清胰岛素水平不同,肥胖大鼠的血清甘油三酯水平随年龄增加。肥胖大鼠表现出肾脏和肾上腺皮质肥大,组织学异常。该研究表明,肥胖的雌性SHR/N-cp大鼠表现出一些与人类非胰岛素依赖型糖尿病相关的代谢和组织病理学变化,并且作为膳食碳水化合物来源的蔗糖喂养进一步放大了该模型中糖尿病的表现。

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