T2DM-SHR/N-cp(肥胖)大鼠褐色脂肪组织发育的研究进展

O. Tulp
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摘要

棕色脂肪组织(BAT)在人类和动物对饮食和环境扰动的非寒战产热反应中起着重要作用。SHR/N-cp大鼠是肥胖和2型糖尿病的动物模型,有报道称其对饮食和环境参数的产热反应受损。将瘦型和肥胖型雄性SHR/N-cp大鼠饲养在钢丝网箱中,饲喂1 ~ 9月龄营养完全的饲粮,饲粮中CHO含量为54%,蛋白质含量为22%,混合脂肪含量为16.5%,必需纤维含量为4.5%,外加维生素、矿物质和必需微量元素。监测体重,并在研究结束时测定24小时尿香草扁桃酸(VMA)。动物被斩首处死,肩胛间BAT库被完整切除,以测量脂肪细胞的大小、数量和脂质含量。在整个研究过程中,肥胖的幼崽的体重、净增重和相对肥胖程度都明显高于它们的瘦崽。瘦>肥胖大鼠尿VMA。IBAT体重和IBAT体重:肥胖者体重>瘦者体重。肥胖>>瘦肉大鼠IBAT细胞数、细胞脂含量及%脂含量。本研究结果表明,虽然肥胖糖尿病动物的IBAT质量和细胞结构的发展被夸大了,但T2DM的累加,包括可能的胰岛素抵抗,可能进一步损害肥胖糖尿病动物充分表达bat介导的非寒战产热作用的能力。
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A Review of Brown Adipose Tissue Development in T2DM-SHR/N-cp (Corpulent) Rats
Brown adipose tissue (BAT) plays a significant role in the expression of non-shivering thermogenesis in response to perturbations in diet and environment in man and animals. The SHR/N-cp rat is an animal model of obesity and T2DM and has been reported to exhibit an impaired thermogenic response to parameters of diet and environment. Groups of lean and obese male SHR/N-cp rats were maintained in hanging wire-bottomed steel cages and fed a nutritionally complete diet containing 54% CHO, 22% protein,16.5% mixed fats, and 4.5% essential fiber, plus vitamins, minerals, and essential micronutrients from 1 to 9 months of age. Measures of body weight were monitored and 24-hour urinary vanil mandelic acid (VMA) were determined at the end of the study. Animals were sacrificed by decapitation and the Interscapular BAT depots excised in their entirety for measures of adipocyte size, number, and lipid content. Bode weights, net weight gain and relative adiposity of Obese was significantly greater than their lean littermates throughout the study. Urinary VMA of lean > obese rats. The IBAT weight and IBAT weight: Body weight of obese >> lean. IBAT cell number, cell lipid content and % lipid of IBAT tissues of obese >> lean rats. The results of this study indicate that while the development of IBAT mass and cellularity becomes exaggerated in the obese-diabetic animals, the superimposition of the T2DM stigmata including likely insulin resistance may further compromise the capacity of the obese diabetic animals to fully express BAT-mediated contributions to nonshivering thermogenesis .
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