表型对wistar脂肪大鼠褐色和白色脂肪组织细胞发育及非寒战产热的影响

Orien L Tulp
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引用次数: 1

摘要

棕色脂肪组织(BAT)已经被解剖学家在尸体标本中发现了数百年,现在已知在包括人类和动物在内的恒温物种中,当饮食和环境扰动时,棕色脂肪组织是表达非寒颤产热的主要外周组织。Wistar肥胖大鼠(WFR)是一种肥胖、胰岛素抵抗(IR)和NIDDM的动物模型,在NIH/Wistar背景下表达(-fa)肥胖特征。据报道,这种染色在肥胖表型中表现出NIDDM和对饮食和环境参数的产热反应受损。将瘦肉和肥肉雄性WFR大鼠分别饲养在悬吊钢丝笼中,22 ~ 30周龄饲喂营养完全的饲粮,饲粮中CHO含量为54%,玉米淀粉(ST)和蔗糖(SUC)的比例为50:60 w/w,外加维生素、矿物质、纤维和必需微量营养素。监测体重和静息量,测定去甲肾上腺素刺激下的VO2。通过斩首处死动物,并将其肩胛骨间BAT库(IBAT)和原发白色脂肪组织(WAT)库全部切除,测量脂肪含量,包括脂肪细胞大小和每个IBAT和WAT库的数量。研究包括测量脂肪细胞脂质含量和脂肪细胞数量的WAT库,包括背(DOR),附睾(EPI)和内脏腹膜后(VRP)库。在整个研究过程中,肥胖鼠的最终体重、净增重和相对脂肪量均显著大于瘦鼠,其中VRP库中WAT细胞脂质含量和脂肪细胞数量增加最多。肥胖幼崽IBAT细胞数、IBAT组织细胞脂质含量及IBAT:BW比。两种表型的空腹血糖相似,但肥胖+NIDDM动物的空腹胰岛素和胰岛素:葡萄糖(I: G)比值明显升高。肥胖+NIDDM的静息VO2和NE的热响应。NE对两种表型的血浆葡萄糖浓度均有显著的影响,其中肥胖+NIDDM表型的增加最大。本研究结果表明,在肥胖-NIDDM动物中,IBAT和WAT的质量和细胞数量通过增生和肥厚而被夸大,而早期贪食和NIDDM斑痕的叠加(可能包括显著IR的发展)是一个促成因素。肥胖+NIDDM表型的I: G和IR升高可能进一步促进WAT和BAT仓库中的脂肪细胞增生和肥大,并可能进一步损害肥胖糖尿病动物充分表达BAT介导的NST的能力。此外,肥胖+NIDDM患者BAT质量和细胞数量的增加本身并不是饮食和环境热反应的可靠预测指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of phenotype on development of brown and white adipose tissue cellularity and nonshivering thermogenesis in the wistar fatty rat
Brown adipose tissue (BAT) has been noted in cadaveric specimens by anatomists for hundreds of years and is now known to be a primary peripheral tissue in the expression of non-shivering thermogenesis in response to perturbations in diet and environment in homeothermic species including man and animals. The Wistar Fatty Rat (WFR) is an animal model of obesity, insulin resistance (IR) and NIDDM and expresses the (-fa) obesity trait in an NIH/Wistar background. This stain has been reported to exhibit NIDDM and an impaired thermogenic response to parameters of diet and environment in the obese phenotype. Groups of lean and obese male WFR rats were maintained in hanging wire-bottomed steel cages and fed a nutritionally complete diet containing 54% CHO as equal parts cornstarch (ST) and sucrose (SUC) (50:60 w/w) plus vitamins, minerals, fiber, and essential micronutrients from 22 to 30 weeks of age. Measures of body weight were monitored and measures of resting, and norepinephrine stimulated VO2 determined. Animals were sacrificed by decapitation and the Interscapular BAT depot (IBAT) and primary white adipose tissue (WAT) depots excised in their entirety for measures of adiposity including adipocyte size and number per IBAT and WAT depots. The studies included measures of adipocyte lipid content and adipocyte number of WAT depots including the dorsal (DOR), epididymal (EPI) and visceral retroperitoneal (VRP) depots. Final Body weights, net weight gain and relative adiposity of obese were significantly greater than their lean littermates throughout the study with the greatest increase in WAT cell lipid content and adipocyte number in the VRP depot. IBAT cell number, cell lipid content of IBAT tissues and IBAT:BW ratio of obese >> lean littermates. Fasting glucose was similar in both phenotypes, but fasting insulin and the Insulin: Glucose (I: G) ratios were markedly elevated in obese+NIDDM animals. Resting VO2 and the thermic response to NE of lean >> Obese+NIDDM. A robust NE response in plasma glucose concentrations occurred in both phenotypes following NE with the greatest increase in the obese+NIDDM phenotype. The results of this study indicate that while the development of IBAT and WAT mass and cellularity became exaggerated via hyperplasia and hypertrophy in the obese-NIDDM animals, the superimposition of early hyperphagia and the NIDDM stigmata which likely includes the development of significant IR is a contributing factor. The elevations in I: G and IR of the Obese+NIDDM phenotype may further facilitate adipocyte hyperplasia and hypertrophy in both WAT and BAT depots and may further compromise the capacity of the obese diabetic animals to fully express BAT-mediated contributions to NST. Moreover, the increased BAT mass and cellularity in the Obese+NIDDM was not by itself a reliable predictor of the thermic responses to diet and environment.
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