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作 者:朱亭[1] 谢宇[1] 刘娟[1] 钟毅[2] 丁国宪[1]
机构地区:[1]南京医科大学第一附属医院老年医学科,江苏南京210029 [2]中国药科大学药化教研室,江苏南京210009
出 处:《南京医科大学学报(自然科学版)》2008年第8期968-972,共5页Journal of Nanjing Medical University(Natural Sciences)
基 金:国家自然科学基金资助(30570878)
摘 要:目的:观察BVT.2733对饮食诱导的肥胖小鼠胰岛素抵抗及炎症指标的影响。方法:建立饮食诱导的肥胖模型小鼠,并将其分为肥胖组和BVT.2733治疗组。肥胖组给予安慰剂;治疗组给予BVT.2733灌胃两周,另设正常饲养的小鼠为正常组,检测小鼠体内代谢及炎症相关指标,观察三组小鼠在胰岛素抵抗以及炎症方面的差异。结果:与正常组相比,肥胖组小鼠脂肪细胞明显增大,体重增加,空腹血糖、血清胰岛素及TNF-α升高,脂肪组织TLR4 mRNA表达增高,经BVT.2733治疗后,肥胖鼠脂肪细胞体积减小,体重减轻,空腹血糖、血清胰岛素明显下降,脂肪组织TLR4 mRNA表达减少,而血TNF-α没有显著变化。结论:BVT.2733能改善肥胖小鼠的胰岛素抵抗并且降低脂肪组织TLR4 mRNA的表达,而对于血清TNF-α水平没有明显的影响。Objective:To investigate the effect of BVT.2733 on insulin resistance (IR) and inflammation in diet-induced obesity (DIO)mice. Methods:Male mice were divided into normal mice and model mice after fed with normal diet and high-fat diet for 20 weeks,respectively. The model mice were subdivided into BVT.2733 mice administrated with BVT.2733 and obesity mice with placebo for 2 weeks. Indexes related with metabolism and inflammation were measured. Results:Compared with normal mice, adipocytes were significantly enlarged in obesity mice, and body weight also increased. Similarly, blood glucose, serum insulin and TNF-α, the expression of TLR4 mRNA in adipose tissue were all increased. After administration of BVT.2733,adipocytes were diminished; body weight, blood glucose,serum insulin,and the expression of TLR4 mRNA in adipose tissue were all decreased. But there was no significant change in serum TNF-α. Conclusion:BVT.2733 can improve IR and decrease the expression of TLR4 mRNA in adipose tissue,but have little effect on serum TNF-α in DIO mice.
关 键 词:肥胖 胰岛素抵抗 炎症 11β-HSD1抑制剂
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