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机构地区:[1]白云区人民医院,广东广州510500 [2]暨南大学药学院,广东广州510632
出 处:《中国新药与临床杂志》2011年第6期449-452,共4页Chinese Journal of New Drugs and Clinical Remedies
基 金:广州市白云区科技计划项目(2009-sz-13)
摘 要:目的探讨茶多酚对奥氮平诱导肥胖大鼠的减肥作用及其机制。方法 SD雌性大鼠50只,随机分为正常对照组(10只)和奥氮平诱导肥胖模型组(40只)。肥胖模型组于黑暗时相前1h奥氮平1.2 mg·kg^(-1)·d^(-1)灌胃,正常对照组给予等容量蒸馏水,连续2 wk。于wk 3开始,再将肥胖模型大鼠随机分为4组:模型组、西布曲明(2.5 mg·kg^(-1)·d^(-1))组、茶多酚低(150 mg·kg^(-1)·d^(-1))剂量组和茶多酚高(300 mg·kg^(-1)·d^(-1))剂量组,每组10只。连续给药5 wk。观察大鼠体重、肾和子宫周围脂肪湿重,计算Lee's指数和脂肪系数,测定血清瘦素、脂联素水平以及超氧化物歧化酶(SOD)活性和丙二醛(MDA)含量。结果与正常对照组相比,模型组大鼠体重和脂肪湿重及Lee's指数和脂肪系数均增加,血清瘦素水平升高,脂联素水平降低(P<0.05)。与模型组比较,茶多酚低、高剂量组大鼠体重和脂肪湿重降低,Lee's指数、脂肪系数降低,SOD活性增加,MDA含量减少(P<0.05)。与模型组比较,茶多酚高剂量组血清脂联素水平升高(P<0.05),瘦素水平无显著差异(P>0.05)。结论茶多酚对奥氮平诱导的肥胖大鼠有减肥作用,其作用机制可能与增强脂联素的调节和提高抗氧化能力有关。AIM To study the anti-obesity effects of tea polyphenols (TP) on olanzapine induced weight gain in rats and its mechanism. METHODS Fifty female SD rats were randomized into 2 groups, 10 rats in the normal control group and 40 rats in the obesity model group. The obesity model rats received olanzapine (1.2 mg·kg^-1·d^-1) daily via gavage 1 h before the beginning of the dark-phase for 2 weeks, while the rats in the normal control group received an equivalent volume of distilled water. At the beginning of wk 3, the obesity model rats were randomized into 4 groups: model group (distilled water), sibutramine (2.5 mg·kg^-1·d^-1)group, low-dose (150 mg·kg^-1·d^-1) group and high-dose (300 mg·kg^-1·d^-1) group of TP, 10 rats in each group, and the rats were administered with olanzapine continuously. TP and sibutramine were given by garage for 5 weeks. The body weight and fat weight around the kidney and uterus were measured, and Lee' s index and fat coefficient were calculated. The levels of serum leptin and adiponectin (ADP) , superoxide dismutase (SOD) activity and malondialchehyche (MDA) content were tested respectively. RESULTS Compared with the normal control group, the body weight, fat weight, Lee' s index, fat coefficient, the level of serum leptin were significantly increased and serum ADP decreased significantly in the model group (P 〈 0.05). Compared with the model group, the body weight, fat weight, Lee' s index, fat coefficient and the content of MDA decreased significantly, while the SOD activity increased significantly in the low-dose group and high-dose group of TP (P 〈 0.05). Compared with the model grouP, the level of serum ADP increased significantly in the high-dose group (P 〈 0.05) , but there was no obvious difference in the level of leptin (P 〉 0.05) . CONCLUSION TP can reduce olanzapine induced weight gain in rats, which may be associated with the enhanced regulation of ADP and antioxidative ability.
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