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维生素 E 可调节饮食诱导肥胖大鼠模型脂肪细胞因子的表达。

Vitamin E regulates adipocytokine expression in a rat model of dietary-induced obesity.

机构信息

Clinical Nutrition Center, Shanghai XinHua Hospital, Shanghai 200092, China.

出版信息

Exp Biol Med (Maywood). 2010 Jan;235(1):47-51. doi: 10.1258/ebm.2009.009122.

Abstract

The aim of this study was to determine the effect of the antioxidant vitamin E (VE) on adiponectin and leptin expression in obese rats. Thirty weaning male Sprague-Dawley rats were divided into three groups as follows: (1) a control group, fed with normal chow; (2) a diet-induced obesity group (DIO), fed with a high-fat diet and (3) an intervention group, fed with a high-fat diet supplemented with VE (350 mg/kg). After 10 weeks of being fed according to these group assignments, rats were weighed and euthanized. Blood and adipose tissues were then immediately collected; mRNA and protein levels of leptin and adiponectin were measured by realtime reverse transcription-polymerase chain reaction and Western blotting. Biomarkers of oxidative stress, including serum levels of 8-epi-prostaglandin-F(2)alpha (8-epi-PGF(2)alpha) and glutathione peroxidase activity, were also examined. Adiponectin and leptin levels were lower in the DIO group than in the control group. VE intervention increased the expression of both leptin and adiponectin (P values < 0.05). Association analysis showed that serum leptin levels correlated positively with body fat mass (r = 0.601, P < 0.05). Both serum leptin and adiponectin levels were associated with the presence of serum 8-epi-PGF2 alpha (leptin, r = 0.513, P < 0.05; adiponectin, r = -0.422, P < 0.05). Administration of VE decreases leptin and adiponectin expression in obese rats. This finding is consistent with the view that antioxidants can play an important role in the treatment of obesity-related diseases.

摘要

本研究旨在探讨抗氧化维生素 E(VE)对肥胖大鼠脂联素和瘦素表达的影响。30 只断奶雄性 Sprague-Dawley 大鼠随机分为三组:(1)对照组,给予正常饲料;(2)饮食诱导肥胖组(DIO),给予高脂肪饮食;(3)干预组,给予高脂肪饮食并补充 VE(350mg/kg)。按照分组进行 10 周喂养后,称重并处死大鼠。立即采集血液和脂肪组织;通过实时逆转录-聚合酶链反应和 Western 印迹法测定瘦素和脂联素的 mRNA 和蛋白水平。还检测了氧化应激生物标志物,包括血清 8-epi-前列腺素 F2alpha(8-epi-PGF2alpha)水平和谷胱甘肽过氧化物酶活性。DIO 组大鼠的脂联素和瘦素水平低于对照组。VE 干预增加了瘦素和脂联素的表达(P 值均<0.05)。相关性分析显示,血清瘦素水平与体脂质量呈正相关(r=0.601,P<0.05)。血清瘦素和脂联素水平均与血清 8-epi-PGF2alpha 相关(瘦素,r=0.513,P<0.05;脂联素,r=-0.422,P<0.05)。VE 的给予降低了肥胖大鼠的瘦素和脂联素表达。这一发现与抗氧化剂在治疗肥胖相关疾病中发挥重要作用的观点一致。

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