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中文处方抗糖丸对 2 型糖尿病 db/db 小鼠脂代谢的影响。

Effect of Chinese prescription Kangen-karyu on lipid metabolism in type 2 diabetic db/db mice.

机构信息

Institute of Natural Medicine, University of Toyama, Sugitani, Toyama, Japan.

出版信息

J Ethnopharmacol. 2010 Jun 16;129(3):299-305. doi: 10.1016/j.jep.2010.03.032. Epub 2010 Apr 2.

Abstract

AIM OF THE STUDY

Chinese prescription Kangen-karyu is clinically used as a treatment for cardiovascular diseases, and we have reported the beneficial effects on chemically induced hyperlipidemic animal models. The present study was investigated to evaluate the hypolipidemic effect of Kangen-karyu in type 2 diabetic db/db mice which has not been explored yet.

MATERIALS AND METHODS

Male db/db mice were divided into three groups, vehicle (control), Kangen-karyu 100, or 200 mg/kg body weight/day, and orally administered for 5 weeks every day. Age-matched non-diabetic m/m mice were used as a normal group.

RESULTS

Serum triglyceride (TG) and total cholesterol levels in db/db mice were increased compared with those of m/m mice. However, the administration of Kangen-karyu reduced hyperlipidemia in db/db mice through a decline in the serum levels of TG and total cholesterol. The hepatic TG and total cholesterol levels of db/db mice were markedly higher than those of m/m mice, but these elevated lipid levels were significantly reduced by 200 mg/kg Kangen-karyu administration. Also, oil red O staining showed that the increased lipid deposition level in the liver of db/db control mice was improved by Kangen-karyu administration. The expression of sterol regulatory element-binding protein-1 in the liver of db/db mice was significantly down-regulated by the administration of Kangen-karyu at a dose of 200 mg/kg body weight. Kangen-karyu caused a slight elevation in the expression of peroxisome proliferator-activated receptor alpha in the liver of db/db mice.

CONCLUSIONS

This study provides scientific evidence that Kangen-karyu improves hyperlipidemia and lipid deposition via the regulation of hepatic SREBP-1 expression in type 2 diabetic db/db mice.

摘要

目的

中药方剂“还原精”临床上用于治疗心血管疾病,我们已报道其对化学诱导的高脂血症动物模型具有有益作用。本研究旨在评估还原精对尚未研究过的 2 型糖尿病 db/db 小鼠的降血脂作用。

材料与方法

雄性 db/db 小鼠分为三组,即 vehicle(对照组)、还原精 100 或 200mg/kg 体重/天,每天口服给药 5 周。年龄匹配的非糖尿病 m/m 小鼠作为正常组。

结果

与 m/m 小鼠相比,db/db 小鼠的血清三酰甘油(TG)和总胆固醇水平升高。然而,还原精的给药降低了 db/db 小鼠的高脂血症,表现为血清 TG 和总胆固醇水平降低。db/db 小鼠的肝 TG 和总胆固醇水平明显高于 m/m 小鼠,但还原精 200mg/kg 给药可显著降低这些升高的脂质水平。此外,油红 O 染色显示,db/db 对照组小鼠肝脏中脂质沉积水平的增加通过还原精给药得到改善。还原精给药剂量为 200mg/kg 时,db/db 小鼠肝脏中固醇调节元件结合蛋白-1 的表达显著下调。还原精给药还使 db/db 小鼠肝脏中过氧化物酶体增殖物激活受体α的表达略有升高。

结论

本研究提供了科学证据,表明还原精通过调节 2 型糖尿病 db/db 小鼠肝脏中 SREBP-1 的表达来改善高脂血症和脂质沉积。

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