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[8-羟基二氢小檗碱改善高游离脂肪酸和高葡萄糖诱导的3T3-L1脂肪细胞胰岛素抵抗]

[8-hydroxy-dihydroberberine ameliorated insulin resistance induced by high FFA and high glucose in 3T3-L1 adipocytes].

作者信息

Xu Li-jun, Lu Fu-er, Yi Ping, Wang Zeng-si, Wei Shi-chao, Chen Guang, Dong Hui, Zou Xin

机构信息

Institute of Integrated Traditional Chinese and Western Medicine, Huazhong University of Science and Technology, Wuhan 430030, China.

出版信息

Yao Xue Xue Bao. 2009 Nov;44(11):1304-8.

Abstract

The purpose of the study is to investigate the effect of 8-hydroxy-dihydroberberine on insulin resistance induced by high free fatty acid (FFA) and high glucose in 3T3-L1 adipocytes and its possible molecular mechanism. Palmic acid or glucose in combination with insulin was used to induce insulin resistance in 3T3-L1 adipocytes. 8-Hydroxy-dihydroberberine and berberine were added to the cultured medium separately, which were considered as treated group and positive control group. The rate of glucose uptake was determined by 2-deoxy-[3H]-D-glucose method. The amount of glucose consumption in the medium was measured by glucose oxidase method. Cell growth and proliferation of 3T3-L1 adipocytes were detected with Cell Counting Kit-8 (CCK-8) assay. After incubated with palmic acid for 24 hours or glucose with insulin for 18 hours, the rate of glucose transport in 3T3-L1 adipocytes was inhibited by 67% and 58%, respectively. The amount of glucose consumption in 3T3-L1 adipose cells was decreased by 41% after cells were incubated with palmic acid for 24 h. However, the above changes were reversed by pretreatment with 8-hydroxy-dihydroberberine for 24 and 48 h. Significant difference existed between groups. Insulin resistance in 3T3-L1 adipocytes, which is induced by high FFA and high glucose, could be ameliorated by 8-hydroxy-dihydroberberine.

摘要

本研究旨在探讨8-羟基二氢小檗碱对3T3-L1脂肪细胞中高游离脂肪酸(FFA)和高糖诱导的胰岛素抵抗的影响及其可能的分子机制。采用棕榈酸或葡萄糖联合胰岛素诱导3T3-L1脂肪细胞产生胰岛素抵抗。将8-羟基二氢小檗碱和小檗碱分别加入培养基中,分别作为处理组和阳性对照组。采用2-脱氧-[3H]-D-葡萄糖法测定葡萄糖摄取率。用葡萄糖氧化酶法测定培养基中葡萄糖消耗量。用细胞计数试剂盒-8(CCK-8)检测3T3-L1脂肪细胞的生长和增殖情况。在用棕榈酸孵育24小时或用葡萄糖与胰岛素孵育18小时后,3T3-L1脂肪细胞中的葡萄糖转运率分别被抑制了67%和58%。在用棕榈酸孵育细胞24小时后,3T3-L1脂肪细胞中的葡萄糖消耗量减少了41%。然而,上述变化在经过24小时和48小时的8-羟基二氢小檗碱预处理后得到逆转。各组之间存在显著差异。8-羟基二氢小檗碱可改善高FFA和高糖诱导的3T3-L1脂肪细胞中的胰岛素抵抗。

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