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小檗碱通过抑制脂肪储存和调节人前脂肪细胞和代谢综合征患者的脂肪因子谱来改善胰岛素敏感性。

Berberine improves insulin sensitivity by inhibiting fat store and adjusting adipokines profile in human preadipocytes and metabolic syndrome patients.

机构信息

First Affiliated Hospital, Shanxi University of Medical, Taiyuan 030001, China.

出版信息

Evid Based Complement Alternat Med. 2012;2012:363845. doi: 10.1155/2012/363845. Epub 2012 Mar 8.

Abstract

Berberine is known to inhibit the differentiation of 3T3-L1 cells in vitro, improve glycemic control, and attenuate dyslipidemia in clinical study. The aim of this study was to investigate the effects of berberine on preadipocytes isolated from human omental fat and in metabolic syndrome patients treated with berberine for 3 months. We have shown that treatment with 10 μM berberine resulted in a major inhibition of human preadipocyte differentiation and leptin and adiponectin secretion accompanied by downregulation of PPARγ2, C/EBPα, adiponectin, and leptin mRNA expression. After 3 months of treatment, metabolic syndrome patients showed decrease in their BMI (31.5 ± 3.6 versus 27.4 ± 2.4 kg/m(2)) and leptin levels (8.01 versus 5.12 μg/L), as well as leptin/adiponectin ratio and HOMA-IR. These results suggest that berberine improves insulin sensitivity by inhibiting fat store and adjusting adipokine profile in human preadipocytes and metabolic syndrome patients.

摘要

小檗碱已知可抑制 3T3-L1 细胞的体外分化,改善血糖控制,并在临床研究中减轻血脂异常。本研究旨在探讨小檗碱对人网膜脂肪来源前体脂肪细胞的影响,以及对接受小檗碱治疗 3 个月的代谢综合征患者的影响。我们已经表明,用 10 μM 小檗碱处理可显著抑制人前体脂肪细胞的分化和瘦素及脂联素的分泌,并伴有 PPARγ2、C/EBPα、脂联素和瘦素 mRNA 表达下调。经过 3 个月的治疗,代谢综合征患者的 BMI(31.5 ± 3.6 对 27.4 ± 2.4 kg/m2)和瘦素水平(8.01 对 5.12 μg/L),以及瘦素/脂联素比值和 HOMA-IR 均有所下降。这些结果表明,小檗碱通过抑制脂肪储存和调节人前体脂肪细胞和代谢综合征患者的脂肪细胞因子谱来改善胰岛素敏感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3adb/3310165/ad20090a70f1/ECAM2012-363845.001.jpg

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