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在暴露于棕榈酸酯的3T3-L1脂肪细胞中,阿萨伊因可改善葡萄糖和脂质代谢。

Aspalathin improves glucose and lipid metabolism in 3T3-L1 adipocytes exposed to palmitate.

作者信息

Mazibuko Sithandiwe E, Joubert Elizabeth, Johnson Rabia, Louw Johan, Opoku Andrew R, Muller Christo J F

机构信息

Diabetes Discovery Platform, South African Medical Research Council, Tygerberg, South Africa.

Department of Biochemistry and Microbiology, University of Zululand, Kwa-Dlangezwa, South Africa.

出版信息

Mol Nutr Food Res. 2015 Nov;59(11):2199-208. doi: 10.1002/mnfr.201500258. Epub 2015 Sep 15.

Abstract

SCOPE

Saturated-free fatty acids, such as palmitate, are associated with insulin resistance. This study aimed to establish if an aspalathin-enriched green rooibos extract (GRE) and, its major flavanoid, aspalathin (ASP) could contribute significantly to the amelioration of experimentally induced insulin resistance in 3T3-L1 adipocytes.

METHODS AND RESULTS

3T3-L1 adipocytes were cultured in DMEM containing 0.75 mM palmitate for 16 h to induce insulin resistance before treatment for 3 h with GRE (10 μg/mL) or ASP (10 μM). GRE and ASP reversed the palmitate-induced insulin resistance. At a protein level GRE and ASP suppressed nuclear factor kappa beta (NF-κB), insulin receptor substrate one (serine 307) (IRS1 (Ser (307) )) and AMP-activated protein kinase phosphorylation and increased serine/threonine kinase AKT (AKT) activation, while only GRE increased glucose transporter four (Glut4) protein expression. Peroxisome proliferator-activated receptor alpha and gamma (PPARα and γ), and carnitine palmitoyltransferase one (CPT1) expression were increased by ASP alone.

CONCLUSION

Together these effects offer a plausible explanation for the ameliorative effect of GRE and ASP on insulin-resistance, an underlying cause for obesity and type 2 diabetes.

摘要

范围

饱和游离脂肪酸,如棕榈酸酯,与胰岛素抵抗有关。本研究旨在确定富含阿萨伊因的南非红茶提取物(GRE)及其主要类黄酮阿萨伊因(ASP)是否能显著改善3T3-L1脂肪细胞实验性诱导的胰岛素抵抗。

方法与结果

将3T3-L1脂肪细胞在含有0.75 mM棕榈酸酯的DMEM中培养16小时以诱导胰岛素抵抗,然后用GRE(10μg/mL)或ASP(10μM)处理3小时。GRE和ASP逆转了棕榈酸酯诱导的胰岛素抵抗。在蛋白质水平上,GRE和ASP抑制核因子κB(NF-κB)、胰岛素受体底物1(丝氨酸307)(IRS1(Ser(307)))和AMP活化蛋白激酶的磷酸化,并增加丝氨酸/苏氨酸激酶AKT(AKT)的活化,而只有GRE增加葡萄糖转运蛋白4(Glut4)的蛋白表达。单独使用ASP可增加过氧化物酶体增殖物激活受体α和γ(PPARα和γ)以及肉碱棕榈酰转移酶1(CPT1)的表达。

结论

这些作用共同为GRE和ASP对胰岛素抵抗的改善作用提供了一个合理的解释,胰岛素抵抗是肥胖和2型糖尿病的一个潜在原因。

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