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硫辛酸抑制 3T3-L1 脂肪细胞脂联素的产生。

Lipoic acid inhibits adiponectin production in 3T3-L1 adipocytes.

机构信息

Department of Nutrition, Food Science and Physiology, University of Navarra, Pamplona, Spain.

出版信息

J Physiol Biochem. 2013 Sep;69(3):595-600. doi: 10.1007/s13105-012-0230-7. Epub 2013 Jan 12.

Abstract

Lipoic acid (LA) is a naturally occurring compound with antioxidant properties. Recent attention has been focused on the potential beneficial effects of LA on obesity and related metabolic disorders. Dietary supplementation with LA prevents insulin resistance and upregulates adiponectin, an insulin-sensitizing adipokine, in obese rodents. The aim of this study was to investigate the direct effects of LA on adiponectin production in cultured adipocytes, as well as the potential signaling pathways involved. For this purpose, fully differentiated 3T3-L1 adipocytes were treated with LA (1-500 μM) during 24 h. The amount of adiponectin secreted to media was detected by ELISA, while adiponectin mRNA expression was determined by RT-PCR. Treatment with LA induced a dose-dependent inhibition on adiponectin gene expression and protein secretion. Pretreatment with the PI3K inhibitor LY294002 inhibited adiponectin secretion and mRNA levels, and significantly potentiated the inhibitory effect of LA on adiponectin secretion. The AMPK activator AICAR also reduced adiponectin production, but surprisingly, it was able to reverse the LA-induced inhibition of adiponectin. The JNK inhibitor SP600125 and the MAPK inhibitor PD98059 did not modify the inhibitory effect of LA on adiponectin. In conclusion, our results revealed that LA reduces adiponectin secretion in 3T3-L1 adipocytes, which contrasts with the stimulation of adiponectin described after in vivo supplementation with LA, suggesting that an indirect mechanism or some in vivo metabolic processing is involved.

摘要

硫辛酸(LA)是一种具有抗氧化特性的天然化合物。最近,人们关注 LA 对肥胖和相关代谢紊乱的潜在有益作用。肥胖啮齿动物膳食补充 LA 可预防胰岛素抵抗并上调脂联素,一种胰岛素增敏脂肪因子。本研究的目的是研究 LA 对培养脂肪细胞中脂联素产生的直接影响,以及涉及的潜在信号通路。为此,用 LA(1-500 μM)处理完全分化的 3T3-L1 脂肪细胞 24 小时。通过 ELISA 检测分泌到培养基中的脂联素量,通过 RT-PCR 测定脂联素 mRNA 表达。LA 处理诱导脂联素基因表达和蛋白分泌的剂量依赖性抑制。用 PI3K 抑制剂 LY294002 预处理可抑制脂联素分泌和 mRNA 水平,并显著增强 LA 对脂联素分泌的抑制作用。AMPK 激活剂 AICAR 也降低脂联素的产生,但令人惊讶的是,它能够逆转 LA 诱导的脂联素抑制。JNK 抑制剂 SP600125 和 MAPK 抑制剂 PD98059 不改变 LA 对脂联素的抑制作用。总之,我们的结果表明,LA 可减少 3T3-L1 脂肪细胞中脂联素的分泌,这与体内补充 LA 后描述的脂联素刺激相反,表明涉及间接机制或一些体内代谢处理。

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