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脂肪细胞中NADPH氧化酶4的减少有助于双氢青蒿素的抗肥胖作用。

Reduction of NADPH oxidase 4 in adipocytes contributes to the anti-obesity effect of dihydroartemisinin.

作者信息

Hua Hu, Wu Mengqiu, Wu Tong, Ji Yong, Jin Lv, Du Yang, Zhang Yue, Huang Songming, Zhang Aihua, Ding Guixia, Liu Qianqi, Jia Zhanjun

机构信息

Department of Nephrology, Children's Hospital of Nanjing Medical University, Nanjing, China.

Nanjing Key Laboratory of Pediatrics, Children's Hospital of Nanjing Medical University, Nanjing, China.

出版信息

Heliyon. 2023 Feb 25;9(3):e14028. doi: 10.1016/j.heliyon.2023.e14028. eCollection 2023 Mar.

Abstract

Artemisinin derivatives have been found to have anti-obesity effects recently, but the mechanism is still controversial. Herein, long-term DHA treatment in obese mice significantly reduced the body weight and improved glucose metabolism. However, short-term DHA treatment did not affect glucose metabolism in obese mice, suggesting that the improved glucose metabolism in mice with DHA treatment could be secondary to body weight reduction. Consistent with previous reports, we observed that DHA inhibited the differentiation of adipocytes. Mechanistically, DHA significantly reduced the expression of NADPH oxidase 4 (NOX4) in white adipose tissue (WAT) of mice and differentiated adipocytes, and using NOX4 siRNA or the NOX4 inhibitor GKT137831 significantly attenuated adipocyte differentiation. Over-expression of NOX4 partially reversed the inhibition effect of DHA on adipogenic differentiation of preadipocytes. In addition, targeted proteomics analysis showed that DHA improved the abnormality of metabolic pathways. In conclusion, DHA significantly reduced fat mass and improved glucose metabolism in obese mice, possibly by inhibiting NOX4 expression to suppress adipocyte differentiation and lipid accumulation in adipocytes.

摘要

近年来发现青蒿素衍生物具有抗肥胖作用,但其机制仍存在争议。在此,对肥胖小鼠进行长期二十二碳六烯酸(DHA)治疗可显著降低体重并改善葡萄糖代谢。然而,短期DHA治疗对肥胖小鼠的葡萄糖代谢并无影响,这表明DHA治疗小鼠葡萄糖代谢的改善可能继发于体重减轻。与先前报道一致,我们观察到DHA抑制脂肪细胞分化。从机制上讲,DHA显著降低了小鼠白色脂肪组织(WAT)和分化脂肪细胞中NADPH氧化酶4(NOX4)的表达,使用NOX4小干扰RNA(siRNA)或NOX4抑制剂GKT137831可显著减弱脂肪细胞分化。NOX4的过表达部分逆转了DHA对前脂肪细胞成脂分化的抑制作用。此外,靶向蛋白质组学分析表明DHA改善了代谢途径的异常。总之,DHA可显著减少肥胖小鼠的脂肪量并改善葡萄糖代谢,可能是通过抑制NOX4表达来抑制脂肪细胞分化和脂肪细胞内脂质积累实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c36f/10006843/0cb64e012309/gr1.jpg

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