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乳酰基六氢吡啶和乳酰基千里光宁通过调节脂代谢改善游离脂肪酸诱导的 HepG2 细胞脂肪变性。

Lactucin & Lactucopicrin ameliorates FFA-induced steatosis in HepG2 cells via modulating lipid metabolism.

机构信息

School of Pharmacy, Xinjiang Medical University, Urumqi 830017, Xinjiang, China.

Central Laboratory, Xinjiang Medical University, Urumqi, 830011, Xinjiang, China.

出版信息

J Pharmacol Sci. 2022 Oct;150(2):110-122. doi: 10.1016/j.jphs.2022.07.007. Epub 2022 Aug 6.

Abstract

Non-alcoholic fatty liver disease (NAFLD) is one of the most common chronic liver diseases, and there are no effective drugs available so far. Lactucin and Lactucopicrin belong to sesquiterpene lactones and are extracted from Cichorium glandulosum Boiss. et Huet (CG) possesses multiple biopharmacological activities. However, the therapeutic effects of both Lactucin and Lactucopicrin on many diseases and their underlying mechanisms remain largely unknown. Here, we analyzed the both natural compounds hypolipidemic effects on FFA-induced HepG2 cells and their potential mechanisms based on transcriptomics and experimental tests. Our results indicated that Lactucin (10 μM) and Lactucopicrin (20 μM) remarkably reduced TG accumulation. Transcriptomics analysis identified 1960, 1645, and 1791 differentially expressed genes (DEGs) and obtained 611 and 635 specific genes in different comparisons, respectively. The enrichment analysis and experimental validations (RT-qPCR and Western Blot) showed that their hypolipidemic activities were most probably exerted via regulating numerous key DEGs involved in lipid metabolism. Taken together, both Lactucin and Lactucopicrin may represent potent hepatoprotective agents. Both of them exhibited therapeutic effects against liver diseases such as NAFLD by regulating multi-gene and proteins like HADHA, ADAM17, SQSTM1, and GBA and modulating multi-pathways like fatty acid oxidation metabolic signaling.

摘要

非酒精性脂肪性肝病 (NAFLD) 是最常见的慢性肝病之一,目前尚无有效的治疗药物。 菊苣内酯和菊苣酸属于倍半萜内酯,从菊苣腺毛 (CG) 中提取,具有多种生物药理学活性。 然而,菊苣内酯和菊苣酸对许多疾病的治疗效果及其潜在机制在很大程度上仍不清楚。 在这里,我们根据转录组学和实验测试分析了这两种天然化合物对 FFA 诱导的 HepG2 细胞的降血脂作用及其潜在机制。 我们的结果表明,菊苣内酯 (10 μM) 和菊苣酸 (20 μM) 可显著减少 TG 积累。 转录组学分析鉴定了 1960、1645 和 1791 个差异表达基因 (DEGs),并分别在不同比较中获得了 611 和 635 个特异性基因。 富集分析和实验验证 (RT-qPCR 和 Western Blot) 表明,它们的降血脂活性可能是通过调节参与脂质代谢的许多关键 DEGs 发挥作用的。 综上所述,菊苣内酯和菊苣酸可能都代表有效的肝保护剂。 它们通过调节 HADHA、ADAM17、SQSTM1 和 GBA 等多种基因和蛋白质,并调节脂肪酸氧化代谢信号等多种途径,对 NAFLD 等肝脏疾病表现出治疗作用。

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