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荜茇中的哌啶生物碱通过调节脂质代谢和激活 AMP 激活的蛋白激酶来预防高脂饮食诱导的肥胖。

Piperidine alkaloids from Piper retrofractum Vahl. protect against high-fat diet-induced obesity by regulating lipid metabolism and activating AMP-activated protein kinase.

机构信息

Department of Biomaterials Science and Engineering, Yonsei University, Seoul 120-749, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2011 Jul 22;411(1):219-25. doi: 10.1016/j.bbrc.2011.06.153. Epub 2011 Jun 29.

Abstract

The fruits of Piper retrofractum Vahl. have been used for their anti-flatulent, expectorant, antitussive, antifungal, and appetizing properties in traditional medicine, and they are reported to possess gastroprotective and cholesterol-lowering properties. However, their anti-obesity activity remains unexplored. The present study was conducted to isolate the anti-obesity constituents from P. retrofractum Vahl. and evaluate their effects in high-fat diet (HFD)-induced obese mice. Piperidine alkaloids from P. retrofractum Vahl. (PRPAs), including piperine, pipernonaline, and dehydropipernonaline, were isolated as the anti-obesity constituents through a peroxisome proliferator-activated receptor δ (PPARδ) transactivation assay. The molecular mechanism was investigated in 3T3-L1 adipocytes and L6 myocytes. PRPA treatment activated AMP-activated protein kinase (AMPK) signaling and PPARδ protein and also regulated the expression of lipid metabolism-related proteins. In the animal model, oral PRPA administration (50, 100, or 300mg/kg/day for 8weeks) significantly reduced HFD-induced body weight gain without altering the amount of food intake. Fat pad mass was reduced in the PRPA treatment groups, as evidenced by reduced adipocyte size. In addition, elevated serum levels of total cholesterol, low-density lipoprotein cholesterol, total lipid, leptin, and lipase were suppressed by PRPA treatment. PRPA also protected against the development of nonalcoholic fatty liver by decreasing hepatic triglyceride accumulation. Consistent with the in vitro results, PRPA activated AMPK signaling and altered the expression of lipid metabolism-related proteins in liver and skeletal muscle. Taken together, these findings demonstrate that PRPAs attenuate HFD-induced obesity by activating AMPK and PPARδ, and regulate lipid metabolism, suggesting their potential anti-obesity effects.

摘要

荜茇果实在传统医学中被用于治疗肠胃气胀、祛痰、镇咳、抗真菌和增进食欲,并且据报道具有胃保护和降低胆固醇的特性。然而,其抗肥胖活性尚未得到探索。本研究旨在从荜茇中分离出具有抗肥胖活性的成分,并评估其在高脂饮食(HFD)诱导肥胖小鼠中的作用。通过过氧化物酶体增殖物激活受体δ(PPARδ)转录激活测定,从荜茇中分离出具有抗肥胖活性的哌啶生物碱,包括胡椒碱、胡椒诺林和脱水胡椒诺林。在 3T3-L1 脂肪细胞和 L6 肌细胞中研究了其分子机制。PRPA 处理激活了 AMP 激活蛋白激酶(AMPK)信号和 PPARδ 蛋白,并调节了脂质代谢相关蛋白的表达。在动物模型中,口服 PRPA 给药(50、100 或 300mg/kg/天,持续 8 周)可显著减轻 HFD 诱导的体重增加,而不改变食物摄入量。PRPA 处理组脂肪垫质量减少,表现为脂肪细胞体积减小。此外,PRPA 治疗还降低了血清总胆固醇、低密度脂蛋白胆固醇、总脂质、瘦素和脂肪酶的水平。PRPA 还通过减少肝甘油三酯积累来预防非酒精性脂肪肝的发生。与体外结果一致,PRPA 激活了 AMPK 信号,并改变了肝脏和骨骼肌中脂质代谢相关蛋白的表达。综上所述,这些发现表明 PRPAs 通过激活 AMPK 和 PPARδ 来减轻 HFD 诱导的肥胖,并调节脂质代谢,提示其具有潜在的抗肥胖作用。

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