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揭示食用根茎类植物生物活性皂苷对抗肥胖的分子机制。

Revealing Molecular Mechanisms of the Bioactive Saponins from Edible Root of in Combating Obesity.

作者信息

Han Bincheng, Luo Jinhai, Xu Baojun

机构信息

Guangdong Provincial Key Laboratory IRADS and Department of Life Sciences, BNU-HKBU United International College, Zhuhai 519087, China.

出版信息

Plants (Basel). 2024 Apr 17;13(8):1123. doi: 10.3390/plants13081123.

Abstract

Obesity has emerged as a significant health concern, as it is a disease linked to metabolic disorders in the body and is characterized by the excessive accumulation of lipids. As a plant-derived food, (PG) was reported by many studies, indicating that the saponins from PG can improve obesity effectively. However, the anti-obesity saponins from PG and its anti-obesity mechanisms have not been fully identified. This study identified the active saponins and their molecular targets for treating obesity. The TCMSP database was used to obtain information on 18 saponins in PG. The anti-obesity target of the PG saponins was 115 targets and 44 core targets. GO and KEGG analyses using 44 core anti-obesity genes and targets of PG-active saponins screened from GeneCards, OMIM, Drugbank, and DisGeNet showed that the PI3K-Akt pathway, the JAK-STAT pathway, and the MAPK pathway were the major pathways involved in the anti-obesity effects of PG saponins. BIOVIA Discovery Studio Visualizer and AutoDock Vina were used to perform molecular docking and process the molecular docking results. The molecular docking results showed that the active saponins of PG could bind to the major therapeutic obesity targets to play an obesity-inhibitory role. The results of this study laid the foundation for further research on the anti-obesity saponins in PG and their anti-obesity mechanism and provided a new direction for the development of functional plant-derived food. This research studied the molecular mechanism of PG saponins combating obesity through various signaling pathways, and prosapogenin D can be used to develop as a new potential anti-obesity drug.

摘要

肥胖已成为一个重大的健康问题,因为它是一种与身体代谢紊乱相关的疾病,其特征是脂质过度积累。作为一种植物源性食物,许多研究报道了(PG),表明PG中的皂苷可以有效改善肥胖。然而,PG中的抗肥胖皂苷及其抗肥胖机制尚未完全明确。本研究确定了治疗肥胖的活性皂苷及其分子靶点。利用中药系统药理学数据库与分析平台(TCMSP)获取PG中18种皂苷的信息。PG皂苷的抗肥胖靶点有115个,核心靶点有44个。使用从基因卡片(GeneCards)、在线人类孟德尔遗传数据库(OMIM)、药物银行(Drugbank)和疾病基因数据库(DisGeNet)筛选出的44个PG活性皂苷的核心抗肥胖基因和靶点进行基因本体(GO)和京都基因与基因组百科全书(KEGG)分析,结果表明磷脂酰肌醇-3激酶-蛋白激酶B(PI3K-Akt)信号通路、Janus激酶-信号转导和转录激活因子(JAK-STAT)信号通路以及丝裂原活化蛋白激酶(MAPK)信号通路是PG皂苷抗肥胖作用的主要信号通路。使用BIOVIA Discovery Studio Visualizer和AutoDock Vina进行分子对接并处理分子对接结果。分子对接结果表明,PG活性皂苷可与主要的肥胖治疗靶点结合,发挥抑制肥胖的作用。本研究结果为进一步研究PG中的抗肥胖皂苷及其抗肥胖机制奠定了基础,为功能性植物源性食品的开发提供了新方向。本研究通过各种信号通路研究了PG皂苷对抗肥胖的分子机制,原皂苷元D可开发成为一种新的潜在抗肥胖药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6d0/11053671/bbafd3a08392/plants-13-01123-g001.jpg

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