痛苦
芹菜素
化学
药理学
啮齿动物
受体
类黄酮
生物
生物化学
生态学
政治学
政治
法学
抗氧化剂
作者
Shamima Khatoon,Nabanita Das,Sourav Chattopadhyay,Amit Joharapurkar,Abhinav Singh,Vishal Patel,Abhishek Nirwan,Akhilesh Kumar,Madhav Nilakanth Mugale,Durga Prasad Mishra,Jagavelu Kumaravelu,Rajdeep Guha,Mukul Rameshchandra Jain,Naibedya Chattopadhyay,Sabyasachi Sanyal
标识
DOI:10.1016/j.ejphar.2024.176800
摘要
Adiponectin plays key roles in energy metabolism and ameliorates inflammation, oxidative stress, and mitochondrial dysfunction via its primary receptors, adiponectin receptors -1 and 2 (AdipoR1 and AdipoR2). Systemic depletion of adiponectin causes various metabolic disorders, including MASLD; however adiponectin supplementation is not yet achievable owing to its large size and oligomerization-associated complexities. Small-molecule AdipoR agonists, thus, may provide viable therapeutic options against metabolic disorders. Using a novel luciferase reporter-based assay here, we have identified Apigenin-6-C-glucoside (ACG), but not apigenin, as a specific agonist for the liver-rich AdipoR isoform, AdipoR2 (EC
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