代谢综合征
核受体
受体
脂肪组织
转录因子
代谢途径
生物信息学
脂肪细胞
信号转导
内分泌学
糖尿病
内科学
化学
机制(生物学)
作用机理
肝X受体
病理生理学
胰岛素受体
神经科学
代谢活性
胰岛素抵抗
生物
胰岛素
医学
表型
计算生物学
葡萄糖摄取
脂质代谢
褐色脂肪组织
作者
Swati Singh,Rohini Agrawal
标识
DOI:10.1080/15257770.2026.2620694
摘要
Metabolic Syndrome can be defined as a cluster of abnormalities which includes obesity, dyslipidemia, hypertension, and insulin resistance. The intricate connections between genetic and environmental variables are involved in the development of metabolic syndrome (MetS). Nuclear receptors (NR), a family of transcription factors, are the key participants in onset and progression of MetS because their major mechanism of action is to modulate various metabolic pathways. The main characteristic features of MetS include abnormal distribution of adipose tissue, aberrant lipid profiles, decreased glucose tolerance, and inflammation, and these all develop due to dysregulation of NR signaling. This review is an attempt to understand the principles of molecular mechanisms and functions of nuclear receptors that can be utilized in the treatment of MetS, because numerous critical processes, such as adipocyte development, lipid metabolism, glucose homeostasis, and inflammation, are strongly mediated by nuclear receptors, e.g. FXR, LXR, GR, and PPARs. In addition, understanding how nuclear receptors interact with other signaling pathways may lead to findings of new therapeutic targets for MetS. Understanding specific methods by which nuclear receptors affect metabolic pathways would further our knowledge of the pathophysiology of MetS, and open the door to future development of novel treatment approaches.
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