Your browser doesn't support javascript.
loading
[Research progresses on PGC-1α, a key energy metabolic regulator].
Wang, Hui-Ting; Zhang, Yan-Chen; Xu, Meng-Yi; Zhang, Wen-Xiang; Liu, Chang; Chen, Si-Yu.
Afiliación
  • Wang HT; College of Life Sciences, China Pharmaceutical University, Nanjing 211198, China.
  • Zhang YC; College of Life Sciences, China Pharmaceutical University, Nanjing 211198, China.
  • Xu MY; College of Life Sciences, China Pharmaceutical University, Nanjing 211198, China.
  • Zhang WX; College of Life Sciences, China Pharmaceutical University, Nanjing 211198, China.
  • Liu C; College of Life Sciences, China Pharmaceutical University, Nanjing 211198, China.
  • Chen SY; College of Life Sciences, China Pharmaceutical University, Nanjing 211198, China. siyuchen@cpu.edu.cn.
Sheng Li Xue Bao ; 72(6): 804-816, 2020 Dec 25.
Article en Zh | MEDLINE | ID: mdl-33349839
ABSTRACT
Disturbance of the energy balance, when the energy intake exceeds its expenditure, is a major risk factor for the development of metabolic syndrome (MS). The peroxisome proliferator activated receptor γ (PPARγ) coactivator-1α (PGC-1α) functions as a key regulator of energy metabolism and has become a hotspot in current researches. PGC-1α sensitively responds to the environmental stimuli and nutrient signals, and further selectively binds to different transcription factors to regulate various physiological processes, including glucose metabolism, lipid metabolism, and circadian clock. In this review, we described the gene and protein structure of PGC-1α, and reviewed its tissue-specific function in the regulation of energy homeostasis in various mammalian metabolic organs, including liver, skeletal muscle and heart, etc. At the meanwhile, we summarized the application of potential small molecule compounds targeting PGC-1α in the treatment of metabolic diseases. This review will provide theoretical basis and potential drug targets for the treatment of metabolic diseases.
Asunto(s)
Buscar en Google
Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Metabolismo Energético Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: Zh Revista: Sheng Li Xue Bao Año: 2020 Tipo del documento: Article País de afiliación: China
Buscar en Google
Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Metabolismo Energético Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: Zh Revista: Sheng Li Xue Bao Año: 2020 Tipo del documento: Article País de afiliación: China