孕妇X受体激活重塑葡萄糖代谢,促进肥胖小鼠的NAFLD发展
Mikko Karpale1, Outi Kummu1, Olli Kärkkäinen2
1Research Unit of Biomedicine and Internal Medicine, Biocenter Oulu, Medical Research Center Oulu, University of Oulu and Oulu University Hospital, Oulu, Finland.
Molecular metabolism
|July 19, 2023
概括
肥胖和化学激活的孕妇X受体 (PXR) 协同恶化非酒精性脂肪肝疾病 (NAFLD). PXR激活重组葡萄糖代谢,可能增加肥胖个体对代谢功能障碍的易感性.
科学领域:
- 肝病学 肝病学是一种肝病学.
- 代谢性疾病 代谢性疾病
- 药理学 药理学是指药理学的学科.
背景情况:
- 非酒精性脂肪性肝病 (NAFLD) 与肥胖和化学物质暴露有关.
- 孕妇X受体 (PXR) 调节新陈代谢,是破坏新陈代谢的化学物质的目标.
- 现有的肥胖症可能会改变PXR激活的代谢效应.
研究的目的:
- 研究PXR激活如何改变肥胖的代谢后果.
- 了解PXR在肥胖引起的NAFLD和代谢功能障碍中的作用.
主要方法:
- 在使用高脂肪饮食的野生型和PXR淘汰赛小鼠中诱导肥胖和代谢功能障碍.
- 通过使用孕龙-16α-碳烯激活了PXR.
- 综合性分析包括葡萄糖代谢,肝硬化,胰岛素信号传递,代谢学和转录学.
主要成果:
- 通过增加脂质生成和减少脂肪酸排放,PXR激活加剧了由肥胖引起的肝肥胖症.
- 肝脏胰岛素敏感性受损,肝脏酶增加.
- PXR激活改变了葡萄糖代谢,导致肝脏和全身胰岛素敏感性之间的分离.
结论:
- 肥胖和PXR激活对NAFLD发展具有协同作用.
- PXR激活重组葡萄糖代谢,可能掩盖系统代谢改善.
- 肥胖个体可能更容易受到PXR激活剂的不良影响.
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