老龄化扰乱了小鼠肝脏线粒体中的循环节律
1College of Life Sciences, Wuhan University, Wuhan 430072, China.
Molecules (Basel, Switzerland)
|June 10, 2023
概括
衰老扰乱了哺乳动物的昼夜节律,影响了线粒体功能,增加了氧化应激. 慢性炎症和NADase CD38升高调节加剧了这些与年龄相关的线粒体功能障碍.
科学领域:
- 时间生物学 时间生物学
- 线粒体生物学 线粒体生物学
- 衰老研究研究 衰老研究
背景情况:
- 昼夜时钟控制着哺乳动物的日常生理节奏.
- 衰老显著改变细胞昼夜节律,特别是线粒体功能和氧化应激.
- 之前的研究结果表明,尽管外围分子时钟完好无损,但衰老对小鼠的肝脏线粒体节律有深远的影响.
研究的目的:
- 审查最近关于昼夜时钟与衰老之间的相互作用的发现.
- 探索老化过程中的线粒体节律调节和氧化还原平衡.
- 研究慢性炎症和NADase CD38在与年龄相关的线粒体功能障碍中的作用.
主要方法:
- 最近研究发现的文献综述.
- 对昼夜节律,衰老和线粒体功能研究的分析.
- 检查炎症和特定分子参与者的影响,如CD38.
主要成果:
- 衰老改变了外围和中心组织中的基因表达节奏.
- 慢性无菌炎症导致线粒体功能障碍和衰老中的氧化应激.
- 通过衰老过程中的炎症对NADase CD38的上调与线粒体失调有关.
结论:
- 衰老破坏了线粒体功能的昼夜调节,导致氧化应激增加.
- 虽然分子钟仍然具有功能,但衰老会改变节律性基因表达.
- 炎症诱导的CD38上调是与年龄相关的线粒体衰退的关键因素.
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