了解氧化应激,衰老和与衰老相关的疾病的进展
Jianying Yang1, Juyue Luo1, Xutong Tian1
1School of Medical Technology and Engineering, Henan University of Science and Technology, Luoyang 471023, China.
Antioxidants (Basel, Switzerland)
|April 27, 2024
概括
过度反应性氧物种 (ROS) 或氧化应激会损害细胞,导致衰老和相关疾病. 这篇评论探讨了ROS触发因素,它们的影响以及抗氧化剂策略,用于衰老研究.
科学领域:
- 生物化学 生物化学
- 细胞生物学 细胞生物学
- 老年学是一门学科.
背景情况:
- 反应性氧物种 (ROS) 是正常的代谢副产品,但过度生产会导致氧化应激 (OS).
- 氧化应激会导致细胞损伤,包括线粒体功能障碍,DNA损伤和亡.
- OS与诸如神经退行,心血管疾病和癌症等众多与衰老相关的疾病有关.
研究的目的:
- 审查人类和动物中ROS产生的内部和外部触发因素.
- 阐明氧化应激,衰老和与年龄相关的疾病之间的关系.
- 在衰老研究中统计分析当前的抗氧化剂干预措施.
主要方法:
- 对ROS,氧化应激和衰老研究的文献综述.
- 分析影响生物系统ROS水平的因素.
- 在老化模型中对抗氧化剂疗法的统计评估.
主要成果:
- 确定了导致ROS失衡的关键内源和外源因素.
- 在OS和细胞衰老标志物之间建立了强烈的相关性.
- 证明了OS与各种与年龄相关疾病的发病之间的联系.
- 介绍了关于新兴抗氧化剂措施有效性的统计数据.
结论:
- 氧化应激是细胞衰老和疾病发展的关键因素.
- 了解ROS触发因素对于开发有效的抗衰老策略至关重要.
- 抗氧化剂干预措施在缓解OS相关的衰老表型和疾病方面表现有前途.
相关概念视频
Aging
49
Aging is a complex biological phenomenon influenced by various processes that affect cellular and systemic functions. Several prominent theories attempt to explain its mechanisms, highlighting cellular limitations, oxidative damage, and hormonal changes as central factors in aging.
Cellular Clock Theory
The cellular clock theory posits that the human lifespan is closely tied to the finite capacity of cells to divide, a phenomenon governed by telomeres, which are protective caps at the ends of...
Cellular Clock Theory
The cellular clock theory posits that the human lifespan is closely tied to the finite capacity of cells to divide, a phenomenon governed by telomeres, which are protective caps at the ends of...
49
Mitochondria
12.3K
Mitochondria are eukaryotic cellular organelles that are known to produce energy through a process called oxidative phosphorylation. Besides their primary function, mitochondria are involved in various cellular processes, including cell growth, differentiation, signaling, metabolism, and senescence. Age-related changes cause a decline in mitochondrial quality and integrity due to increased mitochondrial mutations and oxidative damage. Thus, aging can severely impact mitochondrial functions,...
12.3K
Electron Transport Chain: Complex III and IV
7.4K
During the electron transport chain, electrons from NADH and FADH2 are first transferred to complexes I and II, respectively. These two complexes then transfer the electrons to ubiquinol, which carries them further to complex III. Complex III passes the electrons across the intermembrane space to Cyt c, which carries them further to complex IV. Complex IV donates electrons to oxygen and reduces it to water. As electrons pass through complexes I, III, and IV, the energy released aids the pumping...
7.4K
Electron Transport Chain: Complex I and II
13.1K
The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
ROS generation is regulated and maintained at moderate levels necessary...
13.1K
Chronic Obstructive Pulmonary Disease-II: Pathophysiology
2.8K
Chronic Obstructive Pulmonary Disease (COPD) pathophysiology is intricate and multifaceted, involving a complex interplay of physiological processes. Understanding these mechanisms is crucial for effectively managing and treating COPD. Here is an in-depth look at the critical elements in the pathophysiology of COPD:
Chronic Inflammation
Chronic Inflammation
2.8K
Phase I Oxidative Reactions: Overview
268
Phase I biotransformation, or functionalization, is a crucial chemical process that converts drugs and other xenobiotics into more water-soluble forms, facilitating expulsion from the body. It involves oxidative, reductive, and hydrolytic reactions that add or unveil polar functional groups on lipophilic substrates. Key players in phase I reactions are the mixed-function oxidases. Situated in liver cell microsomes, these enzymes predominantly carry out drug metabolism. They require molecular...
268


