氧化应激:骨肌肉缩中的作用
Han Zhang1, Guangdong Qi2, Kexin Wang1
1Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, NMPA Key Laboratory for Research and Evaluation of Tissue Engineering Technology Products, Medical College, Nantong University, Nantong, Jiangsu Province 226001, China.
Biochemical pharmacology
|June 18, 2023
概括
氧化应激是肌肉缩的关键驱动因素,影响各种细胞过程. 这篇评论探讨了其来源,机制和治疗策略,如抗氧化剂和用于肌肉消耗条件的干细胞.
科学领域:
- 肌肉生物学 肌肉生物学
- 细胞生理学 细胞生理学
- 病理学 病理学 病理学
背景情况:
- 肌肉缩涉及氧化应激,炎症和线粒体功能障碍.
- 氧化应激是骨肌肉缩的早期触发因素,其机制尚未完全理解.
研究的目的:
- 审查骨肌肉缩中氧化应激的来源和机制.
- 讨论氧化应激在导致肌肉缩的各种病理状况中的作用.
- 提出治疗策略,以缓解肌肉缩中的氧化应激.
主要方法:
- 在肌肉缩中对氧化应激的文献综述.
- 氧化应激和细胞过程 (炎症,线粒体功能,蛋白质合成/降解) 之间的相关性分析.
- 在各种缩诱导条件下对氧化应激的检查.
主要成果:
- 氧化应激与炎症,线粒体功能障碍,自,蛋白质合成和肌肉缩中的蛋白质分解密切相关.
- 它在与缩,卸载,慢性疾病,肉症,神经肌肉疾病和癌症缓解症相关的缩中发挥着重要作用.
结论:
- 了解氧化应激机制对于开发有效的肌肉缩疗法至关重要.
- 抗氧化剂,草药提取物,干细胞和细胞外囊泡通过向氧化应激来缓解肌肉缩,显示出有前途.
相关概念视频
Cross-bridge Cycle
117.7K
As muscle contracts, the overlap between the thin and thick filaments increases, decreasing the length of the sarcomere—the contractile unit of the muscle—using energy in the form of ATP. At the molecular level, this is a cyclic, multistep process that involves binding and hydrolysis of ATP, and movement of actin by myosin.
117.7K
Muscle Recovery and Fatigue
2.2K
Muscle fatigue refers to the decline in a muscle's ability to maintain the force of contraction after prolonged activity. It primarily stems from changes within muscle fibers. Even before experiencing muscle fatigue, one may feel tired and have the urge to stop the activity. This response, known as central fatigue, occurs due to changes in the central nervous system, namely the brain and spinal cord. While there is no single mechanism that induces fatigue, it may serve as a protective...
2.2K
Mitochondria
14.0K
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,...
14.0K
Electron Transport Chain: Complex I and II
14.6K
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...
14.6K
Oxygen Requirements and Growth Patterns
164
Microorganisms exhibit diverse oxygen requirements and growth patterns driven by their metabolic strategies and environmental adaptations. Oxygen, while essential for many organisms, can also be toxic under certain conditions, shaping how microorganisms grow and survive.Oxygen Requirements of MicroorganismsMicroorganisms are classified based on their ability to use or tolerate oxygen:Obligate aerobes like Mycobacterium tuberculosis need oxygen for energy production, as it serves as the terminal...
164
Satellite Stem Cells and Muscular Dystrophy
2.0K
Satellite stem cells or myosatellite cells are quiescent stem cells that Alexander Mauro first identified in 1961. These cells are located between the sarcolemma, the plasma membrane of muscle fibers, and the basal lamina, the connective tissue sheath covering it. These mononucleated cells are activated in response to muscle injury, can transform into myoblasts, and may form or repair muscle fibers. Myosatellite cells can provide additional myonuclei for muscle regeneration or return to a...
2.0K


