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TRPA1作为缺血/再输的有前途标:一个全面的审查
Azin Alizadehasl1,2, Maryam Sadat Alavi2, Mohaddeseh Sadat Alavi3
1Cardio-Oncology Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.
Iranian journal of basic medical sciences
|February 9, 2024
概括
暂时受体潜能A1 (TRPA1) 通道在缺血/再输液损伤中起着双重作用. 根据激活水平和持续时间等因素,TRPA1可以保护或恶化器官损伤.
科学领域:
- 心血管生物学 心血管生物学
- 神经科学是一个神经科学.
- 分子生物学分子生物学
背景情况:
- 缺血性疾病是导致死亡的首要原因,反液矛盾地导致进一步的组织损伤.
- 反 perfusion 损伤涉及反应性氧物种 (ROS),炎症和内分泌网膜压力.
- 针对多种病理途径对于有效的缺血/反疗法至关重要.
研究的目的:
- 审查短暂受体潜能A1 (TRPA1) 在缺血/再输 (I/R) 损伤中的作用和机制.
- 探索TRPA1在I/R中的双重保护或有害功能.
主要方法:
- 在PubMed,Scopus,Web of Science和Google Scholar的综合文献搜索到2023年8月.
- 分析研究TRPA1激活及其在缺血病条件下的后果的研究.
主要成果:
- TRPA1通道被与缺血相关的因素激活,包括氧化应激和特定化学物质.
- TRPA1对I/R损伤的贡献取决于环境,受激活水平和缺血性参数的影响.
- 有证据表明,TRPA1在再注射过程中可以表现出保护性和有害性.
结论:
- 在缺血/再输血中TRPA1的作用是复杂的和多方面的.
- 了解TRPA1在不同I/R场景中的特定功能是开发向治疗的关键.
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