Melatonin and mitochondrial function during ischemia/reperfusion injury |
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Authors: | Zhiqiang Ma Zhenlong Xin Wencheng Di Xiaolong Yan Xiaofei Li Russel J. Reiter Yang Yang |
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Affiliation: | 1.Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, Faculty of Life Sciences,UT Health San Antonio,Xi’an,China;2.Department of Thoracic Surgery, Tangdu Hospital,Fourth Military Medical University,Xi’an,China;3.Department of Biomedical Engineering,Fourth Military Medical University,Xi’an,China;4.Department of Cardiology, Affiliated Drum Tower Hospital,Nanjing University Medical School,Nanjing,China;5.Department of Cellular and Structural Biology,UT Health Science Center,San Antonio,USA |
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Abstract: | Ischemia/reperfusion (IR) injury occurs in many organs and tissues, and contributes to morbidity and mortality worldwide. Melatonin, an endogenously produced indolamine, provides a strong defense against IR injury. Mitochondrion, an organelle for ATP production and a decider for cell fate, has been validated to be a crucial target for melatonin to exert its protection against IR injury. In this review, we first clarify the mechanisms underlying mitochondrial dysfunction during IR and melatonin’s protection of mitochondria under this condition. Thereafter, special focus is placed on the protective actions of melatonin against IR injury in brain, heart, liver, and others. Finally, we explore several potential future directions of research in this area. Collectively, the information compiled here will serve as a comprehensive reference for the actions of melatonin in IR injury identified to date and will hopefully aid in the design of future research and increase the potential of melatonin as a therapeutic agent. |
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