论线粒体与缺血再灌注损伤的联系及肾移植中的研究进展
The Relationship between Mitochondria and Ischemia-Reperfusion Injury and the Research Progress in Kidney Transplantation
DOI: 10.12677/ACM.2023.1381847, PDF,    科研立项经费支持
作者: 雷小楠:西安医学院研究生院,陕西 西安;杜 春*, 梁学海:陕西省人民医院泌尿外科,陕西 西安;高文胜:凤翔区人民医院普外科,陕西 宝鸡
关键词: 线粒体缺血再灌注损伤肾移植ROSNS11021mPTPMitochondria Ischemia-Reperfusion Injury Kidney Transplantation ROS NS11021 mPTP
摘要: 近年来尽管针对线粒体的研究取得了很大的进展,但对于改善缺血再灌注损伤所提供的临床治疗方式的相关研究仍未取得明显突破,缺血/再灌注损伤是肾移植术后不可避免的相关后果,影响短期和长期移植效果。而线粒体相关研究中,我们收集了这一领域的相关知识,并综合讨论了当前线粒体与缺血再灌注损伤的相关联系以及对于改善肾移植提供思路,这些策略可能为未来I/R损伤提供潜在治疗方法,以及为其他组织以及器官的缺血再灌注损伤提供潜在的思路以及治疗方式。
Abstract: In recent years, although great progress has been made in the research on mitochondria, there has been no significant breakthrough in the clinical treatment provided by relevant research to im-prove ischemia-reperfusion injury. Ischemia-reperfusion injury is an inevitable consequence after kidney transplantation, affecting both short- and long-term transplantation results. In the mito-chondria-related studies, we collected relevant knowledge in this field and comprehensively dis-cussed the current correlation between mitochondria and ischemia-reperfusion injury and provid-ed ideas for improving kidney transplantation. These strategies may provide potential therapies for future I/R injury. It also provides potential ideas and treatments for ischemia-reperfusion injury in other tissues and organs.
文章引用:雷小楠, 杜春, 梁学海, 高文胜. 论线粒体与缺血再灌注损伤的联系及肾移植中的研究进展[J]. 临床医学进展, 2023, 13(8): 13221-13228. https://doi.org/10.12677/ACM.2023.1381847

参考文献

[1] Zhang, B., Pan, C., Feng, C., Yan, C., Yu, Y. and Chen, Z. (2022) Role of Mitochondrial Reactive Oxygen Species in Homeostasis Regulation. Redox Report, 27, 45-52. [Google Scholar] [CrossRef] [PubMed]
[2] Walkon, L.L., Strubbe-Rivera, J.O. and Bazil, J.N. (2022) Calcium Overload and Mitochondrial Metabolism. Biomolecules, 12, Article No. 1891. [Google Scholar] [CrossRef] [PubMed]
[3] Zheng, J., Cao, Y., Yang, J. and Jiang, H. (2022) UBXD8 Mediates Mitochondria-Associated Degradation to Restrain Apoptosis and Mitophagy. EMBO Reports, 23, e54859. [Google Scholar] [CrossRef] [PubMed]
[4] Kosieradzki, M. and Rowinski, W. (2008) Ische-mia/Reperfusion Injury in Kidney Transplantation: Mechanisms and Prevention. Transplantation Proceedings, 40, 3279-3288. [Google Scholar] [CrossRef] [PubMed]
[5] Rouslin, W. (1983) Mitochondrial Complexes I, II, III, IV, and V in Myocardial Ischemia and Autolysis. American Journal of Physiology, 244, H743-H748. [Google Scholar] [CrossRef
[6] Duann, P. and Lin, P.H. (2017) Mitochondria Damage and Kidney Disease. Advances in Experimental Medicine and Biology, 982, 529-551. [Google Scholar] [CrossRef] [PubMed]
[7] Bhargava, P. and Schnellmann, R.G. (2017) Mitochondrial Energetics in the Kidney. Nature Reviews Nephrology, 13, 629-646. [Google Scholar] [CrossRef] [PubMed]
[8] Eltzschig, H.K. and Eckle, T. (2011) Ischemia and Reperfu-sion—From Mechanism to Translation. Nature Medicine, 17, 1391-1401. [Google Scholar] [CrossRef] [PubMed]
[9] Anzell, A.R., Maizy, R., Przyklenk, K. and Sanderson, T.H. (2018) Mito-chondrial Quality Control and Disease: Insights into Ischemia-Reperfusion Injury. Molecular Neurobiology, 55, 2547-2564. [Google Scholar] [CrossRef] [PubMed]
[10] Dobashi, K., Ghosh, B., Orak, J.K., Singh, I. and Singh, A.K. (2000) Kidney Ischemia-Reperfusion: Modulation of Antioxidant Defenses. Molecular and Cellular Biochemistry, 205, 1-11. [Google Scholar] [CrossRef
[11] Dare, A.J., Bolton, E.A., Pettigrew, G.J., Bradley, J.A., Saeb-Parsy, K. and Murphy, M.P. (2015) Protection against Renal Ischemia-Reperfusion Injury in Vivo by the Mito-chondria Targeted Antioxidant MitoQ. Redox Biology, 5, 163-168. [Google Scholar] [CrossRef] [PubMed]
[12] Park, E.J., Dusabimana, T., Je, J., Jeong, K., Yun, S.P. and Kim, H.J. (2020) Honokiol Protects the Kidney from Renal Ischemia and Reperfusion Injury by Upregulating the Glutathione Biosynthetic Enzymes. Biomedicines, 8, Article No. 352. [Google Scholar] [CrossRef] [PubMed]
[13] Walker, L.M., York, J.L., Imam, S.Z., Ali, S.F., Muldrew, K.L. and Mayeux, P.R. (2001) Oxidative Stress and Reactive Nitrogen Species Generation during Renal Ischemia. Toxicological Sciences, 63, 143-148. [Google Scholar] [CrossRef] [PubMed]
[14] Zhao, M., Wang, Y., Li, L., Liu, S., Wang, C. and Yuan, Y. (2021) Mitochondrial ROS Promote Mitochondrial Dysfunction and Inflammation in Ischemic Acute Kidney Injury by Disrupt-ing TFAM-Mediated mtDNA Maintenance. Theranostics, 11, 1845-1863. [Google Scholar] [CrossRef] [PubMed]
[15] Calkins, M.J., Manczak, M., Mao, P., Shirendeb, U. and Reddy, P.H. (2011) Impaired Mitochondrial Biogenesis, Defective Axonal Transport of Mitochondria, Abnormal Mitochondrial Dy-namics and Synaptic Degeneration in a Mouse Model of Alzheimer’s Disease. Human Molecular Genetics, 20, 4515-4529. [Google Scholar] [CrossRef] [PubMed]
[16] Cao, M., Jiang, J., Du, Y. and Yan, P. (2012) Mitochon-dria-Targeted Antioxidant Attenuates High Glucose-Induced P38 MAPK Pathway Activation in Human Neuroblastoma Cells. Molecular Medicine Reports, 5, 929-934. [Google Scholar] [CrossRef] [PubMed]
[17] Li, J., Chen, X., Xiao, W., Ma, W., Li, T. and Huang, J. (2011) Mito-chondria-Targeted Antioxidant Peptide SS31 Attenuates High Glucose-Induced Injury on Human Retinal Endothelial Cells. Biochemical and Biophysical Research Communications, 404, 349-356. [Google Scholar] [CrossRef] [PubMed]
[18] Manczak, M., Mao, P., Calkins, M.J., Cornea, A., Reddy, A.P. and Murphy, M.P. (2010) Mitochondria-Targeted Antioxidants Protect against Amyloid-Beta Toxicity in Alzheimer’s Dis-ease Neurons. Journal of Alzheimer’s Disease, 20, S609-S631. [Google Scholar] [CrossRef
[19] Mizuguchi, Y., Chen, J., Seshan, S.V., Poppas, D.P., Szeto, H.H. and Felsen, D. (2008) A Novel Cell-Permeable Antioxidant Peptide Decreases Renal Tubular Apoptosis and Damage in Unilateral Ureteral Obstruction. American Journal of Physiology-Renal Physiology, 295, F1545-F1553. [Google Scholar] [CrossRef] [PubMed]
[20] Whiteman, M., Spencer, J.P., Szeto, H.H. and Armstrong, J.S. (2008) Do Mitochondriotropic Antioxidants Prevent Chlorinative Stress-Induced Mitochondrial and Cellular Injury? An-tioxidants & Redox Signaling, 10, 641-650. [Google Scholar] [CrossRef] [PubMed]
[21] Cho, J., Won, K., Wu, D., Soong, Y., Liu, S. and Szeto, H.H. (2007) Potent Mitochondria-Targeted Peptides Reduce Myocardial Infarction in Rats. Coronary Artery Disease, 18, 215-220. [Google Scholar] [CrossRef] [PubMed]
[22] Cho, S., Szeto, H.H., Kim, E., Kim, H., Tolhurst, A.T. and Pinto, J.T. (2007) A Novel Cell-Permeable Antioxidant Peptide, SS31, Attenuates Ischemic Brain Injury by Down-Regulating CD36. Journal of Biological Chemistry, 282, 4634-4642. [Google Scholar] [CrossRef
[23] Zhao, K., Zhao, G.M., Wu, D., Soong, Y., Birk, A.V. and Schiller, P.W. (2004) Cell-Permeable Peptide Antioxidants Targeted to Inner Mitochondrial Membrane Inhibit Mitochondrial Swelling, Oxidative Cell Death, and Reperfusion Injury. Journal of Biological Chemistry, 279, 34682-34690. [Google Scholar] [CrossRef
[24] Arany, I., Faisal, A., Clark, J.S., Vera, T., Baliga, R. and Nagamine, Y. (2010) p66SHC-Mediated Mitochondrial Dysfunction in Renal Proximal Tubule Cells during Oxidative Injury. American Journal of Physiology-Renal Physiology, 298, F1214-F1221. [Google Scholar] [CrossRef] [PubMed]
[25] Arany, I., Faisal, A., Nagamine, Y. and Safirstein, R.L. (2008) p66shc Inhibits Pro-Survival Epidermal Growth Factor Receptor/ERK Signaling during Severe Oxidative Stress in Mouse Renal Proximal Tubule Cells. Journal of Biological Chemistry, 283, 6110-6117. [Google Scholar] [CrossRef
[26] Sun, L., Xiao, L., Nie, J., Liu, F.Y. and Ling, G.H. (2010) p66Shc Mediates High-Glucose and Angiotensin II-Induced Oxidative Stress Renal Tubular Injury via Mitochondrial-Dependent Apoptotic Pathway. American Journal of Physiology-Renal Physiology, 299, F1014-F1025. [Google Scholar] [CrossRef] [PubMed]
[27] Szeto, H.H., Liu, S., Soong, Y., Wu, D., Darrah, S.F., Cheng, F.Y. and Chen, W.C. (2011) Mitochondria-Targeted Peptide Accelerates ATP Recovery and Reduces Ischemic Kidney Injury. Journal of the American Society of Nephrology, 22, 1041-1052. [Google Scholar] [CrossRef
[28] Yang, S.K., Li, A.M., Han, Y.C., Peng, C.H., Song, N. and Yang, M. (2019) Mitochondria-Targeted Peptide SS31 Attenuates Renal Tubulointerstitial Injury via Inhibiting Mitochondrial Fission in Diabetic Mice. Oxidative Medicine and Cellular Longevity, 2019, Article ID: 2346580. [Google Scholar] [CrossRef] [PubMed]
[29] Granata, S., Votrico, V., Spadaccino, F., Catalano, V., Ranieri, E. and Stallone, G. (2022) Oxidative Stress and Ischemia/Reperfusion Injury in Kidney Transplantation: Focus on Ferroptosis, Mitophagy and New Antioxidants. Antioxidants (Basel), 11, Article No. 769. [Google Scholar] [CrossRef] [PubMed]
[30] Trnka, J., Blaikie, F.H., Smith, R.A. and Murphy, M.P. (2008) A Mitochondria-Targeted Nitroxide Is Reduced to Its Hydroxylamine by Ubiquinol in Mitochondria. Free Radical Biology and Medicine, 44, 1406-1419. [Google Scholar] [CrossRef] [PubMed]
[31] Corsi, L., Zavatti, M., Geminiani, E., Zanoli, P.B. and Araldi, M. (2011) Anti-Inflammatory Activity of the Non-Peptidyl Low Molecular Weight Radical Scavenger IAC in Carrageenan-Induced Oedema in Rats. Journal of Pharmacy and Pharmacology, 63, 417-422. [Google Scholar] [CrossRef] [PubMed]
[32] Tian, Y., Shu, J., Huang, R., Chu, X. and Mei, X. (2020) Protective Effect of Renal Ischemic Postconditioning in Renal Ischemic-Reperfusion Injury. Translational Andrology and Urology, 9, 1356-1365. [Google Scholar] [CrossRef] [PubMed]
[33] Youle, R.J. and Narendra, D.P. (2011) Mechanisms of Mitophagy. Na-ture Reviews Molecular Cell Biology, 12, 9-14. [Google Scholar] [CrossRef] [PubMed]
[34] Ashrafi, G. and Schwarz, T.L. (2013) The Pathways of Mitophagy for Qual-ity Control and Clearance of Mitochondria. Cell Death & Differentiation, 20, 31-42. [Google Scholar] [CrossRef] [PubMed]
[35] Esteban-Martinez, L. and Boya, P. (2018) BNIP3L/NIX-Dependent Mi-tophagy Regulates Cell Differentiation via Metabolic Reprogramming. Autophagy, 14, 915-917. [Google Scholar] [CrossRef] [PubMed]
[36] Acuna Castroviejo, D., Escames, G., Carazo, A., Leon, J., Khaldy, H. and Reiter, R.J. (2002) Melatonin, Mitochondrial Homeostasis and Mitochondrial-Related Diseases. Current Topics in Medicinal Chemistry, 2, 133-151. [Google Scholar] [CrossRef] [PubMed]
[37] Hofmann, J., Otarashvili, G., Meszaros, A., Ebner, S., Weissen-bacher, A. and Cardini, B. (2020) Restoring Mitochondrial Function While Avoiding Redox Stress: The Key to Prevent-ing Ischemia/Reperfusion Injury in Machine Perfused Liver Grafts? International Journal of Molecular Sciences, 21, Ar-ticle No. 3132. [Google Scholar] [CrossRef] [PubMed]
[38] Suliman, H., Ma, Q., Zhang, Z., Ren, J., Morris, B.T. and Crowley, S.D. (2021) Annexin A1 Tripeptide Mimetic Increases Sirtuin-3 and Augments Mitochondrial Function to Limit Ischemic Kidney Injury. Frontiers in Physiology, 12, Article ID: 683098. [Google Scholar] [CrossRef] [PubMed]
[39] Yu, W., Sheng, M., Xu, R., Yu, J., Cui, K. and Tong, J. (2013) Berberine Protects Human Renal Proximal Tubular Cells from Hypoxia/Reoxygenation Injury via Inhibiting Endoplasmic Reticulum and Mitochondrial Stress Pathways. Journal of Translational Medicine, 11, Article No. 24. [Google Scholar] [CrossRef] [PubMed]
[40] Shakeri, F., Bianconi, V., Pirro, M. and Sahebkar, A. (2020) Effects of Plant and Animal Natural Products on Mitophagy. Oxidative Medicine and Cellular Longevity, 2020, Article ID: 6969402. [Google Scholar] [CrossRef] [PubMed]
[41] Pabla, N. and Bajwa, A. (2022) Role of Mitochondrial Ther-apy for Ischemic-Reperfusion Injury and Acute Kidney Injury. Nephron, 146, 253-258. [Google Scholar] [CrossRef] [PubMed]
[42] McCully, J.D., Del Nido, P.J. and Emani, S.M. (2022) Mitochondrial Transplantation for Organ Rescue. Mitochondrion, 64, 27-33. [Google Scholar] [CrossRef] [PubMed]