Sirt3在褪黑素减少线粒体损伤的研究进展
Progress of Melatonin in Reducing Mitochondrial Injury by Interacting with Sirt3
DOI: 10.12677/ACM.2019.91006, PDF,    国家自然科学基金支持
作者: 胡亚楠, 韩 非:哈尔滨医科大学附属肿瘤医院麻醉科,黑龙江 哈尔滨
关键词: 褪黑激素Sirt3线粒体功能保护Melatonin Sirtuin 3 Protection of Mitochondria
摘要: 背景:褪黑激素是一种起源于松果腺的特殊吲哚胺,具有抗氧化,抗衰老和调控代谢的特性,近年来,与褪黑激素在细胞中作用的相关研究逐渐集中于线粒体。在线粒体中,褪黑激素可以刺激沉默信息调控蛋白3 (Sirt3)活性,通过加强其去乙酰化作用调控Foxo3a、SOD2及TCA周期中大部分代谢酶的活性,进而在心血管疾病、肝肾损伤、重金属危害等疾病中发挥保护作用。目的:对褪黑激素与Sirt3相互作用减少线粒体损伤的相关文献进行综述。内容:整理和阐述了褪黑激素与Sirt3在线粒体的表达、转移、共定位,及对不同器官的保护作用机制。趋向:褪黑激素与Sirt3在线粒体内共享多种信号通路,两者的相互作用可能是未来一个富有成效的研究领域。
Abstract: Background: Melatonin is a special indole amine derived from the pineal gland, with multiple properties of antioxidant, anti-aging and metabolic. Recent years, studies related to the role of melatonin in cells have gradually focused on mitochondria. In mitochondria, melatonin stimulates Sirt3 activity. It regulates the activity of Foxo3a, SOD2 and the most metabolic enzymes in TCA cy-cles by strengthening the deacetylation effect of Sirt3, and thus plays a protective role in diseases such as cardiovascular disease, liver and kidney injury, and heavy metal hazards. Objective: To re-view the related literatures on the interaction between melatonin and Sirt3 in reducing mito-chondria injury. Content: Based on series studies, this article illuminated the expression, metastasis and co-localization of melatonin and Sirt3 in mitochondria, and summarized the protective mechanism of melatonin in multiple organs. Trend: The interaction between Melatonin and Sirt3 will be one of the most valuable research field in mitochondria protection with both shared multiple signal pathways.
文章引用:胡亚楠, 韩非. Sirt3在褪黑素减少线粒体损伤的研究进展[J]. 临床医学进展, 2019, 9(1): 27-32. https://doi.org/10.12677/ACM.2019.91006

参考文献

[1] Borges Lda S, Dermargos, A., da Silva Junior, E.P., Weimann, E., Lambertucci, R.H. and Hatanaka, E. (2015) Melatonin Decreases Muscular Oxidative Stress and Inflammation Induced by Strenuous Exercise and Stimulates Growth Factor Synthesis. Journal of Pineal Research, 58, 166-172. [Google Scholar] [CrossRef] [PubMed]
[2] Ortiz, F., Acu-na-Castroviejo, D., Doerrier, C., Dayoub, J.C., Lopez, L.C., Venegas, C., et al. (2015) Melatonin Blunts the Mitochon-drial/NLRP3 Connection and Protects against Radiation-Induced Oral Mucositis. Journal of Pineal Research, 58, 34-49. [Google Scholar] [CrossRef] [PubMed]
[3] Tricoire, H., Moller, M., Chemineau, P. and Malpaux, B. (2003) Origin of Cerebrospinal Fluid Melatonin and Possible Function in the Integration of Photoperiod. Reproduction, 61, 311-321.
[4] Hevia, D., Gonzalez-Menendez, P., Quiros-Gonzalez, I., Miar, A., Rodriguez-Garcia, A., Tan, D.X., et al. (2015) Melatonin Uptake through Glucose Transporters: A New Target for Melatonin Inhibition of Cancer. Journal of Pineal Research, 58, 234-250. [Google Scholar] [CrossRef] [PubMed]
[5] Huo, X., Wang, C., Yu, Z., Peng, Y., Wang, S., Feng, S., et al. (2017) Human Transporters, PEPT1/2, Facilitate Melatonin Transportation into Mitochondria of Cancer Cells: An Implication of the Therapeutic Potential. Journal of Pineal Research, 62. [Google Scholar] [CrossRef] [PubMed]
[6] Suofu, Y., Li, W., Jean-Alphonse, F.G., Jia, J., Khattar, N.K., Li, J., et al. (2017) Dual Role of Mitochondria in Producing Melatonin and Driving GPCR Signaling to Block Cytochrome c Release. Proceedings of the National Academy of Sciences of the United States of America, 114, E7997-E8006. [Google Scholar] [CrossRef] [PubMed]
[7] He, C., Wang, J., Zhang, Z., Yang, M., Li, Y., Tian, X., et al. (2016) Mitochondria Synthesize Melatonin to Ameliorate Its Function and Improve Mice Oocyte’s Quality under In Vitro Conditions. International Journal of Molecular Sciences, 17, 939. [Google Scholar] [CrossRef] [PubMed]
[8] Carrico, C., Meyer, J.G., He, W., Gibson, B.W. and Verdin, E. (2018) The Mitochondrial Acylome Emerges: Proteomics, Regulation by Sirtuins, and Metabolic and Disease Implications. Cell Metabolism, 27, 497-512. [Google Scholar] [CrossRef] [PubMed]
[9] Nogueiras, R., Habegger, K.M., Chaudhary, N., Finan, B., Banks, A.S., Dietrich, M.O., et al. (2012) Sirtuin 1 and Sirtuin 3: Physiological Modulators of Metabolism. Physiological Re-views, 92, 1479-1514. [Google Scholar] [CrossRef] [PubMed]
[10] Reiter, R.J., Rosales-Corral, S., Tan, D.X., Jou, M.J., Galano, A. and Xu, B. (2017) Melatonin as a Mitochondria-Targeted Antioxidant: One of Evolution’s Best Ideas. Cellular and Molecular Life Sciences: CMLS, 74, 3863-3881. [Google Scholar] [CrossRef] [PubMed]
[11] Dwaich, K.H., Al-Amran, F.G., Al-Sheibani, B.I. and Al-Aubaidy, H.A. (2016) Melatonin Effects on Myocardial Ischemia-Reperfusion Injury: Impact on the Outcome in Patients Undergoing Coronary Artery Bypass Grafting Surgery. International Journal of Cardiology, 221, 977-986. [Google Scholar] [CrossRef] [PubMed]
[12] Feng, D., Wang, B., Wang, L., Abraham, N., Tao, K., Huang, L., et al. (2017) Pre-Ischemia Melatonin Treatment Alleviated Acute Neuronal Injury after Ischemic Stroke by Inhibiting Endoplasmic Reticulum Stress-Dependent Autophagy via PERK and IRE1 Signalings. Journal of Pineal Research, 62. [Google Scholar] [CrossRef] [PubMed]
[13] Yip, H.K., Chang, Y.C., Wallace, C.G., Chang, L.T., Tsai, T.H., Chen, Y.L., et al. (2013) Melatonin Treatment Improves Adipose-Derived Mesenchymal Stem Cell Therapy for Acute Lung Ischemia-Reperfusion Injury. Journal of Pineal Research, 54, 207-221. [Google Scholar] [CrossRef] [PubMed]
[14] Dominguez-Rodriguez, A., Abreu-Gonzalez, P., de la Torre-Hernandez, J.M., Consuegra-Sanchez, L., Piccolo, R., Gonzalez-Gonzalez, J., et al. (2017) Usefulness of Early Treatment With Melatonin to Reduce Infarct Size in Patients With ST-Segment Elevation Myocardial Infarction Receiving Percutaneous Coronary Intervention (From the Melatonin Adjunct in the Acute Myocardial Infarction Treated With Angioplasty Trial). The American Journal of Cardiology, 120, 522-526. [Google Scholar] [CrossRef] [PubMed]
[15] Lv, Y., Zhang, P., Guo, J., Zhu, Z., Li, X., Xu, D., et al. (2018) Melatonin Protects Mouse Spermatogonial Stem Cells against Hexavalent Chromium-Induced Apoptosis and Epigenetic Histone Modification. Toxicology and Applied Pharmacology, 340, 30-38. [Google Scholar] [CrossRef] [PubMed]
[16] Meki, A.R. and Hussein, A.A. (2001) Melatonin Reduces Oxidative Stress Induced by Ochratoxin A in Rat Liver and Kidney. Comparative Biochemistry and Physiology Toxicology & Pharmacology: CBP, 130, 305-313. [Google Scholar] [CrossRef
[17] Vairetti, M., Ferrigno, A., Bertone, R., Rizzo, V., Richelmi, P., Berte, F., et al. (2005) Exogenous Melatonin Enhances Bile Flow and ATP Levels after Cold Storage and Reperfu-sion in Rat Liver: Implications for Liver Transplantation. Journal of Pineal Research, 38, 223-230. [Google Scholar] [CrossRef
[18] Zhang, Y., Wei, Z., Liu, W., Wang, J., He, X., Huang, H., et al. (2017) Melatonin Protects against Arsenic Trioxide-Induced Liver Injury by the Upregulation of Nrf2 Expression through the Activation of PI3K/AKT Pathway. Oncotarget, 8, 3773-3780. [Google Scholar] [CrossRef] [PubMed]
[19] Han, L., Wang, H., Li, L., Li, X., Ge, J., Reiter, R.J., et al. (2017) Melatonin Protects against Maternal Obesity-Associated Oxidative Stress and Meiotic Defects in Oocytes via the SIRT3-SOD2-Dependent Pathway. Journal of Pineal Research, 63. [Google Scholar] [CrossRef] [PubMed]
[20] Yu, L., Gong, B., Duan, W., Fan, C., Zhang, J., Li, Z., et al. (2017) Melatonin Ameliorates Myocardial Ischemia/Reperfusion Injury in Type 1 Diabetic Rats by Preserving Mitochondrial Function: Role of AMPK-PGC-1alpha-SIRT3 Signaling. Scientific Reports, 7, Article No. 41337. [Google Scholar] [CrossRef] [PubMed]
[21] Zhang, M., Lin, J., Wang, S., Cheng, Z., Hu, J., Wang, T., et al. (2017) Melatonin Protects against Diabetic Cardiomyopathy through Mst1/Sirt3 Signaling. Journal of Pineal Research, 63. [Google Scholar] [CrossRef] [PubMed]
[22] Garcia, J.J., Lopez-Pingarron, L., Almeida-Souza, P., Tres, A., Escudero, P., Garcia-Gil, F.A., et al. (2014) Protective Effects of Melatonin in Reducing Oxidative Stress and in Preserving the Fluidity of Biological Membranes: A Review. Journal of Pineal Research, 56, 225-237. [Google Scholar] [CrossRef] [PubMed]
[23] Lee, F.Y., Sun, C.K., Sung, P.H., Chen, K.H., Chua, S., Sheu, J.J., et al. (2018) Daily Melatonin Protects the Endothelial Lineage and Functional Integrity against the Aging Process, Oxidative Stress, and Toxic Environment and Restores Blood Flow in Critical Limb Ischemia Area in Mice. Journal of Pineal Research, 65, e12489. [Google Scholar] [CrossRef] [PubMed]
[24] Bharti, V.K., Srivastava, R.S., Kumar, H., Bag, S., Majumdar, A.C., Singh, G., et al. (2014) Effects of Melatonin and Epiphyseal Proteins on Fluoride-Induced Adverse Changes in Antioxidant Status of Heart, Liver, and Kidney of Rats. Advances in Pharmacological Sciences, 2014, Article ID: 532969. [Google Scholar] [CrossRef] [PubMed]
[25] Song, C., Zhao, J., Fu, B., Li, D., Mao, T., Peng, W., et al. (2017) Mel-atonin-Mediated Upregulation of Sirt3 Attenuates Sodium Fluoride-Induced Hepatotoxicity by Activating the MT1-PI3K/AKT-PGC-1alpha Signaling Pathway. Free Radical Biology & Medicine, 112, 616-630. [Google Scholar] [CrossRef] [PubMed]
[26] Song, C., Peng, W., Yin, S., Zhao, J., Fu, B., Zhang, J., et al. (2016) Melatonin Improves Age-Induced Fertility Decline and Attenuates Ovarian Mitochondrial Oxidative Stress in Mice. Scientific Reports, 6, Article No. 35165. [Google Scholar] [CrossRef] [PubMed]
[27] Tamura, H., Kawamoto, M., Sato, S., Tamura, I., Maekawa, R., Taketani, T., et al. (2017) Long-Term Melatonin Treatment Delays Ovarian Aging. Journal of Pineal Research, 62, e12381. [Google Scholar] [CrossRef] [PubMed]
[28] Mayo, J.C., Sainz, R.M., Gonzalez Menendez, P., Cepas, V., Tan, D.X. and Reiter, R.J. (2017) Melatonin and Sirtuins: A “Not-So Unexpected” Relationship. Journal of Pineal Research, 62, e12391. [Google Scholar] [CrossRef] [PubMed]