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Melatonin Mitigates Mitochondrial Meltdown: Interactions with SIRT3

Department of Cell Systems and Anatomy, UT Health San Antonio, San Antonio, TX 78229, USA
Centro de Investigacion Biomedica de Occidente, Instituto Mexicano del Seguro Social, Guardalajara, 4436 Jalisco, Mexico
Departamento de Quimica, Universidad Antonoma Metropolitana-Unidad Iztapalapa, San Rafael Atlixco 186, Col. Vicentina, Iztapalapa, C.P. 09340 Mexico D.F., Mexico
Department of Physiology and Pharmacology, Chang Gung University, 259 Wen-Hwa 1st Road, Kwei-Shan, Tao-Yuan 333, Taiwan
Departamento de Fisiologia, Instituto de Biotecnologia, Universidad de Granada, Avenida de Conocimiento S/U, 18016 Granada, Spain
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2018, 19(8), 2439;
Received: 9 July 2018 / Revised: 3 August 2018 / Accepted: 8 August 2018 / Published: 18 August 2018
Melatonin exhibits extraordinary diversity in terms of its functions and distribution. When discovered, it was thought to be uniquely of pineal gland origin. Subsequently, melatonin synthesis was identified in a variety of organs and recently it was shown to be produced in the mitochondria. Since mitochondria exist in every cell, with a few exceptions, it means that every vertebrate, invertebrate, and plant cell produces melatonin. The mitochondrial synthesis of melatonin is not photoperiod-dependent, but it may be inducible under conditions of stress. Mitochondria-produced melatonin is not released into the systemic circulation, but rather is used primarily in its cell of origin. Melatonin’s functions in the mitochondria are highly diverse, not unlike those of sirtuin 3 (SIRT3). SIRT3 is an NAD+-dependent deacetylase which regulates, among many functions, the redox state of the mitochondria. Recent data proves that melatonin and SIRT3 post-translationally collaborate in regulating free radical generation and removal from mitochondria. Since melatonin and SIRT3 have cohabitated in the mitochondria for many eons, we predict that these molecules interact in many other ways to control mitochondrial physiology. It is predicted that these mutual functions will be intensely investigated in the next decade and importantly, we assume that the findings will have significant applications for preventing/delaying some age-related diseases and aging itself. View Full-Text
Keywords: reactive oxygen species; oxidative stress; molecular pathways; sirtuins; antioxidant enzymes; oxidative phosphorylation reactive oxygen species; oxidative stress; molecular pathways; sirtuins; antioxidant enzymes; oxidative phosphorylation
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MDPI and ACS Style

Reiter, R.J.; Tan, D.X.; Rosales-Corral, S.; Galano, A.; Jou, M.-J.; Acuna-Castroviejo, D. Melatonin Mitigates Mitochondrial Meltdown: Interactions with SIRT3. Int. J. Mol. Sci. 2018, 19, 2439.

AMA Style

Reiter RJ, Tan DX, Rosales-Corral S, Galano A, Jou M-J, Acuna-Castroviejo D. Melatonin Mitigates Mitochondrial Meltdown: Interactions with SIRT3. International Journal of Molecular Sciences. 2018; 19(8):2439.

Chicago/Turabian Style

Reiter, Russel J., Dun X. Tan, Sergio Rosales-Corral, Annia Galano, Mei-Jie Jou, and Dario Acuna-Castroviejo. 2018. "Melatonin Mitigates Mitochondrial Meltdown: Interactions with SIRT3" International Journal of Molecular Sciences 19, no. 8: 2439.

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