Melatonin, Mitochondrial Homeostasis and Mitochondrial-Related Diseases

Dario   Acuna   Castroviejo; Germaine      Escames; Angel      Carazo; Josefa      Leon; Huda      Khaldy; Russel   J.   Reiter

doi:10.2174/1568026023394344

Abstract

The recently described ‘hydrogen hypothesis’ invokes metabolic symbiosis as the driving force for a symbiotic association between an anaerobic, strictly hydrogen-dependent organism (the host) and an eubacterium (the symbiont) that is able to respire, but which generates molecular hydrogen as an end product of anaerobic metabolism. The resulting proto-eukaryotic cell would have acquired the essentials of eukaryotic energy metabolism, evolving not only aerobic respiration, but also the cost of oxygen consumption, i.e., generation of reactive oxygen species (ROS) and oxidative damage. Mitochondria contain their own genome with a modified genetic code that is highly conserved among mammals. Control of gene expression suggests that transcription of certain mitochondrial genes may be regulated in response to the redox potential of the mitochondrial membrane. Mitochondria are involved in energy production and conservation, and they have an uncoupling mechanism to produce heat instead of ATP. Al so, mitochondria are involved in programmed cell death. Increasing evidence suggests the participation of mitochondria in neurodegenerative and neuromuscular diseases involving alterations in both nuclear (nDNA) and mitochondrial (mtDNA) DNA. Melatonin is now known as a powerful antioxidant and increasing experimental evidence shows its beneficial effects against oxidative stress-induced macromolecular damage and diseases, including those in which mitochondrial function is affected. This review summarizes the data and mechanisms of action of melatonin in relation to mitochondrial pathologies.

Keywords: Mitochondrial Homeostasis, hydrogen-dependent organism, macromolecular damage, 8-Hydroxydeoxyguanosine, Calcium-camodulin complex, Ubiquinone, Cytochrome, Superoxide anion, Peroxynitrite, Glutathione peroxidase, Dopamine