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Please use this identifier to cite or link to this item: https://elib.bsu.by/handle/123456789/259025
Title: Metabolism of melatonin in the skin: Why is it important?
Authors: Slominski, A. T.
Semak, I.
Fischer, T. W.
Kim, T.-K.
Kleszczyński, K.
Hardeland, R.
Reiter, R. J.
Issue Date: 2017
Publisher: Blackwell Publishing Ltd
Citation: Exp Dermatol 2017;26(7):563-568.
Abstract: Melatonin is produced in almost all living taxa and is probably 2-3 billion years old. Its pleiotropic activities are related to its local concentration that is secondary to its local synthesis, delivery from distant sites and metabolic or non-enzymatic consumption. This consumption generates metabolites through indolic, kynuric and cytochrome P450 (CYP) mediated hydroxylations and O-demethylation or non-enzymatic processes, with potentially diverse phenotypic effects. While melatonin acts through receptor-dependent and receptor-independent mechanisms, receptors for melatonin metabolites remain to be identified, while their receptor-independent activities are well documented. The human skin with its main cellular components including malignant cells can both produce and rapidly metabolize melatonin in cell-type and context-dependent fashion. The predominant metabolism in human skin occurs through indolic, CYP-mediated and kynuric pathways with main metabolites represented by 6-hydroxymelatonin, N1-acetyl-N2-formyl-5-methoxykynuramine (AFMK), N1-acetyl-5-methoxykynuramine (AMK), 5-methoxytryptamine, 5-methoxytryptophol and 2-hydroxymelatonin. AFMK, 6-hydroxymelatonin, 2-hydroxymelatonin and probably 4-hydroxymelatonin can potentially be produced in epidermis through UVB-induced non-enzymatic melatonin transformation. The skin metabolites are also the same as those produced in lower organisms and plants indicating phylogenetic conservation across diverse species and adaptation by skin of the primordial defense mechanism. As melatonin and its metabolites counteract or buffer environmental stresses to maintain its homeostasis through broad-spectrum activities, both melatoninergic and degradative pathways must be precisely regulated, because the nature of phenotypic regulations will depend on local concentration of melatonin and its metabolites. These can be receptor-mediated or represent non-receptor regulatory mechanisms.
URI: https://elib.bsu.by/handle/123456789/259025
Scopus: 10.1111/exd.13208
metadata.dc.identifier.scopus: 85017349771
Sponsorship: 2014_A146; National Institutes of Health (NIH) 1R21AR0666505-01A1; National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) R01AR056666,R21AR066505; Bundesministerium für Bildung und Forschung (BMBF) BMBF-LPD 9901/8-113
Appears in Collections:Статьи биологического факультета

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