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      Local Melatoninergic System as the Protector of Skin Integrity

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          Abstract

          The human skin is not only a target for the protective actions of melatonin, but also a site of melatonin synthesis and metabolism, suggesting an important role for a local melatoninergic system in protection against ultraviolet radiation (UVR) induced damages. While melatonin exerts many effects on cell physiology and tissue homeostasis via membrane bound melatonin receptors, the strong protective effects of melatonin against the UVR-induced skin damage including DNA repair/protection seen at its high (pharmocological) concentrations indicate that these are mainly mediated through receptor-independent mechanisms or perhaps through activation of putative melatonin nuclear receptors. The destructive effects of the UVR are significantly counteracted or modulated by melatonin in the context of a complex intracutaneous melatoninergic anti-oxidative system with UVR-enhanced or UVR-independent melatonin metabolites. Therefore, endogenous intracutaneous melatonin production, together with topically-applied exogenous melatonin or metabolites would be expected to represent one of the most potent anti-oxidative defense systems against the UV-induced damage to the skin. In summary, we propose that melatonin can be exploited therapeutically as a protective agent or as a survival factor with anti-genotoxic properties or as a “guardian” of the genome and cellular integrity with clinical applications in UVR-induced pathology that includes carcinogenesis and skin aging.

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          Most cited references146

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          Extrapineal melatonin: sources, regulation, and potential functions.

          Endogenous melatonin is synthesized from tryptophan via 5-hydroxytryptamine. It is considered an indoleamine from a biochemical point of view because the melatonin molecule contains a substituted indolic ring with an amino group. The circadian production of melatonin by the pineal gland explains its chronobiotic influence on organismal activity, including the endocrine and non-endocrine rhythms. Other functions of melatonin, including its antioxidant and anti-inflammatory properties, its genomic effects, and its capacity to modulate mitochondrial homeostasis, are linked to the redox status of cells and tissues. With the aid of specific melatonin antibodies, the presence of melatonin has been detected in multiple extrapineal tissues including the brain, retina, lens, cochlea, Harderian gland, airway epithelium, skin, gastrointestinal tract, liver, kidney, thyroid, pancreas, thymus, spleen, immune system cells, carotid body, reproductive tract, and endothelial cells. In most of these tissues, the melatonin-synthesizing enzymes have been identified. Melatonin is present in essentially all biological fluids including cerebrospinal fluid, saliva, bile, synovial fluid, amniotic fluid, and breast milk. In several of these fluids, melatonin concentrations exceed those in the blood. The importance of the continual availability of melatonin at the cellular level is important for its physiological regulation of cell homeostasis, and may be relevant to its therapeutic applications. Because of this, it is essential to compile information related to its peripheral production and regulation of this ubiquitously acting indoleamine. Thus, this review emphasizes the presence of melatonin in extrapineal organs, tissues, and fluids of mammals including humans.
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            Synthesis of serotonin by a second tryptophan hydroxylase isoform.

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              On the free radical scavenging activities of melatonin's metabolites, AFMK and AMK.

              The reactions of N(1) -acetyl-N(2) -formyl-5-methoxykynuramine (AFMK) and N(1) -acetyl-5-methoxykynuramine (AMK) with (•) OH, (•) OOH, and •OOCCl3 radicals have been studied using the density functional theory. Three mechanisms of reaction have been considered: radical adduct formation (RAF), hydrogen transfer (HT), and single electron transfer (SET). Their relative importance for the free radical scavenging activity of AFMK and AMK has been assessed. It was found that AFMK and AMK react with •OH at diffusion-limited rates, regardless of the polarity of the environment, which supports their excellent •OH radical scavenging activity. Both compounds were found to be also very efficient for scavenging •OOCCl3 , but rather ineffective for scavenging •OOH. Regarding their relative activity, it was found that AFMK systematically is a poorer scavenger than AMK and melatonin. In aqueous solution, AMK was found to react faster than melatonin with all the studied free radicals, while in nonpolar environments, the relative efficiency of AMK and melatonin as free radical scavengers depends on the radical with which they are reacting. Under such conditions, melatonin is predicted to be a better •OOH and •OOCCl3 scavenger than AMK, while AMK is predicted to be slightly better than melatonin for scavenging •OH. Accordingly it seems that melatonin and its metabolite AMK constitute an efficient team of scavengers able of deactivating a wide variety of reactive oxygen species, under different conditions. Thus, the presented results support the continuous protection exerted by melatonin, through the free radical scavenging cascade. © 2012 John Wiley & Sons A/S.
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                Author and article information

                Contributors
                Role: External Editor
                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                30 September 2014
                October 2014
                : 15
                : 10
                : 17705-17732
                Affiliations
                [1 ]Department of Pathology and Laboratory Medicine, Cancer Research Building, University of Tennessee HSC, 930 Madison Avenue, Memphis, TN 38163, USA; E-Mails: zjanjeto@ 123456uthsc.edu (Z.J.); tkim10@ 123456uthsc.edu (T.-K.K.); radomir.slominski@ 123456gmail.com (R.M.S.)
                [2 ]Department of Medicine, Division of Rheumatology, University of Tennessee HSC, 930 Madison Avenue, Memphis, TN 38163, USA
                [3 ]Department of Dermatology, Allergology and Venerology, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany; E-Mails: Konrad.Kleszczynski@ 123456uksh.de (K.K.); Tobias.Fischer@ 123456uksh.de (T.W.F.)
                [4 ]Department of Biochemistry, Belarusian State University, Minsk 220030, Belarus; E-Mail: semak@ 123456bsu.by
                [5 ]Department of Histology, Medical University of Gdańsk, Gdańsk 80-211, Poland; E-Mail: mzmijewski@ 123456gumed.edu.pl
                [6 ]Department of Cellular and Structural Biology, UT Health Science Center, San Antonio, TX 78229, USA; E-Mail: REITER@ 123456uthscsa.edu
                Author notes
                [* ]Author to whom correspondence should be addressed; E-Mail: aslominski@ 123456uthsc.edu ; Tel./Fax: +1-901-448-3741.
                Article
                ijms-15-17705
                10.3390/ijms151017705
                4227185
                25272227
                e01ae6c3-b896-4628-9635-95bf76cb618c
                © 2014 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 15 August 2014
                : 09 September 2014
                : 16 September 2014
                Categories
                Review

                Molecular biology
                melatonin,keratinocytes,afmk,6-hydroxymelatonin,human full-thickness skin,ultraviolet radiation,oxidative stress

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