alexa Melatonin Pre-treatment Alleviates UVA Radiation Induced Oxidative Stress and Apoptosis in the Skin of a Diurnal Tropical Rodent Funambulus pennanti
ISSN: 2155-9619

Journal of Nuclear Medicine & Radiation Therapy
Open Access

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Research Article

Melatonin Pre-treatment Alleviates UVA Radiation Induced Oxidative Stress and Apoptosis in the Skin of a Diurnal Tropical Rodent Funambulus pennanti

Soumik Goswami and Chandana Haldar*

Pineal Research Lab, Department of Zoology, Banaras Hindu University, Varanasi, 221005, Uttar Pradesh, India

*Corresponding Author:
Chandana Haldar
Pineal Research Lab
Department of Zoology
Banaras Hindu University
Varanasi 221005
Uttar Pradesh, India
Tel: 91-8052222271, +91-9415222261
E-mail: [email protected]

Received date: June 04, 2016; Accepted date: October 24, 2016; Published date: November 04, 2016

Citation: Gowsami S, Haldar C (2016) Melatonin Pre-treatment Alleviates UVA Radiation Induced Oxidative Stress and Apoptosis in the Skin of a Diurnal Tropical Rodent Funambulus pennanti. J Nucl Med Radiat Ther 8:318. doi:10.4172/2155-9619.1000318

Copyright: © 2016 Goswami S. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.



UV radiation has been established as a pro-oxidant that mediates tissue injury by triggering the generation of free radicals. However UVA induced oxidative injury has never been investigated before in the skin of a tropical diurnal rodent which spends longer time directly under the sun for foraging. The present study aimed to note the level of oxidative stress induced by 6.36 Jcm-2 UVA radiations on the skin and its possible prevention by melatonin. The oxidative load was assessed by the activities of key antioxidant enzymes (superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) and catalase (CAT)) and generation of thiobarbituric acid reactive substances (TBARS). Cutaneous apoptosis if any was checked by the expression of Bcl-2, p53 and Heme oxygenase-I (HO-I). Melatonin membrane receptor expression (MT1) and AANAT activity was also investigated to elucidate the protective effect of melatonin. UVA radiation increased the lipid peroxidation, suppressed the enzymatic antioxidant defense system and increased the HO-I expression. Melatonin restored redox balance and up regulated Bcl-2 and down regulated p53 levels. The restoration of AANAT activity also proved beneficial. In summary melatonin can be a part of topical applications or oral supplements that might help to reduce the UVA radiation mediated cutaneous oxidative damages.


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