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bioRxivPhysiology

Skin protective effects of RM191A, a novel superoxide dismutase mimetic

A. Shariev, A. J. Laos, D. Lai, S. Hua, A. Zinger, C. R. Mcrae, L. S. Casbolt, V. Combes, T.-t. Hung, K. M. Dixon, P. Thordarson, R. S. Mason, A. Das

PDFDOIPreprint

Abstract

Superoxide dismutase (SOD) is known to be protective against oxidative stress-mediated skin dysfunction. Here we explore the potential therapeutic activities of RM191A, a novel SOD mimetic, on skin. RM191A is a water soluble, dimeric copper (Cu2+-Cu3+)-centred polyglycine coordination complex. It displays 10-fold higher superoxide quenching activity compared to SOD as well as significant anti-inflammatory activity through beneficial modulation of several significant inflammatory pathways in cells. We tested the therapeutic potential of RM191A in a topical gel using a human skin explant model and observed that it significantly inhibits UV-induced DNA damage in the epidermis and dermis, including cyclobutane pyrimidine dimers (CPD), 8-oxo-guanine (8-oxoG) and 8-nitroguanine (8NGO). RM191A topical gel is found to be safe and non-toxic in mice following month-long daily dosing at 0.19 mL/kg body weight. Moreover, it significantly accelerates excisional wound healing, and reduces 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced skin inflammation in mice. HighlightsO_LISuperoxide dismutase mimetic RM191A is a highly stable copper (Cu2+-Cu3+)-polyglycine coordination complex C_LIO_LIRM191A exhibits potent antioxidant (10-fold more than that of superoxide dismutase) properties in vitro C_LIO_LIRM191A exhibits potent anti-inflammatory properties in vitro and in vivo C_LIO_LIRM191A protects human skin explants against UV-induced oxidative stress and DNA damage C_LIO_LIRM191A is non-toxic and readily bioavailable in mice C_LIO_LIRM191A attenuates TPA-induced skin inflammation and improves wound healing in mice C_LI

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