Molecules | |
Derinat Protects Skin against Ultraviolet-B (UVB)-Induced Cellular Damage | |
Wen-Li Hsu3  Jian-He Lu6  Mami Noda1  Ching-Ying Wu6  Jia-Dai Liu1  Manabu Sakakibara7  Ming-Hsien Tsai4  Hsin-Su Yu5  Ming-Wei Lin2  Yaw-Bin Huang2  Shian-Jang Yan3  Tohru Yoshioka4  | |
[1] Laboratory of Pathophysiology, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8581, Japan;School of Pharmacy, Kaohsiung Medical University, Kaohsiung 80708, Taiwan;The Institute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan;Lipid Science and Aging Research Center, Kaohsiung Medical University, Kaohsiung 80708, Taiwan;Department of Dermatology, Kaohsiung Medical University, No. 100, Shih-Chuan 1st Road, Kaohsiung 80708, Taiwan;Graduate Institute of Medicine, School of Medicine, Kaohsiung Medical University, No. 100, Shih-Chuan 1st Road, Kaohsiung 80708, Taiwan;School of High-Technology for Human Welfare, Tokai University, 410-0321 Numazu, Shizuoka, Japan; | |
关键词: Derinat; UVB; ROS; calcium; TRPCs; | |
DOI : 10.3390/molecules201119693 | |
来源: mdpi | |
【 摘 要 】
Ultraviolet-B (UVB) is one of the most cytotoxic and mutagenic stresses that contribute to skin damage and aging through increasing intracellular Ca2+ and reactive oxygen species (ROS). Derinat (sodium deoxyribonucleate) has been utilized as an immunomodulator for the treatment of ROS-associated diseases in clinics. However, the molecular mechanism by which Derinat protects skin cells from UVB-induced damage is poorly understood. Here, we show that Derinat significantly attenuated UVB-induced intracellular ROS production and decreased DNA damage in primary skin cells. Furthermore, Derinat reduced intracellular ROS, cyclooxygenase-2 (COX-2) expression and DNA damage in the skin of the BALB/c-nu mice exposed to UVB for seven days
【 授权许可】
CC BY
© 2015 by the authors; licensee MDPI, Basel, Switzerland.
【 预 览 】
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RO202003190003420ZK.pdf | 2643KB | download |