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Oxidative Medicine and Cellular Longevity
Volume 2017, Article ID 9703609, 17 pages
https://doi.org/10.1155/2017/9703609
Research Article

Fish Scale Collagen Peptides Protect against CoCl2/TNF-α-Induced Cytotoxicity and Inflammation via Inhibition of ROS, MAPK, and NF-κB Pathways in HaCaT Cells

1Department of Anatomy, Pusan National University School of Medicine, Yangsan, Gyeongsangnam-do 50612, Republic of Korea
2Pioneer Research Center, Suwon 16499, Republic of Korea
3Department of Mechanical Engineering, Korea Polytechnic University, Siheung 15073, Republic of Korea
4Kyungpook National University, Daegu 41566, Republic of Korea
5Department of Pharmacology, Ajou University School of Medicine, Suwon 16499, Republic of Korea

Correspondence should be addressed to Sik Yoon; rk.ca.nasup@nooykis

Received 24 January 2017; Revised 20 March 2017; Accepted 26 April 2017; Published 22 June 2017

Academic Editor: Giuseppe Filomeni

Copyright © 2017 Fazli Subhan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Skin diseases associated with inflammation or oxidative stress represent the most common problem in dermatology. The present study demonstrates that fish scale collagen peptides (FSCP) protect against CoCl2-induced cytotoxicity and TNF-α-induced inflammatory responses in human HaCaT keratinocyte cells. Our study is the first to report that FSCP increase cell viability and ameliorate oxidative injury in HaCaT cells through mechanisms mediated by the downregulation of key proinflammatory cytokines, namely, TNF-α, IL-1β, IL-8, and iNOS. FSCP also prevent cell apoptosis by repressing Bax expression, caspase-3 activity, and cytochrome c release and by upregulating Bcl-2 protein levels in CoCl2- or TNF-α-stimulated HaCaT cells. In addition, the inhibitory effects of FSCP on cytotoxicity and the induction of proinflammatory cytokine expression were found to be associated with suppression of the ROS, MAPK (p38/MAPK, ERK, and JNK), and NF-κB signaling pathways. Taken together, our data suggest that FSCP are useful as immunomodulatory agents in inflammatory or immune-mediated skin diseases. Furthermore, our results provide new insights into the potential therapeutic use of FSCP in the prevention and treatment of various oxidative- or inflammatory stress-related inflammation and injuries.