光老化
MAPK/ERK通路
p38丝裂原活化蛋白激酶
化学
信号转导
细胞生物学
基质金属蛋白酶
磷酸化
皮肤老化
抗氧化剂
生物化学
医学
生物
皮肤病科
作者
Yu Fu,Chongyang Li,Qiang Wang,Ruichang Gao,Xixi Cai,Shaoyun Wang,Yuhao Zhang
标识
DOI:10.1016/j.jff.2022.105101
摘要
The aim of this study was to investigate the protective effect and mechanism of bigeye tuna (Thunnus obesus) skin collagen peptides (TSCP) and bone collagen peptides (TBCP) on skin photoaging. In UVB-damaged NIH/3T3 cells, TSCP and TBCP could effectively scavenge excessive reactive oxygen species, suppress mRNA and protein expression of MMP-1, and inhibit the decreased mRNA and protein expression of TGF-β1 and type I collagen. In the ICR mice model exposed to UVB, TSCP and TBCP could effectively improve moisture content, Hyp content and total antioxidant capacity level, activate TGF-β1 signaling pathway, and inhibit MAPK signaling pathway, thereby retarding UVB-induced skin photoaging. TSCP exhibited more excellent antioxidant activity, inhibited p-p38 activation and promoted TGF-β1 expression via TGF-β signaling pathway. By contrast, TBCP was more potent to down-regulate protein expression of p-ERK, p-JNK and MMP-1. The present work provides a theoretical basis for employment of collagen peptides to attenuate UVB-induced photoaging.
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