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Protective effect of Saussurea involucrata polysaccharide against skin dryness induced by ultraviolet radiation

Affiliation
School of Pharmaceutical Sciences ,Wenzhou Medical University ,Wenzhou ,China
Wang, Lusheng;
Affiliation
Infinitus (China) Company Ltd. ,Guangzhou ,China
Yang, Kaiye;
Affiliation
College of Life and Environmental Sciences ,Wenzhou University ,Wenzhou ,China
Jing, Rongrong;
Affiliation
College of Life and Environmental Sciences ,Wenzhou University ,Wenzhou ,China
Zhao, Wengang;
Affiliation
College of Life and Environmental Sciences ,Wenzhou University ,Wenzhou ,China
Guo, Keke;
Affiliation
College of Life and Environmental Sciences ,Wenzhou University ,Wenzhou ,China
Hu, Zhenlin;
Affiliation
Infinitus (China) Company Ltd. ,Guangzhou ,China
Liu, Guangrong;
Affiliation
College of Life and Environmental Sciences ,Wenzhou University ,Wenzhou ,China
Xu, Nuo;
Affiliation
Chevidence Lab of Child and Adolescent Health ,Children’s Hospital of Chongqing Medical University ,Chongqing ,China
Zhao, Jungang;
Affiliation
School of Pharmaceutical Sciences ,Wenzhou Medical University ,Wenzhou ,China
Lin, Li;
Affiliation
School of Pharmaceutical Sciences ,Wenzhou Medical University ,Wenzhou ,China
Gao, Shuang

Background: Exposure to ultraviolet B (UVB) radiation can damage the epidermis barrier function and eventually result in skin dryness. At present, little work is being devoted to skin dryness. Searching for active ingredients that can protect the skin against UVB-induced dryness will have scientific significance. Methods: Saussurea involucrata polysaccharide (SIP) has been shown to have significant antioxidant and anti-photodamage effects on the skin following UVB irradiation. To evaluate the effect of SIP on UVB-induced skin dryness ex vivo, SIP-containing hydrogel was applied in a mouse model following exposure to UVB and the levels of histopathological changes, DNA damage, inflammation, keratinocyte differentiation, lipid content were then evaluated. The underlying mechanisms of SIP to protect the cells against UVB induced-dryness were determined in HaCaT cells. Results: SIP was found to lower UVB-induced oxidative stress and DNA damage while increasing keratinocyte differentiation and lipid production. Western blot analysis of UVB-irradiated skin tissue revealed a significant increase in peroxisome proliferator-activated receptor-α (PPAR-α) levels, indicating that the underlying mechanism may be related to PPAR-α signaling pathway activation. Conclusions: By activating the PPAR-α pathway, SIP could alleviate UVB-induced oxidative stress and inhibit the inflammatory response, regulate proliferation and differentiation of keratinocytes, and mitigate lipid synthesis disorder. These findings could provide candidate active ingredients with relatively clear mechanistic actions for the development of skin sunscreen moisturizers.

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License Holder: Copyright © 2023 Wang, Yang, Jing, Zhao, Guo, Hu, Liu, Xu, Zhao, Lin and Gao.

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