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Protective Effects of Mogroside V on Oxidative Stress Induced by H 2 O 2 in Skin Fibroblasts.

Authors :
Mo Q
Fu H
Zhao D
Zhang J
Wang C
Wang D
Li M
Source :
Drug design, development and therapy [Drug Des Devel Ther] 2021 Dec 01; Vol. 15, pp. 4901-4909. Date of Electronic Publication: 2021 Dec 01 (Print Publication: 2021).
Publication Year :
2021

Abstract

Purpose: Damage caused by oxidative stress leads to the premature aging of cells. Mogrosides, the main active components of Siraitia grosvenorii , have strong antioxidant activity; however, it is unclear whether mogroside V (MV) exerts these effects in skin cells. This was investigated in the present study by evaluating the protective effects of MV against oxidative damage induced by hydrogen peroxide (H <subscript>2</subscript> O <subscript>2</subscript> ) in skin fibroblasts.<br />Methods: Mouse skin fibroblasts (MSFs) were treated with H <subscript>2</subscript> O <subscript>2</subscript> and cell viability, total antioxidant capacity, reactive oxygen species (ROS) production, malondialdehyde (MDA) content, and antioxidant enzyme activity were assessed.<br />Results: Treatment with MV reduced the ROS level and MDA content in MSFs treated with H <subscript>2</subscript> O <subscript>2</subscript> . This was accompanied by increased superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and catalase (CAT) activities.<br />Conclusion: MV reduces H <subscript>2</subscript> O <subscript>2</subscript> -induced oxidative stress and enhances endogenous antioxidant activity in skin fibroblasts. Thus, MV can potentially be used as an ingredient in anti-aging cosmetic products.<br />Competing Interests: Ms Qiuting Mo reports grants from the Research Foundation for Youth Scholars of Beijing Technology and Business University (QNJJ2020-04), during the conduct of the study. The authors report no other conflicts of interest in relation to this work.<br /> (© 2021 Mo et al.)

Details

Language :
English
ISSN :
1177-8881
Volume :
15
Database :
MEDLINE
Journal :
Drug design, development and therapy
Publication Type :
Academic Journal
Accession number :
34880600
Full Text :
https://doi.org/10.2147/DDDT.S337524