Protective Effect of Castanopsis sieboldii Extract against UVB-Induced Photodamage in Keratinocytes

Author:

Lee Hye Rim1,Yang Ji Hye2,Lee Ji Hyun1,Kim Kyu Min3,Cho Sam Seok1,Baek Jin Sol1,Kim Jae Min1,Choi Moon-Hee4ORCID,Shin Hyun-Jae4ORCID,Ki Sung Hwan1ORCID

Affiliation:

1. College of Pharmacy, Chosun University, Gwangju 61452, Republic of Korea

2. College of Korean Medicine, Dongshin University, Naju 58245, Republic of Korea

3. Department of Biomedical Science, College of Natural Science, Chosun University, Gwangju 61452, Republic of Korea

4. Department of Biochemical Engineering, College of Engineering, Chosun University, Gwangju 61452, Republic of Korea

Abstract

Ultraviolet B (UVB) rays disrupt the skin by causing photodamage via processes such as reactive oxygen species (ROS) production, endoplasmic reticulum (ER) stress, DNA damage, and/or collagen degradation. Castanopsis sieboldii is an evergreen tree native to the southern Korean peninsula. Although it is known to have antioxidant and anti-inflammatory effects, its protective effect against photodamage in keratinocytes has not been investigated. Thus, in the present study, we investigated the effect of 70% ethanol extract of C. sieboldii leaf (CSL3) on UVB-mediated skin injuries and elucidated the underlying molecular mechanisms. CSL3 treatment restored the cell viability decreased by UVB irradiation. Moreover, CSL3 significantly inhibited UVB- or tert-butyl hydroperoxide-mediated ROS generation in HaCaT cells. ER stress was inhibited, whereas autophagy was upregulated by CSL3 treatment against UVB irradiation. Additionally, CSL3 increased collagen accumulation and cell migration, which were decreased by UVB exposure. Notably, epigallocatechin gallate, the major component of CSL3, improved the cell viability decreased by UVB irradiation through regulation of ER stress and autophagy. Conclusively, CSL3 may represent a promising therapeutic candidate for the treatment of UVB-induced skin damage.

Funder

Korea Forestry Promotion Institute

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

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