Ginkgo biloba extract ameliorates skin fibrosis in a bleomycin-induced mouse model of systemic sclerosis

Bibliographic Details
Title: Ginkgo biloba extract ameliorates skin fibrosis in a bleomycin-induced mouse model of systemic sclerosis
Authors: Beomgu Lee, Jong Seong Roh, Hoim Jeong, Yerin Kim, Jihyeon Lee, Changun Yun, Jiyoung Park, Da-sol Kim, Jungsoo Lee, Min Wook So, Aran Kim, Dong Hyun Sohn, Seung-Geun Lee
Source: Animal Cells and Systems, Vol 28, Iss 1, Pp 152-160 (2024)
Publisher Information: Taylor & Francis Group, 2024.
Publication Year: 2024
Collection: LCC:Medicine (General)
LCC:Biology (General)
Subject Terms: Systemic sclerosis (SSc), Ginkgo biloba extract (GBE), transforming growth factor (TGF)-β, skin fibroblast, adipocyte-myofibroblast transition (AMT), Medicine (General), R5-920, Biology (General), QH301-705.5
More Details: Systemic sclerosis (SSc) is a chronic autoimmune disease characterized by skin and internal organ fibrosis and obliterative vasculopathy. Few effective treatments are currently available for fibrosis in SSc, therefore, demand persists for novel therapies. Although use of Ginkgo biloba extract (GBE) has been reported to improve blood circulation and alleviate liver and lung fibrosis, its effect on skin fibrosis in SSc remains unclear. In this study, the effects and underlying mechanisms of GBE on skin fibrosis in bleomycin (BLM)-induced mouse model of SSc was investigated. GBE significantly reduced dermal thickness and protein levels of profibrotic factors in the BLM-induced SSc mouse model. Moreover, GBE inhibited the gene expression of profibrotic factors, such as COL1A1, α-SMA, and connective tissue growth factor (CTGF), in fibroblasts by suppressing transforming growth factor (TGF)-β signaling. Furthermore, GBE inhibited the transdifferentiation of adipocytes into myofibroblasts. Thus, our findings suggest that GBE is a promising therapeutic candidate for the treatment of SSc.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 19768354
2151-2485
1976-8354
Relation: https://doaj.org/toc/1976-8354; https://doaj.org/toc/2151-2485
DOI: 10.1080/19768354.2024.2337761
Access URL: https://doaj.org/article/2bf7767d0625499d8c5425daca7c30e5
Accession Number: edsdoj.2bf7767d0625499d8c5425daca7c30e5
Database: Directory of Open Access Journals
Full text is not displayed to guests.
More Details
ISSN:19768354
21512485
DOI:10.1080/19768354.2024.2337761
Published in:Animal Cells and Systems
Language:English