Jageum-Jung, the herbal pharmaceuticals, inhibits the hepatic fibrogenesis as mediated with TGF-beta 1/smad signaling
- Authors
- Song, Yu Rim; Jang, Mi Hee; Jang, Boyun; Bae, Su Jin; Bak, Seon Been; Lee, Sung Min; Yun, Un-Jung; Lee, Ju Hee; Park, Sang Mi; Jung, Dae Hwa; Sa, Bok Suk; Song, Jong Kuk; Lee, Eun Hye; Kim, Kwang Youn; Park, Kwang-Il; Kim, Young Woo; Kim, Sang Chan
- Issue Date
- Apr-2022
- Publisher
- KOREAN SOCIETY TOXICOGENOMICS & TOXICOPROTEOMICS-KSTT
- Keywords
- Herbal pharmaceutical; Jageum-Jung; Liver fibrosis; TGF-beta 1/smad
- Citation
- MOLECULAR & CELLULAR TOXICOLOGY, v.18, no.2, pp.243 - 251
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- MOLECULAR & CELLULAR TOXICOLOGY
- Volume
- 18
- Number
- 2
- Start Page
- 243
- End Page
- 251
- URI
- https://scholarworks.bwise.kr/gnu/handle/sw.gnu/1418
- DOI
- 10.1007/s13273-021-00196-9
- ISSN
- 1738-642X
- Abstract
- Background Herbal prescriptions have various effects and their efficacy is potentiated by the use of combinations of medicinal herbs. Objective Jageum-Jung (JGJ) is a traditional oriental medical prescription composed of five herbs. It has been used for detoxification, and as an anti-inflammatory and antitumor agent. However, the effect of JGJ on hepatic fibrogenesis is unclear. Results We investigated the role of JGJ in TGF-beta 1/smad signaling, which is implicated in fibrogenesis, and its hepatoprotective effect in CCl4-treated mice with liver fibrosis. Treatment of LX-2 cells with TGF-beta induced expression of mediators (alpha-SMA, PAI-1, and MMP-2) of fibrogenesis and activation of proinflammatory cytokines (TNF-alpha, IL-1 beta, and IL-6). However, these were downregulated by pretreatment with JGJ. In mice, oral administration of JGJ prevented liver injury induced by CCl4, as indicated by decreases in the ALT and AST levels. Conclusions JGJ inhibits hepatic fibrogenesis and TGF-beta 1/Smad signaling.
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Collections - 수의과대학 > Department of Veterinary Medicine > Journal Articles
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