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Herbal compound 861 regulates mRNA expression of collagen synthesis- and degradation-related genes in human hepatic stellate cells.
Wang, Lin; Wang, Bao-En; Wang, Jian; Xiao, Pei-Gen; Tan, Xue-Hai.
Afiliação
  • Wang L; Beijing Genomic Institute, Beijing 101300, China.
World J Gastroenterol ; 14(11): 1790-4, 2008 Mar 21.
Article em En | MEDLINE | ID: mdl-18350612
ABSTRACT

AIM:

To identify the role of herbal compound 861 (Cpd 861) in the regulation of mRNA expression of collagen synthesis- and degradation-related genes in human hepatic stellate cells (HSCs).

METHODS:

mRNA levels of collagen types I and III, matrix metalloproteinase 1 (MMP-1), matrix metalloproteinase 2 (MMP-2), membrane type-1 matrix metalloproteinase (MT1-MMP), tissue inhibitor of metalloproteinase 1 (TIMP-1), and transforming growth factor beta1 (TGF-beta1) in cultured-activated HSCs treated with Cpd 861 or interferon-gamma (IFN-gamma) were determined by real-time PCR.

RESULTS:

Both Cpd 861 and IFN-gamma reduced the mRNA levels of collagen type III, MMP-2 and TGF-beta1. Moreover, Cpd 861 significantly enhanced the MMP-1 mRNA levels while down-regulated the TIMP-1 mRNA expression, increasing the ratio of MMP-1 to TIMP-1 to (6.3 + 0.3)- fold compared to the control group.

CONCLUSION:

The anti-fibrosis function of Cpd 861 may be mediated by both decreased interstitial collagen sythesis by inhibiting the transcription of collagen type III and TGF-beta1 and increased degradation of these collagens by up-regulating MMP-1 and down-regulating TIMP-1 mRNA levels.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transcrição Gênica / RNA Mensageiro / Medicamentos de Ervas Chinesas / Colágeno / Fígado Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2008 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transcrição Gênica / RNA Mensageiro / Medicamentos de Ervas Chinesas / Colágeno / Fígado Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2008 Tipo de documento: Article