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Effect of tetramethylpyrazine and rat CTGF miRNA plasmids on connective tissue growth factor, transforming growth factor-beta in high glucose stimulated hepatic stellate cells / 生物医学工程学杂志
J. biomed. eng ; Sheng wu yi xue gong cheng xue za zhi;(6): 394-399, 2014.
Article de Zh | WPRIM | ID: wpr-290746
Bibliothèque responsable: WPRO
ABSTRACT
The aim of this research is to evaluate the effect of tetramethylpyrazine (TMP) and connective tissue growth factor (CTGF) miRNA plasmids on the expressive levels of CTGF, transforming growth factor-beta (TGFbeta) and type I collagen of rat hepatic stellate cells (HSC) which are stimulated by high glucose. The rat HSCs which were successfully transfected rat CTGF miRNA plasmids and the rat HSCs which were successfully transfected negative plasmids were cultured in vitro. After stimulus of the TMP and the high glucose, the protein levels and gene expressive levels of CTGF, TGF-beta and type I collagen were tested. The results indicated that high glucose increased the expression of CTGF mRNA, CTGF protein, TGF-beta mRNA,TGF-beta protein and type I collagen (P < 0.05). The expressive levels of CTGF mRNA, CTGF protein, TGF-beta mRNA, TGF-beta and type I collagen in TMP group were lower than those in high glucose group and showed statistically significant differences (P < 0.05). Compared with high glucose group, the expressive levels of CTGF mRNA, CTGF protein, TGF-beta mRNA, TGF-beta and type I collagen in rat CTGF miRNA plasmid interference group were significantly lower (P < 0.05). However, no statistically significant difference was found in CTGF mRNA and CTGF protein levels between TMP group and CTGF miRNA group (P > 0.05), while type I collagen levels showed statistically significant differences (P < 0.05). It is concluded that high glucose could promote the expressions of CTGF, TGF-beta and type I collagen, and TMP and rat CTGF miRNA plasmids could reduce the expressions of CTGF, TGF-beta, type I collagen.
Sujet(s)
Texte intégral: 1 Indice: WPRIM Sujet Principal: Pharmacologie / Plasmides / Pyrazines / ARN messager / Transfection / Cellules cultivées / Facteur de croissance transformant bêta / Milieux de culture / Collagène de type I / MicroARN Limites du sujet: Animals langue: Zh Texte intégral: J. biomed. eng / Sheng wu yi xue gong cheng xue za zhi Année: 2014 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Pharmacologie / Plasmides / Pyrazines / ARN messager / Transfection / Cellules cultivées / Facteur de croissance transformant bêta / Milieux de culture / Collagène de type I / MicroARN Limites du sujet: Animals langue: Zh Texte intégral: J. biomed. eng / Sheng wu yi xue gong cheng xue za zhi Année: 2014 Type: Article