Effects of atorvastatin on TGF-β RI mRNA expression in neonatal rat cardiac fibroblasts
Jun Du
Abstract
Jun Du
Abstract
[Objective]To investigate the effects of atorvastatin on the expression of transforming growth factorbeta receptor type Ⅰ (TGF-β RⅠ) mRNA induced by aldosterone in cultured neonatal rat cardiac fibroblasts. [Methods]The neonatal rat cardiac fibroblasts were isolated by trypsin digestion method. The expression of TGF-β RⅠ mRNA was detected by RT-PCR method. [Results]After TGF-β RⅠ mRNA expression increased in 4 hour, and which reached the maximal level at 8 hour. Aldosterone (10-7 mol/L) after Atorvastatin down-regulated TGF-β RⅠ mRNA expression in a concentration-dependent fashion, whereas mevalonate reversed it. [Conclusion]Atorvastatin can inhibit the aldosterone-induced expression of TGF-β RⅠ mRNA in cardiac fibroblasts by a mevalonate mechanism.
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[Objective]To investigate the effects of atorvastatin on the expression of transforming growth factorbeta receptor type Ⅰ (TGF-β RⅠ) mRNA induced by aldosterone in cultured neonatal rat cardiac fibroblasts. [Methods]The neonatal rat cardiac fibroblasts were isolated by trypsin digestion method. The expression of TGF-β RⅠ mRNA was detected by RT-PCR method. [Results]After TGF-β RⅠ mRNA expression increased in 4 hour, and which reached the maximal level at 8 hour. Aldosterone (10-7 mol/L) after Atorvastatin down-regulated TGF-β RⅠ mRNA expression in a concentration-dependent fashion, whereas mevalonate reversed it. [Conclusion]Atorvastatin can inhibit the aldosterone-induced expression of TGF-β RⅠ mRNA in cardiac fibroblasts by a mevalonate mechanism.
Key concepts: Atorvastatin, Messenger RNA, Aldosterone, Transforming growth factor, Internal medicine, Endocrinology, Chemistry, Biology