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[尾加压素II对培养的心脏成纤维细胞增殖及I型胶原mRNA表达的影响]

[Effects of urotensin II on cultured cardiac fibroblast proliferation and collagen type I mRNA expression].

作者信息

He Yan-hua, Hong Jie-min, Guo Heng-shan, Wei Jian-rui, Chen Hui, Zuo Hui-hua, Li Zhi-liang

机构信息

Department of Cardiology, Guangzhou Red-Cross Hospital/Fourth Affiliated Hospital of Jinan University, Guangzhou 510220, China.

出版信息

Di Yi Jun Yi Da Xue Xue Bao. 2004 May;24(5):505-8.

Abstract

OBJECTIVE

To observe the effect of urotensin II on cultured cardiac fibroblast collagen type I mRNA expression and proliferation, thereby to explore the role of urotensin II in myocardial remodeling in the event of cardiac failure.

METHODS

Cardiac fibroblasts of neonatal Sprague-Dawley rats isolated by trypsin digestion method were stimulated by urotensin II at varied concentrations when the cells reached growth arrest. MTT assay was employed to measure the proliferation and determine the number of the cells, and reverse transcriptional (RT)-PCR used to detect the collagen mRNA expression.

RESULTS

With the increase of urotensin II concentration, the optical density at 570 nm of the fibroblasts as shown by MTT assay first increased but then decreased, and remained at a significantly higher level in the cells treated with 1x10(-8) or 1x10(-9) mol/L urotensin II as compared with the control (P<0.05). The collagen type I mRNA levels of the cells treated with 1x10(-7), 1x10(-8) or 1x10(-9) mol/L urotensin II were significantly higher than that of the control cells (P<0.01).

CONCLUSION

Urotensin II can directly induce cardiac fibroblast proliferation and significantly increase collagen type I mRNA expression, suggesting the crucial role of urotensin II in myocardial remodeling.

摘要

目的

观察尾加压素II对培养的心脏成纤维细胞I型胶原mRNA表达及增殖的影响,从而探讨尾加压素II在心力衰竭时心肌重构中的作用。

方法

采用胰蛋白酶消化法分离新生Sprague-Dawley大鼠的心脏成纤维细胞,待细胞生长停滞时用不同浓度的尾加压素II刺激。采用MTT法检测细胞增殖情况并确定细胞数量,用逆转录(RT)-PCR检测胶原mRNA表达。

结果

随着尾加压素II浓度的增加,MTT法检测的成纤维细胞在570nm处的光密度先升高后降低,与对照组相比,用1×10⁻⁸或1×10⁻⁹mol/L尾加压素II处理的细胞光密度仍显著更高(P<0.05)。用1×10⁻⁷、1×10⁻⁸或1×10⁻⁹mol/L尾加压素II处理的细胞I型胶原mRNA水平显著高于对照细胞(P<0.01)。

结论

尾加压素II可直接诱导心脏成纤维细胞增殖并显著增加I型胶原mRNA表达,提示尾加压素II在心肌重构中起关键作用。

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