2006Journal of Military Surgeon in Southwest ChinaRequires access

Rat Cardiac Fibroblasts Proliferation by Aldosterone

HU Yong-xia

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Abstract

Objective To investigate the effect of aldosterone on proliferation of rat cardiac fibroblasts.Methods Upon the model of cultured rat FBs,aldosterone was used to stimulate proliferation of FBs,()~3H-Leucine(()~3H-Leu) and()~3H-Thymidine(()~3H-TdR) incorporation as the target to evaluate FBs proliferation.Results Synthesis rates of protein and nucleic acid of FBs stimulated by aldosterone increased in a dose dependent manner significantly in contrast to control(P0.01);spironoactone markedly inhibited syntheses of protein and nucleic acid mediated by aldosterone in FBs with a significant difference from aldosterone-stimulated group(P0.01).Conclusions Spironoactone inhibits the proliferation of FBs induced by aldosterone.

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Objective To investigate the effect of aldosterone on proliferation of rat cardiac fibroblasts.Methods Upon the model of cultured rat FBs,aldosterone was used to stimulate proliferation of FBs,()~3H-Leucine(()~3H-Leu) and()~3H-Thymidine(()~3H-TdR) incorporation as the target to evaluate FBs proliferation.Results Synthesis rates of protein and nucleic acid of FBs stimulated by aldosterone increased in a dose dependent manner significantly in contrast to control(P0.01);spironoactone markedly inhibited syntheses of protein and nucleic acid mediated by aldosterone in FBs with a significant difference from aldosterone-stimulated group(P0.01).Conclusions Spironoactone inhibits the proliferation of FBs induced by aldosterone.

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Available abstract

Objective To investigate the effect of aldosterone on proliferation of rat cardiac fibroblasts.Methods Upon the model of cultured rat FBs,aldosterone was used to stimulate proliferation of FBs,()~3H-Leucine(()~3H-Leu) and()~3H-Thymidine(()~3H-TdR) incorporation as the target to evaluate FBs proliferation.Results Synthesis rates of protein and nucleic acid of FBs stimulated by aldosterone increased in a dose dependent manner significantly in contrast to control(P0.01);spironoactone markedly inhibited syntheses of protein and nucleic acid mediated by aldosterone in FBs with a significant difference from aldosterone-stimulated group(P0.01).Conclusions Spironoactone inhibits the proliferation of FBs induced by aldosterone.

Key concepts: Aldosterone, Thymidine, Internal medicine, Endocrinology, Cell growth, Medicine, Nucleic acid, Biology

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