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Inhibition of specific over-expression of heat shock protein 27 in heart for doxorubicin-induced myocardial apoptosis in transgenic mice model

Cheng Yun-li

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Abstract

Objective To determine the effects of heat shock protein 27(Hsp27)on the myocardial apoptosis induced by doxorubicin(Dox)in transgenic(TG)mice model.Methods Wild type(WT)and TG mice of cardiac specific over-expression Hsp27 were treated with Dox 25 mg/kg or saline.Three days later,the myocardial apoptosis by TUNEL stain and the expression of inducible heat shock proteins(iHsps)were detected and compared between each group.Results Specific over-expression of Hsp27 in heart was found in TG.Apoptosis significantly increased in Dox-treated groups compared with their control groups(P 0.01)and apoptosis induced by Dox was inhibited in TG compared with WT [(5.22±0.60)‰ vs(10.67±2.41)‰,P 0.01].The expressions of Hsp70 and heme oxygenases-1(HO-1)were enhanced by Dox and much more promoted in TG than in WT(Hsp70:1.793±0.237 vs 1.013±0.14,P 0.01;HO-1:6.884±1.104 vs 4.385±0.463,P 0.05),but αBC displayed no difference between the groups.Conclusions Specific over-expression of Hsp27 in heart can protect myocardial apoptosis induced by Dox in transgenic mice model.

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Objective To determine the effects of heat shock protein 27(Hsp27)on the myocardial apoptosis induced by doxorubicin(Dox)in transgenic(TG)mice model.Methods Wild type(WT)and TG mice of cardiac specific over-expression Hsp27 were treated with Dox 25 mg/kg or saline.Three days later,the myocardial apoptosis by TUNEL stain and the expression of inducible heat shock proteins(iHsps)were detected and compared between each group.Results Specific over-expression of Hsp27 in heart was found in TG.Apoptosis significantly increased in Dox-treated groups compared with their control groups(P 0.01)and apoptosis induced by Dox was inhibited in TG compared with WT [(5.22±0.60)‰ vs(10.67±2.41)‰,P 0.01].The expressions of Hsp70 and heme oxygenases-1(HO-1)were enhanced by Dox and much more promoted in TG than in WT(Hsp70:1.793±0.237 vs 1.013±0.14,P 0.01;HO-1:6.884±1.104 vs 4.385±0.463,P 0.05),but αBC displayed no difference between the groups.Conclusions Specific over-expression of Hsp27 in heart can protect myocardial apoptosis induced by Dox in transgenic mice model.

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Available abstract

Objective To determine the effects of heat shock protein 27(Hsp27)on the myocardial apoptosis induced by doxorubicin(Dox)in transgenic(TG)mice model.Methods Wild type(WT)and TG mice of cardiac specific over-expression Hsp27 were treated with Dox 25 mg/kg or saline.Three days later,the myocardial apoptosis by TUNEL stain and the expression of inducible heat shock proteins(iHsps)were detected and compared between each group.Results Specific over-expression of Hsp27 in heart was found in TG.Apoptosis significantly increased in Dox-treated groups compared with their control groups(P 0.01)and apoptosis induced by Dox was inhibited in TG compared with WT [(5.22±0.60)‰ vs(10.67±2.41)‰,P 0.01].The expressions of Hsp70 and heme oxygenases-1(HO-1)were enhanced by Dox and much more promoted in TG than in WT(Hsp70:1.793±0.237 vs 1.013±0.14,P 0.01;HO-1:6.884±1.104 vs 4.385±0.463,P 0.05),but αBC displayed no difference between the groups.Conclusions Specific over-expression of Hsp27 in heart can protect myocardial apoptosis induced by Dox in transgenic mice model.

Key concepts: Apoptosis, Hsp27, Heat shock protein, Hsp70, TUNEL assay, Medicine, Doxorubicin, Genetically modified mouse

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