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Effect of Moniliformin on Myocardial Contractility in Rats
引用本文:FANLILI LIJUAN 等. Effect of Moniliformin on Myocardial Contractility in Rats[J]. Biomedical and environmental sciences : BES, 1991, 4(3): 290-294
作者姓名:FANLILI LIJUAN 等
作者单位:[1]InstituteofMateriaMedica,ChineseAcademyofMedicalSciences,1XianNongTanStreet,Beijing100050 [2]Instituteo,ChineseAcademyofMedicalSciences,1XianNongTanStreet,Beijing100050
摘    要:The present study was carried out on rat heart to in situ determine the myocardial toxicity of moniliformin, a synthesized compound, originally isolated from mouldy corn and soil samples in the Keshan disease prevalent area in China. Perfusion of moniliformin 10-7 mol/liter in isolated heart decreased myocardial contractile force by 52±17%. Intravenous injection of moniliformin at 1/6 and 1/4 LD_(50) markedly inhibited cardiac hemodynamic variables relative to myocardial contractile function. Particularly, it decreased 4±LV dP/dt max by 52±6%, and induced ventricular arrhythmia. These data indicate that moniliformin is toxic to mammalian heart and might be an important factor relative to Keshan disease.

关 键 词:串珠镰刀菌素 大鼠 心肌收缩力 作用机理

Effect of moniliformin on myocardial contractility in rats.
L L Fan,J Li,L H Sun. Effect of moniliformin on myocardial contractility in rats.[J]. Biomedical and environmental sciences : BES, 1991, 4(3): 290-294
Authors:L L Fan  J Li  L H Sun
Affiliation:Institute of Materia Medica, Chinese Academy of Medical Sciences, Beijing.
Abstract:The present study was carried out on rat heart to in situ determine the myocardial toxicity of moniliformin, a synthesized compound, originally isolated from mouldy corn and soil samples in the Keshan disease prevalent area in China. Perfusion of moniliformin 10(-7) mol/liter in isolated heart decreased myocardial contractile force by 52 +/- 17%. Intravenous injection of moniliformin at 1/6 and 1/4 LD50 markedly inhibited cardiac hemodynamic variables relative to myocardial contractile function. Particularly, it decreased +/- LV dP/dt max by 52 +/- 6%, and induced ventricular arrhythmia. These data indicate that moniliformin is toxic to mammalian heart and might be an important factor relative to Keshan disease.
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