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5—羟色胺增强去甲肾上腺素诱导的肥厚心肌L—型钙电流
引用本文:Zhao MG,Mei QB,Zhang YF,Xiong XY,Lu BH,Xing B,Zhao DH. 5—羟色胺增强去甲肾上腺素诱导的肥厚心肌L—型钙电流[J]. Acta pharmacologica Sinica, 2002, 23(6): 523-528
作者姓名:Zhao MG  Mei QB  Zhang YF  Xiong XY  Lu BH  Xing B  Zhao DH
作者单位:第四军医大学药理学教研室,第四军医大学药理学教研室,第四军医大学药理学教研室,第四军医大学药理学教研室,第四军医大学药理学教研室,第四军医大学药理学教研室 西安,中国 710032,西安,中国 710032,西安,中国 710032,西安,中国 710032,西安,中国 710032,西安,中国 710032
基金项目:Project supported by the National Natural Science Foundation of China, № 39500177.
摘    要:目的:研究5-羟色胺(5-HT)对去甲肾上腺素(NE)诱导的大鼠肥厚心肌L-型钙电流(I_(Ca))的影响.方法:大鼠腹腔注射NE建立心肌肥厚模型;酶解分离单个心室肌细胞;全细胞膜片箝记录I_(Ca).结果:(1)腹腔注射NE第15天,大鼠左心室与体重比增加31.8%(2)肥厚心肌细胞I_(Ca)与正常心肌细胞相比,明显增加0mV时分别为4.5pA/pF±0.5pA/pF和3.5pA/pF±0.3pA/pF(P<0.01).(3)5-HT可显著增加肥厚和正常心肌细胞I_(Ca),并使最大激活电流从0mV降低至-10mV;此外,5-HT增加I_(Ca)作用在肥厚心肌细胞更为显著.(4)稳态激活和失活实验发现,5-HT对稳态激活曲线无显著影响,而影响稳态失活曲线,使半失活电压从-39.5mV±1.8mV升高至-27.8mV±1.7mV(P<0.05),而不改变钙通道电压依赖性(斜率因子k无显著变化).结论:5-HT通过改变L-型钙通道稳态失活特征而显著增加I_(Ca),此作用在肥厚心肌细胞更显著,提示在肥厚心肌5-HT更易于诱导心律失常发生.

关 键 词:血清素  心肥大  钙通道  膜片箝技术

5-Hydroxytryptamine enhances L-type calcium current in norepinephrine-induced hypertrophic ventricular myocytes
Zhao Ming-Gao,Mei Qi-Bing,Zhang Yan-Feng,Xiong Xiao-Yun,Lu Bao-Hua,Xing Bin,Zhao De-Hua. 5-Hydroxytryptamine enhances L-type calcium current in norepinephrine-induced hypertrophic ventricular myocytes[J]. Acta pharmacologica Sinica, 2002, 23(6): 523-528
Authors:Zhao Ming-Gao  Mei Qi-Bing  Zhang Yan-Feng  Xiong Xiao-Yun  Lu Bao-Hua  Xing Bin  Zhao De-Hua
Affiliation:Department of Pharmacology, The Fourth Military Medical University, Xi-an 710032, China. mgzhao@hotmail.com
Abstract:AIM: To study the effects of 5-hydroxytryptamine (5-HT) on L-type calcium current (ICa) in norepinephrine (NE)-induced hypertrophic ventricular myocytes. METHODS: Left ventricular hypertrophy was induced by injecting NE intraperitoneally in rats. The single myocytes were isolated enzymatically from left ventricle. ICa was recorded with the whole-cell configuration of the patch-cl amp technique. RESULTS: (1) The ratio of left heart weight to body weight (LHW/BW) was higher (P < 0.01) in the NE-treated rats compared with the control rats on d 15. LHW/BW was increased 31.8 % in NE-treated rats. (2) ICa was larger in hypertrophic cells than that in normal cells (4.5 p A/pF +/- 0.5 pA/pF vs 3.5 pA/pF +/- 0.3 pA/pF, respectively, at testing potential of 0 mV; P < 0.01). (3) 5-HT (1, 10 micromol/L) increased ICa and decreased the peak current potential from 0 mV to -10 mV in both myocytes. The augmentation of ICa induced by 5-HT was larger in hypertrophic ones. (4) 5-HT did not markedly influence the steady-state activation kinetics. However, 5-HT shifted steady-state inactivation curve with half inactivation voltage V 1/2 changing from -39.5 mV +/- 1.8 mV to -27.8 mV +/- 1.7 m V (P < 0.05), while not changing the voltage responsiveness of calcium channel (slope factor k was not changed markedly). CONCLUSION: 5 -HT increased ICa in ventricular myocytes by changing the kinetics of steady-st ate inactivation. A larger alteration of ICa induced by 5-HT i n hypertrophic ventricular myocytes suggests that 5-HT be more prone to induce arrhythmia in hypertrophic heart than in normal one.
Keywords:serotonin  cardiomegaly  calcium channels  patch-clamp techniques
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