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首页> 外文期刊>Pharmacology: International Journal of Experimental and Clinical Pharmacology >Modulation of the Negative Inotropic Effect of Haloperidol by Drugs with Positive Inotropic Effects in Isolated Rabbit Heart.
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Modulation of the Negative Inotropic Effect of Haloperidol by Drugs with Positive Inotropic Effects in Isolated Rabbit Heart.

机译:具有正性肌力作用的药物对离体兔心脏中氟哌啶醇的负性肌力作用的调节。

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摘要

Haloperidol is a typical antipsychotic drug with inhibitory effects on dopamine and calcium homeostasis. In this study, the effect of haloperidol on the inotropism of rabbits' isolated heart was investigated by measuring the isovolumetric left ventricular pressure using a balloon in a modified Langendorff perfusion apparatus. Haloperidol at 0.01-0.3 &mgr;mol/l induced a negative inotropic effect (E(max) = 77.95 +/- 0.19; EC(50) = 0.043 +/- 0.002 &mgr;mol/l). The effect of haloperidol was decreased by Ca(2+) (E(max) = 42.93 +/- 3.22; EC(50) = 0.37 +/- 0.07 &mgr;mol/l; pD'(2) = 7.01 +/- 0.16), Bay K 8644 (E(max) = 30.75 +/- 1.33; EC(50) = 10.43 +/- 1.5 &mgr;mol/l, pD'(2) = 7.13 +/- 0.12), and digoxin (E(max ) = 42.03 +/- 3.72, EC(50) = 0.32 +/- 0.05 &mgr;mol/l, pD'(2) = 6.81 +/- 0.14). The effect of haloperidol was also reduced by norepinephrine (E(max) = 37.16 +/- 1.84; EC(50) = 1.73 +/- 0.24 &mgr;mol/l, pD'(2) = 6.97 +/- 0.08) and dopamine (E(max) = 35.68 +/- 2.78; EC(50) = 0.69 +/- 0.01 &mgr;mol/l, pD'(2 )7.48 +/- 0.15). However, the effect of haloperidol was nonsignificantly reduced by dobutamine (E(max) = 58.89 +/- 5.18; EC(50) = 0.15 +/- 0.06 &mgr;mol/l, pD'(2) = 5.88 +/- 0.47). These results show that the drugs that increase the influx of Ca(2+) into the cardiomyocyte decrease the negative inotropic effect of haloperidol, suggesting that the effect of haloperidol could be mediated via mechanisms involving actions on Ca(2+) entry into the cardiomyocyte. Haloperidol should be used carefully when prescribed for patients with cardiovascular disorders. Copyright 2002 S. Karger AG, Basel
机译:氟哌啶醇是一种典型的抗精神病药物,对多巴胺和钙稳态具有抑制作用。在这项研究中,氟哌啶醇对家兔离体心脏正性肌力的影响是通过在改良的Langendorff灌注仪中使用气球测量等容左心室压力来研究的。氟哌啶醇在0.01-0.3 mg / mol时引起负性肌力作用(E(max)= 77.95 +/- 0.19; EC(50)= 0.043 +/- 0.002 mg / l)。 Ca(2+)降低了氟哌啶醇的作用(E(max)= 42.93 +/- 3.22; EC(50)= 0.37 +/- 0.07&mgr; mol / l; pD'(2)= 7.01 +/- 0.16),Bay K 8644(E(max)= 30.75 +/- 1.33; EC(50)= 10.43 +/- 1.5&mol / mol,pD'(2)= 7.13 +/- 0.12)和地高辛( E(max)= 42.03 +/- 3.72,EC(50)= 0.32 +/- 0.05μmol/ l,pD'(2)= 6.81 +/- 0.14)。去甲肾上腺素(E(max)= 37.16 +/- 1.84; EC(50)= 1.73 +/- 0.24&mgr; mol / l,pD'(2)= 6.97 +/- 0.08)也降低了氟哌啶醇的作用多巴胺(E(max)= 35.68 +/- 2.78; EC(50)= 0.69 +/- 0.01&mol / l,pD'(2)7.48 +/- 0.15)。但是,多巴酚丁胺对氟哌啶醇的作用没有显着降低(E(max)= 58.89 +/- 5.18; EC(50)= 0.15 +/- 0.06 mg / l,pD'(2)= 5.88 +/- 0.47 )。这些结果表明,增加Ca(2+)流入心肌细胞的药物可降低氟哌啶醇的负性肌力作用,表明氟哌啶醇的作用可通过涉及对Ca(2+)进入心肌细胞的作用的机制来介导。 。心血管疾病患者开处方时应谨慎使用氟哌啶醇。版权所有2002 S. Karger AG,巴塞尔

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