首页> 外文期刊>The Journal of Veterinary Medical Science >Inhibitory Effects of Psychotropic Drugs on the Acetylcholine Receptor-Operated Potassium Current (IK.ACh) in Guinea-Pig Atrial Myocytes
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Inhibitory Effects of Psychotropic Drugs on the Acetylcholine Receptor-Operated Potassium Current (IK.ACh) in Guinea-Pig Atrial Myocytes

机译:精神药物对豚鼠心房肌细胞乙酰胆碱受体操纵性钾电流(IK.ACh)的抑制作用

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References(34) Cited-By(1) Influences of psychotropic drugs, six antipsychotics and three antidepressants, on acetylcholine receptor-operated potassium current (IK.ACh) were examined by a whole-cell patch clamp method in freshly isolated guinea-pig atrial myocyte. IK.ACh was induced by a superfusion of carbachol (CCh) or by an intracellular application of guanosine 5’-[thio] triphosphate (GTPγS). To elucidate mechanism for anticholinergic action, IC50 ratio, the ratio of IC50 for GTPγS-activated IK.ACh to CCh-induced IK.ACh, was calculated. Antipsychotics and antidepressants inhibited CCh-induced IK.ACh in a concentration-dependent manner. The IC50 values were as follows; chlorpromazine 0.53 μM, clozapine 0.06 μM, fluphenazine 2.69 μM, haloperidol 2.66 μM, sulpiride 42.3 μM, thioridazine 0.07 μM, amitriptyline 0.03 μM, imipramine 0.22 μM and maprotiline 1.81 μM. The drugs, except for sulpiride, inhibited GTPγS-activated IK.ACh with following IC50 values; chlorpromazine 1.71 μM, clozapine 14.9 μM, fluphenazine 3.55 μM, haloperidol 2.73 μM, thioridazine 1.90 μM, amitriptyline 7.55 μM, imipramine 7.09 μM and maprotiline 5.93 μM. The IC50 ratio for fluphenazine and haloperidol was close to unity. The IC50 ratio for chlorpromazine, clozapine, thioridazine, amitriptyline, imipramine and maprotiline was much higher than unity. The present findings suggest that the psychotropics studied suppress IK.ACh. Chlorpromazine, clozapine, thioridazine, amitriptyline, imipramine, maprotiline and sulpiride are preferentially acting on muscarinic receptor. Fluphenazine and haloperidol may act on G protein and/or potassium channel.
机译:参考文献(34)被引用(1)在新分离的豚鼠心房中,采用全细胞膜片钳法研究了精神药物,六种抗精神病药和三种抗抑郁药对乙酰胆碱受体操纵的钾电流(IK.ACh)的影响。肌细胞。 IK.ACh是通过卡巴胆碱(CCh)的过度融合或鸟苷5'-[硫代]三磷酸鸟苷(GTPγS)的细胞内应用诱导的。为了阐明抗胆碱作用的机制,计算了IC50比率,即GTPγS激活的IK.ACh与CCh诱导的IK.ACh的IC50比率。抗精神病药和抗抑郁药以浓度依赖性方式抑制CCh诱导的IK.ACh。 IC50值如下。氯丙嗪0.53μM,氯氮平0.06μM,氟奋乃静2.69μM,氟哌啶醇2.66μM,舒必利42.3μM,硫代哒嗪0.07μM,阿米替林0.03μM,丙咪嗪0.22μM和马普替林1.81μM。除舒必利外,这些药物均抑制GTPγS活化的IK.ACh,其IC50值如下:氯丙嗪1.71μM,氯氮平14.9μM,氟奋乃静3.55μM,氟哌啶醇2.73μM,硫代哒嗪1.90μM,阿米替林7.55μM,丙咪嗪7.09μM和马普替林5.93μM。氟奋乃静和氟哌啶醇的IC50比率接近于1。氯丙嗪,氯氮平,硫代达嗪,阿米替林,丙咪嗪和马普替林的IC50比率远高于统一。目前的发现表明,所研究的精神药物可以抑制IK.ACh。氯丙嗪,氯氮平,硫代达嗪,阿米替林,丙咪嗪,马普替林和舒必利优先作用于毒蕈碱受体。氟奋乃静和氟哌啶醇可能作用于G蛋白和/或钾通道。

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