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N-乙基马来酰亚胺对大鼠心房毒蕈碱受体刺激引起的变时性和变力性反应的区分作用

Discrimination by N-ethylmaleimide between the chronotropic and inotropic response to muscarinic receptor stimulation in rat atrium.

作者信息

Doods H N, Davidesko D, Mathy M J, Batink H D, de Jonge A, van Zwieten P A

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1986 Jun;333(2):182-5. doi: 10.1007/BF00506524.

Abstract

N-ethylmaleimide (NEM) rapidly blocked the negative chronotropic effect of carbachol on rat right atrium. In contrast, NEM did not reduce the negative inotropic response to muscarinic (M) receptor stimulation. Carbachol inhibited the specific binding of [3H]-N-methylscopolamine [( 3H]-NMS) to membranes of rat atria as reflected by a shallow inhibition curve. Both guanosine triphosphate (GTP) and NEM shifted the [3H]-NMS inhibition curves of carbachol to the right. Pretreatment of the atrial membranes with NEM abolished the GTP-induced rightward shift. However, when instead of the membranes the intact atria were pre-incubated with NEM, no interaction between NEM and GTP in the membranal preparation was observed. The results indicate that NEM sharply discriminated between the inotropic and chronotropic effects to M-receptor stimulation in rat atria. The inhibitory effect of NEM on the M-receptor-mediated negative chronotropic effect in rat atrium cannot be explained by an interaction of the sulfhydryl reagent with GTP-binding proteins, like Ni or No.

摘要

N-乙基马来酰亚胺(NEM)迅速阻断了卡巴胆碱对大鼠右心房的负性变时作用。相比之下,NEM并未降低对毒蕈碱(M)受体刺激的负性变力反应。卡巴胆碱抑制了[3H]-N-甲基东莨菪碱[(3H]-NMS)与大鼠心房膜的特异性结合,这表现为一条浅的抑制曲线。鸟苷三磷酸(GTP)和NEM均使卡巴胆碱的[3H]-NMS抑制曲线右移。用NEM预处理心房膜消除了GTP诱导的右移。然而,当用NEM预孵育完整心房而非心房膜时,在膜制备物中未观察到NEM与GTP之间的相互作用。结果表明,NEM在大鼠心房中对M受体刺激的变力和变时作用有明显区分。NEM对大鼠心房中M受体介导的负性变时作用的抑制作用不能用巯基试剂与GTP结合蛋白(如Ni或No)的相互作用来解释。

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