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一种新型毒蕈碱受体拮抗剂AF-DX 116可不同程度地阻断兔交感神经节中的慢抑制性和慢兴奋性突触后电位。

A novel muscarinic receptor antagonist AF-DX 116 differentially blocks slow inhibitory and slow excitatory postsynaptic potentials in the rabbit sympathetic ganglia.

作者信息

Mochida S, Kobayashi H

机构信息

Department of Physiology, Tokyo Medical College, Japan.

出版信息

Life Sci. 1988;42(22):2195-201. doi: 10.1016/0024-3205(88)90370-0.

Abstract

Muscarinic, slow postsynaptic potentials (s-epsp and s-ipsp) in the rabbit superior cervical ganglia were shown to be differentially depressed by a novel cardioselective M2-type antagonist AF-DX 116: it antagonized the s-ipsp with IC50 value of 1.5 X 10(-7) M, which is 16-fold more potent in depressing the s-ipsp than the s-epsp. A hyperpolarizing component in the biphasic potential changes induced by a muscarinic agonist, methacholine, was selectively eliminated by this antagonist. AF-DX 116 was thus shown to be an useful tool for discriminating the M2-type muscarinic responses from those of M1-type in the nervous system.

摘要

在兔颈上神经节中,毒蕈碱型慢突触后电位(慢兴奋性突触后电位和慢抑制性突触后电位)被一种新型心脏选择性M2型拮抗剂AF-DX 116差异性抑制:它拮抗慢抑制性突触后电位,IC50值为1.5×10⁻⁷M,在抑制慢抑制性突触后电位方面比慢兴奋性突触后电位强16倍。毒蕈碱激动剂乙酰甲胆碱诱导的双相电位变化中的超极化成分被该拮抗剂选择性消除。因此,AF-DX 116被证明是一种用于区分神经系统中M2型毒蕈碱反应和M1型反应的有用工具。

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