Characterization of tachykinin receptors in urinary bladder from guinea pig.

Characterization of tachykinin receptors in urinary bladder from guinea pig.
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豚鼠膀胱中速激肽受体的表征。

DOI:
10.1254/jjp.54.241
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发表时间:
1990
期刊:
Japanese journal of pharmacology
影响因子:
--
通讯作者:
I. Takayanagi
I. Takayanagi
中科院分区:
--
文献类型:
--
作者:
M. Shinkai;I. Takayanagi

文献摘要

被引文献

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研究了豚鼠逼尿肌条对P物质(SP)、神经激肽A (NKA)、tyr -神经激肽B (Tyr-NKB)、senktide (NK3受体选择性激动剂)和SP甲酯(SPOMe, NK1受体选择性激动剂)的收缩反应。除senktide外,所有药物均呈浓度相关收缩,其效价大小顺序为:SPOMe > SP > NKA >或等于Tyr-NKB。NK1受体与SPOMe脱敏后,效力等级为NKA大于等于tyr1 - nkb大于SP大于SPOMe。豚鼠逼尿肌条中同时存在NK1和NK2受体。
The contractile responses to substance P (SP), neurokinin A (NKA), Tyro-neurokinin B (Tyr-NKB), senktide (NK3 receptor selective agonist) and SP methyl ester (SPOMe, NK1 receptor selective agonist) were investigated in detrusor strips from guinea pigs. Except for senktide, all drugs induced a concentration-related contraction with the following rank order of potency: SPOMe greater than SP greater than NKA greater than or equal to Tyr-NKB. After desensitization of NK1 receptors with SPOMe, the rank order of potency was NKA greater than or equal to Tyr-NKB greater than SP greater than SPOMe. Both NK1 and NK2 receptors exist in the detrusor strip from guinea pigs.