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苄非他明对兔离体输精管和隐静脉中存在的NPY-Y1受体亚型的区分作用。

Discrimination by benextramine between the NPY-Y1 receptor subtypes present in rabbit isolated vas deferens and saphenous vein.

作者信息

Palea S, Corsi M, Rimland J M, Trist D G

机构信息

Glaxo Research Laboratories, Verona, Italy.

出版信息

Br J Pharmacol. 1995 May;115(1):3-10. doi: 10.1111/j.1476-5381.1995.tb16311.x.

Abstract
  1. In order to characterize the neuropeptide Y (NPY) Y1 receptors known to be present in rabbit isolated vas deferens and saphenous vein, the pharmacological activity of the selective NPY Y1 receptor agonists, [Leu31,Pro34] NPY and various other peptide agonists, together with the putative NPY antagonist, benextramine, were compared in the two tissues. 2. In rabbit isolated saphenous vein, cumulative dose-response curves to various NPY agonists were obtained. All the peptides tested caused contractions which developed quite slowly. The rank order of potency obtained was: PYY > NPY > [Leu31,Pro34] NPY = NPY2-36 > hPP >> NPY13-36 = NPY18-36. Incubation with benextramine (BXT) at 100 microM for 30 min irreversibly abolished the contractile response to [Leu31,Pro34] NPY but was ineffective against NPY18-36-induced contractions. 3. Cumulative dose-response curves to [Leu31,Pro34] NPY were performed in the same preparation before and after incubation with 100 microM BXT for 20 min in order to inactivate NPY Y1 receptors. The pKA (-logKA) estimation for [Leu31,Pro34] NPY was 7.60 +/- 0.30 using the operational model and 7.20 +/- 0.33 using the null method; the difference between the two methods was not statistically significant (P = 0.36). 4. Prostatic segments of rabbit vas deferens were electrically stimulated with single pulses. Immediately after stabilization of the contractile response, a cumulative dose-response curve to various NPY agonists was obtained in each tissue. The rank order of potency for twitch inhibition was: PYY> [Leu31,Pro34]NPY > NPY > hPP>NPY2- 36 >>NPY13-36>> NPY 18-36 which indicates the presence of a prejunctional NPY Y1 receptor. BXT at 100 microM incubated for 10 or 60 min did not antagonize the response to[Leu31,Pro34] NPY.5. We conclude that rabbit isolated saphenous vein contains a population of post-junctional NPY Y1 receptors irreversibly blocked by BXT, as well as a population of post-junctional NPY Y2 receptors,which are insensitive to BXT. In contrast, the rabbit isolated vas deferens express a pre-junctional NPYY1 receptor subtype which is not blocked by BXT. Tetramine disulphides such as BXT could be useful tools in classifying NPY receptors.
摘要
  1. 为了表征已知存在于兔离体输精管和隐静脉中的神经肽Y(NPY)Y1受体,在这两种组织中比较了选择性NPY Y1受体激动剂[Leu31,Pro34]NPY和其他各种肽类激动剂以及推定的NPY拮抗剂苄非他明的药理活性。2. 在兔离体隐静脉中,获得了对各种NPY激动剂的累积剂量 - 反应曲线。所有测试的肽均引起收缩,收缩发展相当缓慢。获得的效价顺序为:PYY>NPY>[Leu31,Pro34]NPY = NPY2 - 36>人胰多肽(hPP)>>NPY13 - 36 = NPY18 - 36。用100μM苄非他明(BXT)孵育30分钟可不可逆地消除对[Leu31,Pro34]NPY的收缩反应,但对NPY18 - 36诱导的收缩无效。3. 为了使NPY Y1受体失活,在与100μM BXT孵育20分钟之前和之后,在同一制备物中对[Leu31,Pro34]NPY进行累积剂量 - 反应曲线实验。使用操作模型对[Leu31,Pro34]NPY的pKA(-logKA)估计值为7.60±0.30,使用零方法为7.20±0.33;两种方法之间的差异无统计学意义(P = 0.36)。4. 用单脉冲电刺激兔输精管的前列腺段。在收缩反应稳定后,立即在每个组织中获得对各种NPY激动剂的累积剂量 - 反应曲线。对抽搐抑制的效价顺序为:PYY>[Leu31,Pro34]NPY>NPY>hPP>NPY2 - 36>>NPY13 - 36>>NPY18 - 36,这表明存在突触前NPY Y1受体。100μM的BXT孵育10或60分钟并未拮抗对[Leu31,Pro34]NPY的反应。5. 我们得出结论:兔离体隐静脉含有一群可被BXT不可逆阻断的突触后NPY Y1受体以及一群对BXT不敏感的突触后NPY Y2受体。相比之下,兔离体输精管表达一种不被BXT阻断的突触前NPY Y1受体亚型。诸如BXT的二硫代四胺类化合物可能是分类NPY受体的有用工具。

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