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负鼠食管黏膜肌层中速激肽受体的分类

Classification of tachykinin receptors in muscularis mucosae of opossum oesophagus.

作者信息

Daniel E E, Cipris S, Manaka Y, Bowker P, Regoli D

机构信息

Department of Neurosciences, McMaster University, Hamilton, Ontario, Canada.

出版信息

Br J Pharmacol. 1989 Aug;97(4):1013-8. doi: 10.1111/j.1476-5381.1989.tb12556.x.

Abstract
  1. Muscularis mucosae of the distal oesophagus of the opossum contracts in response to substance P and to a variety of tachykinins. To delineate the nature of the receptors present in this tissue, we evaluated contractile responses to substance P, neurokinin A, neurokinin B, eledoisin and analogues believed to be highly selective for NK-1, NK-2 and NK-3 receptors. In addition, the effects of prolonged exposure to each of these agents (10(-6) M or 10(-5) M) on contractile responses to substance P and to itself were evaluated. Similarly effects of prolonged exposure to the various tachykinins and their analogues on the field-stimulated responses of this muscle were studied. 2. All naturally occurring tachykinins were full agonists and differed in potency (comparing ED50 values) by less than ten fold. In nearly all cases there was cross tachyphylaxis between substance P and the other tachykinins and each reduced tonic responses to field stimulation, a response previously shown to be mediated by a substance P like agent. Eledoisin failed to cause tachyphylaxis under the conditions of these experiments. 3. When highly selective tachykinin analogues were used, only that believed to activate NK-1 receptors was a full agonist. [beta-Ala4,Sar9,MetO2(11)]SP(4-11) was also only slightly less potent than substance P. In contrast, an agonist selective for NK-2 (NK-A) receptors, [Nle10]NKA(4-10), and one selective for NK-3 (NK-B) receptors, [beta-Asp4, MePhe7]NKB(4-10) were unable to produce a response equal to 50% of the maximum even at 10(-5) M. However, all three selective tachykinin analogues reduced responses to substance P but not to carbachol. They usually reduced both phasic and tonic responses to field stimulation. 4. We conclude, based on this and earlier study, that the tachykinin receptors of opossum oesophagus muscularis mucosae recognize all naturally occurring tachykinins but may represent only NK-1 receptors. The ability of analogues selective for other types of tachykinin receptors to reduce responses to substance P raises the possibility that their selectivity depends in part on diminished efficacy rather than totally on diminished affinity at some classes of receptor.
摘要
  1. 负鼠远端食管的黏膜肌层会对P物质和多种速激肽产生收缩反应。为了阐明该组织中存在的受体的性质,我们评估了对P物质、神经激肽A、神经激肽B、eledoisin以及据信对NK-1、NK-2和NK-3受体具有高度选择性的类似物的收缩反应。此外,还评估了长时间暴露于这些药物中的每一种(10⁻⁶ M或10⁻⁵ M)对P物质及其自身收缩反应的影响。同样,研究了长时间暴露于各种速激肽及其类似物对该肌肉场刺激反应的影响。2. 所有天然存在的速激肽都是完全激动剂,其效力(比较ED50值)相差不到十倍。在几乎所有情况下,P物质与其他速激肽之间都存在交叉快速耐受性,并且每种速激肽都会降低对场刺激的强直反应,先前已证明这种反应是由一种类似P物质的介质介导的。在这些实验条件下,eledoisin未引起快速耐受性。3. 当使用高度选择性的速激肽类似物时,只有被认为能激活NK-1受体的类似物是完全激动剂。[β-丙氨酸⁴,Sar⁹,MetO₂(¹¹)]SP(4 - 11)的效力也仅略低于P物质。相比之下,一种对NK-2(NK-A)受体具有选择性的激动剂,[Nle¹⁰]NKA(4 - 10),以及一种对NK-3(NK-B)受体具有选择性的激动剂,[β-天冬氨酸⁴,MePhe⁷]NKB(4 - 10),即使在10⁻⁵ M时也无法产生等于最大反应50%的反应。然而,所有三种选择性速激肽类似物都会降低对P物质的反应,但不会降低对卡巴胆碱的反应。它们通常会降低对场刺激的相性和强直反应。4. 基于本研究及早期研究,我们得出结论,负鼠食管黏膜肌层的速激肽受体能识别所有天然存在的速激肽,但可能仅代表NK-1受体。对其他类型速激肽受体具有选择性的类似物降低对P物质反应的能力,增加了其选择性部分取决于效力降低而非完全取决于对某些受体类别的亲和力降低的可能性。

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