首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >A comparison of A2 adenosine receptor-induced cyclic AMP generation in cerebral cortex and relaxation of pre-contracted aorta.
【2h】

A comparison of A2 adenosine receptor-induced cyclic AMP generation in cerebral cortex and relaxation of pre-contracted aorta.

机译:A2腺苷受体诱导的大脑皮层中环状AMP生成与预收缩主动脉松弛的比较。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

1. A comparative study was carried out between the adenosine receptor mediating a stimulation of cyclic AMP formation in guinea-pig cerebral cortical slices with the adenosine receptor mediating relaxation of phenylephrine precontracted guinea-pig aortic rings. 2. [3H]-cyclic AMP accumulation in [3H]-adenine-prelabelled guinea-pig cerebral cortical slices was stimulated by adenosine and its analogues with the following EC50 values (microM): 5'-N-ethylcarboxamidoadenosine (3.1 +/- 0.3) > 2-chloroadenosine (10 +/- 2) > adenosine (109 +/- 15). 3. 2-Chloroadenosine and adenosine elicited maximal responses for [3H]-cyclic AMP accumulation that were 100 +/- 7 and 71 +/- 6% of the maximal response to 5'-N-ethylcarboxamidoadenosine, respectively. CGS 21680 (100 microM) and DPMA (100 microM) elicited -2 +/- 2 and 12 +/- 3% of the response to 100 microM 5'-N-ethylcarboxamidoadenosine. 4. Estimation of antagonist potencies at the A2 adenosine receptor of cerebral cortex showed a rank order of potency (K1, nM): xanthine amino congener (35 +/- 3) > 8-cyclopentyl-1,3-dipropylxanthine (130 +/- 22) > PD 115,199 (407 +/- 82) > 3,7-dimethyl-1-propargylxanthine (13 +/- 2 microM). 5. Adenosine analogues produced long-lasting relaxation of phenylephrine-precontracted aortic rings with the following rank order of potency (EC50 values, microM): 5'-N-ethylcarboxamidoadenosine (0.68 +/- 0.06) > 2-chloroadenosine (4.3 +/- 0.6) > adenosine (104 +/- 13). Maximal relaxations elicited by these agents were 71 +/- 3, 98 +/- 1, and 100 +/- 1%, respectively. CGS 21680 and DPMA at 100 microM elicited smaller relaxations of the precontracted tissues (12 +/- 2 and 43 +/- 15%, respectively). 6. Antagonism by xanthine derivatives of the 5'-N-ethylcarboxamidoadenosine-induced relaxation of aortic rings showed the following rank order of potency (Ki, nM): xanthine amino congener (17 +/- 4) > 8-cyclopentyl-1,3-dipropylxanthine (171 +/- 36) > PD 115,199 (341 +/- 64) > 3,7-dimethyl-1-propargylxanthine (5520 +/- 820).(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.在腺苷受体介导豚鼠脑皮质切片中环AMP形成的刺激与腺苷受体介导去氧肾上腺素预收缩的豚鼠主动脉环松弛之间进行了比较研究。 2.腺苷及其类似物具有以下EC50值(microM)刺激[3H]-腺嘌呤预标记的豚鼠大脑皮层切片中的[3H]-环AMP积累:5'-N-乙基羧酰胺基腺苷(3.1 +/- 0.3)> 2-氯腺苷(10 +/- 2)>腺苷(109 +/- 15)。 3. 2-氯代腺苷和腺苷引起[3H]-环AMP积累的最大响应,分别是对5'-N-乙基羧酰胺基腺苷最大响应的100 +/- 7和71 +/- 6%。 CGS 21680(100 microM)和DPMA(100 microM)引起对100 microM 5'-N-乙基羧酰胺基腺苷反应的-2 +/- 2和12 +/- 3%。 4.估计大脑皮质A2腺苷受体的拮抗药效价显示效价等级排序(K1,nM):黄嘌呤氨基同源物(35 +/- 3)> 8-环戊基-1,3-二丙基黄嘌呤(130 + / -22)> PD 115,199(407 +/- 82)> 3,7-二甲基-1-炔丙基黄嘌呤(13 +/- 2 microM)。 5.腺苷类似物使苯肾上腺素预收缩的主动脉环持久松弛,其效力如下(EC50值,microM):5'-N-乙基羧酰胺基腺苷(0.68 +/- 0.06)> 2-氯腺苷(4.3 + / -0.6)>腺苷(104 +/- 13)。这些试剂引起的最大舒张分别为71 +/- 3、98 +/- 1和100 +/- 1%。 100 microM的CGS 21680和DPMA引起预收缩组织的松弛较小(分别为12 +/- 2和43 +/- 15%)。 6.黄嘌呤衍生物对5'-N-乙基羧酰胺基腺苷诱导的主动脉环松弛的拮抗作用显示出以下等级的效力(Ki,nM):黄嘌呤氨基同源物(17 +/- 4)> 8-环戊基-1, 3-二丙基黄嘌呤(171 +/- 36)> PD 115,199(341 +/- 64)> 3,7-二甲基-1-炔丙基黄嘌呤(5520 +/- 820)。(截短为250字)

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号