首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Receptor interactions of imidazolines: alpha-adrenoceptors of rat and rabbit aortae differentiated by relative potencies affinities and efficacies of imidazoline agonists.
【2h】

Receptor interactions of imidazolines: alpha-adrenoceptors of rat and rabbit aortae differentiated by relative potencies affinities and efficacies of imidazoline agonists.

机译:咪唑啉受体相互作用:通过咪唑啉激动剂的相对效力亲和力和效率区分大鼠和兔主动脉的α-肾上腺素受体。

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 Noradrenaline and a series of imidazolines were used to characterized and differentiate the postsynaptic alpha-adrenoceptors of rat and rabbit aortae. 2 Dose-response curves in each tissue revealed marked differences in the profile of agonist activity among the compounds. Based on the ED50 values for each compound, a rank order of potency of oxymetazoline greater than noradrenaline greater than tramazoline greater than tetrahydrozoline greater than clonidine was obtained in rabbit aorta and an order of noradrenaline greater than clonidine greater than tramazoline greater than oxymetazoline was obtained in rat aorta. Tetrahydrozoline had no agonist activity in rat aorta. 3 Dissociation constants were determined for each agonist in rat and rabbit aortae. Again, differences between the tissues were observed to the extent that the rank order of affinities for the imidazolines were exactly opposite for the two tissues. In rabbit aorta the order was, oxymetazoline greater than tramazoline greater than tetrahydrozoline greater than clonidine, whereas in rat aorta it was, clonidine greater than tetrahydrozoline greater then tramazoline greater than oxymetazoline. The extremes in tissue selectivity were observed with clonidine, which had approximately 125 fold higher affinity in rat aorta, and oxymetazoline, which had approximately 4 times higher affinity in rabbit aorta. 4 The absolute values of relative efficacies of the imidazolines studied, and their rank order, also differed between the two tissues. The relative efficacies of oxymetazoline and tramazoline were more than 15 fold greater in rabbit aorta than in rat aorta. Furthermore, tetrahydrozoline had a greater relative efficacy than clonidine in rabbit aorta while the converse was true in rat aorta. 5 Differences in the rank order of potency, affinity and relative efficacy of noradrenaline and a series of imidazolines in rat and rabbit aortae indicate that the postsynaptic alpha-adrenoceptors in these tissues are different. While the postsynaptic alpha-adrenoceptor of rabbit aorta is clearly of the alpha 1-subtype, the exact nature of the postsynaptic alpha-receptor of rat aorta is not clear. The unique alpha-receptor of rat aorta has properties of both alpha 1- and alpha 2-adrenoceptors.
机译:1去甲肾上腺素和一系列咪唑啉用于表征和区分大鼠和兔主动脉突触后的α-肾上腺素能受体。在每个组织中的2个剂量反应曲线显示出化合物之间激动剂活性的分布存在显着差异。根据每种化合物的ED50值,在兔主动脉中获得的羟甲唑啉大于去甲肾上腺素大于曲马唑啉大于四氢唑啉大于可乐定的效价等级次序,在甲酚中获得了去甲肾上腺素大于可乐定的阶数大于苯并咪唑啉的效价等级。大鼠主动脉。四氢唑啉在大鼠主动脉中没有激动剂活性。测定了大鼠和兔子主动脉中每种激动剂的解离常数。再次,观察到组织之间的差异,以至于对于咪唑啉的亲和力的等级顺序对于两个组织完全相反。在兔子主动脉中的顺序是,羟甲唑啉大于曲唑啉大于四氢唑啉大于可乐定,而在大鼠主动脉中,则是可乐定大于四氢唑啉大于曲马唑啉大于羟甲唑啉。用可乐定观察到极端的组织选择性,可乐定对大鼠主动脉的亲和力高约125倍,而羟甲唑啉对兔主动脉的亲和力高约4倍。 4研究的咪唑啉相对效率的绝对值及其等级顺序在两个组织之间也有所不同。羟甲唑啉和曲唑啉在兔主动脉中的相对效力比在大鼠主动脉中高15倍以上。此外,四氢唑啉在兔主动脉中具有比可乐定更大的相对功效,而在大鼠主动脉中则相反。 5去甲肾上腺素和一系列咪唑啉在大鼠和兔主动脉中的效力,亲和力和相对功效的等级顺序差异表明,这些组织中的突触后α-肾上腺素受体是不同的。虽然兔主动脉的突触后α-肾上腺素受体显然是α1-亚型,但大鼠主动脉的突触后α-受体的确切性质尚不清楚。大鼠主动脉的独特α受体同时具有α1和α2肾上腺素受体的特性。

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