Suppr超能文献

B2受体在缓激肽诱导的豚鼠离体气管舒张中的作用。

Involvement of B2 receptors in the bradykinin-induced relaxation of guinea-pig isolated trachea.

作者信息

Da Silva A, Amrani Y, Trifilieff A, Landry Y

机构信息

Laboratoire de Neuroimmunopharmacologie, INSERM-U405, Université Louis Pasteur Strasbourg I, Faculté de Pharmacie, Illkirch, France.

出版信息

Br J Pharmacol. 1995 Jan;114(1):103-8. doi: 10.1111/j.1476-5381.1995.tb14912.x.

Abstract
  1. The aim of this study was to determine the receptor type and involvement of arachidonic acid metabolites in bradykinin-induced relaxation of the guinea-pig isolated trachea. 2. In the resting tracheal preparation, bradykinin (0.1 nM-30 microM induced a concentration-related contractile response (pD2 = 8.8 +/- 0.3). The maximal tension (1056 +/- 321 mg) was observed at 0.3 microM bradykinin. In contrast, when tracheal preparations were pre-contracted with histamine (30 microM leading to a half-maximum response), a concentration-related relaxation was observed with bradykinin. At the highest concentration of bradykinin used (3 microM), a reversal of 63 +/- 13% of the contractile response to histamine was observed. Both effects of bradykinin were inhibited by the cyclo-oxygenase inhibitor, indomethacin (1 microM). In concentration-response curves, melittin (10 nM-1 microM), a direct activator of phospholipase A2, mimicked both effects of bradykinin. The highest concentration of melittin used (1 microM), induced a tension of 813 +/- 120 mg and led to the reversal of 41 +/- 8% of the contractile response to histamine. The contractile effect of melittin was inhibited in the presence of both indomethacin (1 microM) and AA861 (1 microM), a 5-lipoxygenase inhibitor. 3. [Des Arg9]-bradykinin (1 nM-3 microM), a B1-receptor agonist, was unable to relax precontracted guinea-pig tracheal preparations. The relaxation induced by bradykinin was antagonized by the B2 receptor antagonists, Hoe 140 (D-Arg0[Hyp3,Thi5,D-Tic7,Oic8]bradykinin) and NPC 17761 (D-Arg0[Hyp3,D-HypE(trans-thiophenyl)7,Oic8]bradykinin ). Hoe 140 (0.1 microM to 0.6 microM) behaved as a non-competitive antagonist with an apparent pA2 = 7.2 +/- 0.4, whereas NPC 17761 (0.3 to 1 microM) competitively antagonized bradykinin-induced relaxation with a pKB = 7.3 +/- 0.2. The Schild regression slope did not differ from unity, 0.96 +/- 0.20, P<0.05.4. These data demonstrate that bradykinin-induced relaxation of guinea-pig trachea occurs via the activation of bradykinin B2-receptors. The stimulation of B2-bradykinin receptors induces the activation of the cyclo-oxygenase pathway, leading either to contraction or relaxation depending on the tone of the trachea.
摘要
  1. 本研究的目的是确定受体类型以及花生四烯酸代谢产物在缓激肽诱导的豚鼠离体气管舒张中的作用。2. 在静息气管标本中,缓激肽(0.1 nM - 30 μM)诱导出浓度依赖性收缩反应(pD2 = 8.8 ± 0.3)。在0.3 μM缓激肽时观察到最大张力(1056 ± 321 mg)。相反,当气管标本用组胺(30 μM,导致半数最大反应)预收缩时,缓激肽可诱导出浓度依赖性舒张。在所用的最高缓激肽浓度(3 μM)下,观察到对组胺收缩反应的63 ± 13%的逆转。缓激肽的这两种作用均被环氧化酶抑制剂吲哚美辛(1 μM)抑制。在浓度 - 反应曲线中,蜂毒肽(10 nM - 1 μM),一种磷脂酶A2的直接激活剂,模拟了缓激肽的两种作用。所用的最高蜂毒肽浓度(1 μM)诱导出813 ± 120 mg的张力,并导致对组胺收缩反应的41 ± 8%的逆转。在吲哚美辛(1 μM)和5 - 脂氧合酶抑制剂AA861(1 μM)存在时,蜂毒肽的收缩作用被抑制。3. [去精氨酸9] - 缓激肽(1 nM - 3 μM),一种B1受体激动剂,不能使预收缩的豚鼠气管标本舒张。缓激肽诱导的舒张被B2受体拮抗剂Hoe 140(D - 精氨酸0[Hyp3,Thi5,D - Tic7,Oic8]缓激肽)和NPC 17761(D - 精氨酸0[Hyp3,D - HypE(反式 - 噻吩基)7,Oic8]缓激肽)拮抗。Hoe 140(0.1 μM至0.6 μM)表现为非竞争性拮抗剂,表观pA2 = 7.2 ± 0.4,而NPC 17761(0.3至1 μM)竞争性拮抗缓激肽诱导的舒张,pKB = 7.3 ± 0.2。Schild回归斜率与1无差异,为0.96 ± 0.20,P<0.05。4. 这些数据表明,缓激肽诱导的豚鼠气管舒张是通过缓激肽B2受体的激活而发生的。B2缓激肽受体的刺激诱导环氧化酶途径的激活,根据气管的张力状态导致收缩或舒张。

相似文献

本文引用的文献

2
Some quantitative uses of drug antagonists.药物拮抗剂的一些定量应用。
Br J Pharmacol Chemother. 1959 Mar;14(1):48-58. doi: 10.1111/j.1476-5381.1959.tb00928.x.
10
Pharmacological profile of AA-861, a 5-lipoxygenase inhibitor.5-脂氧合酶抑制剂AA-861的药理学特性
Prostaglandins. 1983 Dec;26(6):955-72. doi: 10.1016/0090-6980(83)90157-0.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验