Pyne S, Pyne N J
Department of Physiology and Pharmacology, University of Strathclyde, Royal College, Glasgow, U.K.
Cell Signal. 1994 Mar;6(3):269-77. doi: 10.1016/0898-6568(94)90031-0.
Bradykinin-treatment of cultured airway smooth muscle (ASM) induced the formation of [3H]1,2-diacylglycerol ([3H]1,2-DG), [3H]1,3-diacylglycerol ([3H]1,3-DG) and [3H]phosphatidic acid ([3H]PtdOH) in [3H]palmitate-labelled cells and of [3H]choline in [3H]methyl choline-labelled cells. [3H]1,2-DG and [3H]1,3-DG responses were biphasic with an initial transient phase from 0-2 min and a second sustained phase to 10 min. In contrast, [3H]PtdOH accumulation plateaued at 2 min stimulation as did [3H]choline formation. The bradykinin-stimulated [3H]1,2-DG and [3H]PtdOH responses exhibited similar concentration dependencies (EC50 values: [3H]1,2-DG 5.14 +/- 2.82 nM; [3H]1,3-DG 4.95 +/- 1.12 nM; [3H]PtdOH 1.52 +/- 0.82 nM). In contrast, PMA elicited a [3H]PtdOH response, but was without effect upon [3H]DG levels. Bradykinin-induced accumulation of [3H]1,2-DG and [3H]PtdOH was insensitive to blockade by a bradykinin B2-receptor antagonist, NPC567 (40 microM) and the B1-receptor agonist, Des-Arg9-bradykinin, (10 microM) failed to elicit a response. These observations are similar to those obtained previously for bradykinin-stimulated phospholipase D activity in ASM (Pyne S. and Pyne N. J., Br. J. Pharmac. 110, 477-481, 1993). Thus, both bradykinin-stimulated 1,2-DG and PtdOH accumulation may also be regulated via a novel B3-receptor. Bradykinin-stimulated formation of [3H]PtdOH was partially inhibited by butan-1-ol (by 47.25 +/- 12.7%, n = 3) which had no effect upon basal or bradykinin-stimulated levels of [3H]1,2-DG or upon basal [3H]PtdOH.(ABSTRACT TRUNCATED AT 250 WORDS)
用缓激肽处理培养的气道平滑肌(ASM),在[3H]棕榈酸酯标记的细胞中诱导形成[3H]1,2 - 二酰甘油([3H]1,2 - DG)、[3H]1,3 - 二酰甘油([3H]1,3 - DG)和[3H]磷脂酸([3H]PtdOH),在[3H]甲基胆碱标记的细胞中诱导形成[3H]胆碱。[3H]1,2 - DG和[3H]1,3 - DG的反应呈双相性,初始短暂阶段为0 - 2分钟,第二个持续阶段至10分钟。相比之下,[3H]PtdOH的积累在刺激2分钟时达到平台期,[3H]胆碱的形成也是如此。缓激肽刺激的[3H]1,2 - DG和[3H]PtdOH反应表现出相似的浓度依赖性(EC50值:[3H]1,2 - DG为5.14±2.82 nM;[3H]1,3 - DG为4.95±1.12 nM;[3H]PtdOH为1.52±0.82 nM)。相比之下,佛波醇酯(PMA)引发了[3H]PtdOH反应,但对[3H]DG水平没有影响。缓激肽诱导的[3H]1,2 - DG和[3H]PtdOH积累对缓激肽B2受体拮抗剂NPC567(40 microM)的阻断不敏感,B1受体激动剂去精氨酸9 - 缓激肽(10 microM)未能引发反应。这些观察结果与先前在ASM中缓激肽刺激的磷脂酶D活性的观察结果相似(派恩S.和派恩N. J.,《英国药理学杂志》110,477 - 481,1993)。因此,缓激肽刺激的1,2 - DG和PtdOH积累也可能通过一种新型B3受体进行调节。缓激肽刺激的[3H]PtdOH形成被丁醇部分抑制(抑制47.25±12.7%,n = 3),丁醇对基础或缓激肽刺激的[3H]1,2 - DG水平或基础[3H]PtdOH没有影响。(摘要截取自250字)