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佛波醇12,13 - 二丁酸酯诱导的人及大鼠肺动脉血管平滑肌收缩。

Contraction of vascular smooth muscle induced by phorbol 12,13 dibutyrate in human and rat pulmonary arteries.

作者信息

Savineau J P, Marthan R, Crevel H

机构信息

Laboratoire de Physiologie, Université de Bordeaux, France.

出版信息

Br J Pharmacol. 1991 Nov;104(3):639-44. doi: 10.1111/j.1476-5381.1991.tb12482.x.

Abstract
  1. The effect of phorbol 12,13 dibutyrate (PDB) on vascular tone was studied in both human and rat isolated pulmonary arterial strips (HPA and RPA, respectively). 2. PDB (1 nM to 2 microM) produced slowly developing, sustained and concentration-dependent contractions in HPA (mean EC50 = 3.5 nM, n = 5) and RPA (mean EC50 = 120 nM, n = 5). The maximal response was 185.6 +/- 25% and 207 +/- 27.5% (n = 5) of that induced by K(+)-rich (80mM) solution, and 223 +/- 34.5% and 176.5 +/- 38.6% of the noradrenaline (10 microM)-induced contraction in HPA and RPA, respectively. 3. PDB-induced contractions were not altered either by the presence of atropine (10 microM), propranolol (5 microM), phentolamine (5 microM) or tetrodotoxin (10 microM) in the bathing solution, or by the removal of endothelium from pulmonary arteries. 4. In HPA, the amplitude of PDB-induced contractions was significantly reduced by removal of external calcium ions, addition of verapamil (10 microM) or trifluoperazine (TFP, 5 microM) and significantly increased by Bay K 8644 (0.5 microM). In contrast, in RPA, calcium-free solution and verapamil had only a moderate effect on the maximal PDB-induced contraction (approximately 20% reduction), whereas Bay K 8644 and TFP had no significant effect. In both HPA and RPA, PDB-contractions in calcium-free solutions were not modified by ryanodine (25 microM) or by 8-(N,N diethylamino)octyl-3,4,5, trimethoxybenzoate hydrochloride (TMB-8, 50 microM). 5. PDB-induced contractions were inhibited by protein kinase C (PKC) antagonists. The maximal response was decreased by 60 +/- 10.5% and 35 +/- 11.5% (n = 5) by 145-isoquinolinesulphonyl)-2-methylpiperazine (H7, 50 microM), 70.5 +/- 12.2% and 56 +/- 18% (n = 5) by phloretin (100 microM) and 80.7 +/- 8.4% and 71 +/- 14% (n = 5) by staurosporine (25 nM) in HPA and RPA, respectively.6. Long term treatment (15-20 h) of arterial strips with phorbol esters (phorbol 12,13 didecanoate, or PDB) abolished the contractile response to subsequent addition of PDB.7. These results show that PDB is a potent vasoconstrictor agent in human and rat pulmonary arteries. Unlike the rat, part of the PDB response depends on calcium influx in human preparations. PDB action appears mainly mediated by the activation of protein kinase C. PKC could thus play a major role in the control of vascular pulmonary reactivity.
摘要
  1. 研究了佛波醇12,13 - 二丁酸酯(PDB)对人及大鼠离体肺动脉条(分别为HPA和RPA)血管张力的影响。2. PDB(1 nM至2 microM)在HPA(平均EC50 = 3.5 nM,n = 5)和RPA(平均EC50 = 120 nM,n = 5)中产生缓慢发展、持续且浓度依赖性的收缩。最大反应分别为富含钾(80mM)溶液诱导反应的185.6 +/- 25%和207 +/- 27.5%(n = 5),以及去甲肾上腺素(10 microM)诱导收缩的223 +/- 34.5%和176.5 +/- 38.6%,分别在HPA和RPA中。3. 浴液中存在阿托品(10 microM)、普萘洛尔(5 microM)、酚妥拉明(5 microM)或河豚毒素(10 microM),或去除肺动脉内皮,均不改变PDB诱导的收缩。4. 在HPA中,去除细胞外钙离子、添加维拉帕米(10 microM)或三氟拉嗪(TFP,5 microM)可显著降低PDB诱导收缩的幅度,而添加Bay K 8644(0.5 microM)则显著增加。相反,在RPA中,无钙溶液和维拉帕米对PDB诱导的最大收缩仅有中等程度的影响(约降低20%),而Bay K 8644和TFP无显著影响。在HPA和RPA中,无钙溶液中的PDB收缩不受ryanodine(25 microM)或盐酸8 - (N,N - 二乙氨基)辛基 - 3,4,5 - 三甲氧基苯甲酸酯(TMB - 8,50 microM)的影响。5. PDB诱导的收缩受蛋白激酶C(PKC)拮抗剂抑制。在HPA和RPA中,145 - 异喹啉磺酰基)- 2 - 甲基哌嗪(H7,50 microM)使最大反应分别降低60 +/- 10.5%和35 +/- 11.5%(n = 5),根皮素(100 microM)使其降低70.5 +/- 12.2%和56 +/- 18%(n = 5),星形孢菌素(25 nM)使其降低80.7 +/- 8.4%和71 +/- 14%(n = 5)。6. 用佛波醇酯(佛波醇12,13 - 十二烷酸酯或PDB)对动脉条进行长期处理(15 - 20小时)可消除对随后添加PDB的收缩反应。7. 这些结果表明,PDB是人和大鼠肺动脉中的一种强效血管收缩剂。与大鼠不同,人肺动脉中PDB反应的一部分依赖于钙内流。PDB的作用似乎主要由蛋白激酶C的激活介导。因此,PKC可能在控制肺血管反应性中起主要作用。

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