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新型选择性磷酸二酯酶IV型抑制剂RP 73401的抗炎及支气管扩张特性

Anti-inflammatory and bronchodilator properties of RP 73401, a novel and selective phosphodiesterase type IV inhibitor.

作者信息

Raeburn D, Underwood S L, Lewis S A, Woodman V R, Battram C H, Tomkinson A, Sharma S, Jordan R, Souness J E, Webber S E

机构信息

Rhône-Poulenc Rorer Ltd., Dagenham Research Centre, Essex.

出版信息

Br J Pharmacol. 1994 Dec;113(4):1423-31. doi: 10.1111/j.1476-5381.1994.tb17156.x.

DOI:10.1111/j.1476-5381.1994.tb17156.x
PMID:7889300
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1510545/
Abstract
  1. We have investigated the effects of RP 73401, a novel, potent and highly selective cyclic nucleotide phosphodiesterase (PDE) type IV inhibitor, in guinea-pig and rat models of bronchoconstriction and allergic inflammation. In some models, the effects of RP 73401 have been compared with those of the standard PDE type IV inhibitor, rolipram. 2. RP 73401 (0.4-400 micrograms kg-1, intratracheally (i.t.) on lactose) inhibited antigen-induced bronchospasm in previously sensitized conscious guinea-pigs (ID50: 7 +/- 1 micrograms kg-1) and in anaesthetized rats (ID50: 100 +/- 25 micrograms kg-1). Rolipram inhibited the antigen-induced bronchospasm in guinea-pigs with an ID50 of 5 +/- 1 micrograms kg-1. In guinea-pig bronchoalveolar lavage (BAL) fluid, total inflammatory cell and eosinophil numbers were reduced by RP 73401 (ID50s: 3.9 +/- 0.8 micrograms kg-1 and 3.2 +/- 0.7 micrograms kg-1, respectively). In the rat, inflammatory cell numbers are less affected. Only the highest dose of RP 73401 (400 micrograms kg-1) significantly inhibited eosinophil influx (41 +/- 16% inhibition). 3. RP 73401 (0.02-100 micrograms kg-1, i.v.) inhibited PAF-induced bronchial hyperreactivity to bombesin in the anaesthetized guinea-pig (ID50: 0.09 +/- 0.03 micrograms kg-1) and inhibited (0.4-40 micrograms kg-1, i.t.) histamine-induced airway microvascular leakage in the anaesthetized guinea-pig by approximately 60% at all doses. 4. RP 73401 relaxed guinea-pig isolated trachea under basal tone (EC50: 9 nM) and when precontracted with histamine (IC50: 2 nM), methacholine (IC50: 29 nM) or leukotriene D4 (LTD4, IC50: 4 nM). 5. RP 73401 (0.4-100 microg kg-1, i.t.) inhibited bronchospasm induced by histamine (ID.%: 34 +/- 6 microg kg-1), methacholine (ID50: 66 +/- 12 pg kg-1) and LTD4 (ID50: <4 microg kg-1) in the anaesthetized guinea pig.Against these same bronchoconstrictors, rolipram (i.t.) had ID5o values of 44 +/- 4, 72 +/- 18 and<4 pg kg- respectively. RP 73401 (4 and 40 pg kg-, i.t.) increased the magnitude and duration of bronchodilatation produced by salbutamol in the anaesthetized guinea-pig. At doses producing significant bronchodilatation, RP 73401 was without effect on heart rate or blood pressure in the anaesthetized guinea-pig. RP 73401 (0.01 -0.25 mg kg-1, i.v.) did not affect heart rate and produced only a small fall in blood pressure in the anaesthetized rat.6. These data demonstrate that RP 73401 and rolipram inhibit antigen- and mediator-induced bronchospasmin guinea-pigs with the same potency. Furthermore, RP 73401 administered directly into the airways, protects against allergic airway inflammation. These results indicate the importance of PDE IV in regulating smooth muscle and inflammatory cell activity. At doses suppressing the inflammatory response in the lung, RP 73401 had little effect in the cardiovascular system. RP 73401 may have a role as a bronchodilator and, more importantly, as a prophylactic anti-inflammatory agent in the treatment of asthma.
摘要
  1. 我们研究了新型、强效且高度选择性的环核苷酸磷酸二酯酶(PDE)IV型抑制剂RP 73401在豚鼠和大鼠支气管收缩及过敏性炎症模型中的作用。在一些模型中,已将RP 73401的作用与标准PDE IV型抑制剂咯利普兰的作用进行了比较。2. RP 73401(0.4 - 400微克/千克,经气管内(i.t.)溶于乳糖)可抑制预先致敏的清醒豚鼠(半数抑制剂量(ID50):7±1微克/千克)和麻醉大鼠(ID50:100±25微克/千克)中抗原诱导的支气管痉挛。咯利普兰抑制豚鼠抗原诱导的支气管痉挛的ID50为5±1微克/千克。在豚鼠支气管肺泡灌洗(BAL)液中,RP 73401可降低总炎症细胞和嗜酸性粒细胞数量(ID50分别为:3.9±0.8微克/千克和3.2±0.7微克/千克)。在大鼠中,炎症细胞数量受影响较小。仅最高剂量的RP 73401(400微克/千克)可显著抑制嗜酸性粒细胞流入(抑制率为41±16%)。3. RP 73401(0.02 - 100微克/千克,静脉注射)可抑制麻醉豚鼠中血小板活化因子(PAF)诱导的对蛙皮素的支气管高反应性(ID50:0.09±0.03微克/千克),并在所有剂量下均抑制(0.4 - 40微克/千克,经气管内)组胺诱导的麻醉豚鼠气道微血管渗漏约60%。4. RP 73401可使豚鼠离体气管在基础张力下舒张(半数有效浓度(EC50):9纳摩尔),以及在预先用组胺(半数抑制浓度(IC50):2纳摩尔)、乙酰甲胆碱(IC50:29纳摩尔)或白三烯D4(LTD4,IC50:4纳摩尔)预收缩后舒张。5. RP 73401(0.4 - 100微克/千克,经气管内)可抑制麻醉豚鼠中组胺(ID50:34±6微克/千克)、乙酰甲胆碱(ID50:66±12微克/千克)和LTD4(ID50:<4微克/千克)诱导的支气管痉挛。针对这些相同的支气管收缩剂,咯利普兰(经气管内)的ID50值分别为44±4、72±18和<4微克/千克。RP 73401(4和40微克/千克,经气管内)可增加沙丁胺醇在麻醉豚鼠中产生的支气管舒张的幅度和持续时间。在产生显著支气管舒张的剂量下,RP 73401对麻醉豚鼠的心率或血压无影响。RP 73401(0.01 -  0.25毫克/千克,静脉注射)对麻醉大鼠的心率无影响,仅使血压略有下降。6. 这些数据表明,RP 73401和咯利普兰以相同效力抑制豚鼠中抗原和介质诱导的支气管痉挛。此外,直接气道内给药的RP 73401可预防过敏性气道炎症。这些结果表明PDE IV在调节平滑肌和炎症细胞活性中的重要性。在抑制肺部炎症反应的剂量下,RP 73401对心血管系统影响很小。RP 73401可能作为支气管扩张剂发挥作用,更重要的是,作为预防哮喘的抗炎剂。

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