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选择性磷酸二酯酶抑制剂与其他抗哮喘药物相比对豚鼠气道变应原诱导的嗜酸性粒细胞增多的影响。

The effect of selective phosphodiesterase inhibitors in comparison with other anti-asthma drugs on allergen-induced eosinophilia in guinea-pig airways.

作者信息

Banner K H, Marchini F, Buschi A, Moriggi E, Semeraro C, Page C P

机构信息

Department of Pharmacology, King's College London, UK.

出版信息

Pulm Pharmacol. 1995 Feb;8(1):37-42. doi: 10.1006/pulp.1995.1005.

Abstract

The effects of isoenzyme selective phosphodiesterase (PDE) inhibitors and other anti-asthma drugs on antigen-induced eosinophil recruitment and activation in guinea-pig airways was studied. Guinea-pigs were sensitized and subsequently challenged with aerosolized ovalbumin (OVA). Bronchoalveolar lavage (BAL) was performed 24 h later. A significant increase in eosinophils and eosinophil peroxidase (EPO) was detected in BAL fluid and BAL fluid supernatant respectively from OVA immunized guinea-pigs compared with sham treated animals. Guinea-pigs were treated for 7 days prior to antigen challenge with either the following drugs or the appropriate vehicle (i.p.). The selective beta 2 agonist, salbutamol (0.3 mg/kg), the PDE III inhibitor, milrinone (15 mg/kg) and the non-selective PDE inhibitor, trequinsin (1 mg/kg) had no effect on eosinophil number or EPO levels. The PDE IV inhibitor, rolipram (15 mg/kg), the mixed type III/IV PDE inhibitor, benzafentrine (15 mg/kg) and the non-selective PDE inhibitor, aminophylline (31.5 mg/kg) had no effect on eosinophil number but reduced the amount of EPO detected. The anti-inflammatory glucocorticosteroids, beclomethasone (10 mg/kg) and betamethasone (4 mg/kg) and the type IV PDE inhibitor, RP 73401 (5 mg/kg) reduced both eosinophil numbers and EPO levels. These results suggest a role for the type IV PDE isoenzyme in the control of eosinophil recruitment and possibly activation in the airways.

摘要

研究了同工酶选择性磷酸二酯酶(PDE)抑制剂及其他抗哮喘药物对豚鼠气道中抗原诱导的嗜酸性粒细胞募集和激活的影响。豚鼠致敏后,随后用雾化卵清蛋白(OVA)进行激发。24小时后进行支气管肺泡灌洗(BAL)。与假处理动物相比,在OVA免疫的豚鼠的BAL液和BAL液上清液中分别检测到嗜酸性粒细胞和嗜酸性粒细胞过氧化物酶(EPO)显著增加。在抗原激发前7天,用以下药物或适当的赋形剂(腹腔注射)对豚鼠进行治疗。选择性β2激动剂沙丁胺醇(0.3mg/kg)、PDE III抑制剂米力农(15mg/kg)和非选择性PDE抑制剂曲喹辛(1mg/kg)对嗜酸性粒细胞数量或EPO水平无影响。PDE IV抑制剂咯利普兰(15mg/kg)、III/IV型混合PDE抑制剂苄非他明(15mg/kg)和非选择性PDE抑制剂氨茶碱(31.5mg/kg)对嗜酸性粒细胞数量无影响,但降低了检测到的EPO量。抗炎糖皮质激素倍氯米松(10mg/kg)和倍他米松(4mg/kg)以及IV型PDE抑制剂RP 73401(5mg/kg)降低了嗜酸性粒细胞数量和EPO水平。这些结果表明IV型PDE同工酶在控制气道中嗜酸性粒细胞募集以及可能的激活中起作用。

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