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糖皮质激素布地奈德和新型磷酸二酯酶4抑制剂CDP840对新生期免疫家兔抗原诱导的气道反应的影响。

Effect of the glucocorticosteroid budesonide and a novel phosphodiesterase type 4 inhibitor CDP840 on antigen-induced airway responses in neonatally immunised rabbits.

作者信息

Gozzard N, el-Hashim A, Herd C M, Blake S M, Holbrook M, Hughes B, Higgs G A, Page C P

机构信息

Celltech Therapeutics Ltd., Slough, London.

出版信息

Br J Pharmacol. 1996 Jul;118(5):1201-8. doi: 10.1111/j.1476-5381.1996.tb15524.x.

DOI:10.1111/j.1476-5381.1996.tb15524.x
PMID:8818344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1909605/
Abstract
  1. The effects of the inhaled corticosteroid budesonide and a novel PDE 4 inhibitor CDP840 given systematically, were evaluated in a model of antigen-induced airway inflammation in the rabbit. 2. Adult litter-matched NZW rabbits (2.4-3.5 kg) immunised within 24 h of birth with Alternaria tenuis antigen were pretreated with budesonide (total dose 100 micrograms, inhaled over 2 days) or CDP840 (total dose 7 mg kg-1, i.p. over 3 days), before antigen challenge. For each drug-treated group a parallel group of rabbits was pretreated with the appropriate vehicle. In all groups airway responsiveness to inhaled histamine was assessed and bronchoalveolar lavage (BAL) performed 24 h before and after antigen challenge. 3. Basal lung function in terms of total lung resistance (RL; cmH2O l 1s-1) and dynamic compliance (Cdyn; ml cmH2O-1) were unaltered by pretreatment with budesonide or CDP840 compared to their respective vehicles 24 h before or after antigen challenge. 4. The RL component of the acute bronchoconstriction induced by inhaled Alternaria tenuis aerosol was unaffected by pretreatment with budesonide. However, budesonide prevented the fall in Cdyn due to antigen. Treatment with CDP840 significantly reduced antigen-induced acute bronchoconstriction in terms of both RL and Cdyn. 5. Airway hyperresponsiveness (AHR) to inhaled histamine was indicated by reduced RL PC50 (2.4-4.5 fold) and Cdyn PC35 (2.1-3.9 fold) values 24 h after antigen challenge. Treatment with either budesonide or CDP840 abolished the antigen-induced increase in responsiveness to inhaled histamine. 6. Total cells recovered per ml of BAL fluid increased 24 h after antigen challenge. Antigen-induced pulmonary eosinophilia was reduced (93%) in budesonide and (85%) in CDP840 treated rabbits. Antigen-induced increases in neutrophil numbers were reduced (76%) with budesonide but not CDP840 pretreatment. 7. Inhalation of Alternaria tenuis aerosol elicited an acute bronchoconstriction, followed 24 hours later by an increased responsiveness to inhaled histamine and pulmonary neutrophil and eosinophil recruitment. CDP840 was more effective than budesonide in preventing the antigen-induced increase in total lung resistance (RL); however, both drugs prevented the antigen-induced reduction in dynamic compliance (Cdyn). CDP840 and budesonide also prevented antigen-induced AHR and eosinophilia in the immunised rabbit.
摘要
  1. 在兔抗原诱导的气道炎症模型中,评估了吸入性皮质类固醇布地奈德和一种新型磷酸二酯酶4(PDE 4)抑制剂CDP840经系统给药后的效果。2. 成年同窝出生体重匹配的新西兰白兔(2.4 - 3.5千克)在出生后24小时内用链格孢菌抗原免疫,在抗原激发前,用布地奈德(总剂量100微克,2天内吸入)或CDP840(总剂量7毫克/千克,3天内腹腔注射)进行预处理。对于每个药物治疗组,有一组平行的兔子用相应的赋形剂进行预处理。在所有组中,在抗原激发前和激发后24小时评估气道对吸入组胺的反应性,并进行支气管肺泡灌洗(BAL)。3. 与各自的赋形剂相比,在抗原激发前或激发后24小时,用布地奈德或CDP840预处理对以总肺阻力(RL;厘米水柱·升⁻¹·秒⁻¹)和动态顺应性(Cdyn;毫升·厘米水柱⁻¹)衡量的基础肺功能没有影响。4. 吸入链格孢菌气雾剂诱导的急性支气管收缩的RL成分不受布地奈德预处理的影响。然而,布地奈德可防止由于抗原导致的Cdyn下降。用CDP840治疗在RL和Cdyn方面均显著降低了抗原诱导的急性支气管收缩。5. 抗原激发后24小时,气道对吸入组胺的高反应性(AHR)表现为RL PC50(2.4 - 4.5倍)和Cdyn PC35(2.1 - 3.9倍)值降低。用布地奈德或CDP840治疗均可消除抗原诱导的对吸入组胺反应性的增加。6. 抗原激发后24小时,每毫升BAL液中回收的总细胞数增加。在布地奈德治疗的兔子中,抗原诱导的肺嗜酸性粒细胞增多减少了93%,在CDP840治疗的兔子中减少了85%。用布地奈德预处理可使抗原诱导的中性粒细胞数量增加减少76%,但CDP840预处理则无此效果。7. 吸入链格孢菌气雾剂引发急性支气管收缩,24小时后对吸入组胺的反应性增加,同时肺部中性粒细胞和嗜酸性粒细胞募集增加。在预防抗原诱导的总肺阻力(RL)增加方面,CDP840比布地奈德更有效;然而,两种药物均可防止抗原诱导的动态顺应性(Cdyn)降低。CDP840和布地奈德还可预防免疫兔中抗原诱导的AHR和嗜酸性粒细胞增多。

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本文引用的文献

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2
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Br J Pharmacol. 1996 Jul;118(5):1183-91. doi: 10.1111/j.1476-5381.1996.tb15522.x.
3
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