Clark J M, Abraham W M, Fishman C E, Forteza R, Ahmed A, Cortes A, Warne R L, Moore W R, Tanaka R D
Department of Molecular Pharmacology, Arris Pharmaecutical Corporation, South San Francisco, California 94080, USA.
Am J Respir Crit Care Med. 1995 Dec;152(6 Pt 1):2076-83. doi: 10.1164/ajrccm.152.6.8520778.
Tryptase, a mast cell serine protease, has been implicated in the pathophysiology of allergic asthma, but formal evidence to support this hypothesis has been limited by the lack of specific inhibitors for use in vivo. Therefore, in this study we examined the effects of two inhibitors of tryptase, APC 366 [N-(1-hydroxy-2-naphthoyl)-L-arginyl-L-prolinamide hydrochloride] and BABIM [bis(5-amidino-2-benzimidazolyl)methane] on antigen-induced early and late responses, airway responsiveness as measured by carbachol provocation, microvascular permeability as measured by bronchoalveolar lavage (BAL) albumin concentrations, and tissue eosinophilia from biopsies in allergic sheep. APC 366 and BABIM were administered by aerosol in all experiments. In vehicle control trials, antigen challenge resulted in peak early and late increases in specific lung resistance (SRL) of (mean +/- SE, n = 6) 259 +/- 30% and 183 +/- 27% over baseline, respectively. Treatment with APC 366 (9 mg/3 ml H2O given 0.5 h before, 4 h after, and 24 h after antigen challenge) slightly reduced the peak early response (194 +/- 41%), but significantly inhibited the late response (38 +/- 6%, p < 0.05 versus control trials). Twenty-four hours after challenge, APC 366 also completely blocked the antigen-induced airway hyperresponsiveness to inhaled carbachol observed in the control trial.(ABSTRACT TRUNCATED AT 250 WORDS)
类胰蛋白酶是一种肥大细胞丝氨酸蛋白酶,与过敏性哮喘的病理生理学有关,但由于缺乏可用于体内的特异性抑制剂,支持这一假说的正式证据一直有限。因此,在本研究中,我们检测了两种类胰蛋白酶抑制剂,APC 366 [N-(1-羟基-2-萘甲酰基)-L-精氨酰-L-脯氨酰胺盐酸盐] 和BABIM [双(5-脒基-2-苯并咪唑基)甲烷] 对变应原诱导的早期和晚期反应、通过卡巴胆碱激发测定的气道反应性、通过支气管肺泡灌洗 (BAL) 白蛋白浓度测定的微血管通透性以及变应性绵羊活检组织中的嗜酸性粒细胞增多的影响。在所有实验中,APC 366和BABIM均通过气雾剂给药。在赋形剂对照试验中,抗原激发导致特异性肺阻力 (SRL) 的早期和晚期峰值分别比基线增加 (平均值±标准误,n = 6) 259±30% 和183±27%。用APC 366治疗 (在抗原激发前0.5小时、激发后4小时和24小时给予9 mg/3 ml水) 略微降低了早期反应峰值 (194±41%),但显著抑制了晚期反应 (38±6%,与对照试验相比p < 0.05)。激发后24小时,APC 366还完全阻断了对照试验中观察到的抗原诱导的气道对吸入卡巴胆碱的高反应性。(摘要截断于250字)