Zia S, Hyde D M, Giri S N
Department of Veterinary Pharmacology and Toxicology, School of Veterinary Medicine, University of California, Davis 95616.
Pharmacol Toxicol. 1992 Jul;71(1):11-8. doi: 10.1111/j.1600-0773.1992.tb00513.x.
The antifibrotic effect of an interferon inducer, bropirimine (2-amino-5-bromo-6-phenyl-4(3H)-pyrimidinone, ABPP) was evaluated in bleomycin (BLM)-hamster model of lung fibrosis. ABPP is an orally active biological response modifier and has immunomodulatory, antiviral, and antineoplastic activities. The hamsters were randomized in four groups and treated with either bropirimine (100 mg/kg, intraperitoneally) suspended in carboxymethylcellulose (CMC, 10 mg/10 mg/ml) or CMC alone each day for sixteen days. After two days, the hamsters received either single bolus of BLM (7.5 U/5 ml/kg) or an equivalent volume of saline by the transoral endotracheal route. Groupings were assigned as: CMC + saline (CS), ABPP + saline (AS), CMC + BLM (CB) and ABPP + BLM (AB). Animals were sacrificed at fourteen days after intratracheal installation of either BLM or saline. Their lungs were lavaged and processed for morphometric and biochemical studies. ABPP had little effect in preventing BLM-induced weight loss and lung injury. ABPP was found to reduce the BLM-induced accumulation of collagen in the lung as measured by hydroxyproline content. The hamsters in AB group had significantly less collagen than the hamsters in CB group: 995 and 1157 micrograms hydroxyproline/lung, respectively. Administration of ABPP prevented the BLM-induced increase in the lung prolyl hydroxylase activity. The total number of monocytes and eosinophils recovered from the bronchoalveolar lavage fluid (BALF) of the AB group were significantly lower than that of the animals in CB group. However, the BALF supernatant protein content from animals in AB group (7.9 mg/lung) was significantly higher than that of CB group (4.5 mg/lung).(ABSTRACT TRUNCATED AT 250 WORDS)
在博来霉素(BLM)诱导的仓鼠肺纤维化模型中评估了一种干扰素诱导剂布罗匹明(2-氨基-5-溴-6-苯基-4(3H)-嘧啶酮,ABPP)的抗纤维化作用。ABPP是一种口服活性生物反应调节剂,具有免疫调节、抗病毒和抗肿瘤活性。将仓鼠随机分为四组,每天分别用悬浮于羧甲基纤维素(CMC,10mg/10mg/ml)中的布罗匹明(100mg/kg,腹腔注射)或单独的CMC处理16天。两天后,仓鼠经口气管内途径接受单次大剂量的BLM(7.5U/5ml/kg)或等量的生理盐水。分组如下:CMC+生理盐水(CS)、ABPP+生理盐水(AS)、CMC+BLM(CB)和ABPP+BLM(AB)。在气管内注入BLM或生理盐水14天后处死动物。对其肺进行灌洗并进行形态计量学和生化研究。ABPP在预防BLM诱导的体重减轻和肺损伤方面作用甚微。通过羟脯氨酸含量测定发现,ABPP可减少BLM诱导的肺中胶原蛋白的积累。AB组仓鼠的胶原蛋白含量明显低于CB组仓鼠:分别为995和1157微克羟脯氨酸/肺。给予ABPP可防止BLM诱导的肺脯氨酰羟化酶活性增加。从AB组支气管肺泡灌洗液(BALF)中回收的单核细胞和嗜酸性粒细胞总数明显低于CB组动物。然而,AB组动物的BALF上清液蛋白含量(7.9mg/肺)明显高于CB组(4.5mg/肺)。(摘要截断于250字)