Wild J S, Hyde D M, Giri S N
Department of Molecular Biosciences, School of Veterinary Medicine, University of California, Davis 95616.
Pharmacol Toxicol. 1994 Jul;75(1):42-8. doi: 10.1111/j.1600-0773.1994.tb00322.x.
The antifibrotic effects of an interferon inducer, polyinosinic-polycytidylic acid complexed with poly-L-lysine (poly ICLC), was evaluated in a bleomycin-hamster model of pulmonary fibrosis. Hamsters received three consecutive intratracheal doses of bleomycin (2.5, 2.0, and 1.5 U/kg/5 ml) or saline at weekly intervals. Poly ICLC at three doses (0.5, 1.0, and 1.5 mg/kg body weight) or saline was injected intraperitoneally by daily and semiweekly regimens for four weeks, and animals were sacrificed at five weeks. In both the daily and semiweekly poly ICLC regimens, hamsters receiving bleomycin plus poly ICLC demonstrated increased mortality and decreased weight gain compared to the vehicle and bleomycin control groups. The groups receiving bleomycin plus daily poly ICLC demonstrated poly ICLC-dose related effects for weight changes, lung hydroxyproline and lung prolyl hydroxylase activity. Depending on the poly ICLC dose, bleomycin plus daily poly ICLC produced significantly decreased hydroxyproline or significantly increased hydroxyproline and prolyl hydroxylase activity compared to the bleomycin control group. In contrast, the groups receiving bleomycin plus semiweekly poly ICLC did not demonstrate poly ICLC-dose related effects or significant differences from the bleomycin control group for any of the biochemical assays performed. The results of this study indicate that, depending on dose and regimen, poly ICLC can reduce collagen accumulation or produce a synergistic toxicity when administered with multiple doses of bleomycin. The toxic effects may restrict the therapeutic potential of poly ICLC in combination with bleomycin for anticancer therapy.
在博来霉素诱导的仓鼠肺纤维化模型中评估了一种干扰素诱导剂——与聚-L-赖氨酸复合的聚肌苷酸-聚胞苷酸(聚肌胞苷酸)的抗纤维化作用。仓鼠每周接受连续三次气管内注射博来霉素(2.5、2.0和1.5 U/kg/5 ml)或生理盐水。以每日和半周给药方案,连续四周腹腔注射三种剂量(0.5、1.0和1.5 mg/kg体重)的聚肌胞苷酸或生理盐水,在五周时处死动物。在每日和半周聚肌胞苷酸给药方案中,与赋形剂和博来霉素对照组相比,接受博来霉素加聚肌胞苷酸的仓鼠死亡率增加且体重增加减少。接受博来霉素加每日聚肌胞苷酸的组在体重变化、肺羟脯氨酸和肺脯氨酰羟化酶活性方面表现出与聚肌胞苷酸剂量相关的效应。根据聚肌胞苷酸剂量,与博来霉素对照组相比,博来霉素加每日聚肌胞苷酸可使羟脯氨酸显著降低或使羟脯氨酸和脯氨酰羟化酶活性显著增加。相比之下,接受博来霉素加半周聚肌胞苷酸的组在任何生化检测中均未表现出与聚肌胞苷酸剂量相关的效应,也与博来霉素对照组无显著差异。本研究结果表明,根据剂量和给药方案,聚肌胞苷酸与多剂量博来霉素联合使用时可减少胶原蛋白积累或产生协同毒性。这些毒性作用可能会限制聚肌胞苷酸与博来霉素联合用于抗癌治疗的治疗潜力。