Canonico P G, Kastello M D, Cosgriff T M, Donovan J C, Ross P E, Spears C T, Stephen E L
Toxicol Appl Pharmacol. 1984 Jun 30;74(2):163-72. doi: 10.1016/0041-008x(84)90139-x.
Ribavirin (Virazole, 1-beta-D-ribofuranosyl-1,2,4-triazole-3-carboxamide), a broad-spectrum antiviral compound, was evaluated for effects on blood and bone marrow of rhesus monkeys when administered by intramuscular injection for 10 days in doses of 30 or 100 mg/kg/day (four monkeys/group). Both groups developed a normochromic, normocytic anemia that was mild in the low-dose group and severe in the high-dose group. A dose-related erythroid hypoplasia occurred during the treatment period. Myeloid precursors were not affected. Differential counts of erythroid precursors showed a significant decrease in late erythroid forms while early erythroid forms were either unchanged or increased. Megakaryocyte numbers were increased in both groups. Qualitative changes in marrow cells included vacuolization of erythroid precursors and of occasional white cell precursors and megakaryocytes, and the appearance of bone marrow histiocytes containing red cells in various stages of disintegration. Thrombocytosis occurred in both treatment groups, with platelet counts returning to control values after drug withdrawal. Platelet function was not affected by treatment. No drug-related changes were seen during the treatment period for total and differential leukocyte counts, mean corpuscular hemoglobin and mean corpuscular hemoglobin concentration. Reticulocyte counts and mean corpuscular volume increased after treatment then returned to control values. Osmotic fragility of erythrocytes was not changed. These data show that in monkey, ribavirin causes a dose-related decrease in circulating red blood cell mass that is due in part to suppression of late erythroid precursors in bone marrow. These effects are reversible when treatment is discontinued and are not predictive of potentially serious or lasting untoward effects of ribavirin.
利巴韦林(病毒唑,1-β-D-呋喃核糖基-1,2,4-三唑-3-甲酰胺)是一种广谱抗病毒化合物,对恒河猴肌肉注射给药10天,剂量为30或100mg/kg/天(每组4只猴子),评估其对血液和骨髓的影响。两组均出现正色素正细胞性贫血,低剂量组症状较轻,高剂量组症状严重。治疗期间出现了与剂量相关的红系造血功能低下。髓系前体细胞未受影响。红系前体细胞分类计数显示,晚期红系细胞形态显著减少,而早期红系细胞形态要么未变,要么增加。两组巨核细胞数量均增加。骨髓细胞的定性变化包括红系前体细胞、偶尔的白细胞前体细胞和巨核细胞的空泡化,以及出现含有处于不同崩解阶段红细胞的骨髓组织细胞。两个治疗组均出现血小板增多症,停药后血小板计数恢复到对照值。血小板功能不受治疗影响。治疗期间白细胞总数和分类计数、平均红细胞血红蛋白含量和平均红细胞血红蛋白浓度未见与药物相关的变化。治疗后网织红细胞计数和平均红细胞体积增加,然后恢复到对照值。红细胞渗透脆性未改变。这些数据表明,在猴子中,利巴韦林会导致循环红细胞量出现与剂量相关的减少,部分原因是骨髓中晚期红系前体细胞受到抑制。停药后这些影响是可逆的,且不能预测利巴韦林潜在的严重或持久的不良影响。