Shirai M, Ohmori K, Hirano S, Iguchi H, Hori S, Sato H
Jpn J Antibiot. 1980 Feb;33(2):151-62.
Wistar rats, both male and female, were treated with aclacinomycin A at 4 dosage levels (0.375, 0.75, 1.5 and 3.0 mg/kg/day) by daily intraperitoneal injection for 30 days. Several rats died in the two higher dose groups (1.5 mg/kg/day: male 2/8 and 3.0 mg/kg: male 8/8, female 8/8. Piloerection, anorexia, depression of spontaneous activity, diarrhea and slight incontinence were observed in rats in 3.0 mg/kg/day dose group. Body weight gain decreased after day 3 in rats receiving 1.5 and 3.0 mg/kg/day. A significant decrease in the total WBC count and a slight decrease in RBC count were observed in animals of 1.5 mg/kg/day dose group which were survived for 30 days. Autopsy findings demonstrated atrophy of the thymus and spleen, and hyperemia and hemorrhage in the intestine. The atrophy of the thymus and decreased hematopoiesis in the bone marrow were histologically noted in the two highest dose groups. No cardiotoxicity was observed.
选用雄性和雌性Wistar大鼠,通过每日腹腔注射给予4种剂量水平(0.375、0.75、1.5和3.0mg/kg/天)的阿克拉霉素A,持续30天。两个较高剂量组中有几只大鼠死亡(1.5mg/kg/天:雄性2/8;3.0mg/kg:雄性8/8,雌性8/8)。在3.0mg/kg/天剂量组的大鼠中观察到竖毛、厌食、自发活动减少、腹泻和轻度大小便失禁。接受1.5和3.0mg/kg/天的大鼠在第3天后体重增加减少。在存活30天的1.5mg/kg/天剂量组动物中观察到白细胞总数显著减少,红细胞计数略有减少。尸检结果显示胸腺和脾脏萎缩,肠道充血和出血。在两个最高剂量组中,组织学上发现胸腺萎缩和骨髓造血减少。未观察到心脏毒性。