Mathes L E, Hayes K A, Swenson C L, Polas P J, Weisbrode S E, Kociba G J
Department of Veterinary Pathobiology, Ohio State University, Columbus 43210.
Antimicrob Agents Chemother. 1991 Oct;35(10):2147-50. doi: 10.1128/AAC.35.10.2147.
The feline leukemia virus (FeLV) disease model was used to conduct a toxicity and antiretrovirus efficacy trial of dextran sulfate (DS; molecular mass, 7,000 to 8,000 Da). In vitro, FeLV infection of feline lymphoid cells was inhibited by 10 micrograms of DS per ml. DS was administered to cats by continuous intravenous infusion at doses of 600, 120, 24, or 4.8 mg/kg of body weight per day, beginning 24 h before FeLV challenge. Doses of 24 mg/kg/day and more were excessively toxic, causing intestinal lesions and death. Similar changes were observed in unchallenged animals receiving 24 mg/kg/day, indicating that toxicity was DS mediated. The dosage of 4.8 mg/kg/day was subtoxic but did not prevent the induction and persistence of FeLV viremia. The results demonstrate that DS by continuous intravenous infusion is excessively toxic at high doses and ineffective at preventing FeLV infection at a subtoxic dose in the FeLV cat model.
猫白血病病毒(FeLV)疾病模型被用于进行硫酸葡聚糖(DS;分子量7000至8000道尔顿)的毒性和抗逆转录病毒疗效试验。在体外,每毫升10微克的DS可抑制猫淋巴细胞的FeLV感染。在FeLV攻击前24小时开始,以每天600、120、24或4.8毫克/千克体重的剂量通过连续静脉输注将DS给予猫。24毫克/千克/天及更高的剂量毒性过大,会导致肠道病变和死亡。在接受24毫克/千克/天的未受攻击动物中也观察到了类似变化,表明毒性是由DS介导的。4.8毫克/千克/天的剂量具有亚毒性,但不能阻止FeLV病毒血症的诱导和持续存在。结果表明,在FeLV猫模型中,通过连续静脉输注的DS在高剂量时毒性过大,而在亚毒性剂量下预防FeLV感染无效。