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齐多夫定对感染猫白血病病毒的猫的毒性

Zidovudine toxicity to cats infected with feline leukemia virus.

作者信息

Haschek W M, Weigel R M, Scherba G, DeVera M C, Feinmehl R, Solter P, Tompkins M B, Tompkins W A

机构信息

Department of Pathobiology, College of Veterinary Medicine, University of Illinois, Urbana 61801.

出版信息

Fundam Appl Toxicol. 1990 May;14(4):764-75. doi: 10.1016/0272-0590(90)90301-y.

Abstract

Feline leukemia virus (FeLV) infection of cats is a model for the acquired immunodeficiency syndrome in humans. The toxicity of zidovudine was evaluated in SPF cats experimentally infected with FeLV. At initiation of the zidovudine study, all cats were antibody positive for FeLV antigens but clinically asymptomatic. Four cats were also viremic. Thirteen, 6- to 10-month-old cats were divided into five dosage groups and given zidovudine po at 0, 7.5, 15, 30, or 60 mg/kg daily in three equally divided doses for 32 to 34 days. Titers of circulating virus antigen remained constant; however, three of six cats receiving the higher doses of zidovudine (greater than or equal to 30 mg/kg) showed an increase in antibody titers to FeLV. Administration of zidovudine resulted in a progressive anemia, dependent upon dose and time. Macrocytes were observed prior to the development of anemia and were also found in several nonanemic cats. Repeated measures regression analyses indicated that an increased dose of zidovudine was associated with decreased packed cell volume, red blood cell count, and hemoglobin. As determined from the packed cell volume, the analyses indicate that anemia is induced only by the two highest doses of zidovudine. The regression model indicates that daily doses of 60 and 30 mg/kg are expected to induce anemia by Day 4 and Day 13, respectively. Progressive absolute neutropenia was observed in the greater than or equal to 30 mg/kg groups. Histopathologic lesions consisted of marked bone marrow hypercellularity in cats given greater than or equal to 30 mg/kg zidovudine and splenic extramedullary hematopoiesis in cats given greater than or equal to 15 mg/kg. Thus, oral toxicity of zidovudine in the cat is manifested by a dose-related anemia and neutropenia as observed in humans.

摘要

猫白血病病毒(FeLV)感染猫是人类获得性免疫缺陷综合征的一个模型。在实验感染FeLV的无特定病原体(SPF)猫中评估了齐多夫定的毒性。在齐多夫定研究开始时,所有猫的FeLV抗原抗体均呈阳性,但临床上无症状。四只猫也存在病毒血症。将13只6至10月龄的猫分为五个剂量组,分别给予每日0、7.5、15、30或60mg/kg的齐多夫定,分三次等量给药,持续32至34天。循环病毒抗原滴度保持恒定;然而,接受较高剂量齐多夫定(大于或等于30mg/kg)的六只猫中有三只显示出针对FeLV的抗体滴度增加。齐多夫定的给药导致进行性贫血,这取决于剂量和时间。在贫血发生之前观察到了巨红细胞,并且在几只非贫血猫中也发现了巨红细胞。重复测量回归分析表明,齐多夫定剂量增加与红细胞压积、红细胞计数和血红蛋白降低有关。根据红细胞压积确定,分析表明仅两种最高剂量的齐多夫定可诱发贫血。回归模型表明,每日60mg/kg和30mg/kg的剂量预计分别在第4天和第13天诱发贫血。在大于或等于30mg/kg的组中观察到进行性绝对中性粒细胞减少。组织病理学病变包括给予大于或等于30mg/kg齐多夫定的猫出现明显的骨髓细胞增多,以及给予大于或等于15mg/kg齐多夫定的猫出现脾脏髓外造血。因此,正如在人类中观察到的那样,猫体内齐多夫定的口服毒性表现为剂量相关的贫血和中性粒细胞减少。

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