Gould D H, Fettman M J, Daxenbichler M E, Bartuska B M
Toxicol Appl Pharmacol. 1985 Apr;78(2):190-201. doi: 10.1016/0041-008x(85)90283-2.
The organonitriles, 2S-1-Cyano-2-hydroxy-3,4-epithiobutane (erythro and threo) (CHEB), isolated from the seed of Crambe abyssinica were administered by gavage to male Fischer-344 rats. Rats given 50 mg/kg/day were killed at 24, 48, and 72 hr. The rats given 100 mg/kg/day were killed at 48 and 72 hr. Serum urea nitrogen and creatinine were increased by 48 hr and further elevated by 72 hr. Glomerular filtration rate (GFR) of the 50 mg/kg CHEB rats was elevated at 24 hr but fell to subnormal values by 72 hr. The GFR of the 100-mg/kg group was decreased at 48 and 72 hr. Urine output of the 50-mg/kg group increased continuously through 72 hr, while urine output of the 100-mg/kg group was increased to a lesser degree. Urinary N-acetyl-beta-D-glucosaminidase (NAG) activity (nmol/hr/mg creatinine) was significantly elevated in both groups by 48 hr, and further increased by 72 hr. Twenty-four hours after administration of 50 mg/kg, renal proximal tubular epithelial cells of some rats had fine cytoplasmic vacuolation. At 48 and 72 hr, necrosis and coarse vacuolation of proximal tubular epithelial cells occurred in both dose groups. The necrosis was most severe at the apexes of the medullary rays and the coarse vacuolation extended deeply toward the outer stripe of the outer zone of the medulla. Higher doses and/or longer times of CHEB administration resulted in a more extensive lesion distribution. It is concluded that CHEB induces nephrotoxicity in rats characterized by nonoliguric, acute renal failure, and morphological lesions preferentially involving the pars recta of the proximal tubules.
从阿比西尼亚芥种子中分离得到的有机腈类化合物2S-1-氰基-2-羟基-3,4-环氧硫丁烷(赤藓型和苏阿糖型)(CHEB),通过灌胃给予雄性Fischer-344大鼠。给予50mg/kg/天的大鼠在24、48和72小时处死。给予100mg/kg/天的大鼠在48和72小时处死。血清尿素氮和肌酐在48小时时升高,并在72小时时进一步升高。给予50mg/kg CHEB的大鼠的肾小球滤过率(GFR)在24小时时升高,但在72小时时降至低于正常的值。100mg/kg组的GFR在48和72小时时降低。50mg/kg组的尿量在72小时内持续增加,而100mg/kg组的尿量增加程度较小。两组的尿N-乙酰-β-D-氨基葡萄糖苷酶(NAG)活性(nmol/小时/毫克肌酐)在48小时时均显著升高,并在72小时时进一步增加。给予50mg/kg 24小时后,一些大鼠的肾近端小管上皮细胞出现细小的细胞质空泡化。在48和72小时时,两个剂量组均出现近端小管上皮细胞坏死和粗大空泡化。坏死在髓放线顶端最为严重,粗大空泡化向髓质外带的外条纹深部延伸。给予更高剂量和/或更长时间的CHEB导致更广泛的病变分布。结论是,CHEB在大鼠中诱导肾毒性,其特征为非少尿型急性肾衰竭,形态学病变优先累及近端小管的直部。