Ishmael J, Lock E A
Toxicol Pathol. 1986;14(2):258-62. doi: 10.1177/019262338601400216.
The nephrotoxicity of hexachloro-1,3-butadiene (HCBD), its glutathione conjugate (HCBD-GSH), cysteine conjugate (HCBD-CYS), and its N-acetyl cysteine conjugate (HCBD-NAC) were compared in male and female Alderley Park rats. Rats, six to eight weeks of age, were given a single intra-peritoneal injection of HCBD or its conjugates and killed 24 hours later. Nephrotoxicity was assessed by histological examination and plasma urea. All three glutathione-derived conjugates produced an elevation of plasma urea and proximal renal tubular necrosis with a similar localization in the pars recta as seen with HCBD. All the conjugates were more nephrotoxic than HCBD itself. HCBD was about four times more toxic to female rats than males. This sex difference was also shown by all the HCBD metabolites.
在雄性和雌性奥尔德利公园大鼠中比较了六氯-1,3-丁二烯(HCBD)、其谷胱甘肽共轭物(HCBD-GSH)、半胱氨酸共轭物(HCBD-CYS)及其N-乙酰半胱氨酸共轭物(HCBD-NAC)的肾毒性。6至8周龄的大鼠单次腹腔注射HCBD或其共轭物,24小时后处死。通过组织学检查和血浆尿素评估肾毒性。所有三种谷胱甘肽衍生的共轭物均导致血浆尿素升高和近端肾小管坏死,在直部的定位与HCBD相似。所有共轭物的肾毒性均比HCBD本身更强。HCBD对雌性大鼠毒性约为雄性大鼠的四倍。所有HCBD代谢物也表现出这种性别差异。