Kojima S, Inoue T, Kiyozumi M, Shimada H
Department of Hygienic Chemistry, Faculty of Pharmaceutical Sciences, Kumamoto University, Japan.
Chem Pharm Bull (Tokyo). 1990 Nov;38(11):3127-9. doi: 10.1248/cpb.38.3127.
The protective effect of N-benzyl-D-glucamine dithiocarbamate (BGD) against gastrointestinal and bone marrow toxicities produced by cis-diamminedichloroplatinum (DDP) injection in rats was studied. Rats were injected i.p. with BGD (2 mmol/kg) immediately after i.v. injection of DDP (20 mumol/kg). A scanning electron micrograph of the jejunum after DDP treatment showed damage in the villi, and that BGD protected the DDP-induced jejunal damage. BGD treatment also had a protective effect against DDP-induced diarrhea. BGD significantly reversed the reduction in maltase and sucrase activities of jejunal mucosa of rats treated with DDP. Platinum (Pt) concentrations in the gastrointestine as well as in the kidney and liver after DDP injection decreased following BGD treatment. The reduction of leukocytes following DDP injection returned to control values after BGD treatment. Biliary and urinary excretions of Pt after DDP injection was remarkably increased by BGD treatment. The results of this study indicated that the injection of BGD to rats treated with DDP can effectively remove Pt from the body through biliary and urinary excretions, resulting in protection of the gastrointestinal and bone marrow toxicities induced by DDP treatment.
研究了N-苄基-D-葡糖胺二硫代氨基甲酸盐(BGD)对大鼠静脉注射顺二氨二氯铂(DDP)所产生的胃肠道和骨髓毒性的保护作用。大鼠静脉注射DDP(20 μmol/kg)后立即腹腔注射BGD(2 mmol/kg)。DDP处理后空肠的扫描电子显微镜照片显示绒毛受损,而BGD可保护DDP诱导的空肠损伤。BGD处理对DDP诱导的腹泻也有保护作用。BGD显著逆转了DDP处理大鼠空肠黏膜中麦芽糖酶和蔗糖酶活性的降低。BGD处理后,DDP注射后胃肠道以及肾脏和肝脏中的铂(Pt)浓度降低。DDP注射后白细胞的减少在BGD处理后恢复到对照值。BGD处理显著增加了DDP注射后Pt的胆汁和尿液排泄。本研究结果表明,给用DDP处理的大鼠注射BGD可通过胆汁和尿液排泄有效地将Pt从体内清除,从而保护DDP处理诱导的胃肠道和骨髓毒性。