Manesh C, Kuttan G
Amala Cancer Research Centre, Amala Nagar, Thrissur, Kerala, India.
J Exp Clin Cancer Res. 2002 Dec;21(4):509-17.
Treatment of Swiss albino mice with naturally occurring sulphur compounds such as Diallyl sulphide (DAS) (500 microg/dose/animal, i.p) and Diallyl Disulphide (DADS) (250 microg/dose/animal, i.p) for five days along with cyclophosphamide (CTX) (1.5 mmol/kg.body.wt; i.p) reduced the CTX induced urotoxicity. Morphological analysis of the urinary bladders of the CTX treated group showed severe inflammation and dark colouration whereas the sulphur compounds treated group showed almost normal bladder morphology. Treatment with DAS and DADS was found to reduce the urine urea N2 level DAS (15.31+/-0.01 g/l), DADS (12.38+/-0.17 g/l) 4 hrs after CTX administration which was elevated in the CTX alone treated group (26.87+/-1.86 g/l). Urine protein level, which was enhanced drastically (8.66+/-0.47 g/l) after the CTX treatment, was significantly reduced (2.9+/-0.25 g/l) by the treatment with DADS. Similarly GSH content (which was drastically reduced by the CTX administration) in both bladder (0.87+/-0.1 nmol/mg protein) and liver (2.47+/-0.6 nmol/mg protein) was enhanced significantly (P<0.001) by the treatment with DAS and DADS both in bladder (DAS--1.56+/-0.17 nmol/mg protein; DADS--2.65+/-0.21 nmol/mg protein) and liver (DAS--5.30+/-0.07 nmol/mg protein; DADS--6.93+/-0.06 nmol/mg protein). Histopathological analysis of the bladder of the CTX alone treated group showed severe necrosis of the tissue whereas the sulphur compounds treated group showed normal bladder pathology.
用天然存在的硫化合物如二烯丙基硫醚(DAS)(500微克/剂量/动物,腹腔注射)和二烯丙基二硫醚(DADS)(250微克/剂量/动物,腹腔注射)对瑞士白化小鼠进行为期五天的治疗,并同时注射环磷酰胺(CTX)(1.5毫摩尔/千克体重;腹腔注射),可降低CTX诱导的尿路毒性。CTX治疗组膀胱的形态学分析显示有严重炎症和颜色变深,而硫化合物治疗组的膀胱形态几乎正常。发现用DAS和DADS治疗可降低CTX给药4小时后的尿尿素氮水平,DAS为(15.31±0.01克/升),DADS为(12.38±0.17克/升),而仅用CTX治疗的组该水平升高(26.87±1.86克/升)。CTX治疗后急剧升高的尿蛋白水平(8.66±0.47克/升),经DADS治疗后显著降低(2.9±0.25克/升)。同样,膀胱(0.87±0.1纳摩尔/毫克蛋白)和肝脏(2.47±0.6纳摩尔/毫克蛋白)中谷胱甘肽含量(经CTX给药后急剧降低),经DAS和DADS治疗后在膀胱(DAS为1.56±0.17纳摩尔/毫克蛋白;DADS为2.65±0.21纳摩尔/毫克蛋白)和肝脏(DAS为5.30±0.07纳摩尔/毫克蛋白;DADS为6.93±0.06纳摩尔/毫克蛋白)中均显著升高(P<0.001)。仅用CTX治疗组膀胱的组织病理学分析显示组织严重坏死,而硫化合物治疗组的膀胱病理学正常。