Brock N, Pohl J
IARC Sci Publ. 1986(78):269-79.
Urotoxic side effects, particularly haemorrhagic cystitis, have been a limiting factor for the therapeutic use of the oxazaphosphorine cytostatics cyclophosphamide, ifosfamide and trofosfamide. The development of mesna (Uromitexan) has made it possible to carry out regional detoxification in the kidneys and the efferent urinary tract and thus to achieve clinically prophylaxis against the urotoxic side effects of oxazaphosphorines. In the body, mesna is rapidly converted to the biologically inactive disulfide form (dimesna). After glomerular filtration, dimesna is reduced by interaction with the glutathione system of the renal tubular cells and is excreted in the urine as mesna, the free thiol compound. This compound is then capable of definitively detoxifying the oxazaphosphorine metabolites in the urine. In extensive experiments on rats, it has been demonstrated that the cyclophosphamide-induced occurrence of urinary bladder tumours could be reduced or even eliminated by simultaneous administration of mesna. Detoxification by mesna enables the clinical use of higher doses and, consequently, a possible increase in therapeutic efficiency.
泌尿毒性副作用,尤其是出血性膀胱炎,一直是氧氮磷啶类细胞抑制剂环磷酰胺、异环磷酰胺和曲磷胺治疗应用的限制因素。美司钠(巯乙磺酸钠)的研发使得在肾脏和传出尿路进行局部解毒成为可能,从而实现对氧氮磷啶类药物泌尿毒性副作用的临床预防。在体内,美司钠迅速转化为无生物活性的二硫化物形式(二巯乙磺酸钠)。经肾小球滤过后,二巯乙磺酸钠通过与肾小管细胞的谷胱甘肽系统相互作用而被还原,并以美司钠(游离硫醇化合物)的形式随尿液排出。然后,这种化合物能够最终使尿液中的氧氮磷啶类代谢产物解毒。在对大鼠进行的广泛实验中,已证明同时给予美司钠可减少甚至消除环磷酰胺诱导的膀胱肿瘤的发生。美司钠解毒使得临床能够使用更高剂量,从而可能提高治疗效果。