Okamura T, Masui T, St John M K, Cohen S M, Taylor R J
Department of Urology, Nagoya City University Medical School.
Hinyokika Kiyo. 1995 Apr;41(4):289-96.
Hemorrhagic cystitis is a common problem following cyclophosphamide or radiation therapy. Chitosan has been shown to be an effective hemostatic agent and promoter of wound healing in animal experiments. We evaluated the safety and efficacy of intravesical chitosan in an animal model of cyclophosphamide cystitis. Hemorrhagic cystitis was induced in female F344 rats by intraperitoneal cyclophosphamide, 100 mg/kg. Chitosan solution (0.3 ml) was instilled intravesically on day 1 (Group 1), on days 1, 3, and 5 (Group 2), or 1 hour after the administration of cyclophosphamide (Group 3). The rats in group 4 were treated with chitosan diluent on day 1 after cyclophosphamide, and the rats in group 5 received intravesical chitosan without cyclophosphamide. Sequential examination revealed decreased mortality and lower incidences of severe bladder bleeding, necrosis and inflammation in Group 3. Treatment delayed until after the appearance of the cystitis, especially repeated treatments, appeared to make the cyclophosphamide-induced changes worse. Used within 1 hour of cyclophosphamide administration, before the cystitis develops, chitosan seemed to have the possibility to inhibit the appearance of hemorrhagic cystitis. In addition to the changes in the bladder, severe changes occurred in the kidneys secondary to cyclophosphamide.
出血性膀胱炎是环磷酰胺治疗或放射治疗后常见的问题。在动物实验中,壳聚糖已被证明是一种有效的止血剂和伤口愈合促进剂。我们在环磷酰胺诱导的膀胱炎动物模型中评估了膀胱内灌注壳聚糖的安全性和有效性。通过腹腔注射100mg/kg环磷酰胺在雌性F344大鼠中诱导出血性膀胱炎。在第1天膀胱内灌注壳聚糖溶液(0.3ml)(第1组),在第1、3和5天灌注(第2组),或在给予环磷酰胺后1小时灌注(第3组)。第4组大鼠在环磷酰胺后第1天用壳聚糖稀释剂治疗,第5组大鼠未用环磷酰胺而接受膀胱内壳聚糖治疗。连续检查显示第3组死亡率降低,严重膀胱出血、坏死和炎症的发生率较低。膀胱炎出现后延迟治疗,尤其是重复治疗,似乎会使环磷酰胺诱导的变化更严重。在膀胱炎发生前,在环磷酰胺给药后1小时内使用壳聚糖,似乎有可能抑制出血性膀胱炎的出现。除膀胱变化外,环磷酰胺还导致肾脏发生严重变化。