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巯乙磺酸钠(美司钠)对环磷酰胺给药后大鼠膀胱尿路上皮增殖的影响。

Effect of the uroprotector sodium 2-mercaptoethane sulfonate (Mesna) on the proliferation of the bladder urothelium in the rat after administration of cyclophosphamide.

作者信息

Kunze E, Köhnecke B, Engelhardt W, Steinröder H, Brock N, Pohl J

出版信息

Urol Int. 1984;39(2):61-7. doi: 10.1159/000280947.

Abstract

The chemotherapy of malignant tumors with oxazaphosphorine cytostatics, e.g., cyclophosphamide (CP) and ifosfamide, is limited by their severe urotoxic side effects. As a result of cytotoxic damage, the proliferation of the urinary bladder urothelium is considerably stimulated during an intensive reparative regeneration. The recently developed uroprotector sodium 2-mercaptoethane sulfonate (Mesna) allows regional detoxification limited to the kidneys and lower urinary tract and thus protects against damage by aggressive oxazaphosphorine metabolites. The object of the present quantitative autoradiographic investigation was to study urothelial proliferation in the bladder of rats after administration of CP alone and in combination with Mesna. 20 h after intraperitoneal injection of a single dose of CP alone (100 mg/kg), the urothelium showed a steep rise of the 3H-thymidine (3H-TdR) labeling index which reached a peak of 17.6% at 30 h. Thereafter, the 3H-TdR index rapidly dropped. A second peak of 4.4% was observed after 7 days. With supplementary intravenous administration of a single dose of Mesna (100 mg/kg) 15 min before treatment with CP, the labeling index was substantially lower than after administration of CP alone. Thus, maximal values of only 1.6 and 1.9% were observed at 35 h and 7 days, respectively. Histopathological examination of the bladders showed severe necrotizing and ulcerative cystitis, 10, 20 and 25 h after administration of CP alone whereas with additional treatment with Mesna only slight edema of the lamina propria developed. The results obtained clearly demonstrate the protective action of Mesna on the urothelium of the lower urinary tract against the urotoxic effects of CP.

摘要

用氮杂磷三环类细胞抑制剂(如环磷酰胺(CP)和异环磷酰胺)进行恶性肿瘤化疗时,会受到其严重的尿路毒性副作用的限制。由于细胞毒性损伤,在强烈的修复性再生过程中,膀胱尿路上皮的增殖会受到显著刺激。最近研发的尿路保护剂2-巯基乙烷磺酸钠(美司钠)可使解毒作用局限于肾脏和下尿路,从而防止受到具有侵袭性的氮杂磷三环代谢物的损害。本定量放射自显影研究的目的是研究单独给予CP以及CP与美司钠联合给药后大鼠膀胱尿路上皮的增殖情况。单独腹腔注射单剂量CP(每千克体重100毫克)20小时后,尿路上皮的3H-胸腺嘧啶核苷(3H-TdR)标记指数急剧上升,在30小时时达到17.6%的峰值。此后,3H-TdR指数迅速下降。7天后观察到第二个峰值为4.4%。在CP治疗前15分钟补充静脉注射单剂量美司钠(每千克体重100毫克),标记指数显著低于单独给予CP后。因此,在35小时和7天时分别仅观察到1.6%和1.9%的最大值。单独给予CP后10、20和25小时,膀胱的组织病理学检查显示有严重的坏死性和溃疡性膀胱炎,而额外给予美司钠治疗时,仅出现固有层轻度水肿。所获得的结果清楚地证明了美司钠对下尿路尿路上皮具有保护作用,可抵抗CP的尿路毒性作用。

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