ASIA unversity:Item 310904400/115274
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    题名: The Uroprotective Efficacy of Total Ginsenosides in Chinese Ginseng on Chemotherapy with Cyclophosphamide
    作者: 陳永祥;Chen, Yung-Hsian;Chen, Wen-Chi;Chen, Wen-Chi;Chen, Szu-Ju;Chen, Szu-Ju;Wa, Shih-Jing;Wang, Shih-Jing;Liu, Po-Len;Liu, Po-Len;Tsa, Ming-Yen;Tsai, Ming-Yen;Li, Chun-Ting;Liu, Chun-Ting;Der-Cherng, Cherng C;Chen, Der-Cherng;Chen, Huey-Yi;Chen, Huey-Yi
    贡献者: 醫學暨健康學院心理學系
    关键词: cyclophosphamide;uroprotection;urothelial damage;total ginsenosides in Chinese ginseng
    日期: 2022-08-01
    上传时间: 2023-03-29 01:17:52 (UTC+0)
    出版者: 亞洲大學
    摘要: Hemorrhagic cystitis is a recognizable complication of cyclophosphamide (CYP) attributable to its lively metabolite acrolein, which produces urothelial injury. The study intended to examine the uroprotective efficacy of total ginsenosides in Chinese ginseng (TGCG) in CYP-induced hemorrhagic cystitis. In total, 24 virgin female rats were randomized into four groups as follows: group 1 (control group; injected with normal saline), group 2 (injected with CYP plus a placebo with normal saline), group 3 (given CYP and TGCG (200 mg/kg)), and group 4 (given CYP and 2-mercaptoethane sulfonate sodium (Mesna, 30 mg/kg)). An evaluation by cystometry was conducted. Values of the voiding interval were assessed in anesthetized rats and histological examinations of the bladders were measured. In the cystometry analysis, the voiding interval was significantly reduced in the CYP group. TGCG and Mesna significantly increased in the voiding interval values, individually. Bladder edema and urothelial injury were examined after contact with CYP. Contrasted to the group given CYP, CYP-induced hemorrhagic cystitis, TGCG significantly increased the urothelial thickness, and significantly reduced scores of mucosal break and submucosal edema in the bladder. In conclusion, these findings mean that the treatment with TGCG in CYP rats can avoid hemorrhagic cystitis. TGCG decreases urothelial injury. TGCG may participate as the chief character of uroprotection in CYP-induced hemorrhagic cystitis.
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