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金家贵, 孟延发, 郭卫, 等. 聚乙二醇修饰对苦瓜核糖体失活蛋白的肝细胞毒性影响[J]. 四川大学学报(医学版), 2013, 44(4): 536-539,544.
引用本文: 金家贵, 孟延发, 郭卫, 等. 聚乙二醇修饰对苦瓜核糖体失活蛋白的肝细胞毒性影响[J]. 四川大学学报(医学版), 2013, 44(4): 536-539,544.
JIN Jia-gui, MENG Yan-fa, GUO Wei, et al. Effect of PEGylation of α-Momorcharin against Its Hepatotoxicity in Rats[J]. Journal of Sichuan University (Medical Sciences), 2013, 44(4): 536-539,544.
Citation: JIN Jia-gui, MENG Yan-fa, GUO Wei, et al. Effect of PEGylation of α-Momorcharin against Its Hepatotoxicity in Rats[J]. Journal of Sichuan University (Medical Sciences), 2013, 44(4): 536-539,544.

聚乙二醇修饰对苦瓜核糖体失活蛋白的肝细胞毒性影响

Effect of PEGylation of α-Momorcharin against Its Hepatotoxicity in Rats

  • 摘要: 目的 探讨聚乙二醇(PEG)修饰对α型苦瓜核糖体失活蛋白(α-momorcharin,α-MMC)的大鼠肝细胞毒性的影响。 方法 将SD大鼠随机分为生理盐水阴性对照组,α-MMC高、中、低剂量组(蛋白含量分别为6.25、2.08、0.70 mg/kg)和PEG修饰后的α-MMC-PEG高、中、低剂量组(蛋白含量相同),每组24只,隔日经尾静脉注射给药一次,连续28 d,停药后恢复14 d,观测动物的一般状况,并分别在给药期末和恢复期末进行肝功能和肝组织病理学检查。 结果 在给药第28 d,与生理盐水阴性对照组比较,α-MMC高、中剂量组有明显的肝功能异常,如血清白蛋白(ALB)含量降低,血清球蛋白(GLB)增加,A/G比值降低,谷草转氨酶(AST)、总胆红素(BIL)和胆固醇(CHO)增加;HE染色可见弥散性肝细胞水肿、变性,炎性细胞浸润,甚至点状坏死。与α-MMC不同,经PEG修饰后的α-MMC-PEG各组的毒性则明显减轻,其高剂量组肝功损害指标及病理改变仅与α-MMC低剂量组接近,而中剂量和低剂量组与阴性对照组一致。 结论 PEG修饰能够明显降低α-MMC对大鼠的肝细胞毒性。

     

    Abstract: Objective To explore the effect of PEGylation of α-Momorcharin (α-MMC), one of ribosome-inactivating proteins from bitter melon seed, against its hepatotoxicity in rats. Methods SD rats were randomized into NS group, α-MMC treated groups, and α-MMC-PEG treated groups. The doses of α-MMC and α-MMC-PEG were high, middle, and low dose(6.25, 2.08, 0.70 mg/kg). The rats were given different dose of α-MMC, or α-MMC-PEG via caudal vein every other day for consecutive 28 days and then left for 14 days recovery. The general condition of animals was observed, blood and liver samples were collected for liver function study and pathological examination on day 28 after initiation of administration and on day 14 after withdrawal. Results On day 28 after initiation of administration, the liver function damages were found in high-dose and middle-dose of α-MMC treated groups, such as the decreasing of ALB, increasing of GLB, A/G ratio decreasing and the dose-dependant increasing of AST, BIL and CHO. The pathological changes of hepatotoxicity were also observed in these two groups, including the massive hepatocyte, swelling degeneration, inflammatory cell infiltration, congestion and diffusive necrosis. However, the liver function and pathological changes in α-MMC-PEG treated groups were better than those in α-MMC treated groups. Conclusion PEGylation could reduce the hepatotoxicity of α-MMC to rats.

     

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