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甲苯咪唑、阿苯达唑和吡喹酮对小鼠体内细粒棘球绦虫囊肿壁中富马酸水合酶、丙酮酸激酶和磷酸烯醇式丙酮酸羧激酶的影响。

Effects of mebendazole, albendazole, and praziquantel on fumarate hydratase, pyruvate kinase, and phosphoenolpyruvate carboxykinase of Echinococcus granulosus cyst wall harbored in mice.

作者信息

Xiao S H, Feng J J, Guo H F, Jiao P Y, Yao M Y, Jiao W

机构信息

Institute of Parasitic Diseases, Chinese Academy of Preventive Medicine, Shanghai.

出版信息

Zhongguo Yao Li Xue Bao. 1994 Jan;15(1):69-72.

PMID:8010090
Abstract

Echinococcus granulosus cyst wall exhibited activities of fumarate hydratase (FH), pyruvate kinase (PK), and phosphoenolpyruvate carboxykinase (PEPCK) with 911-1433, 151-215, and 54-98U, respectively. The ratio of PK/PEPCK was 2.2-2.7, indicating that glycolysis is the main pathway of carbohydrate metabolism in the cyst wall. When infected mice were treated ig with mebendazole, albendazole or praziquantel at the respective daily dose of 25-50, 300, and 500 mg.kg-1 for 7-14 d, no apparent change of FH activity in the cyst wall was found, while PK and PEPCK activities in the cyst wall were markedly inhibited by mebendazole and albendazole. The inhibition rates of PK and PEPCK activities in mebendazole group were 85-88% and 90-92%, respectively, while in albendazole group were 55.3 and 71.6%, respectively. The results suggest that PK or PEPCK in the cyst wall may the important site attacked by effective anti-hydatid drugs.

摘要

细粒棘球绦虫囊肿壁表现出延胡索酸水合酶(FH)、丙酮酸激酶(PK)和磷酸烯醇式丙酮酸羧激酶(PEPCK)的活性,分别为911 - 1433、151 - 215和54 - 98U。PK/PEPCK的比值为2.2 - 2.7,表明糖酵解是囊肿壁碳水化合物代谢的主要途径。当感染小鼠分别以25 - 50、300和500mg·kg-1的日剂量灌胃给予甲苯咪唑、阿苯达唑或吡喹酮7 - 14天时,囊肿壁FH活性未发现明显变化,而甲苯咪唑和阿苯达唑显著抑制了囊肿壁PK和PEPCK的活性。甲苯咪唑组PK和PEPCK活性的抑制率分别为85 - 88%和90 - 92%,而阿苯达唑组分别为55.3%和71.6%。结果表明,囊肿壁中的PK或PEPCK可能是有效抗包虫药物攻击的重要靶点。

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