中国寄生虫学与寄生虫病杂志 ›› 1983, Vol. 1 ›› Issue (3): 158-163.

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日本血吸虫嘧啶合成代谢及其抑制的研究

黄左钺,常惠玲,周依燕,莫启忠   

  1. 中国医学科学院寄生虫病研究所; 中国医学科学院寄生虫病研究所; 中国医学科学院寄生虫病研究所; 上海中医学院
  • 收稿日期:2017-01-12 修回日期:2017-01-12 出版日期:1983-08-31 发布日期:2017-01-12

PYRIMIDINE METABOLISM IN SCHISTOSOMA JAPONICUM

  • Received:2017-01-12 Revised:2017-01-12 Online:1983-08-31 Published:2017-01-12

摘要: 实验证明标记物[~(14)C]碳酸氢钠、[5-~3H]乳清酸和[5-~3H]尿嘧啶都能掺入日木血吸虫虫体,并进入核酸。匀浆的酶活力测定,证明了虫体存在嘧啶自身合成途径的酶系:氨甲酰磷酸合成酶Ⅱ-氯甲酰天冬氨酸转移酶(ATCase)-二氢乳清酸酶酶组,二氢乳清酸脱氢酶(DHOdehase)以及乳清酸磷酸核糖转移酶(OPRTase)-乳清酸核苷-5′-磷酸脱羧酸酶(ODCase)组。虫体还存在补救途径的酶。对这两条途径在虫体嘧啶合成代谢中的重要性进行了讨论。感染日本血吸虫病的小鼠口服硝唑咪和硝硫氰胺后,对血吸虫的乳清酸磷酸核糖转移酶-乳清酸核苷-5′-磷酸脱羧酶有一定的抑制作用,该酶组有可能作为抗

关键词: 日本血吸虫, 乳清酸, 酶活力, 磷酸核糖, 碳酸氢钠, 转移酶, 合成代谢, 合成途径, 硝硫氰胺, 酸合成酶

Abstract: Experiments on the pyrimidine metabolism in Schistosoma japonicum have demonstrated that labelled bicarbonate, orotic acid and uracil are all incorporated into the nucleic acids of worms. This indicates that carbamyl phosphate synthetase II-aspartate carbamyl transferase-dihydroorotase complex, dihydroorotate dehydrogenase as well as orotate phosphoribosyl-transferase-orotidylate decarboxylase complex do exist.S. japonicum not only possesses all the enzymes of the pyrimidine de novo pathway but also the capacity of salvaging the preformed pyrimidines. It is evident that host blood may supply sufficient amount of bicarbonate to meet the requirements of de novo synthesis, but it is questionable whether blood contains enough quantity of pyrimidine bases and nucleosides for the salvage pathway.The effect of schistosomicides (niridazole and amoscanate) on the pyrimidine de novo pathway in vivo has also been studied. It is suggested that the orotate phosphoribosyl-transferase-orotidylate decarboxylase complex is a vulnerable point which might be attacked by chemotherapeutic agents. Since the structure of niridazole is similar to that of orotic acid, analogues of orotic acid may be of selective significance.