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The Ultrastructure and Development of Schistosoma japonicum Pigment

机译:日本血吸虫色素的超微结构和发展

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Schistosome japonicum is the etiological agent for schistosomiasis, a parasitic disease still prevalent in some parts of world. Today 200 million people are infected worldwide. Pmaziquanteh, as the specific drug for treatment of schistosomiasis, has been used extensively. Continuous use of the single drug inevitably increases the risk of developing resistance to Pmaziquanteh. Thus, it is important to speed up new drugs research and development as soon as possible. Recent researches indicate that inhibition of formation of Schistosome pigment (SP) leads to remarkable decrease in total protein, SP content and viability of the worms, as well as in parasitemia and deposition of eggs in mouse livers. The results suggest that formation of SP is a potential target for chemotherapy. Recent work regarding SP has mostly been centered on its chemical composition, structure and mechanism of formation.
机译:血吸虫粳米是血吸虫病的病因,寄生疾病在世界某些地区仍然普遍存在。今天有200万人受到全世界的感染。作为用于治疗血吸虫病的特定药物的pmaziquantiquationAniquantiquationAntiquantiquationAntiquanti。连续使用单一药物不可避免地增加对PMAZIQUANTEH的抗性的风险。因此,尽快加快新的药物研发。最近的研究表明,血吸虫色素(SP)形成的抑制导致蠕虫的总蛋白质,SP含量和活力的显着降低,以及在小鼠肝脏中的寄生症和鸡蛋的沉积。结果表明,SP的形成是化疗的潜在目标。最近关于SP的工作主要是以其化学成分,结构和形成机制为中心。

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