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Ultrastructural effects of acetamizuril on endogenous phases of Eimeria tenella

机译:乙胺嘧啶对艾美耳球虫内源期的超微结构影响

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摘要

To explore the primary stage or site of action of acetamizuril (AZL), a novel triazine anticoccidial compound, the ultrastructural development of Eimeria tenella at different endogenous stages was studied in experimentally infected chickens treated with a single oral dose of 15 mg/kg AZL. As a result of drug action, the differentiations of second-generation schizonts and microgamonts were largely inhibited and merozoites became irregular in shape. Meanwhile, the outer membrane blistering and perinuclear space enlargement were obvious in the second-generation schizonts and microgamonts, which were never observed in the classic triazine anticoccidiosis drug diclazuril-treated E. tenella. The chromatin aggregation, anachromasis, and marginalization were visible in merozoites and microgamonts. Furthermore, the abnormal evagination of microgametes finally resulted in the degeneration of microgamonts and the failure of subsequent fertilization. The most marked micromorphological alteration occurring in the macrogamonts was the WFB2. Even if the fertilization occurred, the formation of oocyst wall became malformed and the zygote proceeded to the obvious degeneration. In addition, mitochondria swelling and cytoplasm vacuolization were discerned in respective intracellular stages, while endoplasmic reticulum and Golgi body swelling was less seen. These alterations may be the causes leading to the final death of E. tenella and also provide some information for further exploring the mechanism of action of AZL at the molecular level.
机译:为了探索一种新的三嗪类抗球虫药乙酰胺(AZL)的主要阶段或作用部位,在单剂量口服15 mg / kg AZL治疗的实验感染鸡中研究了艾美球虫在不同内源阶段的超微结构发展。由于药物作用,第二代裂殖体和微gamonts的分化受到很大抑制,裂殖子的形状变得不规则。同时,在第二代裂殖体和微gamont中,外膜起泡和核周空间增大是很明显的,而在经典的三嗪类抗球虫病药物地克珠利治疗的大肠杆菌中则从未观察到。在裂殖子和微gamonts中可见染色质聚集,无色性和边缘化。此外,微配子的异常撤离最终导致微配子的退化和随后的受精失败。在大峡谷中发生的最明显的微观形态变化是WFB2。即使发生受精,卵囊壁的形成也变得畸形,合子继续发生明显的变性。此外,线粒体肿胀和细胞质空泡化分别在细胞内阶段可见,而内质网和高尔基体肿胀较少。这些改变可能是导致E. tenella最终死亡的原因,也为进一步探索AZL在分子水平上的作用机理提供了一些信息。

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