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青蒿琥酯给药后感染日本血吸虫的小鼠体内童虫的超微结构改变。

Ultrastructural alterations of juvenile Schistosoma japonicum harbored in mice following mefloquine administration.

机构信息

National Institute of Parasitic Diseases, Chinese Center for Disease, Control and Prevention, Key Laboratory of Parasite and Vector Biology, MOH, WHO Collaborating Centre for Malaria, Schistosomiasis, and Filariasis, Shanghai 200025, People's Republic of China.

出版信息

Parasitol Res. 2012 Feb;110(2):637-44. doi: 10.1007/s00436-011-2534-x. Epub 2011 Jul 13.

Abstract

The aim of the present study was to assess the ultrastructural alterations of juvenile Schistosoma japonicum induced by mefloquine. Mice infected with 14-day-old S. japonicum were treated orally with mefloquine at a single dose of 400 mg/kg. Between 8 h and 7 days after treatment, groups of two mice were sacrificed, and schistosomula were recovered for transmission electron microscopic observations. Ultrastructural damage was seen in the tegument, subtegumental musculature, parenchymal tissues, and gut epithelial cell. It was already prominent 8 h after drug administration and increased in severity rapidly to reach a peak 3 days post-treatment. Tegumental alterations were characterized by emergence of irregular and elongated cytoplasmic processes, which further fused together accompanied by indistinction of matrix and roughness of external plasma membrane. Meanwhile, in the subtegument, damage to the syncytium, swelling, and lysis of muscle bundles and parenchymal tissues were universal, which further aggravated the lesion on the tegument, followed by collapse or disintegration of damaged tegument to form numerous fragment or debris of cytoplasmic process detached from the worm surface. Severe damage to the gut epithelial cell was also observed 8 h post-mefloquine treatment, which included focal lysis of cytoplasm accompanied by formation of vacuoles and degeneration of mitochondria, emergence of enlarged and contracted nucleus with indistinct or focal disrupted nuclear membrane, and decrease in microvilli. All these alterations further increased in severity and reached the peak 3 days post-treatment. The findings of our study indicate that mefloquine exhibits a fast and potent ability to cause extensive ultrastructural damage to juvenile S. japonicum, which correlates with its high efficacy against juvenile schistosomes.

摘要

本研究旨在评估甲氟喹对感染日本血吸虫 14 日龄童虫的超微结构改变。感染日本血吸虫的小鼠经口给予甲氟喹,剂量为 400mg/kg,单次给药。给药后 8 小时至 7 天,每组处死 2 只小鼠,回收童虫进行透射电镜观察。在表皮、皮下肌肉、实质组织和肠上皮细胞中均观察到超微结构损伤。给药后 8 小时即可观察到明显的损伤,且损伤严重程度迅速增加,在给药后 3 天达到高峰。表皮改变的特征是出现不规则和伸长的细胞质突起,进一步融合,同时基质不清,外质膜粗糙。同时,在皮下组织中,合胞体损伤、肌束和实质组织肿胀和溶解普遍存在,这进一步加重了表皮的病变,随后受损表皮塌陷或崩解,形成大量从虫体表面脱离的细胞质突起碎片或残骸。给药后 8 小时也观察到肠上皮细胞严重损伤,包括细胞质局灶性溶解,伴有空泡形成和线粒体变性,细胞核增大和收缩,核膜模糊或局灶性破坏,微绒毛减少。所有这些改变的严重程度进一步增加,在给药后 3 天达到高峰。本研究结果表明,甲氟喹对感染日本血吸虫 14 日龄童虫具有快速而强大的广泛超微结构损伤能力,这与其对童虫的高效作用相关。

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