中国寄生虫学与寄生虫病杂志 ›› 2013, Vol. 31 ›› Issue (6): 2-419-427.

• 论著 • 上一篇    下一篇

OZ78单剂口服治疗对小鼠体内日本血吸虫成虫超微结构的损害(英文)

肖树华,孙军,薛剑,杜喜玲,张皓冰   

  1.  1  中国疾病预防控制中心寄生虫病预防控制所,卫生部寄生虫病原与媒介生物学重点实验室,世界卫生组织疟疾、血吸虫病和丝虫病合作中心,上海 200025;2 同济大学医学院传染病与疫苗研究所,上海 200092;3 同济大学生命科学与技术学院,上海 200092
  • 出版日期:2013-12-30 发布日期:2014-02-28

Ultrastructural Alterations of Adult Schistosoma japonicum Harbored  in Mice Treated with a Single Oral Dose of OZ78

XIAO Shu-hua*,SUN Jun,XUE Jian,DU Xi-ling,ZHANG Hao-bing   

  1. 1 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,China;2 Institute for Infectious Disease and Vaccine Development,School of Medicine,Tongji University,Shanghai 200092,China;3 School of Life Science and Technology,Tongji University,Shanghai 200092,China
  • Online:2013-12-30 Published:2014-02-28

摘要: 目的  观察合成的螺金刚烷臭氧化物OZ78对日本血吸虫成虫所引起的超微结构变化。 方法  10只小鼠每鼠感染40~60条日本血吸虫尾蚴,感染后35 d,取8只小鼠,每鼠口服单剂OZ78 400 mg/kg,治后24 h、3 d、7 d和14 d各剖杀2只小鼠,用灌注法收集血吸虫,并按常规方法固定和处置虫体,透射电镜观察。从另2只未治疗的感染小鼠体内取虫作对照。 结果  感染鼠经OZ78治后24 h,雌、雄虫皮层的明显变化是因细胞质突起肿胀致使体表平坦、远端细胞质突起不规则膨大伴有杆状和盘状分泌体减少、皮层基质局灶性溶解、一些细胞质突起融合成大片状、基底膜破裂或消失,感觉器内部结构受损。在皮层下,肌束无或呈轻度肿胀,并查见肌束局灶性溶解,而肌层下的皮层细胞示核肿大、部分核膜模糊和染色质局灶性溶解形成小空泡,在核周胞质内出现变性线粒体。实质组织的主要变化是线粒体变性,以及一些小空泡与髓鞘样结构的形成。肠上皮细胞的明显变化是细胞核的不规则肿大、核仁轻度溶解和部分双层核膜融合、细胞质中的线粒体变性和微绒毛破溃。此时雌虫卵黄细胞最明显的变化为许多卵黄滴破裂,卵黄球释出,继而溶解和融合。治后3~7 d,虫体受损的范围和程度加重。雄虫和雌虫的明显损害是细胞质突起的融合、受损细胞质突起剥落或破溃以致肌束显露、感觉器和皮层细胞的严重破坏、肌束局灶性或广泛肿胀和溶解、出现一些大片变性的实质组织和严重受损的肠上皮细胞。雌虫的卵黄细胞则示卵黄滴减少、细胞核局灶性溶解及卵黄细胞间实质组织的广泛溶解。经OZ78治后14 d,存活雌、雄虫的受损皮层和皮层下组织均有一些恢复,而大多数肠上皮细胞和卵黄细胞仍示有明显损害。 结论  OZ78对日本血吸虫成虫的皮层和皮层下组织,包括皮层细胞、实质组织、肠上皮细胞和卵黄细胞具有广泛的损害作用。

关键词: 合成的螺金刚烷臭氧化物, OZ78, 日本血吸虫, 超微结构变化, 透射电镜

Abstract: 【Abstract】  Objective  To observe the ultrastructural alterations of adult Schistosoma japonicum induced by synthetic trioxolane OZ78.  Methods  Eight out of ten mice infected with 40-60 S. japonicum cercariae for 35 d were treated orally with OZ78 at a single dose of 400 mg/kg. Four groups of two mice were killed at 24 h, 3 d, 7 d, and 14 d post treatment, and schistosomes were recovered by perfusion technique, fixed, and examined by transmission electron microscopy. Schistosomes obtained from the remaining two untreated mice served as control.  Results  After infected mice were treated with OZ78 for 24 h, the prominent alterations in tegument of both male and female worms were observed, which revealed in flattened surface due to swelling of cytoplasmic processes, irregular expansion in distal end of cytoplasmic processes accompanied by decrease in rod-like and discoid-like secretory bodies, focal lysis of tegumental matrix; fusion of some cytoplasmic processes to form a large piece, disruption or disappearance of basal membrane, and destruction of internal structures in sensory organelles. In the subtegument, no or slight swelling and focal lysis of muscle bundles were seen, while the syncytium beneath the muscle showed enlargement of nucleus with indistinction of partial nuclear membrane, formation of small vacuoles due to focal lysis of chromatin, and emergence of degenerated mitochondria in perinuclear cytoplasm. As to parenchymal tissues, the major alterations included degeneration of mitochondria, formation of some small vacuoles and myelin-like structures. In gut epithelial cells, the prominent alterations were irregular enlargement of nucleus with light lysis of nucleoli and fusion of partial bi-layer nuclear membrane, degeneration of mitochondria in cytoplasm and collapse of microvilli. At this time point, in the vitelline cells of female worms, the most significant alteration was the collapse of many vitelline droplets, which led to release of the vitelline balls, followed by their lysis and fusion. Three to 7 d post treatment, the damage to the worms aggravated either in extent or in severity along with time. The significant damages to male and female worms were fusion of cytoplasmic processes, peeling or collapse of damaged cytoplasmic processes resulting in exposure of muscle bundles, severe destruction of sensory organelles and syncytium, focal or extensive swelling and lysis of muscle bundles, emergence of some larger piece of degenerated parenchymal tissues and severe damage to the gut epithelial cell. While in the vitelline cells of female worms, decrease in the number of vitelline droplet, focal lysis of nucleus and extensive lysis of parenchymal tissues among the vitelline cells were also observed. Fourteen days post OZ78 dosing, male and female worms which survived the treatment showed some renovation in damaged tegument and subtegument, while most gut epithelial cells and vitelline cells still revealed in prominent injury.  Conclusion  The results demonstrate that OZ78 possesses an extensive damage to the ultrastructure in tegument and subtegument tissues including syncytium, parenchymal tissues, gut epithelial cells, and vitelline cells of adult S. japonicum.

Key words: Synthetic trioxolane, OZ78, Schistosoma japonicum, Ultrastructural alteration, Transmis-sion electron microscopy