Shibayama M, Navarro-García F, López-Revilla R, Martínez-Palomo A, Tsutsumi V
Department of Experimental Pathology, Centro de Investigación y de Estudios Avanzados del IPN, México DF, Mexico.
Parasitol Res. 1997;83(2):170-6. doi: 10.1007/s004360050228.
One of the main drawbacks of experimental amebiasis is the lack of an adequate animal model for invasive intestinal lesions. Mongolian gerbils are useful because both intestinal and hepatic amebiasis can be produced experimentally with Entamoeba histolytica trophozoites. In this paper we show results obtained with in vivo and in vitro models of intestinal amebiasis in gerbils. We inoculated gerbils intracecally with monoxenic cultures of a highly virulent E. histolytica HM1:IMSS substrain. In the in vivo model an increase in mucus production was observed during the first 6 h of interaction. Microulcerative mucosal lesions appeared at 24-72 h postinoculation. Inflammatory infiltrate and edema of the lamina propria were associated with superficial foci of necrosis. At 96 h the cecal mucosa had an almost normal appearance and live amebas were no longer detected. In the in vitro model, early damage was detected in cecal strips mounted in Ussing chambers as a rapid fall in potential difference, short-circuit current, and transepithelial resistance that correlated with the extent of the microscopic lesions produced. The latter consisted of cellular edema and the appearance of small, translucent vacuoles at the base of epithelial cells. Further damage led to loss of intercellular junctions, destruction of interglandular epithelial cells, and edema of the lamina propria. The present results demonstrate that the gerbil is useful as an experimental model for the analysis of early stages of invasive intestinal amebiasis both in vivo and in vitro.
实验性阿米巴病的主要缺点之一是缺乏用于侵袭性肠道病变的合适动物模型。蒙古沙鼠很有用,因为肠道和肝脏阿米巴病都可以通过溶组织内阿米巴滋养体在实验中诱发。在本文中,我们展示了在沙鼠肠道阿米巴病的体内和体外模型中获得的结果。我们向沙鼠盲肠内接种了高毒力溶组织内阿米巴HM1:IMSS亚株的单菌培养物。在体内模型中,在相互作用的最初6小时内观察到黏液分泌增加。接种后24 - 72小时出现微溃疡性黏膜病变。固有层的炎性浸润和水肿与浅表坏死灶相关。在96小时时,盲肠黏膜外观几乎正常,不再检测到活的阿米巴。在体外模型中,安装在尤斯灌流小室中的盲肠条带出现早期损伤,表现为电位差、短路电流和跨上皮电阻迅速下降,这与所产生的微观病变程度相关。后者包括细胞水肿以及上皮细胞底部出现小的半透明空泡。进一步的损伤导致细胞间连接丧失、腺间上皮细胞破坏以及固有层水肿。目前的结果表明,沙鼠作为体内和体外分析侵袭性肠道阿米巴病早期阶段的实验模型是有用的。