Fontes Carlos Edmundo Rodrigues, Abreu Ana Paula de, Gasparim Aretuza Zaupa
Laboratory of Experimental Surgery.
Post-Graduate Program in Health Sciences, State University of Maringá, Maringá, PR, Brazil.
Arq Bras Cir Dig. 2018 Mar 1;31(1):e1341. doi: 10.1590/0102-672020180001e1341.
Researches on Chagas disease still use several animals and rats, due to size and susceptibility were preferred by many authors.
To develop an experimental model of megacolon in rats inoculated with the strain Y of Trypanosoma cruzi.
Thirty male Wistar rats were distributed in three groups inoculated with different inoculants: Group A: 600000, Group B: 1000000 and Group C: 1500000 blood trypomastigotes of T. cruzi. Animals were sedated intramuscularly at zero inoculation time (T0) and 60 days after inoculation (T60), to perform the barium enema in order to evaluate the dilatation of the different segments of colon in a comparative study of the measurements obtained, using a digital caliper. Evidence of infection was performed by blood smear collected from the animal's tail 18 days after inoculation with observation of blood forms.
Comparing the intestinal diameter of the inoculated animals with 60,0000 trypomastigotes in the T0 of infection with T60 days after the inoculation, significant dilatation was observed between the proximal, medial and distal segments (p<0.01), indicating the establishment of the megacolon model. In addition, comparing intestinal diameter between the different segments, with in the T0 of infection and the T60 after inoculation, significant alterations were observed (p<0.05).
The proposed model was possible for in vivo studies of alterations due to infection by T. cruzi and functional alterations of the colon. In addition, the changes manifested in the colon are not directly proportional to the size of the inoculum, but to the time of infection that the animals were submitted, since the animals inoculated with 60,0000 blood forms were the ones which presented the most significant alterations.
由于许多作者认为大鼠体型合适且易感染,关于恰加斯病的研究仍使用多种动物,其中大鼠较为常用。
建立接种克氏锥虫Y株的大鼠巨结肠实验模型。
将30只雄性Wistar大鼠分为三组,分别接种不同剂量的接种物:A组:600000个、B组:1000000个、C组:1500000个克氏锥虫血液型鞭毛体。在接种零时(T0)和接种后60天(T60)对动物进行肌肉注射镇静,以便进行钡灌肠,使用数字卡尺在比较测量结果的研究中评估结肠不同节段的扩张情况。在接种18天后从动物尾巴采集血涂片观察血相,以确定感染情况。
将接种600000个鞭毛体的感染动物在感染T0时与接种后60天的肠道直径进行比较,近端、中段和远端节段之间观察到显著扩张(p<0.01),表明巨结肠模型建立。此外,比较感染T0时和接种后T60时不同节段之间的肠道直径,观察到显著变化(p<0.05)。
所提出的模型可用于克氏锥虫感染引起的改变及结肠功能改变的体内研究。此外,结肠中表现出的变化与接种物大小不成正比,而是与动物感染的时间有关,因为接种600000个血相的动物表现出最显著变化。