Jiménez-Coello Matilde, Acosta-Viana Karla Yolanda, Pérez G Maria Salud, Guzmán-Marín Eugenia del S
Laboratorio de Biologia Celular, CIR Dr. Hideyo Noguchi, Universidad Autonoma de Yucatán, Ave. Itzaes # 490 x 59, Centro, C P 97000, Merida Yucatan, Mexico.
Afr J Tradit Complement Altern Med. 2011;8(5 Suppl):198-207. doi: 10.4314/ajtcam.v8i5S.26. Epub 2011 Jul 3.
The antiprotozoal activity in vivo against Trypanosoma cruzi of (8-hydroxymethylen)-trieicosanyl acetate was evaluated in BALB/c mice during the acute phase of Chagas' disease (15 days after infection). Animals were treated during 15 days at doses of 16.8 and 33.6 µg/g, reduced parasitemia of 77.6 and 64.1% was observed respectively, in comparison with positive control mice (allopurinol 8.5 µg/g) which reduced only 29.7%. Also, amastigote nests in cardiac tissue were significant reduced in treated mice groups. The regression of effect induced after the suppression of the treatment with the compound was evaluated; animals were infected and simultaneously began the treatment with the compound during 20 days (16.8 and 33.6 µg/g). Mice were monitored after the end of the treatment for one more week. A good antitrypanosomal response was observed (66.1 and 68.9% less than untreated mice) during treatment, but 8 days after suspension of treatment, parasitemia level increased, reducing only 58.6 and 56.29 % respectively in treated animals compared with no treated.
在恰加斯病急性期(感染后15天),对BALB/c小鼠体内(8-羟基亚甲基)-二十三烷基乙酸酯抗克氏锥虫的活性进行了评估。动物以16.8和33.6 µg/g的剂量接受为期15天的治疗,与阳性对照小鼠(别嘌呤醇8.5 µg/g)相比,分别观察到寄生虫血症降低了77.6%和64.1%,而阳性对照小鼠仅降低了29.7%。此外,治疗小鼠组心脏组织中的无鞭毛体巢也显著减少。评估了用该化合物治疗停止后诱导效应的消退情况;动物被感染并同时开始用该化合物治疗20天(16.8和33.6 µg/g)。治疗结束后对小鼠再监测一周。在治疗期间观察到良好的抗锥虫反应(比未治疗小鼠少66.1%和68.9%),但在治疗停止8天后,寄生虫血症水平升高,与未治疗动物相比,治疗动物的寄生虫血症水平仅分别降低了58.6%和56.29%。