...
首页> 外文期刊>Sociedade Brasileira de Medicina Tropical. Revista >Response to different benznidazole doses in animal models of chronic phase Chagas disease: a critical review
【24h】

Response to different benznidazole doses in animal models of chronic phase Chagas disease: a critical review

机译:在慢性恰加斯病动物模型中对不同苯并硝唑剂量的反应:一项重要综述

获取原文

摘要

Chagas disease is a protozoan infection that was identified over a century ago. No drugs are available to treat the indeterminate and determinate chronic phases of the disease. Success of a drug design is dependent on correct biological evaluation. Concerning new drug designs for Chagas disease, it is essential to first identify the most effective, existing, experimental chronic protocols that can be used for comparison purposes. Here, we present a literature review regarding experimental models with chronic Chagas disease to evaluate the efficacy of benznidazole (BZN). We searched literature published in PubMed and Web of Science databases, using these keywords: animal model, BZN, Chagas disease, T. cruzi, and chronic phase, with no timeframe limitations. We excluded articles involving acute phase animal models and/or those without BZN treatment. The selected studies were conducted using different BZN concentrations (10mg-100mg) involving several different periods (5-70 days). Concentrations and durations of use are directly related to side effects, but do not prevent chronic tissue lesions. BZN use during the late/chronic phases of Chagas disease is unable to eliminate amastigote forms present in infected tissues. This study suggests the administration of a lower BZN concentration (100mg/kg/day) during the chronic phase of the animal model, as this had been reported to result in fewer side effects.
机译:恰加斯病是一个多世纪以前发现的原生动物感染。没有药物可用于治疗该疾病的不确定的和确定的慢性期。药物设计的成功取决于正确的生物学评估。关于南美锥虫病的新药设计,至关重要的是首先确定可用于比较目的的最有效,现有的实验性慢性方案。在这里,我们提出了有关慢性恰加斯病实验模型的文献综述,以评估苯并硝唑(BZN)的疗效。我们使用以下关键字搜索PubMed和Web of Science数据库中发表的文献:动物模型,BZN,恰加斯病,克鲁格氏菌和慢性期,没有时间限制。我们排除了涉及急性期动物模型和/或未经BZN治疗的动物的文章。选择的研究使用不同的BZN浓度(10mg-100mg)进行,涉及几个不同的时期(5-70天)。使用浓度和持续时间与副作用直接相关,但不能预防慢性组织损伤。在恰加斯病的晚期/慢性阶段使用BZN无法消除感染组织中存在的鞭毛体形式。这项研究表明,在动物模型的慢性期给予较低的BZN浓度(<100mg / kg /天),因为据报道这会减少副作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号