Monzote Lianet, Montalvo Ana M, Scull Ramón, Miranda Migdalia, Abreu Juan
Parasitology Department, Institute of Medicine Tropical "Pedro Kourí", Apartado Postal No. 601, Marianao 13, Havana City, Cuba.
Biomed Pharmacother. 2007 Feb-Apr;61(2-3):148-53. doi: 10.1016/j.biopha.2006.12.001. Epub 2006 Dec 28.
The World Health Organization has classified the leishmaniasis as a major tropical disease. Current therapy is toxic, expensive and cause several adverse effects. The majority of people in endemic areas of leishmaniasis depend of natural and traditional medicine. This study was developed to examine the activity of the essential oil from Chenopodium ambrosioides in BALB/c mice infected with Leishmania amazonensis. The infected animals received two cycle of treatment by different routes (intraperitoneal, oral or intralesional route). The intraperitoneal administration of the essential oil at dose of 30 mg/Kg prevented lesion development and decrease the parasite burden. Oral administration retarded the infection in the experimental model compared with untreated mice, although it was less effective that the intraperitoneal route. The administration by intralesional route did not show activity. Intraperitoneal and oral treatment at 30 mg/Kg with the essential oil had better antileishmanial effect that treatment with the reference drug, amphotericin B at 1 mg/Kg. Preliminarily, we examined the toxicity and the resistance after treatment. Signs of toxicity were evident only in the animals treated by intraperitoneal route. No resistance was detected in L. amazonensis isolates obtained from treated mice. These data clearly demonstrated that this natural product could be an alternative for the development of a new drug against cutaneous leishmaniasis based in the ethnomedical information.
世界卫生组织已将利什曼病列为一种主要的热带疾病。目前的治疗方法有毒、昂贵且会引发多种不良反应。利什曼病流行地区的大多数人依赖天然药物和传统药物。本研究旨在检测来自土荆芥的精油对感染亚马逊利什曼原虫的BALB/c小鼠的活性。感染的动物通过不同途径(腹腔内、口服或病灶内途径)接受两个疗程的治疗。腹腔内以30mg/Kg的剂量给予精油可预防病灶发展并减轻寄生虫负担。与未治疗的小鼠相比,口服给药在实验模型中延缓了感染,尽管其效果不如腹腔内途径。病灶内途径给药未显示出活性。腹腔内和口服以30mg/Kg的剂量给予精油比以1mg/Kg的参考药物两性霉素B治疗具有更好的抗利什曼原虫效果。初步地,我们检测了治疗后的毒性和耐药性。仅在通过腹腔内途径治疗的动物中出现了毒性迹象。从接受治疗的小鼠中获得的亚马逊利什曼原虫分离株未检测到耐药性。这些数据清楚地表明,基于民族医学信息,这种天然产物可能成为开发一种抗皮肤利什曼病新药的替代品。