Cutaneous Leishmaniasis in the Dorsal Skin of Hamsters: a Useful Model for the Screening of Antileishmanial Drugs

ABSTRACT: Traditionally, hamsters are experimentally inoculated in the snout or the footpad. However in these sites an ulcer not always occurs, measurement of lesion size is a hard procedure and animals show difficulty to eat, breathe and move because of the lesion. In order to optimize the hamster...

Full description

Autores:
Robledo Restrepo, Sara María
Carrillo Bonilla, Lina María
Rodríguez, Berardo de Jesús
Daza Figueredo, Juan Alejandro
Restrepo Agudelo, Adriana María
Muñoz Herrera, Diana Lorena
Tobón Peña, Jairo Andrés
Murillo Arroyave, Javier Darío
López Arias, Anderson
Ríos Úsuga, Carolina
Mesa Castro, Carol Vanesa
Yulieth Alexandra, Upegui Zapata
Valencia Tobón, Alejandro
Mondragón Shem, Karina
Vélez Bernal, Iván Darío
Tipo de recurso:
Article of investigation
Fecha de publicación:
2012
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/33383
Acceso en línea:
https://hdl.handle.net/10495/33383
Palabra clave:
Antiprotozoarios
Antiprotozoal Agents
Leishmaniasis Cutánea
Leishmaniasis, Cutaneous
Cricetinae
Modelos Animales de Enfermedad
Disease Models, Animal
Leishmania - crecimiento y desarrollo
Leishmania - growth and development
Evaluación Preclínica de Medicamentos
Drug Evaluation, Preclinical
Mesocricetus
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-nd/4.0/
Description
Summary:ABSTRACT: Traditionally, hamsters are experimentally inoculated in the snout or the footpad. However in these sites an ulcer not always occurs, measurement of lesion size is a hard procedure and animals show difficulty to eat, breathe and move because of the lesion. In order to optimize the hamster model for cutaneous leishmaniasis, young adult male and female golden hamsters (Mesocricetus auratus) were injected intradermally at the dorsal skin with 1 to 1.5 x l07 promastigotes of Leishmania species and progression of subsequent lesions were evaluated for up to 16 weeks post infection. The golden hamster was selected because it is considered the adequate bio-model to evaluate drugs against Leishmania as they are susceptible to infection by different species. Cutaneous infection of hamsters results in chronic but controlled lesions, and a clinical evolution with signs similar to those observed in humans. Therefore, the establishment of the extent of infection by measuring the size of the lesion according to the area of indurations and ulcers is feasible. This approach has proven its versatility and easy management during inoculation, follow up and characterization of typical lesions (ulcers), application of treatments through different ways and obtaining of clinical samples after different treatments. By using this method the quality of animal life regarding locomotion, search for food and water, play and social activities is also preserved.