Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Med Mycol ; 57(2): 181-195, 2019 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-29529254

RESUMO

As the current therapies for intestinal microsporidiosis are either inconsistent in their efficacies or hampered by several adverse effects, alternative antimicrosporidial agents are being sought. The present study is the first that was designed to evaluate the potency of orlistat, an approved anti-obesity drug, against intestinal microsporidiosis caused by both Enterocytozoon bieneusi and Encephalitozoon intestinalis. Results were assessed through studying fecal and intestinal spore load, intestinal histopathological changes, viability, and infectivity of spores from treated animals. Results showed that orlistat has promising antimicrosporidia potential, with better results in E. intestinalis than E. bieneusi. The animals that received orlistat showed statistically significant decrease in the fecal and intestinal spore load, when compared to the corresponding control infected nontreated mice. The results were insignificant compared to fumagillin and albendazole. Light microscopic examination of stained intestinal sections revealed amelioration of the pathological changes and decreased inflammatory cells detected in the control infected nontreated mice. Spores encountered from stool of orlistat-treated E. bieneusi and E. intestinalis mice showed low viability and significant reduction of infectivity versus their control. Thus, considering the results of the present work, orlistat proved its effectiveness against the intestinal microsporidial infection.


Assuntos
Antifúngicos/uso terapêutico , Encephalitozoon/efeitos dos fármacos , Enterocytozoon/efeitos dos fármacos , Microsporidiose/tratamento farmacológico , Orlistate/uso terapêutico , Animais , Fármacos Antiobesidade , Contagem de Colônia Microbiana , Modelos Animais de Doenças , Reposicionamento de Medicamentos , Encephalitozoon/crescimento & desenvolvimento , Encephalitozoon/isolamento & purificação , Enterocytozoon/crescimento & desenvolvimento , Enterocytozoon/isolamento & purificação , Fezes/microbiologia , Humanos , Intestinos/microbiologia , Intestinos/patologia , Masculino , Camundongos , Viabilidade Microbiana/efeitos dos fármacos , Microsporidiose/microbiologia , Especificidade da Espécie
2.
Parasitol Res ; 111(2): 545-54, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22392135

RESUMO

This study was carried out to evaluate the anti parasitic potential of silver, chitosan, and curcumin nanoparticles as anti-Giardia agents. Non-treated infected control rats were inoculated with Giardia lamblia cysts in a dose of 2 × 10(5) cysts/rat. Experimental group was infected then treated with curcumin, curcumin nanoparticles, chitosan, chitosan nanoparticles, and silver nanoparticles as single or combined therapy. The number of Giardia cysts in stools and trophozoites in intestinal sections were detected. Toxicity of nanoparticles was evaluated by comparing hematological and histopathological parameters of the normal control group and treated non-infected control group. The amount of silver was also measured in the liver, kidney, small intestine, lung, and brain of rats treated with silver nanoparticles. The number of the parasites in stool and small intestinal sections decreased in treated infected rats compared with infected non-treated ones. The effect in the single therapy was better with nanoparticles, and the best effect was detected in nano-silver. The combined therapy gave better results than single. Combination between nanoparticles was better than the combination of nano-forms and native chitosan and curcumin. The best effect was detected in combinations of nano-silver and nano-chitosan but with no full eradication. In conclusion, the highest effect and complete cure was gained by combining the three nano-forms. The parasite was successfully eradicated from stool and intestine. None of the treatments exhibited any toxicity. Accumulated silver in different organs was within the safe limits.


Assuntos
Antiprotozoários/farmacologia , Quitosana/farmacologia , Curcumina/farmacologia , Giardíase/tratamento farmacológico , Nanopartículas/química , Prata/farmacologia , Animais , Antiprotozoários/química , Quitosana/química , Curcumina/química , Quimioterapia Combinada , Giardia lamblia/efeitos dos fármacos , Giardíase/parasitologia , Ratos , Prata/química
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...