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1.
Artículo en Inglés | MEDLINE | ID: mdl-32152088

RESUMEN

Of four genotypes of Encephalitozoon cuniculi, E. cuniculi genotype II is considered to represent a parasite that occurs in many host species in a latent asymptomatic form, whereas E. cuniculi genotype III seems to be more aggressive, and infections caused by this strain can lead to the death of even immunocompetent hosts. Although albendazole has been considered suitable for treatment of Encephalitozoon species, its failure in control of E. cuniculi genotype III infection has been reported. This study determined the effect of a 100× recommended daily dose of albendazole on an Encephalitozoon cuniculi genotype III course of infection in immunocompetent and immunodeficient mice and compared the results with those from experiments performed with a lower dose of albendazole and E. cuniculi genotype II. The administration of the regular dose of abendazole during the acute phase of infection reduced the number of affected organs in all strains of mice and absolute counts of spores in screened organs. However, the effect on genotype III was minor. Surprisingly, no substantial effect was recorded after the use of a 100× dose of albendazole, with larger reductions seen only in the number of affected organs and absolute counts of spores in all strains of mice, implying variations in albendazole resistance between these Encephalitozoon cuniculi genotypes. These results imply that differences in the course of infection and the response to treatment depend not only on the immunological status of the host but also on the genotype causing the infection. Understanding how microsporidia survive in hosts despite targeted antimicrosporidial treatment could significantly contribute to research related to human health.


Asunto(s)
Albendazol/farmacología , Antifúngicos/farmacología , Encephalitozoon cuniculi/efectos de los fármacos , Encephalitozoon cuniculi/genética , Encefalitozoonosis/tratamiento farmacológico , Albendazol/administración & dosificación , Animales , Antifúngicos/administración & dosificación , Antígenos CD4/genética , Antígenos CD8/genética , Línea Celular , Chlorocebus aethiops , Recuento de Colonia Microbiana , Modelos Animales de Enfermedad , Encephalitozoon cuniculi/aislamiento & purificación , Genotipo , Huésped Inmunocomprometido/inmunología , Ratones , Ratones Endogámicos BALB C , Ratones Endogámicos C57BL , Ratones Noqueados , Ratones SCID , Pruebas de Sensibilidad Microbiana , Células Vero
2.
Exp Parasitol ; 182: 16-21, 2017 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-28942047

RESUMEN

Encephalitozoon cuniculi is probably the most common microsporidia which infects a wide range of vertebrates, including human. So far, four genotypes of this parasite have been identified based on the rRNA internal transcribed spacer variations. The course of infection caused by E. cuniculi III had very massive onset in immunocompetent host characterized by the presence of this parasite in all organs and tissues within one week after peroral infection. Encephalitozoonosis caused by E. cuniculi III had very progressive spreading into all organs within first week post inoculation in immunocompromised SCID mice and led to the death of the host. The experimental treatment with albendazole of immunocompetent BALB/c mice infected with E. cuniculi III have shown very weak effect. Our findings clearly showed that the different course of infection and response to treatment depends not only on the immunological status of the host, but also on the genotype of microsporidia. It could be very important especially for individuals under chemotherapy and transplant recipients of organs originating from infected donors.


Asunto(s)
Albendazol/uso terapéutico , Encephalitozoon cuniculi/fisiología , Encefalitozoonosis/inmunología , Inmunocompetencia , Huésped Inmunocomprometido , Albendazol/farmacología , Animales , Antifúngicos/farmacología , Antifúngicos/uso terapéutico , Encephalitozoon cuniculi/efectos de los fármacos , Encephalitozoon cuniculi/genética , Encephalitozoon cuniculi/inmunología , Encefalitozoonosis/tratamiento farmacológico , Encefalitozoonosis/parasitología , Heces/parasitología , Genotipo , Ratones , Ratones Endogámicos BALB C , Ratones SCID , Esporas Fúngicas
3.
Exp Parasitol ; 181: 94-101, 2017 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-28779899

RESUMEN

The present study was conducted to evaluate the methanolic extracts from several plant leaves widely used in traditional medicine to cure digestive tract disorders and in the self-medication of wild animals such as non-human primates, namely Archidendron fagifolium, Diospyros sumatrana, Shorea sumatrana, and Piper betle leaves, with regard to their antimicrosporidial activity against Encephalitozoon cuniculi in immunocompetent BALB/c mice determined using molecular detection of microsporidial DNA (qPCR) in various tissues and body fluids of infected, treated mice. Of the plant extracts tested, Diospyros sumatrana provided the most promising results, reducing spore shedding by 88% compared to untreated controls. Moreover, total burden per 1 g of tissue in the D. sumatrana extract-treated group reached 87% reduction compared to untreated controls, which was comparable to the effect of the standard drug, Albendazole. This data represents the baseline necessary for further research focused on determining the structure, activity and modes of action of the active compounds, mainly of D. sumatrana, enabling subsequent development of antimicrosporidial remedies.


Asunto(s)
Antifúngicos/uso terapéutico , Diospyros/química , Encephalitozoon cuniculi/efectos de los fármacos , Encefalitozoonosis/tratamiento farmacológico , Extractos Vegetales/uso terapéutico , Albendazol/farmacología , Albendazol/uso terapéutico , Animales , Antifúngicos/farmacología , Chlorocebus aethiops , ADN de Hongos/aislamiento & purificación , Dimetilsulfóxido/farmacología , Dimetilsulfóxido/uso terapéutico , Dipterocarpaceae/química , Fabaceae/química , Heces/parasitología , Tracto Gastrointestinal/microbiología , Inmunocompetencia , Indonesia , Ratones , Ratones Endogámicos BALB C , Piper betle/química , Extractos Vegetales/farmacología , Hojas de la Planta/química , Esporas Fúngicas/efectos de los fármacos , Células Vero
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