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1.
Mem. Inst. Oswaldo Cruz ; 108(7): 865-872, 1jan. 2013. tab, graf
Artículo en Inglés | LILACS | ID: lil-696017

RESUMEN

Schistosomiasis is an endemic parasite disease and praziquantel is the only drug currently in use to control this disease. Experimental and epidemiological evidence strongly suggests that Microtus fortis ( Mf ) is a naturally resistant vertebrate host of Schistosoma japonicum . In the present study, we found that Mf serum albumin ( Mf -albumin) and the conditioned medium of pcDNA3.1- Mf -albumin caused 46.2% and 38.7% schistosomula death rates in 96 h, respectively, which were significantly higher than that of the negative control (p < 0.05). We also found that mice injected with Mf -albumin had a 43.5% reduction in worm burden and a 48.1% reduction in liver eggs per gram (p < 0.05) in comparison to the control animals. To characterise the mechanisms involved in clearance, schistosomula were incubated with fluorescein isothiocyanate-labelled Mf -albumin and fluorescent enrichment effects were found in the gut lumen of schistosomula after 48 h of incubation. Next, digestive tract excretions from schistosomula were collected and the sensitivity of Mf -albumin to digestive tract excretions was evaluated. The results indicated that schistosomula digestive tract excretions showed indigestibility of Mf -albumin. The death of schistosomula could be partially attributed to the lack of digestion of Mf -albumin by digestive tract excretions during the development of the schistosomula stage. Therefore, these data indicate the potential of Mf -albumin as one of the major selective forces for schistosomiasis.


Asunto(s)
Animales , Arvicolinae/parasitología , Schistosoma japonicum/efectos de los fármacos , Albúmina Sérica/farmacología , Cromatografía de Afinidad , Albúmina Sérica/aislamiento & purificación
2.
Acta cient. venez ; 46(2): 89-96, 1995. graf
Artículo en Inglés | LILACS | ID: lil-217134

RESUMEN

The pancreatic beta-cell response to stimulation with glucose and GIP, single and combined, was studied in acromegalics and in normal subjects. Acromegalics had higher IRI and GIP basal values with glucose levels and glucose disposal in the normal range. Further, acromegalics showed a greater IRI response to glucose, GIP and glucose combined with GIP. The results suggested that high growth hormone levels cause a greater activity of the entero-insular axis both in the basal state and after meal ingestion, as mimicked by GIP infusion. From these and previous observations, it can be assumed that growth hormone induces a facilitation of the IRI response to metabolite substrates and hormones


Asunto(s)
Humanos , Masculino , Femenino , Persona de Mediana Edad , Adulto , Acromegalia/metabolismo , Polipéptido Inhibidor Gástrico/farmacología , Glucosa/farmacología , Insulina/metabolismo , Albúmina Sérica/farmacología , Glucemia/análisis , Polipéptido Inhibidor Gástrico/sangre , Hormona de Crecimiento Humana/sangre , Islotes Pancreáticos/metabolismo , Factores de Tiempo
3.
J. venom. anim. toxins ; 1(1): 11-22, 1995. tab, ilus
Artículo en Inglés | LILACS | ID: lil-194266

RESUMEN

Thirty-one patients bitten by venomous snakes in Botucatu area (State of Säo Paulo - Brazil), sixteen by Bothrops spp. and fifteen by Crotalus durissus terrificus, were studied. The group comprised twenty-nine males and two females, ranging from fourteen to sixty-three years of age (mean 33 ñ 15.Leukocytosis with neutrophilia and lymphopenia, increase of mucoproteins and C reactive protein, decrease of total serum protein and albumin, were observed on the first day after the accident. In addition, increased serum levels of the cytokines IL-6 and IL-8, but not of IL-1 beta and TNF-alpha, were observed. The alterations were generally more intense in patients bitten by Crotalus durissus terrificus than by Bothrops spp. It is concluded that these snakebite envenomations closely resemble an acute trauma, inducing a typical acute-phase response.


Asunto(s)
Humanos , Masculino , Femenino , Citocinas/fisiología , Elapidae , Interleucina-1/farmacología , Interleucina-6/farmacología , Leucocitosis/fisiopatología , Linfopenia/fisiopatología , Proteína C-Reactiva/farmacología , Proteínas de Fase Aguda/farmacología , Reacción de Fase Aguda/fisiopatología , Albúmina Sérica/farmacología , Interleucina-8/farmacología , Mucoproteínas/farmacología , Neutropenia/fisiopatología , Mordeduras de Serpientes/fisiopatología , Venenos de Serpiente/envenenamiento , Factor de Necrosis Tumoral alfa
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