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1.
Acta cir. bras ; 31(9): 586-596, Sept. 2016. tab, graf
Artículo en Inglés | LILACS | ID: lil-795992

RESUMEN

ABSTRACT PURPOSE: To evaluate the contribution of L-arginine oral or topical rout of administration in the surgical wound healing process. METHODS: L-arginine was orally or topically administrated to mice after a laparotomy model procedure. The wounds were analyzed to evaluate the granulation tissue by HE analysis, collagen deposition, iNOS and cytokines production by immunochemisyry on wound progress. Mice used in this model were healthy, immunosupressed or diabetic and all of them were treated with different concentration of L-arginine and rout of administration. RESULTS: Suggested that groups treated with L-arginine orally or topically improved wound repair when compared with non-treatad mice. L- arginine treatment stimulated TGF-β and restricted NO production leading to a mild Th1 response and collagen deposition in injured area, when it was orally administrated. Topical administration decreased IL-8 and CCR1 expression by wound cells but did not interfere with TNF-α and IL-10 production, ratifying the decrease of inflammatory response, the oral administration however, presented a higher iNOS and TGF-β expression then. L-arginine treatment also improved the improved the wound healing in immunosupressed or diabetic mice. CONCLUSION: L-arginine administrated orally or topically can be considered an important factor in the recuperation of tissues.


Asunto(s)
Animales , Masculino , Ratones , Arginina/administración & dosificación , Cicatrización de Heridas/efectos de los fármacos , Citocinas/metabolismo , Factor de Crecimiento Transformador beta/biosíntesis , Óxido Nítrico Sintasa de Tipo II/biosíntesis , Herida Quirúrgica/tratamiento farmacológico , Arginina/metabolismo , Heridas y Lesiones/patología , Administración Oral , Administración Tópica , Colágeno/biosíntesis , Huésped Inmunocomprometido , Diabetes Mellitus Experimental/metabolismo , Modelos Animales de Enfermedad , Inflamación/metabolismo , Óxido Nítrico/biosíntesis
2.
Acta cir. bras ; 30(11): 762-769, Nov. 2015. tab, graf
Artículo en Inglés | LILACS | ID: lil-767600

RESUMEN

PURPOSE : To evaluate the effects of metoclopramide on metalloproteinases (MMP) and interleukins (IL) gene expression in colonic anastomoses in rats. METHODS : Eighty rats were divided into two groups for euthanasia on the 3rd or 7th postoperative day (POD), then into two subgroups for sepsis induction or not, and then into subgroups to receive either metoclopramide or saline solution. Left colonic anastomosis were performed and then analyzed. RESULTS : On the 3rd POD, metoclopramide was associated with increased expression of MMP-1a, MMP-13, and TNF-α. On the 7th POD, the transcripts of all MMPs, TNF-α, IL-1β, IFN-γ, and IL-10 of the treated animals became negatively modulated. In the presence of sepsis, metoclopramide did not change MMPs and decreased IL-6, IL-1β, IFN-γ and IL-10 gene expression on the 3rd POD. On the 7th POD, increased expression of all MMPs, IFN-γ and IL-10 and negative modulated TNF-α and IL-6 gene expression. CONCLUSION : Administration of metoclopramide increased metalloproteinases and interleukins gene expression on the 3rd postoperative day and negatively modulated them on the 7th POD. In the presence of abdominal sepsis, metoclopramide did not change MMPs and decreased ILs gene expression on the 3rd POD. On the 7th POD, the drug increased expression of all MMPs.


Asunto(s)
Animales , Masculino , Antieméticos/farmacología , Colon/cirugía , Expresión Génica/efectos de los fármacos , Interleucinas/metabolismo , Metaloproteasas/efectos de los fármacos , Metoclopramida/farmacología , Anastomosis Quirúrgica , Modelos Animales de Enfermedad , Infecciones Intraabdominales/etiología , Metaloproteasas/metabolismo , Periodo Posoperatorio , Distribución Aleatoria , Ratas Wistar , Reacción en Cadena en Tiempo Real de la Polimerasa , Sepsis/etiología , Cicatrización de Heridas/efectos de los fármacos
3.
J. bras. patol. med. lab ; 44(1): 59-64, fev. 2008. ilus
Artículo en Portugués | LILACS | ID: lil-482486

RESUMEN

INTRODUÇÃO: Exposição pré-natal ao etanol é freqüentemente associada a microcefalia e atraso na migração celular. O mecanismo pelo qual o etanol induz seus efeitos no desenvolvimento do sistema nervoso não é muito bem entendido. OBJETIVOS: Avaliar o efeito da exposição crônica ao etanol sobre o córtex visual de ratos durante seu desenvolvimento. MATERIAL E MÉTODO: Ratos Wistar provenientes do acasalamento de 30 fêmeas, divididos nos grupos etanol (n = 10) - 3 g/kg/dia - e controle (n = 10), foram utilizados nesse experimento. Os ratos foram perfundidos e o encéfalo, dividido em três partes: anterior, médio e posterior. Os cortes obtidos do fragmento posterior foram expostos à rotina histológica e submetidos a diferentes técnicas de coloração. Na análise estatística foi utilizado o teste t para comparar os pesos encefálicos e corporais. Considerou-se como nível de rejeição de hipótese nula um valor de p < 0,05. RESULTADO: Houve redução de peso cerebral em diferentes períodos analisados, além de ectopia e heterotopia neuronal. Não se observou deposição de fibras. DISCUSSÃO/CONCLUSÃO: O etanol atua de maneira negativa no desenvolvimento dos ratos, incluindo alterações na migração neuronal e microcefalia. Essas alterações podem ajudar a explicar as disfunções relatadas na síndrome do alcoolismo fetal (SAF).


BACKGROUND: Prenatal exposure to ethanol is frequently associated with microencephaly and delayed cell migration. The mechanism by which ethanol affects the development of the nervous system is still not fully understood. OBJECTIVE: To evaluate the effect of chronic exposure to ethanol on the visual cortex of rats during their development. MATERIAL AND METHOD: Wistar rats, born from the mating of 30 females, were divided into two groups: those exposed to ethanol (n = 10) - 3 g/kg/day - and a control group (n = 10). The rats were perfused and brain was divided into three parts: anterior, middle and posterior. Slices taken from the posterior fragment were subjected to histological analysis routine and different staining techniques. A statistical analysis was carried out using t test to compare brain and body weight. A value < 0,05 was considered a rejection of null hypothesis. RESULTS: There was a reduction of brain weight in different analyzed periods. There were no fiber deposits. Ectopia and neuronal heterotopia were observed. DISCUSSION/CONCLUSION: Ethanol has a negative effect on the development of rats, including alterations in neuronal migration and microencephaly. These alterations may help to explain some of the dysfunctions reported in patients with fetal alcohol syndrome (FAS).


Asunto(s)
Animales , Femenino , Embarazo , Recién Nacido , Lactante , Corteza Visual , Encéfalo/crecimiento & desarrollo , Encéfalo , Etanol/efectos adversos , Etanol/toxicidad , Microcefalia/inducido químicamente , Movimiento Celular , Neuronas , Neurópilo , Trastornos del Sistema Nervioso Inducidos por Alcohol/inducido químicamente , Animales Recién Nacidos , Cerebro/anatomía & histología , Cerebro/crecimiento & desarrollo , Efectos Tardíos de la Exposición Prenatal/inducido químicamente , Inmunohistoquímica , Modelos Animales , Ratas Wistar/crecimiento & desarrollo , Tamaño de los Órganos
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