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Purpose To evaluate the effect of chronic alcoholism on morphometry and apoptosis mechanism and correlate with miRNA-21 expression in the corpus cavernosum of rats. Methods Twenty-four rats were divided into two experimental groups: Control (C) and Alcoholic group (A). After two weeks of an adaptive phase, rats from group A received only ethanol solution (20%) during 7 weeks. The morphometric and caspase-3 immunohistochemistry analysis were performed in the corpus cavernosum. The miRNA-21 expression was analyzed in blood and cavernous tissue. Results Chronic ethanol consumption decreased cavernosal smooth muscle area of alcoholic rats. The protein expression of caspase 3 in the corpus cavernosum was higher in A compared to the C group. There was no difference in the expression of miRNA-21 in serum and cavernous tissue between the groups. Conclusion Chronic ethanol consumption reduced smooth muscle area and increased caspase 3 in the corpus cavernosum of rats, without altered serum and cavernosal miR-21 gene expression.(AU)

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To investigate the impact of bone mesenchymal stem cells (BMSCs) intervention on the viscoelasticity of sciatic nerve in rats with chronic alcohol intoxication (CAI). Methods: The CAI rat models were prepared, divided into model groups, and treated with either BMSCs or basic fibroblast growth factor (bFGF). Then the rats underwent electrophysiological test and the serum levels of malondialdehyde (MDA), superoxide dismutase (SOD), and metallothionein (MT) were measured. Histological observation, stress relaxation test, and creep test were performed for the sciatic nerve of the CAI model in each group. Results: The MDA level of group BMSC was significantly lower (p 0.05) than that of groups MOD (the CIA model) and bFGF. The SOD and MT levels were higher in group BMSC than in groups MOD and bFGF (p 0.05). The motor nerve conduction velocity and amplitude were higher in group BMSC than in groups MOD and bFGF (p 0.05). The amounts of 7200s stress reduction and 7200 s strain increase of the sciatic nerve in group BMSC were greater than those in groups bFGF and MOD (p 0.05). Conclusion: Bone mesenchymal stem cells can improve the metabolism of free radicals, restore the tissue morphology and viscoelasticity of the chronic alcohol intoxication animal model, and positively affect the repairing of the injured sciatic nerve.(AU)

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PURPOSE: To evaluated histopathological changes, morphometric and expression of proteins CASPASE-3, BCL-2 and XIAP related to apoptosis in the cerebellum after induction of temporary focal cerebral ischemia followed by reperfusion, with or without a model of chronic alcoholism. METHODS: Fifty Wistar rats were used and divided into: control group (C), sham group (S), ischemic group (I), alcoholic group (A), and ischemic and alcoholic group (IA). The cerebellum samples collected were stained for histopathological and morphometric analysis and immunohistochemistry study. RESULTS: Histopathological changes were observed a greater degree in animals in groups A and IA. The morphometric study showed no difference in the amount of cells in the granular layer of the cerebellum between the groups. The expression of CASPASE-3 was higher than BCL-2 and XIAP in the groups A and IA. CONCLUSION: We observed correlation between histopathological changes and the occurrence of apoptosis in cerebellar cortex.(AU)

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[...] Os objetivos desse estudo foram avaliar quantitativamente os efeitos do consumo crônico de álcool no peso, reparo ósseo e densidade óssea em ratos Wistar, além de observarmos qualitativamente as fibras colágenas e a expressão de OPG e RANKL. Para isso, separamos aleatoriamente 30 ratos Wistar em dois grupos , sendo (G1) 15 ratos consumindo solução de aguardente diluída em água por 100 dias com concentração progressiva e controlada (10ºGL, 15ºGL, 20ºGL, 25ºGL e 30ºGL) e 15 ratos não alcoólatras consumindo como dieta líquida somente água (G2). Após o 92º dia do período de indução do alcoolismo, ambos os grupos foram submetidos a um defeito ósseo realizado na tíbia com um motor rotacional contendo uma broca com tamanho de 3 mm de diâmetro. Após 8 dias após o procedimento cirúrgico os animais foram eutanasiados em câmara de C02, as tíbias foram removidas e aparadas nas proximidades do defeito ósseo para que fossem processadas através de secções histológicas descalcificadas. A porcentagem de osso neoformado e a densidade óssea foram avaliadas histometricamente. Através da imunohistoquimica observamos a expressão de OPG e RANKL e através de reação histoquímica pelo método Picro-sirius Red, estudamos o padrão de birrefringência das fibras colágenas. Como resultados, pudemos observar que o peso dos animais, a densidade e remodelação ósseas foram menores no grupo alcoólico. Encontramos também efeitos negativos em relação à qualidade e organização das fibras colágenas, bem como diferenciação na expressão de RANKL e OPG nos diferentes grupos. Nossos resultados demonstram que o protocolo proposto de ingestão de álcool exerce efeitos negativos no ganho de peso e qualidade óssea quando comparado ao grupo controle

[...] The objective of this study was to verify quantitatively the effects of chronic alcohol consumption on body weight, bone healing and density in rats. It was also observed quantitatively the collagenous fibers and the expression of OPG and RANKL. For this purpose, 30 Wistar rats were randomly divided into two groups: G1 (group 1) consisted in 15 rats which had, for 100 days, a liquid diet of liquor diluted in water with a progressive and controlled concentration (10°GL, 15°GL, 20°GL, 25°GL and 30°GL); G2 (group 2) consisted in 15 rats on a liquid diet of only water and free of alcohol. After the 92nd day of the induction period of alcoholism, tibial defects of 3 mm in diameter were created in both groups and after 8 days from this surgery procedure the animals were euthanized in a CO2 chamber. The tibiae were removed and cut next to the bone defect in order to be processed through decalcified histological sections. The percentage of renovated bone and osseous density were submitted to histometric analysis. Through immunohistochemistry, the expression of OPG and RANKL were analyzed and using Picrosirius red staining method, the birefringence pattern of the collagen fibers was studied. As a result, it was verified that the body weight of the animals, the osseous density and bone remodeling were smaller in G1; negative effects regarding to the collagen fibers quality and organization and a differentiation in the expression of OPG and RANKL were also found in both groups. Conclusion: these results show that the proposed protocol of alcohol intake produces negative effects in the gain of body weight and bone quality when compared to the control group

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Morphometric and quantitative analyses were accomplished to study the effects of the consumption of alcohol above the size and density of the myenteric neurons of cecum of rats. Ten rats with 90 days were divided in the groups: control (C), and alcoholic (A). After 120 days of treatment with ethanol the cecum of both groups were collected, submitted it prepared of membranes that after carried out to Giemsa´s technique, permitted to evaluate the neuronal density, in an area of 13.44mm², and measure the cell body area of 300 neurons by group. The alcoholic rats presented an increase in the number of small neurons and a reduction of the big and medium neurons. The neuronal density verified in alcoholic rats was significantly reduced regarding the controls rats, however, that reduction left of be statistically significant when was projected the neuronal density for the total area of cecum, since the macroscopic observation showed that the alcoholic rats presented a cecum dilated. The alcoholism induced a significant reduction in the final body weight of the rats of the GA, provoked enlargement of cecum of the rats causing to a big dispersion neuronal. The enlargement of cecum of the alcoholic rats is probably associated with the functional alterations of the myenteric neurons that have repercussions in the tone of the intestinal smooth muscle.

Los análisis morfométrico y cuantitativo fueron hechos para estudiar los efectos del consumo de alcohol sobre el tamaño y densidad de las neuronas mientéricas del ciego de ratones. Diez ratones de 90 días, fueron divididos en los grupos: control (C), y alcohólico (A). Después de 120 días de tratamiento con etanol, los ciegos de ambos grupos fueron colectados, sometidos a preparación de membranas que después de coloreados por el método de Giemsa. Fue posible evaluar la densidad neuronal en un área de 13,44 mm2, y medir el área del cuerpo celular de 300 neuronas por grupo. Los ratones alcohólicos presentaron un incremento en el número de neuronas pequeñas y una disminución de las neuronas medianas y grandes. La densidad neuronal verificada en los ratones alcohólicos fue significativamente reducida, en relación a los ratones controles. Esa reducción dejó de ser estadísticamente significativa cuando fue proyectada la densidad de las neuronas para el área del ciego, ya que la observación macroscópica mostraba que los ratones alcohólicos presentaban un ciego dilatado. El alcoholismo indujo una reducción significativa en el peso corporal final de los ratones del grupo A, provocó dilatación del ciego de los ratones, llevando a una gran dispersión neuronal. La dilatación del ciego de los ratones alcohólicos está probablemente asociada a alteraciones funcionales de las neuronas mientéricas que repercuten en el tono de la musculatura lisa intestinal.

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Estima-se que entre 1 milhão de adultos do hemisfério ocidental, 20.000 tenham anomalias nos músculos esqueléticos como conseqüência da ingestão de álcool. Estudos revelam que nestes casos ocorre uma fraqueza progressiva afetando predominantemente os músculos da coxa, ombro e quadris, e uma artrofia das fibras do tipo II ou de contração rápida. Na literatura consultada não foi observado relato do que acontece com os músculos da mastigação, por isso este estudo foi desenvolvido com o intuito de observar se as fibras de contração rápida do músculo digástrico apresentam alterações semelhantes às que ocorrem nos músculos do tronco e membros. Para tanto, amostras dos músculos digástrico e reto do abdome foram retiradas de cinco animais de cada grupo Controle (C), Alcoolizado (A) e Isocalórico (I). As amostras foram submetidas às reações de m-ATPase (com pré-incubações ácida e alcalina) e NADH-TR, para a classificação das fibras de acordo com os resultados obtidos nestas reações em FG (fast-twitch-glycolitic, FOG (fast-oxidative-glycolitic) e SO (slow-oxidative). Os resultados mostraram uma diferença significativa, na área das fibras dos tipos FG e FOG, entre os grupos estudados no músculo digástrico e na área das fibras do tipo FG no músculo reto do abdome; uma diferença sigificativa na freqüência das fibras dos tipos FG e FOG no músculo reto do abdome. Baseando-se nestes resultados, é possivel concluir que o etanol produz uma atrofia nas fibras da contração rápida dos músculos da mastigação, semelhante à dos músculos do tronco, mas com um coeficiente de atrofia diferente...

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Amostras de vários órgäos que compöem o sistema reprodutor masculino, tais como: próstata, glândulas de coagulaçäo, vesículas seminais, uretra, bexiga urinária, parte dos ureteres e ductos deferentes, foram coletados e pesados com o objetivo de avaliar os efeitos do alcoolismo crônico experimental. Foi comprovada estatisticamente uma reduçäo do peso corporal e atrofia generalizada dos órgäos em estudo, em especial da próstata e vesícula seminal

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