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No estudo sobre a origem e ramificações das artérias mesentéricas cranial (AMCr) e caudal (AMCa) do mocó, foram utilizados 20 animais (18 machos e 2 fêmeas) de diferentes idades, que, após morte natural, foram dissecados rebatendo-se as paredes torácica e abdominal, pelo antímero esquerdo, expondo-se a aorta que foi então canulada em seu trajeto pré-diafragmático, procedendo-se a injeção de neoprene látex corado, no sentido caudal. A seguir, foram fixados em solução aquosa de formol a 10 por cento, durante 48 horas, e posteriormente dissecados. Os resultados mostraram que em 18 animais (90 por cento), a AMCr originou-se da aorta abdominal isoladamente, logo após a artéria celíaca, emitindo as artérias cólica média (CoM), pancreaticoduodenal caudal (PDC), duodenojejunal (DJ), jejunal (J) e ileocecocólica (ICeCo). Em um mocó (5 por cento), as AMCr e AC se originaram da aorta abdominal em um tronco comum. Neste caso, a AMCr originou às artérias CoM, PDC, ICeCo e J. Em uma observação (5 por cento), as artérias AMCr e AMCa surgiram em tronco comum. Neste animal, as artérias PDC, DJ, ICeCo, CoM e J foram originadas da AMCr, enquanto as aterias cólica esquerda (CoE) e retal cranial (ARCr) derivaram da AMCa. Dois animais (10 por cento) apresentaram como colaterais da AMCr as artérias CoM, PDC, DJ, J e o tronco ICeCo, que originou às artérias CoD e ileocecal (ICe). No que diz respeito a AMCa, nos 20 casos (100 por cento) originou as artérias CoE e RCr.(AU)

In this study about the origin and ramification of the cranial (CrMA) and caudal (CaMA) mesenteric collateral arteries of the rock cavy, 20 animals (18 males and 2 females) of different ages, originated from the Wild Animals Multiplication Center of the Universidade Federal Rural do Semi-Árido (Cemas/Ufersa), were used. After the natural death, the walls of the abdominal cavity of the animals, in the left antimere, were dissected to cannulate to the aorta in pre-diaphragmatic path. Then they were fixed in 10 percent formaline and conditioned in order to study their anatomy. The results showed that in 18 animals (90 percent) the CrMA arose, separately, of the abdominal aorta, soon after the celiac artery (CA), originating, by this time, the middle colic (MCo), caudal pancreaticduodenal (CPD), duodenojejune (DJ), jejune (J) and ileocecocolic (ICeCo) trunk from which derives the ileocecal (ICe) and the right colic (RCo) arteries. In one rock cavy (5 percent), the CrMA and CA originate from abdominal aorta in a common trunk. In this case the CrMA originated the CPD, MCo, ICeCo, and J. In one observation (5 percent) CrMA and CaMA appear in common trunk. In this animal, CPD, DJ, ICeCo, MCo and J arteries were originated of the CrMA, while the left colic (LCo) and rectal cranial (RCr) arteries were originated of the CaMA. Regarding the CaMA, in 20 cases (100,00 percent) it originates the LCo and the rectal cranial arteries.(AU)

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Objetivo: Este estudo tem por objetivo avaliar os efeitos da homocisteinemia plasmática elevada na formação da placa aterosclerótica na aorta de coelhos. Material e método: Realizou-se estudo experimental comparativo em dois grupos homogêneos de coelhos durante 60 dias. Foram utilizados 20 coelhos da linhagem New Zealand divididos em dois grupos de 10 animais: grupo controle (C) e grupo metionina (M). Todos os animais receberam a mesma dieta sólida e 500 ml de água. Os animais do grupo M receberam 2 ml de uma solução de metionina na concentração de 200 mg/ml a cada 24 horas. Foram colhidas amostras de sangue para a dosagem de colesterol, triglicerídeos, HDL, LDL e homocisteína após 0, 30 e 60 dias. Os animais foram submetidos a eutanásia por dose letal de anestésico no 60° dia. A aorta torácica e a aorta abdominal foram retiradas para estudo anatomopatológico...

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The aim of this work was to determine whether there is a pre-established basal condition of the endothelial cells isolated from aortic abdominal aneurysm that might augment immune effector mechanisms and thus provide us an insight into the possible causes of aneurysm rupture. Endothelial cells isolated from saccular aortic aneurysm fragments were analyzed by cytofluorometry for the expression of different immune response-related molecules. Our results showed that there is a subpopulation of granule-rich, CD105 positive and von Willebrand antigen negative endothelial cells that have an enhanced basal expression of ICAM-1, and Fas antigen, but, interestingly, no apoptotic bodies were detected. Control endothelial cells derived from healthy areas of the same abdominal aortas did not show such enhanced expression. We conclude that in the endothelium that lines abdominal aorta aneurysms there is, at least, one endothelial cell subpopulation with an apparent inhibition of programmed cell death and in a proinflammatory activation status.

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We examined the presence of estrogen receptors (ER) in vascular mast cells and a possible genomic effect of estrogens on the expression of mast cell (MC) mediators such as chymase, TNF alpha, NOS and IL-10, which are known to affect the course of atherosclerosis. Immunocytochemical detection of mast cell tryptase and the co-localization of ERs in MCs from abdominal aortic vessels from 10 fertile woman, 10 postmenopausal women and 15 men was performed. The genomic expression of IL-10, TNF alpha, and NOS was analyzed by RT-PCR and chymase activity by spectrophotometry after 24 h incubation with 17-beta estradiol (0.2-0.5 ng/mL) in rat purified peritoneal MCs. A similar number of MCs were found in both intima and adventitia layers from men, and fertile and postmenopausal women, while ERs were detected only in the arterial walls from fertile women. The mRNA expressions of IL-10 and TNF alpha, as well as chymase activity, were not affected. A moderate increment of NO and both NOS, and a reduction in TNF alpha cytotoxicity was observed after incubating peritoneal MCs with 17-beta estradiol at a concentration of 0.5 ng/mL. Taken together, these results indicate that vascular MCs express ERs. The data demonstrate that estrogens can directly modify vascular MC activity. This is a novel mechanism of synergistic cooperation for the protective role of estrogens in the genesis of atherosclerosis.

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RESUMO

We examined the presence of estrogen receptors (ER) in vascular mast cells and a possible genomic effect of estrogens on the expression of mast cell (MC) mediators such as chymase, TNF alpha, NOS and IL-10, which are known to affect the course of atherosclerosis. Immunocytochemical detection of mast cell tryptase and the co-localization of ERs in MCs from abdominal aortic vessels from 10 fertile woman, 10 postmenopausal women and 15 men was performed. The genomic expression of IL-10, TNF alpha, and NOS was analyzed by RT-PCR and chymase activity by spectrophotometry after 24 h incubation with 17-beta estradiol (0.2-0.5 ng/mL) in rat purified peritoneal MCs. A similar number of MCs were found in both intima and adventitia layers from men, and fertile and postmenopausal women, while ERs were detected only in the arterial walls from fertile women. The mRNA expressions of IL-10 and TNF alpha, as well as chymase activity, were not affected. A moderate increment of NO and both NOS, and a reduction in TNF alpha cytotoxicity was observed after incubating peritoneal MCs with 17-beta estradiol at a concentration of 0.5 ng/mL. Taken together, these results indicate that vascular MCs express ERs. The data demonstrate that estrogens can directly modify vascular MC activity. This is a novel mechanism of synergistic cooperation for the protective role of estrogens in the genesis of atherosclerosis.(AU)

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