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1.
Ciênc. rural (Online) ; 49(3): e20180858, 2019. graf
Article in English | LILACS | ID: biblio-1045309

ABSTRACT

ABSTRACT: Cockatiels (Nymphicus hollandicus) are exotic birds thatoriginated from Australia.Because of their beauty and learning ability, they are one of the most popular pet birds among the Psittaciformes. The objective of this study was to report a case of leiomyosarcoma on the humeral musculature of the left wing of a cockatiel (Nymphicus hollandicus). The animal was admitted to the Wildlife Rehabilitation Center (NURFS-CETAS) of the Universidade Federal de Pelotas withswelling in the humeral region of the left wing. During surgery, the animal died and was transferred to the Laboratório Regional de Diagnóstico, Faculdade de Veterinária (LRD-UFPel). During histopathological evaluation (hematoxylin and eosin routine technique) of the tumor, spindle neoplastic cells were observed, arranged in interlaced bundles amongst degenerate and normal muscle fibers. Using immunohistochemistry, neoplastic cells were positively immunostained for vimentin and alpha smooth muscle actin. Based on of clinical-pathological and immunohistochemical findings, leiomyosarcoma was diagnosed.


RESUMO: As calopsitas (Nymphicus hollandicus) são aves exóticas originárias da Austrália. Devido a beleza e capacidade de aprendizado são uma das principais aves utilizadas como animal de companhia. O objetivo deste trabalho foi relatar um caso de leiomiossarcoma, na musculatura umeral da asa esquerda de uma calopsita. O animal deu entrada no Núcleo de Reabilitação da Fauna Silvestre (NURFS-CETAS) da Universidade Federal de Pelotas (UFPel), por apresentar aumento de volume na região umeral da asa esquerda. Durante o procedimento cirúrgico o animal veio a óbito, sendo encaminhado ao Laboratório Regional de Diagnóstico, Faculdade de Veterinária (LRD-UFPel). Na avaliação histopatológica (Técnica de rotina Hematoxilina e Eosina) da massa tumoral foram observadas células neoplásicas fusiformes, arranjadas em feixes entrelaçados, em meio a fibras musculares degeneradas e normais. Na imunohistoquímica verificou-se imunomarcação positiva das células neoplásicas para vimentina e alfa actina, de músculo liso. Diante dos achados clínico-patológicos e imunohistoquímicos determinou-se o diagnóstico de leiomiossarcoma. O diagnóstico definitivo deste neoplasma requer analise imunohistoquímica.

2.
Int. j. morphol ; 35(2): 403-412, June 2017. ilus
Article in English | LILACS | ID: biblio-892995

ABSTRACT

Obese mice (C57BL/6J-ob/ob) do not express leptin and develops hyperphagia, decreased energy expenditure, obesity, hyperglycemia, hyperinsulinemia, hypothermia, and infertility. Obesity causes reproductive dysfunction with negative impacts on prostatic structure and fertility. We aimed to compare the structure and molecular aspects of the ventral prostate between of lean and obese (ob/ob) mice. Three months old male lean and obese mice had their prostates dissected and prepared for light microscopy and immunofluorescence. In comparison to the lean mouse, the obese mouse showed a substantial structural modification in the ventral prostate starting with an atrophy of the prostate ventral lobe. Histologically, the acini showed a reduction in size, and in the lumen, we found a mixed secretion PAS positive and negative. Epithelial changes consisted of a hypertrophied acinar epithelium with intraepithelial neoplasia focuses. Also, we observed a marked expression of PCNA and Caspase3 in the epithelium indicating even cellular proliferation as cell death. The stroma showed a high activity of the extracellular matrix remodeling with marked deposition of collagen fibers and smooth muscle cells. Around the ventral region, we observed an increase in the presence of adipose tissue. The expressions of interleukin 6 and tumor necrosis factor alpha were present in the ventral prostate of the obese mice indicating inflammation. In conclusion, obesity negatively modulates prostate in ob/ob mice, directly affecting cellular and structural mechanisms necessary for the maintenance of prostate and reproductive structure.


Los ratones obesos (C57BL / 6J-ob / ob) no expresan leptina y desarrollan hiperfagia, disminución del gasto energético, obesidad, hiperglucemia, hiperinsulinemia, hipotermia e infertilidad. La obesidad causa disfunción reproductiva con impacto negativo sobre la estructura prostática y la fertilidad. El objetivo de nuestro trabajo consistió en comparar la estructura y los aspectos moleculares de la próstata ventral en ratones magros y obesos (ob/ob). Se disecaron las próstatas de ratones machos obesos, de tres meses de edad, y fueron preparadas para visualizarlas por microscopía óptica e inmunofluorescencia. En comparación con el ratón magro, el ratón obeso mostró una sustancial modificación estructural en la próstata ventral comenzando con una atrofia del lóbulo ventral de la próstata. Histológicamente, los acinos mostraron una reducción de tamaño, y en el lumen, encontramos una secreción mixta PAS positiva y negativa. Los cambios epiteliales consistieron en un epitelio acinar hipertrofiado con focos de neoplasia intraepitelial. Además, se observó una marcada expresión de PCNA y Caspase3 en el epitelio, que indica tanto la proliferación celular como la muerte celular. El estroma mostró una alta remodelación de la matriz extracelular con marcada deposición de fibras de colágeno y células de músculo liso. Alrededor de la región ventral, se observó un aumento en la presencia de tejido adiposo. Las expresiones de interleuquina 6 y factor de necrosis tumoral alfa estaban presentes en la próstata ventral de los ratones obesos indicando inflamación. En conclusión, la obesidad modula negativamente la próstata en los ratones ob/ob, afectando directamente los mecanismos celulares y estructurales necesarios para el mantenimiento de la estructura de la próstata y la reproducción.


Subject(s)
Animals , Mice , Prostate/pathology , Obesity/pathology , Mice, Inbred C57BL , Mice, Obese
3.
Rio de Janeiro; s.n; 2011. 139 p. ilus.
Thesis in Portuguese | LILACS | ID: lil-689386

ABSTRACT

A insuficiência renal crônica (IRC) é caracterizada por alterações glomerulares secundárias aos mecanismos adaptativos ocasionados por perda de néfrons funcionantes. Alterações na hemodinâmica glomerular, proliferação celular, influxo de células inflamatórias, desequilíbrio na síntese de proteínas da matriz extracelular glomerular (MECG) e perda da seletividade de carga e/ou tamanho da membrana basal glomerular têm sido apontados como mecanismos envolvidos na expansão mesangial e conseqüente glomeruloesclerose. A participação dos hormônios sexuais na função renal e na evolução da insuficiência renal crônica tem sido sugerida. Os glicosaminoglicanos, especialmente o heparan sulfato (HS), têm sido associados à seletividade glomerular de macromoléculas. O remodelamento podocitário precoce e a proteinuria (PTN) se relacionam com a progressão da IRC. Neste contexto, o acúmulo de MECG, proliferação de miofibroblastos e PTN têm sido apontados como mediadores precoces que precedem as lesões glomerulares e túbulo-intersticiais. Neste estudo, avaliamos as alterações renais precoces (30 dias de IRC) gênero-dependentes em ratos (M) e ratas (F) Wistar submetidos à redução de 5/6 da massa renal (IRC) e à castração (c). Os animais foram divididos em 10 grupos: Controles (C) (CM, CF, CMc, CFc) e sham (CM sham, CF sham); e aqueles submetidos à nefrectomia 5/6: IRCM, IRCF, IRCMc, IRCFc. Os animais foram castrados com 5 semanas e submetidos à nefrectomia 5/6 com 7 semanas de idade. Resultados significativos mostraram que os machos com IRC apresentaram maior PTN, acompanhada de maior comprometimento mesangial, imunomarcação positiva para α-actina e maior concentração de heparan sulfato (HS) comparados com as fêmeas IRC (p<0,05). Estas alterações foram reduzidas nos machos castrados. A análise da morfologia podocitária mostrou raras regiões onde ocorreram alterações podocitárias nos grupos IRC. O conjunto de dados sugere que o hormônio masculino pode participar na manutenção...


Chronic renal failure (CRF) is characterized by adaptive mechanisms secondary to the loss of functioning nephrons. Glomerular hemodynamics alterations, cellular proliferation, inflammatory cells influx, imbalance between synthesis and degradation of the glomerular extracellular matrix (GECM) and loss of charge and/or size selectivity of the glomerular basal membrane are pointed as mechanisms leading to mesangial expansion and glomerulosclerosis. Additionally, participation of gender related hormones on renal function and progression of CRF have been suggested. We evaluated the effect of castration in renal alterations in males (M) and females (F) Wistar rats, after 30 days of 5/6 reduction of renal mass (CRF). The animals were castrated (c) at 5 weeks old and 7 weeks old 5/6 and sham nephrectomy were done. Groups: Control (C) CM, CM sham, CMc, CF, CF sham, CFc, CRFM, CRFMc, CRFF, CRFFc. CRFM group showed higher proteinuria followed by increased mesangial expansion and α-actin immunostaining. Concomitant higher concentration of heparan sulfate (HS) was also observed when compared to CRFF (p<0.05). These alterations were reduced in CRFMc group. Podocyte morphology analysis through electronic microscopy showed few disorders of foot processes in CRF groups Overall, CRFF group showed fewer alterations compared to males, and a reduction of HS was observed in association with PTN. Castration did not change this profile in female rats. Data suggest that male hormones may participate in the maintenance of the mesangial equilibrium and that PTN collaborated with the mesangial expansion process. Additionally, the higher concentration of HS in CRFM suggest that the remodeling process of the GECM, included a synthesis of de novo HS, that presented a functioning defect, compromising the glomerular filtration barrier and, ultimately corroborated with the loss of its selectivity and consequently with a higher PTN. This set of results leads us to conclude that PTN appears...


Subject(s)
Animals , Rats , Renal Insufficiency, Chronic , Kidney/physiopathology , Glomerular Mesangium , Glycosaminoglycans , Kidney Glomerulus/injuries , Myofibroblasts , Extracellular Matrix/metabolism , Nephrectomy , Proteinuria , Cell Proliferation , Rats, Wistar , Sex Factors
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