Abstract in English:
ABSTRACT.- Cid M.S., Indurain C., Odriozola E., Brizuela M.A. & Lauge M. 2011. Diagnose of the ingestion of Asclepias mellodora St. Hil. by sheep through microhistological analysis of their digestive contents. Pesquisa Veterinária Brasileira 31(2):111-116. Animal Production Department, Balcarce Integrated Unit (Faculty of Agricultural Sciences, Mar del Plata National University - Balcarce Experimental Station, National Institute of Agricultural Technology), Ruta 226 Km 73.5, cc 276 (7620) Balcarce, Agentina. E-mail: scid@balcarce.inta.gov.ar
Asclepias mellodora St. Hil. is a native acute toxic species frequent in the grasslands of the Buenos Aires province, Argentina, whose toxicity had not been assessed until now. This study evaluates the minimal lethal dose of this species for sheep, and the possibility of microscopically recognizing its fragments in gastrointestinal contents as a complementary diagnostic tool in necropsies. Three Frisona sheep (average LW=55±4.5 kg) were dosed via an esophageal tube with each one of the following doses of asclepias: 8.0, 5.0, 2.0 and 0.8 g DM.kg LW-1. Sheep poisoned with the three higher doses died between 10 and 85 h after intoxication, but those receiving the lower dose did not. During necropsies we: 1) determined the dry weight of the contents of rumen+reticulum, omasum+abomasum, and large intestine, 2) estimated the percentages of asclepias fragments by microanalysis correcting for digestion effects on fragment recognition, and 3) calculated the total mass of asclepias in the digestive tract of each animal. For the three higher doses, the mass of asclepias identified in the total ingesta was 12.3±3.4% of the amount supplied, possibly because of the strong diarrhea its ingestion produced. The percentages of asclepias in rumen+reticulum did not differ from the average quantified for the entire tract. The results of this study indicate that the minimal lethal doses of asclepias for sheep is between 2.0 and 0.8g DM·kg LW-1, and that the microhistological analysis of the rumen+reticulum, the easiest region to sample, can be used to confirm the ingestion of this toxic species, although the estimated percentage will be not a good estimator of the ingested percentage.
Abstract in Portuguese:
RESUMO.- Cid M.S., Indurain C., Odriozola E., Brizuela M.A. & Lauge M. 2011. Diagnose of the ingestion of Asclepias mellodora St. Hil. by sheep through microhistological analysis of their digestive contents. [Diagnose da ingestão de Asclepias mellodora St. Hil. por ovinos através da análise micro-histológica de seu conteúdo digestivo.] Pesquisa Veterinária Brasileira 31(2):111-116. Animal Production Department, Balcarce Integrated Unit (Faculty of Agricultural Sciences, Mar del Plata National University - Balcarce Experimental Station, National Institute of Agricultural Technology), Ruta 226 Km 73.5, cc 276 (7620) Balcarce, Agentina. E-mail: scid@balcarce.inta.gov.ar
Asclepias mellodora St. Hil. é uma espécie nativa de aguda toxicidade, frequente nos campos da província de Buenos Aires, Argentina. A sua toxicidade não foi avaliada até agora. Este estudo avalia a dose mínima letal desta espécie, para os ovinos, bem como a possibilidade de reconhecer microscopicamente seus fragmentos no conteúdo gastrointestinal como uma ferramenta complementar de diagnóstico em necropsias. Três ovinos Frisona (PV média = 55±4,5 kg) foram dosados através de uma sonda esofágica em cada uma das seguintes doses de Asclepias: 8,0, 5,0, 2,0 e 0,8 g DM.kg PV-1. Ovinos intoxicados com as três maiores doses morreram entre 10-85 h após a intoxicação, mas não aqueles que receberam a dose menor. Durante as necropsias se: 1) determinou o peso seco do conteúdo do rúmen + retículo, omaso + abomaso e intestino grosso, 2) estimou as porcentagens de fragmentos de Asclepias por microanálise, fazendo a correção para efeitos de digestão no reconhecimento dos fragmentos, e 3) calculou a massa total de Asclepias no trato digestivo de cada animal. Para as três doses maiores, a massa de Asclepias identificada na ingesta total foi de 12,3±3,4% da quantidade fornecida, possivelmente por causa da forte diarréia produzida pela sua ingestão. As porcentagens de Asclepias no rúmen + retículo não diferiram da média quantificada para o trato completo. Os resultados deste estudo indicam que a dose letal mínima de Asclepias em ovinos é de entre 2,0 e 0,8 g kg PV • DM-1, e que a análise micro-histológica do rúmen + retículo, a região mais fácil de amostrar, pode ser usada para confirmar a ingestão desta espécie tóxica, embora a percentagem estimada não será um bom estimador da porcentagem ingerida.
Abstract in English:
ABSTRACT.- Rocha T.L.,Yamada A.T., Mazaro e Costa R. & Sabóia-Morais S.M.T. 2011. [Analyses of the development and glycoproteins present in the ovarian follicles of Poecilia vivipara (Cyprinodontiformes, Poeciliidae).] Análise do desenvolvimento e das glicoproteínas presentes nos folículos ovarianos de Poecilia vivipara (Cyprinodontiformes, Poeciliidae). Pesquisa Veterinária Brasileira 31(1):87-93. Laboratório de Comportamento Celular, Departamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Goiás, Campus II, ICB IV, Cx. Postal 131, Goiânia, GO 74001-970, Brazil. E-mail: simonesaboias@gmail.com
The morphofunctional aspects of oogenesis of Poecilia vivipara were studied aiming to understand the reproductive biology and development of species with internal fertilization, particularly those belonging to the family Poeciliidae. The stages of gonadal maturation and follicular development were characterized using mesoscopic, histological, histochemical, and lectin cytochemical analyses. Through mesoscopic evaluation the ovarian development was classified in six phases of development: immature, in maturation I, in maturation II, mature I, mature II, and post-spawn. Based on microscopic examination of the ovaries, we identified the presence of oocytes types I and II during the previtellogenic phase and types III, IV, and V during the vitellogenic phase. As oogenesis proceeded the oocyte cytosol increased in volume and presented increased cytoplasmic granule accumulation, characterizing vitellogenesis. The zona radiata (ZR) increased in thickness and complexity, and the follicular epithelium, which was initially thin and consisting of pavimentous cells, in type III oocytes exhibited cubic simple cells. The histochemical and cytochemical analyses revealed alterations in the composition of the molecular structures that form the ovarian follicle throughout the gonadal development. Our study demonstrated differences in the female reproductive system among fish species with internal and external fertilization and we suggest P. vivipara can be used as experimental model to test environmental toxicity.
Abstract in Portuguese:
RESUMO.- Rocha T.L.,Yamada A.T., Mazaro e Costa R. & Sabóia-Morais S.M.T. 2011. [Analyses of the development and glycoproteins present in the ovarian follicles of Poecilia vivipara (Cyprinodontiformes, Poeciliidae).] Análise do desenvolvimento e das glicoproteínas presentes nos folículos ovarianos de Poecilia vivipara (Cyprinodontiformes, Poeciliidae). Pesquisa Veterinária Brasileira 31(1):87-93. Laboratório de Comportamento Celular, Departamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Goiás, Campus II, ICB IV, Cx. Postal 131, Goiânia, GO 74001-970, Brazil. E-mail: simonesaboias@gmail.com
Abstract in English:
ABSTRACT.- Madureira K.M., Gomes V., Castro R.S., Kitamura S.S. & Araújo W.P. 2010. [Analysis of direct and indirect methods for somatic cell counts in the milk of healthy goats.] Análise das metodologias diretas e indiretas para a contagem de células somáticas no leite de cabras hígidas. Pesquisa Veterinária Brasileira 30(4):311-316. Departamento de Clínica Médica, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, Av. Prof. Orlando Marques de Paiva 87, Bloco 12-14, Sala 47, São Paulo, SP 05508-000, Brasil. E-mail: karinamedici@yahoo.com.br
The particular apocrine secretion of goat milk different from the merocrine one observed in cows, may lead to errors in interpreting cellularity evaluations in the milk of this species. Thus, the objective of the present trial was to determine Somatic Cell Counts by means of one indirect methods, the California Mastitis Test (CMT), and direct methods, flow cytometry and direct microscopic count using methyl green-pyronine-Y stain, beyond comparing the methods of cellular counting. A total of 102 samples from 51 Saanen, Brown Alpine and Toggenburg female goats, bred in the state of São Paulo, were analyzed. Goats were separated in groups according to the phase of lactation and to physical examination of the mammary gland, and milk examination. Samples were divided into two aliquots, and were collected after California Mastitis Test evaluation. One aliquot was used in automatic cell counts, and the other, in direct microscopic count using methyl green-pyronine-Y stain. CMT results were as follows: 74.5% of the samples were negative, 8.8% yielded traces, 8.8% were weak positive (1), 6.8% were distinct positive (2) and 0.9% were strong positive (3). Medians of somatic cell counts in goat milk as evaluated by means automatic cell counter and direct microscopy, and grouped according to the different CMT scores, were as follows: 181,000, 578,000, 628,000, 1,421,500, and 5,542,000 cells/mL of milk and 74,991, 271,396, 71,420, 640,995, and 5,049,394 cells/mL of milk in scores negative, traces, 1, 2 and 3, respectively. Medians obtained in automatic cell counts and direct microscopic counts, grouped according to the phase of lactation were 159,500; 508,000; and 277,500 cells/mL of milk and 62,493; 89,275; and 146,411 cells/ml of milk, respectively. The correlation between the automatic and microscopic methods for somatic cell counts was 88%. Based on the results obtained, it could be concluded that there were differences between the automatic and microscopic methods for somatic cell counts, being this most adequate for the determination of the celularidade in the cellularity of goat milk.
Abstract in Portuguese:
RESUMO.- Madureira K.M., Gomes V., Castro R.S., Kitamura S.S. & Araújo W.P. 2010. [Analysis of direct and indirect methods for somatic cell counts in the milk of healthy goats.] Análise das metodologias diretas e indiretas para a contagem de células somáticas no leite de cabras hígidas. Pesquisa Veterinária Brasileira 30(4):311-316. Departamento de Clínica Médica, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, Av. Prof. Orlando Marques de Paiva 87, Bloco 12-14, Sala 47, São Paulo, SP 05508-000, Brasil. E-mail: karinamedici@yahoo.com.br
A particularidade da secreção láctea caprina, do tipo apócrina, diferente da secreção merócrina da vaca, leva a erros de interpretação durante a realização de técnicas de avaliação da celularidade do leite de fêmeas desta espécie. Portanto, o presente trabalho teve o objetivo de determinar a contagem de células somáticas pelo método indireto California Mastitis Test (CMT), e por métodos diretos, incluindo a contagem por citometria de fluxo e a contagem microscópica direta, através da coloração de verde de metil e pironina-Y, além de comparar os métodos de contagem celular. Foram analisadas 102 amostras de 51 fêmeas caprinas, das raças Saanen, Parda Alpina e Toggenburg, criadas no Estado de São Paulo. Os animais foram categorizados segundo a fase da lactação, exame físico da glândula mamária e exame do leite. As amostras foram colhidas, após a realização do exame Califórnia Mastitis Test, em duas alíquotas, uma destinada à contagem celular automática e a outra, a contagem microscópica direta, utilizando-se o corante verde de metil e pironina-Y. De acordo com os diferentes escores do CMT, observou-se 74,5% de amostras negativas, 8,8% de amostras com escore traços, 8,8% de amostras ligeiramente positivas (+), 6,8% de amostras fracamente positivas (++) e 0,9% de amostras fortemente positivas (+++). Os valores medianos das contagens de células somáticas presentes no leite de cabras, avaliadas através de contador automático e microscopia direta, e analisadas de acordo com os diferentes escores do CMT, foram, respectivamente, 181.000, 578.000, 628.000, 1.421.500 e 5.542.000 células/mL de leite e 74.991, 271.396, 71.420, 640.995 e 5.049.394 células/mL de leite, nos escores negativo, traços, +, ++ e +++. Os valores medianos obtidos através da contagem de células somáticas pelo método automático e microscópico direto, de acordo com as fases de lactação foram de 159.500, 508.000 e 277.500 células/mL de leite, e 62.493, 89.275 e 146.411. A correlação obtida entre a contagem celular automática e microscópica direta foi de 88%. A partir dos resultados observados pode-se concluir que existe diferença na contagem celular determinada através do método automático e microscópico sendo este último o mais adequado para a determinação da celularidade no leite de cabras.
Abstract in English:
ABSTRACT.- Moraes L.B., Osório F.S., Salle F.O., Souza G.F., Moraes H.L.S., Fallavena L.C.B., Nascimento V.P., Santos L.R. & Salle C.T.P. 2010. Evaluation of follicular lymphoid depletion in the Bursa of Fabricius: An alternative methodology using digital image analysis and artificial neural networks. Pesquisa Veterinária Brasileira 30(4):340-344. Departamento de Medicina Animal, Universidade Federal do Rio Grande do Sul, Avenida Bento Gonçalves 8824, Porto Alegre, RS 91540-000, Brazil. E-mail: lucasbmoraes@gmail.com
Fifty Bursa of Fabricius (BF) were examined by conventional optical microscopy and digital images were acquired and processed using Matlab® 6.5 software. The Artificial Neuronal Network (ANN) was generated using Neuroshell® Classifier software and the optical and digital data were compared. The ANN was able to make a comparable classification of digital and optical scores. The use of ANN was able to classify correctly the majority of the follicles, reaching sensibility and specificity of 89% and 96%, respectively. When the follicles were scored and grouped in a binary fashion the sensibility increased to 90% and obtained the maximum value for the specificity of 92%. These results demonstrate that the use of digital image analysis and ANN is a useful tool for the pathological classification of the BF lymphoid depletion. In addition it provides objective results that allow measuring the dimension of the error in the diagnosis and classification therefore making comparison between databases feasible.
Abstract in Portuguese:
RESUMO.- Moraes L.B., Osório F.S., Salle F.O., Souza G.F., Moraes H.L.S., Fallavena L.C.B., Nascimento V.P., Santos L.R. & Salle C.T.P. 2010. Evaluation of follicular lymphoid depletion in the Bursa of Fabricius: An alternative methodology using digital image analysis and artificial neural networks. Pesquisa Veterinária Brasileira 30(4):340-344. Departamento de Medicina Animal, Universidade Federal do Rio Grande do Sul, Avenida Bento Gonçalves 8824, Porto Alegre, RS 91540-000, Brazil. E-mail: lucasbmoraes@gmail.com
Cinquenta Bursa de Fabrícius (BF) foram examinadas através de microscopia óptica convencional e imagens digitais foram obtidas e processadas através do software Matlab® 6.5. Redes Neurais Artificiais (ANN) foram geradas com a utilização do software Neuroshell® Classifier, e os dados das análises óptica e digital foram comparados. A ANN classificou corretamente a maioria dos folículos, atingindo sensibilidade e especificidade de 89% e 96%, respectivamente. Quando os folículos foram agrupados de forma binária houve um aumento da sensibilidade para 90% e obteve-se um valor máximo para a especificidade de 92%. Estes resultados demonstram que o uso da análise digital de imagem associada à ANN é uma ferramenta bastante útil para a classificação patológica da depleção linfóide da BF. Além disso, fornece resultados objetivos que permitem medir a dimensão do erro classificatório, tornando possível a comparação entre distintos bancos de dados.
Abstract in English:
ABSTRACT.- Fernandez D.S., Ferraz R.H.S., Melo A.P.F., Rodrigues R.F. & Souza W.M. 2010. [Histological analysis of urethral glands of the capybara (Hydrochoerus hydrochaeris).] Análise histológica das glândulas uretrais da capivara (Hydrochoerus hydrochaeris). Pesquisa Veterinária Brasileira 30(4):373-377. Curso de Medicina Veterinária, Universidade de Rio Preto (Unirp), Centro Universitário de Rio Preto, Rua Gabriel Yvette Atique 45, São José do Rio Preto, SP 15025-400, Brasil. E-mail: alanmelo@unirpnet.com.br
To perform a microscopic study of the glands attached to the male urethra, we used two adult capybaras (Hydrochoerus hydrocaeris) from which fragments of the urethral glands were collected, immersed in Bouin’s fixative solution, washed thoroughly with 70% to absolute alcohol, submitted to routine histological techniques and stained with hematoxylin/eosin and Masson’s trichromic method. The morphological findings were: Vas deferens has a thickening of the wall without granular epithelium and with unchanged lumen; the vesicular gland has a secretory epithelium of pseudostratified columnar type; the prostate gland has a high and ramified mucous membrane covered with pseudostratified cylindrical epithelium. Male capybaras have vesicular, prostate as urethral glands. In the material examined, no secretory epithelium corresponding to bulbourethral glands was identified; morphologically it resembles to the other histricomorphs.
Abstract in Portuguese:
RESUMO.- Fernandez D.S., Ferraz R.H.S., Melo A.P.F., Rodrigues R.F. & Souza W.M. 2010. [Histological analysis of urethral glands of the capybara (Hydrochoerus hydrochaeris).] Análise histológica das glândulas uretrais da capivara (Hydrochoerus hydrochaeris). Pesquisa Veterinária Brasileira 30(4):373-377. Curso de Medicina Veterinária, Universidade de Rio Preto (Unirp), Centro Universitário de Rio Preto, Rua Gabriel Yvette Atique 45, São José do Rio Preto, SP 15025-400, Brasil. E-mail: alanmelo@unirpnet.com.br
Para realização do estudo microscópico das glândulas anexas à uretra masculina, foram utilizadas duas capivaras (Hydrochoerus hydrocaeris), adultas, das quais foram coletados fragmentos das glândulas genitais acessórias, imersos em solução fixadora de Bouin e lavados cuidadosamente em álcool de 70% ao absoluto. A seguir foram submetidos aos processos histológicos de rotina e corados pelos métodos de Hematoxilina/Eosina e Tricrômico de Masson. Os resultados morfológicos encontrados foram: o ducto deferente possui um espessamento da parede, onde a luz permanece inalterada e sem presença de epitélio granular. A glândula vesicular possui um epitélio secretor do tipo pseudoestratificado colunar. A glândula prostática possui mucosa com pregueamentos altos e ramificados, revestido por epitélio pseudoestratificado cilíndrico. Machos de capivaras possuem glândulas vesiculares e próstata como glândulas uretrais. No material examinado não foi identificado epitélio secretor correspondente a glândula bulbouretral e morfologicamente assemelha-se aos outros histricomorfos.
Abstract in English:
ABSTRACT.- Kondo K.R.J., Fonseca C.C., Da Matta S.L.P. & Viloria M.I.V. 2009. [Histomorphometric analysis of the extracellular matrix of popliteal lymph nodes from dogs naturally infected by Leishmania (L.) chagasi.] Análise histomorfométrica da matriz extracelular do linfonodo poplíteo de cães naturalmente infectados por Leishmania (L.) chagasi. Pesquisa Veterinária Brasileira 29(8):610-616. Departamento de Veterinária, Universidade Federal de Viçosa, Av. Peter Henry Rolfs s/n, Campus Universitário, Viçosa, MG 36570-000, Brazil. E-mail: krisregia@hotmail.com
In the Americas, canine visceral leishmaniasis is caused by Leishmania (Leishmania) chagasi, an obligatory intracellular parasite of the phagocytic-monocytic system; the main histological changes associated with this disease occur in the lymphoid organs. Although dogs are considered to be the main carriers and disseminators of leishmaniasis in urban areas, there are few studies on the histopathologic and histomorphometric aspects in dogs naturally infected by L.chagasi analyzing the interaction between parasite and extracellular matrix. The current study characterize and quantify changes in the cellular and extracellular matrix (collagens type I and III) components of the popliteal lymph node from of 22 dogs with the natural infection by L. chagasi confirmed by indirect immuno-fluorescence assay (IFA) and compare theses findings with those fund in the popliteal lymph node from 10 non-infected dogs, that reacted negative in the IFA, and were clinically healthy. Lymph node fragments were longitudinally sliced and sections were processed for routine histopathology and stained by hematoxylin and eosin. For histomorphometry, additional sections from the same lymph node were fixed in glycol methacrylate and stained with toluidine blue. Lymph nodes from affected dogs were systemically enlarged, had increased numbers of lymphoid follicles, capsule hyperplasia and hypertrophy, and significant hyperplasia of lymphoid cells. In the lymph nodes from infected dogs, quantitative analyses of collagen fibers revealed predominance of type I collagen over type III fibers. These results demonstrate that dogs infected by L.chagasi experience degradation of the extracellular matrix components and consequently destruction of the lymphoid framework, thus altering nodal morphology.
Abstract in Portuguese:
RESUMO.- Kondo K.R.J., Fonseca C.C., Da Matta S.L.P. & Viloria M.I.V. 2009. [Histomorphometric analysis of the extracellular matrix of popliteal lymph nodes from dogs naturally infected by Leishmania (L.) chagasi.] Análise histomorfométrica da matriz extracelular do linfonodo poplíteo de cães naturalmente infectados por Leishmania (L.) chagasi. Pesquisa Veterinária Brasileira 29(8):610-616. Departamento de Veterinária, Universidade Federal de Viçosa, Av. Peter Henry Rolfs s/n, Campus Universitário, Viçosa, MG 36570-000, Brazil. E-mail: krisregia@hotmail.com
Nas Américas, a leishmaniose visceral canina é causada por Leishmania (Leishmania) chagasi, um protozoário intracelular obrigatório do sistema fagocítico mononuclear; as principais alterações histológicas associadas a essa doença ocorrem nos em órgãos linfóides. Apesar de o cão ser considerado o principal mantenedor e disseminador da leishmaniose no ambiente urbano, são escassos estudos dos aspectos histopatológicos e histomorfométricos, em cães naturalmente infectados com L. chagasi, que investiguem a interação entre o parasito e a matriz extracelular. Este estudo visou caracterizar e quantificar as alterações dos componentes celulares e da matriz extracelular (colágenos I e III) do linfonodo poplíteo de 22 cães com infecção natural por L. chagasi detectada através da reação de imunofluorescência indireta (RIF) e compará-las com as alterações encontradas no linfonodo poplíteo de 10 cães não-infectados, negativos na RIF e clinicamente saudáveis. Fragmentos dos linfonodos foram seccionados longitudinalmente, processados rotineiramente para exame histológico e corados por hematoxilina-eosina. Cortes adicionais do mesmo linfonodo incluídos em glicol metacrilato foram corados pelo azul de toluidina para histomorfometria. Linfonodos de cães infectados apresentaram linfadenopatia generalizada, aumento do tamanho e do número dos folículos linfóides, hipertrofia da cápsula e hiperplasia linfóide significativa. Nos linfonodos de cães do grupo infectado, a análise quantitativa de fibras colágenas mostrou significativo predomínio do colágeno I sobre o colágeno III. Esses resultados demonstram que cães infectados por L. chagasi apresentam degradação dos constituintes da matriz extracelular e conseqüente destruição do arcabouço linfóide, alterando a morfologia do órgão.
Abstract in English:
ABSTRACT.- Rezende R.S., Coelho H.E, Kamimura R., Severino R.S, Oliveira, P.C.L., Medeiros A.A. & Magalhães A.O.C. 2009. [Microscopic analysis of the left ventricular myocardium in positive serum dogs to distemper disease.] Análise microscópica do miocárdio ventricular esquerdo em cães soropositivos para cinomose. Pesquisa Veterinária Brasileira 29(2):117-119. Instituto de Estudos Avançados em Veterinária José Caetano Borges, Universidade de Uberaba, Av. do Tutunas 720, Uberaba, MG 38061-500, Brazil. E-mail: rezendehvu@hotmail.com
Classified pertaining to the genus Morbillivirus of the Paramyxoviridae family, the canine distemper virus is a RNA single-stranded virus with negative polarity and causes a multisystemic disease, serious and highly contagious for dogs and wild carnivores, with a high mortality rate in non-vaccinated animals or with vaccine fails. With the objective to evaluate heart histopathological alterations, particularly in the left ventricular myocardium, in dogs naturally infected with canine distemper virus, 35 dogs, males and females of different ages, were studied. All the 35 samples sent to the Veterinary Hospital of Uberaba were serum-positive for distemper (immunoassay technique in solid phase) and had in the left ventricular myocardium the following histopathologic alterations: myocarditis, hyalin degeneration, hyperemia and hemorrhage, in 42.8% (15/35), 31.4% (11/35), 14.3% (5/35) and 11.4% (4/35), respectively. Having carried out the Qui-Quadrado test with a significancy level of 0.05, it can be concluded that there is a high correlation (p=0.02) between the infected animals with canine distemper virus and histopathological alterations found in the left ventricular myocardium.
Abstract in Portuguese:
ABSTRACT.- Rezende R.S., Coelho H.E, Kamimura R., Severino R.S, Oliveira, P.C.L., Medeiros A.A. & Magalhães A.O.C. 2009. [Microscopic analysis of the left ventricular myocardium in positive serum dogs to distemper disease.] Análise microscópica do miocárdio ventricular esquerdo em cães soropositivos para cinomose. Pesquisa Veterinária Brasileira 29(2):117-119. Instituto de Estudos Avançados em Veterinária José Caetano Borges, Universidade de Uberaba, Av. do Tutunas 720, Uberaba, MG 38061-500, Brazil. E-mail: rezendehvu@hotmail.com
Classified pertaining to the genus Morbillivirus of the Paramyxoviridae family, the canine distemper virus is a RNA single-stranded virus with negative polarity and causes a multisystemic disease, serious and highly contagious for dogs and wild carnivores, with a high mortality rate in non-vaccinated animals or with vaccine fails. With the objective to evaluate heart histopathological alterations, particularly in the left ventricular myocardium, in dogs naturally infected with canine distemper virus, 35 dogs, males and females of different ages, were studied. All the 35 samples sent to the Veterinary Hospital of Uberaba were serum-positive for distemper (immunoassay technique in solid phase) and had in the left ventricular myocardium the following histopathologic alterations: myocarditis, hyalin degeneration, hyperemia and hemorrhage, in 42.8% (15/35), 31.4% (11/35), 14.3% (5/35) and 11.4% (4/35), respectively. Having carried out the Qui-Quadrado test with a significancy level of 0.05, it can be concluded that there is a high correlation (p=0.02) between the infected animals with canine distemper virus and histopathological alterations found in the left ventricular myocardium.
Abstract in English:
Abstract.- Oliveira E.C., Pescador C.A., Sonne L., Pavarini S.P., Santos A.S., Corbellini L.G. & Driemeier D. 2009. [Immunohistochemical analysis of dogs infected naturally by canine parvovirus.] Análise imuno-histoquímica de cães naturalmente infectados pelo parvovírus canino. Pesquisa Veterinária Brasileira 29(2):131-136. Setor de Patologia Veterinária, Faculdade de Veterinária, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves 9090, Porto Alegre, RS 91540-000, Brazil. E-mail: davetpat@ufrgs.br
Ninety-six dogs with gross lesions suggestive of canine parvovirus infection were selected and necropsied in the Faculty of Veterinary Medicine, Universidade Federal do Rio Grande do Sul, between March 2005 and November 2006. The main gross lesions were enlargement of the Peyer’s patches in the small intestine and hyperemia in the intestinal mucosa and serosa. Microscopically, the small intestine showed necrotizing enteritis in 77% (74/96) of the dogs examined. However, in 17.7% of the histological evaluation in the small intestine were damaged due to autolytic changes making it difficult to obtain an appropriate interpretation. The immunohistochemistry test was performed in tissues of small intestine, mesenteric lymph nodes, thymus, spleen, tonsils, tongue, and bone marrow in all the 96 selected cases. Parvovirus antigen was detected in 91.6% (88/96) of the dogs necropsied. The best result of the IHC test was seen in samples of small intestine which was positive in 77% (74/96) of the cases. The statistical analysis (Fisher test) showed a weak association between intestinal autolysis and positive result of the IHC test. The chance of the autolysed intestine showing a positive result in the immunohistochemistry test was 0.33 less (OR=0.33, 95% CI:0.10-1.17) when compared with small intestine not autolysed.
Abstract in Portuguese:
Abstract.- Oliveira E.C., Pescador C.A., Sonne L., Pavarini S.P., Santos A.S., Corbellini L.G. & Driemeier D. 2009. [Immunohistochemical analysis of dogs infected naturally by canine parvovirus.] Análise imuno-histoquímica de cães naturalmente infectados pelo parvovírus canino. Pesquisa Veterinária Brasileira 29(2):131-136. Setor de Patologia Veterinária, Faculdade de Veterinária, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves 9090, Porto Alegre, RS 91540-000, Brazil. E-mail: davetpat@ufrgs.br
Ninety-six dogs with gross lesions suggestive of canine parvovirus infection were selected and necropsied in the Faculty of Veterinary Medicine, Universidade Federal do Rio Grande do Sul, between March 2005 and November 2006. The main gross lesions were enlargement of the Peyer’s patches in the small intestine and hyperemia in the intestinal mucosa and serosa. Microscopically, the small intestine showed necrotizing enteritis in 77% (74/96) of the dogs examined. However, in 17.7% of the histological evaluation in the small intestine were damaged due to autolytic changes making it difficult to obtain an appropriate interpretation. The immunohistochemistry test was performed in tissues of small intestine, mesenteric lymph nodes, thymus, spleen, tonsils, tongue, and bone marrow in all the 96 selected cases. Parvovirus antigen was detected in 91.6% (88/96) of the dogs necropsied. The best result of the IHC test was seen in samples of small intestine which was positive in 77% (74/96) of the cases. The statistical analysis (Fisher test) showed a weak association between intestinal autolysis and positive result of the IHC test. The chance of the autolysed intestine showing a positive result in the immunohistochemistry test was 0.33 less (OR=0.33, 95% CI:0.10-1.17) when compared with small intestine not autolysed.
Abstract in English:
ABSTRACT.- Iamaguti L.S., Brandão C.V.S., Pellizzon C.H., Ranzani J.J.T. & Minto B.W. 2008. [Histological and morphometric analysis for the use of a biosynthetic cellulose membrane in experimental trochleopasty.] Análises histológica e morfométrica do uso de membrana biossintética de celulose em trocleoplastia experimental de cães. Pesquisa Veterinária Brasileira 28(4):195-200. Departamento de Cirurgia e Anestesiologia, Faculdade de Medicina Veterinária e Zootecnia, Universidade Estadual Paulista, Campus de Botucatu, Distrito de Rubião Jr s/n, Botucatu, SP 18.618-000, Brazil. E-mail: iamaguti_lu@hotmail.com
The aim of this study was to evaluate the use of a locally made biosynthetic cellulose membrane after experimental trochleoplasty, in order to verify whether its use could support migration of chondrogenic cells. Twelve male and female adult healthy dogs and without claudication were used. All dogs were submitted to trochleoplasty in both pelvic limbs after sedation and epidural anesthesia. In the left hind limb, the biosynthetic cellulose membrane was fixed with simple suture using Polyglactin 910 6-0 after performing trochleoplasty (treated group); whereas in the right limb (control group) only trochleoplasty was performed. The dogs were subdivided into 4 subgroups for postoperative evaluation at 15, 30, 60 and 90 days post-surgery. Biopsy was performed after exploratory arthrotomy for histopathologic and morfometric evaluation. At 30 and 60 days post-surgery, more condrocyte-like cells of immature aspect were observed in lesions treated with the cellulose membrane. At 90 days post-surgery the reparative tissue was characterized as mature fibrocartilage-like tissue without difference between the groups. In the control group there was a progressive increase of the number of cells until the end of the evaluation period. Otherwise, when compared to the initial period (15 days), there was an increase in the number of cells until 60 days, followed by a return the initial values at 90 days in the treated group. In comparison to controls, the number of cells was greater in the treated group from 15 to 60 days. Initially, the neoformed repair tissue was thicker in the treated group. From the results of this study, it was concluded that the cellulose membrane shortened the initial tissue repair process in the trochleoplasty area, showing good integration of the neoformed tissue with the adjacent cartilage.
Abstract in Portuguese:
ABSTRACT.- Iamaguti L.S., Brandão C.V.S., Pellizzon C.H., Ranzani J.J.T. & Minto B.W. 2008. [Histological and morphometric analysis for the use of a biosynthetic cellulose membrane in experimental trochleopasty.] Análises histológica e morfométrica do uso de membrana biossintética de celulose em trocleoplastia experimental de cães. Pesquisa Veterinária Brasileira 28(4):195-200. Departamento de Cirurgia e Anestesiologia, Faculdade de Medicina Veterinária e Zootecnia, Universidade Estadual Paulista, Campus de Botucatu, Distrito de Rubião Jr s/n, Botucatu, SP 18.618-000, Brazil. E-mail: iamaguti_lu@hotmail.com
The aim of this study was to evaluate the use of a locally made biosynthetic cellulose membrane after experimental trochleoplasty, in order to verify whether its use could support migration of chondrogenic cells. Twelve male and female adult healthy dogs and without claudication were used. All dogs were submitted to trochleoplasty in both pelvic limbs after sedation and epidural anesthesia. In the left hind limb, the biosynthetic cellulose membrane was fixed with simple suture using Polyglactin 910 6-0 after performing trochleoplasty (treated group); whereas in the right limb (control group) only trochleoplasty was performed. The dogs were subdivided into 4 subgroups for postoperative evaluation at 15, 30, 60 and 90 days post-surgery. Biopsy was performed after exploratory arthrotomy for histopathologic and morfometric evaluation. At 30 and 60 days post-surgery, more condrocyte-like cells of immature aspect were observed in lesions treated with the cellulose membrane. At 90 days post-surgery the reparative tissue was characterized as mature fibrocartilage-like tissue without difference between the groups. In the control group there was a progressive increase of the number of cells until the end of the evaluation period. Otherwise, when compared to the initial period (15 days), there was an increase in the number of cells until 60 days, followed by a return the initial values at 90 days in the treated group. In comparison to controls, the number of cells was greater in the treated group from 15 to 60 days. Initially, the neoformed repair tissue was thicker in the treated group. From the results of this study, it was concluded that the cellulose membrane shortened the initial tissue repair process in the trochleoplasty area, showing good integration of the neoformed tissue with the adjacent cartilage.
Abstract in English:
ABSTRACT.- Moura C.E.B., Albuquerque J.F.G., Magalhães M.S., Silva N.B., Oliveira M.F. & Papa P.C. 2007. [Comparative analysis of the origin of the brachial plexus of the collared peccary (Tayassu tajacu).] Análise comparativa da origem do plexo braquial de catetos (Tayassu tajacu). Pesquisa Veterinária Brasileira 27(9):357-362. Departamento de Morfologia, Universidade Federal do Rio Grande do Norte, Cx. Postal 1524, Campus Universitário Lagoa Nova, Natal, RN 59072-970, Brazil. E-mail: cadumoura@ufrnet.br
Collared peccary (Tayassu tajacu) belongs to the Tayassuidae family, characterized by a “collar” of white hairs that cross behind the neck and extend bilaterally in front of the shoulders. It can be found from south-western United States to Argentina. In the literature a shortage of data is verified regarding the functional anatomy of the collared peccaries, especially of studies that involve the anatomy of the brachial plexus. To elucidate the behavior of this plexus of collared peccaries and with the purpose to contribute for the development of compared anatomy, this study was accomplished. Thirty animals of different ages were used (17 males and 13 females) coming from the Wild Animal Multiplication Center of the “Universidade Federal Rural do Semi-árido” Mossoró, Rio Grande do Norte, Brazil. After slaughter bilateral dissection of the brachial plexuses took place, and the results were registered in schematic drawings and the dispositions grouped in tables for subsequent statistical analysis based on the percentile frequency. It was found that the Plexus brachialis of collared peccaries is the result of established communications, mainly among the Rami ventrales of the last three cervical nerves and of the first two thoracic nerves, having a contribution of the fourth and fifth cervical nerves in 16.67% and 50.00% of the cases, respectively. In 40.00% of the dissections the most frequent plexus was of the type C6, C7, C8, T1 and T2. The main nerves derived from brachial plexus of the collared peccaries and its respective origins had been: Nervus suprascapularis (C6, C7), Nn. subscapulares (C5, C6 e C7 or C6 e C7), N. axillaris (C6, C7), N. musculocutaneus (C7, C8), N. medianus (C7, C8, T1, T2), N. radialis (C8, T1, T2), N. ulnaris (C8, T1, T2), cranialis (C7), and caudalis (C7, C8) Nn. pectorales, N. thoracodorsalis (C6, C7, C8), N. thoracicus longus (C7, C8), and N. thoracicus lateralis (C8, T1, T2).
Abstract in Portuguese:
ABSTRACT.- Moura C.E.B., Albuquerque J.F.G., Magalhães M.S., Silva N.B., Oliveira M.F. & Papa P.C. 2007. [Comparative analysis of the origin of the brachial plexus of the collared peccary (Tayassu tajacu).] Análise comparativa da origem do plexo braquial de catetos (Tayassu tajacu). Pesquisa Veterinária Brasileira 27(9):357-362. Departamento de Morfologia, Universidade Federal do Rio Grande do Norte, Cx. Postal 1524, Campus Universitário Lagoa Nova, Natal, RN 59072-970, Brazil. E-mail: cadumoura@ufrnet.br
Collared peccary (Tayassu tajacu) belongs to the Tayassuidae family, characterized by a “collar” of white hairs that cross behind the neck and extend bilaterally in front of the shoulders. It can be found from south-western United States to Argentina. In the literature a shortage of data is verified regarding the functional anatomy of the collared peccaries, especially of studies that involve the anatomy of the brachial plexus. To elucidate the behavior of this plexus of collared peccaries and with the purpose to contribute for the development of compared anatomy, this study was accomplished. Thirty animals of different ages were used (17 males and 13 females) coming from the Wild Animal Multiplication Center of the “Universidade Federal Rural do Semi-árido” Mossoró, Rio Grande do Norte, Brazil. After slaughter bilateral dissection of the brachial plexuses took place, and the results were registered in schematic drawings and the dispositions grouped in tables for subsequent statistical analysis based on the percentile frequency. It was found that the Plexus brachialis of collared peccaries is the result of established communications, mainly among the Rami ventrales of the last three cervical nerves and of the first two thoracic nerves, having a contribution of the fourth and fifth cervical nerves in 16.67% and 50.00% of the cases, respectively. In 40.00% of the dissections the most frequent plexus was of the type C6, C7, C8, T1 and T2. The main nerves derived from brachial plexus of the collared peccaries and its respective origins had been: Nervus suprascapularis (C6, C7), Nn. subscapulares (C5, C6 e C7 or C6 e C7), N. axillaris (C6, C7), N. musculocutaneus (C7, C8), N. medianus (C7, C8, T1, T2), N. radialis (C8, T1, T2), N. ulnaris (C8, T1, T2), cranialis (C7), and caudalis (C7, C8) Nn. pectorales, N. thoracodorsalis (C6, C7, C8), N. thoracicus longus (C7, C8), and N. thoracicus lateralis (C8, T1, T2).