Resultado da pesquisa (2)

Termo utilizado na pesquisa Zandim B.M.

#1 - Platelet activation: Ultrastructure and morphometry in platelet-rich plasma of horses, 32(1):83-92

Abstract in English:

ABSTRACT.- Zandim B.M., Souza M.V., Magalhães P.C., Benjamin L.A., Maia L., Oliveira A.C., Pinto J.O. & Ribeiro Júnior J.I. 2012. Platelet activation: Ultrastructure and morphometry in platelet-rich plasma of horses. Pesquisa Veterinária Brasileira 32(1):83-92. Departamento de Veterinária, Universidade Federal de Viçosa, Campus Universitário s/n, Viçosa, MG 36570-000, Brazil. E-mail: msouza@ufv.br This study was conducted to investigate the activation ability of the platelet-rich plasma (PRP) by pharmacological agents, as well as to verify the need or not of this activation for therapeutic use. The PRP was obtained from four healthy crossbred geldings aged 13 to 16 years (15±1years), and was processed for observation and quantification of the platelet morphology by using the transmission electron microscopy. All PRP samples were activated with 10% calcium chloride (CaCl2) solution, pure bovine thrombin or associated with CaCl2. The control (pure PRP) was not pharmacologically activated. In the pure PRP samples, 49% of the platelets were classified as state of activation uncertain, 41% as resting, 9% as fully activated and 1% as irreversibly damaged. Treatment with 10% CaCl2 provided a distribution of 54% platelets in state of activation uncertain, 24% as fully activated, 20% as resting, and 2% as irreversibly damaged. The platelet morphology of the bovine thrombin treated samples did not fit into classification adopted, as showing irregular shape with emission of large filamentous pseudopods, appearance of ruptured and whole granules in the remaining cytoplasm and extracellular environment. There was effect of the treatment on the platelet morphology (P=0.03). The 10% CaCl2 is an adequate platelet-activating agent. However, in cases the use of PRP under its liquid form is necessary, the use of pure PRP is recommended, since besides presenting an adequate percentage of fully activated platelets it also has significant amount of the resting type, which can be activated by substances found in the injured tissue.

Abstract in Portuguese:

RESUMO.- Zandim B.M., Souza M.V., Magalhães P.C., Benjamin L.A., Maia L., Oliveira A.C., Pinto J.O. & Ribeiro Júnior J.I. 2012. Platelet activation: Ultrastructure and morphometry in platelet-rich plasma of horses. Pesquisa Veterinária Brasileira 32(1):83-92. Departamento de Veterinária, Universidade Federal de Viçosa, Campus Universitário s/n, Viçosa, MG 36570-000, Brazil. E-mail: msouza@ufv.br O objetivo desse estudo foi investigar a capacidade de ativação do plasma rico em plaquetas (PRP) por substâncias farmacológicas, assim como verificar a necessidade ou não dessa ativação para uso terapêutico. O PRP foi obtido de quatro equinos mestiços hígidos, machos castrados, com 13 a 16 anos (15±1anos) de idade, e processado para observação e quantificação da morfologia plaquetária mediante a utilização da microscopia eletrônica de transmissão. Todas as amostras de PRP foram ativadas com cloreto de cálcio (CaCl2) a 10%, trombina bovina pura ou associada a CaCl2. O controle (PRP puro) não foi ativado farmacologicamente. Nas amostras de PRP puro, 49% das plaquetas foram classificadas como ativação incerta, 41% em repouso, 9% totalmente ativada e 1% com dano irreversível. O tratamento com CaCl2 a 10% proporcionou uma distribuição de 54% de plaquetas com ativação incerta, 24% totalmente ativada, 20% em repouso, e 2% como com dano irreversível. Amostras tratadas com trombina bovina apresentaram morfologia plaquetária que não se enquadraram na classificação adotada, apresentando forma irregular com emissão de grandes pseudópodes filamentosos, aspecto de rompimento e grânulos inteiros no citoplasma remanescente e meio extracelular. Houve efeito do tratamento sobre a morfologia plaquetária (P=0,03). O CaCl2 a 10% é um adequado agente ativador de plaquetas. Entretanto, nos casos onde se faz necessário o uso de PRP na forma mais líquida, recomenda-se o uso do PRP puro, que além de apresentar uma adequada porcentagem de plaquetas totalmente ativadas, também possui importante quantidade do tipo em repouso, que pode ser ativado por substâncias presentes no tecido lesionado.


#2 - Plasma rico em plaquetas no tratamento de tendinite induzida em eqüinos: avaliação ultra-sonográfica, p.241-245

Abstract in English:

ABSTRACT.- Maia L., Souza M.V., Alves G.E.S., Júnior J.I.R., Oliveira A.C., Silva Y.F.R.S. & Zandim B.M. 2009. [Platelet-rich plasma in the treatment of induced tendinitis in equines: Ultrasonographic evaluation.] Plasma rico em plaquetas no tratamento de tendinite induzida em eqüinos: avaliação ultra-sonográfica. Pesquisa Veterinária Brasileira 29(3):241-245. Setor de Clínica e Cirurgia de Grandes Animais, Departamento de Veterinária, Universidade Federal de Viçosa, 36570-000 Viçosa, MG, Brazil. E-mail: msouza@ufv.br The objective of the study was to evaluate the effect of platelet-rich plasma (PRP) in the treatment of induced tendinitis in the superficial digital flexor tendon (SDFT) of horses through ultrasonographic evaluation. Thus, six 8 to15-year-old healthy gelding horses (=12 years) were used. Tendinitis of the SDFT was provoked in both forelimbs via intratendineous administration of 2.5mg of collagenase (2.5mg.mL-1), what was considered as beginning of the experimental phase. Twelve days after induced tendinitis, the horses were submitted to two treatments: (1) in the lesion caused in the right SDFT (treated group, TG), 2.5mL of PRP activated with calcium chloride at 0.0125mol.L-1, at concentrations from 320,000 to 500,000 platelets.µL-1, were administered; (2) in the tendinitis of the left SDFT (control group, CG), 2.5mL of 0.9% saline solution was administered. After 5 days, the animals were submitted to controlled and progressive physical activity during 30 days. Ultrasonographic examinations were carried out before and after tendinitis induction (48 hours after and on experimental days 7, 12, 14, 21 28, 35 and 42), with tendon cross-sectional area (CSA), lesion cross-sectional area (L-CSA), L-CSA percentage, severity and echogenicity of the lesion, as well as collagen fiber alignment being evaluated. The result revealed reduction (P<0.05) in the L-CSA and in the degree of lesion echogenicity in function of time, but with difference (P<0.05) between groups only for L-CSA, with smaller values in TG. The treatment with PRP promotes greater reduction in the area of the lesion measured by ultrasound.

Abstract in Portuguese:

ABSTRACT.- Maia L., Souza M.V., Alves G.E.S., Júnior J.I.R., Oliveira A.C., Silva Y.F.R.S. & Zandim B.M. 2009. [Platelet-rich plasma in the treatment of induced tendinitis in equines: Ultrasonographic evaluation.] Plasma rico em plaquetas no tratamento de tendinite induzida em eqüinos: avaliação ultra-sonográfica. Pesquisa Veterinária Brasileira 29(3):241-245. Setor de Clínica e Cirurgia de Grandes Animais, Departamento de Veterinária, Universidade Federal de Viçosa, 36570-000 Viçosa, MG, Brazil. E-mail: msouza@ufv.br The objective of the study was to evaluate the effect of platelet-rich plasma (PRP) in the treatment of induced tendinitis in the superficial digital flexor tendon (SDFT) of horses through ultrasonographic evaluation. Thus, six 8 to15-year-old healthy gelding horses (=12 years) were used. Tendinitis of the SDFT was provoked in both forelimbs via intratendineous administration of 2.5mg of collagenase (2.5mg.mL-1), what was considered as beginning of the experimental phase. Twelve days after induced tendinitis, the horses were submitted to two treatments: (1) in the lesion caused in the right SDFT (treated group, TG), 2.5mL of PRP activated with calcium chloride at 0.0125mol.L-1, at concentrations from 320,000 to 500,000 platelets.µL-1, were administered; (2) in the tendinitis of the left SDFT (control group, CG), 2.5mL of 0.9% saline solution was administered. After 5 days, the animals were submitted to controlled and progressive physical activity during 30 days. Ultrasonographic examinations were carried out before and after tendinitis induction (48 hours after and on experimental days 7, 12, 14, 21 28, 35 and 42), with tendon cross-sectional area (CSA), lesion cross-sectional area (L-CSA), L-CSA percentage, severity and echogenicity of the lesion, as well as collagen fiber alignment being evaluated. The result revealed reduction (P<0.05) in the L-CSA and in the degree of lesion echogenicity in function of time, but with difference (P<0.05) between groups only for L-CSA, with smaller values in TG. The treatment with PRP promotes greater reduction in the area of the lesion measured by ultrasound.


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