Resultado da pesquisa (2)

Termo utilizado na pesquisa Amniotic membrane

#1 - Amniotic membrane: alternative source of mesenchymal stromal cells in several animals species, 36(6):520-525

Abstract in English:

ABSTRACT.- Faita T., Silva V.N., Sattin W.R., Pinheiro A.O. & Ambrósio C.E. 2016. [Amniotic membrane: alternative source of mesenchymal stromal cells in several animals species.] Membrana amniótica: fonte alternativa de células-tronco mesenquimais em diversas espécies animais. Pesquisa Veterinária Brasileira 36(6):520-525. Departamento de Medicina Veterinária, Universidade de São Paulo, Rua Duque de Caxias Norte 225, Campus Fernando Costa, USP, Pirassununga, SP 13635-900, Brazil. E-maol: ceambrosio@usp.br The increasing interest for the use of stem cells in regenerative medicine, is based on their self-renewal capacity, tissue repair and immunomodulation. The therapy with stem cells is a science in formation considered a promising therapeutic alternative for the treatment of various degenerative, hereditary and inflammatory disorders. The search for alternative sources of stem cells of easy obtention and isolation has led to the study of various tissues, includng embryonic attachments such as the amniotic membrane. However for effective therapeutic application are needed studies of the characteristics in vitro and preclinical and clinical trials. Thus, the aim of this study was a literature review regarding the characterization and clinical application of stem cells from the amniotic membrane in several domestic animal species.

Abstract in Portuguese:

RESUMO.- Faita T., Silva V.N., Sattin W.R., Pinheiro A.O. & Ambrósio C.E. 2016. [Amniotic membrane: alternative source of mesenchymal stromal cells in several animals species.] Membrana amniótica: fonte alternativa de células-tronco mesenquimais em diversas espécies animais. Pesquisa Veterinária Brasileira 36(6):520-525. Departamento de Medicina Veterinária, Universidade de São Paulo, Rua Duque de Caxias Norte 225, Campus Fernando Costa, USP, Pirassununga, SP 13635-900, Brazil. E-maol: ceambrosio@usp.br O crescente interesse do uso de células-tronco (CTs) na medicina regenerativa, estão baseadas na sua capacidade de autorrenovação, reparação tecidual e imunomodulação. A terapia utilizando células-tronco é uma ciência em formação considerada uma alternativa terapêutica promissora no tratamento de diversas patologias degenerativas, hereditárias e inflamatórias. A busca por fontes alternativas de CTs que possuam características como fácil obtenção e isolamento, tem levado ao estudo dos mais variados tecidos, onde se inclui os anexos embrionários como a membrana amniótica. Porém, para sua efetiva aplicação terapêutica são necessários estudos de suas características “in vitro”, além de testes pré-clínicos e clínicos. Com isso, o objetivo deste trabalho é realizar uma revisão bibliográfica sobre a caracterização e aplicação clínica das células-tronco da membrana amniótica em diversas espécies de animais domésticos.


#2 - Effects of topical 0.2% Cyclosporine A on corneal neovascularization induced by xenologous amniotic membrane implantation into a corneal stroma micropocket of rats, p.379-386

Abstract in English:

ABSTRACT.- Milani J.F., Barros P.S.M., Guerra J.L. & Brooks D.E. 2008. Effects of topical 0.2% Cyclosporine A on corneal neovascularization induced by xenologous amniotic membrane implantation into a corneal stroma micropocket of rats. Pesquisa Veterinária Brasileira 28(8):379-386. Laboratório de Investigação em Oftalmologia Comparada, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, Av. Prof. Orlando Marques de Paiva 87, São Paulo, SP 05508-900, Brazil. E-mail: pauloeye@usp.br The objective of the study was to evaluate the topical effects of 0.2% Cyclosporine A (CsA) on corneal neovascularization of rats following surgical implantation of equine amniotic membrane into a corneal stroma micropocket. The implantation of xenologous amniotic membrane was performed bilaterally in 90 rats. In the same day of the surgery each right eye started receiving topical CsA twice a day. The left eye received no medication and served as a control. The evaluation of corneal neovascularization was performed by computerized image analysis and histopathological evaluation at 1, 3, 7, 15, 30 and 60 days postoperatively. For the image analysis 10 animals were used per time period, and for the histopathological examination, five animals were used per time period. Image analysis found that corneal neovascularization began on the 3rd postoperative day, reached its peak on the 7th day, and then progressively and rapidly decreased. Statistic analysis indicated that neovascularization of the CsA treated eye on the 7th day was significantly higher than that observed in untreated eyes. On the 30th day, however, this pattern was reversed with the neovascularization observed in the CsA treated eyes declining to the low levels observed on the 3rd day. The degree of neovascularization in the untreated eyes on the 30th day declined to the baseline levels found on day 3 at the 60th day. Histopathological analysis indicated that deposition of collagen in the implanted tissue was completed by the 15th day. Therefore, we concluded that (1) equine amniotic membrane in rat corneal stroma produced an intense neovascularization until the 15th day postoperatively and then regressed, (2) deposition of collagen of the implanted tissue was completed on the 15th day postoperatively, and (3) use of CsA was associated with increase in the corneal neovascularization initially, followed by a quick and intense regression.

Abstract in Portuguese:

ABSTRACT.- Milani J.F., Barros P.S.M., Guerra J.L. & Brooks D.E. 2008. Effects of topical 0.2% Cyclosporine A on corneal neovascularization induced by xenologous amniotic membrane implantation into a corneal stroma micropocket of rats. Pesquisa Veterinária Brasileira 28(8):379-386. Laboratório de Investigação em Oftalmologia Comparada, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, Av. Prof. Orlando Marques de Paiva 87, São Paulo, SP 05508-900, Brazil. E-mail: pauloeye@usp.br The objective of the study was to evaluate the topical effects of 0.2% Cyclosporine A (CsA) on corneal neovascularization of rats following surgical implantation of equine amniotic membrane into a corneal stroma micropocket. The implantation of xenologous amniotic membrane was performed bilaterally in 90 rats. In the same day of the surgery each right eye started receiving topical CsA twice a day. The left eye received no medication and served as a control. The evaluation of corneal neovascularization was performed by computerized image analysis and histopathological evaluation at 1, 3, 7, 15, 30 and 60 days postoperatively. For the image analysis 10 animals were used per time period, and for the histopathological examination, five animals were used per time period. Image analysis found that corneal neovascularization began on the 3rd postoperative day, reached its peak on the 7th day, and then progressively and rapidly decreased. Statistic analysis indicated that neovascularization of the CsA treated eye on the 7th day was significantly higher than that observed in untreated eyes. On the 30th day, however, this pattern was reversed with the neovascularization observed in the CsA treated eyes declining to the low levels observed on the 3rd day. The degree of neovascularization in the untreated eyes on the 30th day declined to the baseline levels found on day 3 at the 60th day. Histopathological analysis indicated that deposition of collagen in the implanted tissue was completed by the 15th day. Therefore, we concluded that (1) equine amniotic membrane in rat corneal stroma produced an intense neovascularization until the 15th day postoperatively and then regressed, (2) deposition of collagen of the implanted tissue was completed on the 15th day postoperatively, and (3) use of CsA was associated with increase in the corneal neovascularization initially, followed by a quick and intense regression.


Colégio Brasileiro de Patologia Animal SciELO Brasil CAPES CNPQ UNB UFRRJ CFMV