RESUMO

ABSTRACT Purpose: To describe an innovative animal model of eye transplantation used in rabbits. Methods: six Dutch-belted male rabbits were submitted to lateral orbitotomy in the right eye, wide retrobulbar anatomy exposure, dissection of the structures, identification and distal section of the optic nerve followed by anastomosis either by vicryl (group 1) or fibrin glue (group 2). Electroretinography recording was performed before the section of the optic nerve and every 30 seconds after, to monitor the function of retina. Left eye was used as control group. Results: After optic nerve resection and anastomosis, stable ERG amplitude of the right eye was lost after 302 seconds in group 1 and after 296 seconds on group 2. Left eye kept longer stable ERG amplitude curves. Conclusions: The animal model of whole eye transplantation was effective in describing a novel technique to be used in rabbits, with success of the anatomic procedure. Further studies will clarify the best anastomosis methods and maintenance of function of the receptor organ. Translational relevance: this animal model of whole eye transplantation provides a novel perspective for blind patients and the research models, since we describe a novel mammal animal model. This model can be used as basis of a human model of whole eye transplantation in future studies.

RESUMO Objetivo: Descrever uma técnica cirúrgica inovadora para transplante de olho em um modelo animal em coelhos. Métodos: Seis coelhos machos com Dutch Belted foram submetidos à orbitotomia lateral do olho direito, com ampla exposição da anatomia retrobulbar, dissecção do cone muscular, exposição e secção distal do nervo óptico seguida de anastomose por vicryl (Grupo 1) ou cola de fibrina (Grupo 2). O registro da eletrorretinografia foi realizado antes da secção do nervo óptico e a cada 30 segundos após, para monitorar a função da retina. O olho esquerdo foi usado como grupo controle. Resultados: Após a ressecção do nervo óptico, a estabilidade da amplitude da eletrorretinografia foi perdida no olho direito após 302 segundos no Grupo 1 e após 296 segundos no Grupo 2. O olho esquerdo manteve eletrorretinografia estável por períodos mais longos. Conclusão: O modelo animal de transplante total de olho foi eficaz em descrever uma nova técnica cirúrgica para ser utilizada em laboratório com coelhos, com sucesso do procedimento anatômico. Novos estudos esclarecerão os melhores métodos de anastomose e manutenção da função do órgão receptor.

Assuntos

RESUMO

BACKGROUND: Vascularized composite allotransplantation of the eye is an appealing, novel method for reconstruction of the nonfunctioning eye. The authors' group has established the first orthotopic model for eye transplantation in the rat. With advancements in immunomodulation strategies together with new therapies in neuroregeneration, parallel development of human surgical protocols is vital for ensuring momentum toward eye transplantation in actual patients. METHODS: Cadaveric donor tissue harvest (n = 8) was performed with orbital exenteration, combined open craniotomy, and endonasal approach to ligate the ophthalmic artery with a cuff of paraclival internal carotid artery, for transection of the optic nerve at the optic chiasm and transection of cranial nerves III to VI and the superior ophthalmic vein at the cavernous sinus. Candidate recipient vessels (superficial temporal/internal maxillary/facial artery and superficial temporal/facial vein) were exposed. Vein grafts were required for all anastomoses. Donor tissue was secured in recipient orbits followed by sequential venous and arterial anastomoses and nerve coaptation. Pedicle lengths and calibers were measured. All steps were timed, photographed, video recorded, and critically analyzed after each operative session. RESULTS: The technical feasibility of cadaveric donor procurement and transplantation to cadaveric recipient was established. Mean measurements included optic nerve length (39 mm) and caliber (5 mm), donor artery length (33 mm) and caliber (3 mm), and superior ophthalmic vein length (15 mm) and caliber (0.5 mm). Recipient superficial temporal, internal maxillary artery, and facial artery calibers were 0.8, 2, and 2 mm, respectively; and superior temporal and facial vein calibers were 0.8 and 2.5 mm, respectively. CONCLUSION: This surgical protocol serves as a benchmark for optimization of technique, large-animal model development, and ultimately potentiating the possibility of vision restoration transplantation surgery. CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, V.

Assuntos

RESUMO

Vascularized composite allotransplantation represents a potential shift in approaches to reconstruction of complex defects resulting from congenital differences as well as trauma and other acquired pathology. Given the highly specialized function of the eye and its unique anatomical components, vascularized composite allotransplantation of the eye is an appealing method for restoration, replacement, and reconstruction of the nonfunctioning eye. Herein, we describe conventional treatments for eye restoration and their shortcomings as well as recent research and events that have brought eye transplantation closer to a potential clinical reality. In this article, we outline some potential considerations in patient selection, donor facial tissue procurement, eye tissue implantation, surgical procedure, and potential for functional outcomes.

Assuntos

RESUMO

OBJETIVO: Avaliar a reação tecidual à implantação de enxertos homólogos de esclera e dura-máter. MÉTODOS: Foram realizadas cirurgias experimentais em 41 coelhos albinos da raça Nova Zelândia, sendo que dois coelhos foram selecionados, ao acaso, para serem doadores dos enxertos a serem utilizados no experimento. Trinta coelhos foram divididos em dois grupos: grupo D e grupo E, sendo submetidos à implantação dos tecidos homólogos e nove animais constituíram o grupo controle (grupo DE), submetidos à cirurgia sem enxertia. Os olhos foram enucleados e amostras foram colhidas em duas, seis e 12 semanas após o experimento, constituindo os subgrupos I, II e III. RESULTADOS: Foi realizada análise histopatológica qualitativa, além de estudo semiquantitativo comparativo da vascularização e infiltrado inflamatório na esclera e dura-máter transplantadas. Procedeu-se, também, a histomorfometria das medidas do lado dos enxertos com sistema analisador de imagens. Não houve diferença estatisticamente significante comparando-se a vascularização, infiltrado inflamatório e medidas do lado, entre os subgrupos I de esclera em relação à dura-máter, assim como nos subgrupos II. Não foram comparados os subgrupos III, pois foram observados somente fragmentos dos enxertos de dura-máter. CONCLUSÕES: O enxerto de dura-máter mostrou intensa reabsorção e progressiva substituição por tecido conjuntivo frouxo. O enxerto de esclera mostrou discreta reabsorção na periferia com formação de membrana fibrosa mais evidente, integrando este à esclera do hospedeiro.

PURPOSE: To evaluate tissue reaction to implantation of homologous scleral and dura mater grafts. METHODS: Experimental surgeries were performed on 41 albine New Zealand rabbits; two rabbits were selected at random to be graft donors. Thirty rabbits were divided into two groups: group D and group E, receiving grafts of homologous tissues. The remaining nine animals comprised the control group (DE) and were submitted to surgery but with no graft. The eyes were enucleated and samples collected two, six and 12 weeks after the experiment, comprising subgroups I, II and III. RESULTS: A qualitative histopathological analysis was performed together with a comparative semi-quantitative study on vascularization and inflammatory infiltrate in the transplanted sclera and dura mater. Histomorphometry was conducted based on measurements of the grafts with an image analyzing system. There was no statistically significant difference when comparing vascularization, inflammatory infiltrate and measurements between subgroup I in relation to sclera and dura mater, nor in subgroup II. Subgroup III was not compared, since only fragments of dura mater grafts were considered. CONCLUSIONS: The dura mater graft presented intense absorption and progressive replacement of loose connective tissue. And the scleral graft showed discreet absorption in the periphery with formation of a more evident fibrous membrane, integrating the graft into the host sclera.

Assuntos

RESUMO

PURPOSE: To evaluate tissue reaction to implantation of homologous scleral and dura mater grafts. METHODS: Experimental surgeries were performed on 41 albine New Zealand rabbits; two rabbits were selected at random to be graft donors. Thirty rabbits were divided into two groups: group D and group E, receiving grafts of homologous tissues. The remaining nine animals comprised the control group (DE) and were submitted to surgery but with no graft. The eyes were enucleated and samples collected two, six and 12 weeks after the experiment, comprising subgroups I, II and III. RESULTS: A qualitative histopathological analysis was performed together with a comparative semi-quantitative study on vascularization and inflammatory infiltrate in the transplanted sclera and dura mater. Histomorphometry was conducted based on measurements of the grafts with an image analyzing system. There was no statistically significant difference when comparing vascularization, inflammatory infiltrate and measurements between subgroup I in relation to sclera and dura mater, nor in subgroup II. Subgroup III was not compared, since only fragments of dura mater grafts were considered. CONCLUSIONS: The dura mater graft presented intense absorption and progressive replacement of loose connective tissue. And the scleral graft showed discreet absorption in the periphery with formation of a more evident fibrous membrane, integrating the graft into the host sclera.

Assuntos

Assuntos

RESUMO

Cell-lethal developmental mutations, which are presumed to affect the viability of all cells in a mutant embryo, have been distinguished from other development lethals on the basis of the results of parabiosis and transplant experiments. Premature death (p), previously classified as a cell lethal, does not survive parabiosis. However, transplants involving mutant eye, flank epidermis and primordial limb tissue all survived on a normal recipient. The mutant, therefore, cannot be considered a true cell lethal, though it suffers from serious and widespread abnormalities that cannot be corrected by parabiosis. In addition, transplants of mutant branchial mound tissue did not develop into normal gills on a normal recipient. These transplants were the only ones involving mutant endoderm, and their failure supports our hypothesis that the mutation leads to a specific endoderm defect.

Assuntos

Assuntos

RESUMO

1. Gene l is a recessive lethal factor found in the white strain of axolotls. Animals heterozygous for the gene are phenotypically normal. When mated with each other they give offspring 25% of which exhibit the lethal effects of the gene. 2. The l/l homozygotes develop normally to an advanced embryonic stage (Harrison stage 40) before the effects of the gene are first manifested. They then come to display a characteristic combination of abnormalities, including a disproportionately small head, small and poorly developed eyes, abnormal poorly developed gills, undifferentiated limb buds, and reduced overall growth rate. They may feed briefly, but soon stop and invariably die within a few weeks of the time of hatching. 3. The action of gene l has been analyzed by parabiosing mutant and normal embryos, and by grafting various organ primordia reciprocally between mutant and normal embryos. Parabiosis to normal embryos fails to correct the abnormalities of the mutants, although their survival may be somewhat prolonged. Grafts of mutant organ primordia (eye, limb, gill, pronephros, gonad, head) also invariably fail to show improved development or to survive on normal hosts; normal organ primordia develop normally on mutant hosts so long as the mutant survives. These experiments indicate that gene l is a recessive autonomous cell lethal affecting all of the organ systems during late embryonic and early larval development.

Assuntos