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Human saphenous vein organ culture under controlled hemodynamic conditions
Miyakawa, Ayumi Aurea; Dallan, Luis Alberto Oliveira; Lacchini, Silvia; Borin, Thaiz Ferraz; Krieger, Jose Eduardo.
Afiliação
  • Miyakawa, Ayumi Aurea; Universidade de São Paulo. Faculdade de Medicina. Heart Institute. São Paulo. BR
  • Dallan, Luis Alberto Oliveira; Universidade de São Paulo. Faculdade de Medicina. Heart Institute. São Paulo. BR
  • Lacchini, Silvia; Universidade de São Paulo. Faculdade de Medicina. Heart Institute. São Paulo. BR
  • Borin, Thaiz Ferraz; Universidade de São Paulo. Faculdade de Medicina. Heart Institute. São Paulo. BR
  • Krieger, Jose Eduardo; Universidade de São Paulo. Faculdade de Medicina. Heart Institute. São Paulo. BR
Clinics ; Clinics;63(5): 683-688, 2008. ilus, graf
Article em En | LILACS | ID: lil-495045
Biblioteca responsável: BR1.1
ABSTRACT

INTRODUCTION:

Saphenous vein grafting is still widely used to revascularize ischemic myocardium. The effectiveness of this procedure is limited by neointima formation and accelerated atherosclerosis, which frequently leads to graft occlusion. A better understanding of this process is important to clarify the mechanisms of vein graft disease and to aid in the formulation of strategies for prevention and/or therapeutics.

OBJECTIVE:

To develop an ex vivo flow system that allows for controlled hemodynamics in order to mimic arterial and venous conditions.

METHODS:

Human saphenous veins were cultured either under venous (flow 5 ml/min) or arterial hemodynamic conditions (flow 50 ml/min, pressure 80 mmHg) for 1-, 2- and 4-day periods. Cell viability, cell density and apoptosis were compared before and after these intervals using MTT, Hoeschst 33258 stain, and TUNEL assays, respectively.

RESULTS:

Fresh excised tissue segments were well preserved prior to the study. Hoechst 33258 and MTT stains showed progressive losses in cell density and cell viability in veins cultured under arterial hemodynamic conditions from 1 to 4 days, while no alterations were observed in veins cultured under venous conditions. Although the cell density from 1-day cultured veins under arterial conditions was similar to that of freshly excised veins, the TUNEL assay indicated that most of these cells were undergoing apoptosis.

CONCLUSION:

The results observed resemble the events taking place during early in vivo arterial-vein grafting and provide evidence that an ex vivo perfusion system may be useful for the identification of new therapeutic targets that ameliorate vein graft remodeling and increase graft patency over time.
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Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Assunto principal: Técnicas de Cultura de Órgãos / Perfusão / Veia Safena / Hemodinâmica / Modelos Cardiovasculares Limite: Humans Idioma: En Revista: Clinics Assunto da revista: MEDICINA Ano de publicação: 2008 Tipo de documento: Article / Project document País de afiliação: Brasil País de publicação: Brasil
Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Assunto principal: Técnicas de Cultura de Órgãos / Perfusão / Veia Safena / Hemodinâmica / Modelos Cardiovasculares Limite: Humans Idioma: En Revista: Clinics Assunto da revista: MEDICINA Ano de publicação: 2008 Tipo de documento: Article / Project document País de afiliação: Brasil País de publicação: Brasil