Decellularization as an anticalcification method in stentless bovine pericardium valve prosthesis: a study in sheep.

OBJECTIVE: The objective was to analyze the decellularization process with SDS in glutaraldehyde-preserved bovine pericardium as an anticalcification method in a circulatory sheep model. METHODS: The valved tubs were implanted in pulmonary artery position in sheep by 180 days. The animals were divided in two groups of 8 animals: control group--glutaraldehyde-preserved bovine pericardium and the study group--decellularized bovine pericardium with 0,1% SDS and glutaraldehyde-preserved. After explantation the tubs were analized by x-ray macroscopy, hematoxilin-eosin, alizarin-red and Russel-Movatz pentacromic histology. The calcium content was measured by flame atomic absorption spectrometry. RESULTS: There was no early mortality, but two animals in each group died during the study. All cusps in the control group were severely calcified and in some points in the conduits, while the decellularized group did not show macroscopic calcification. Data were proved by x-ray and histologycal exams. The matrix was preserved in histologycal analysis in decellularized group, without gross calcification. The wall conduits calcium content was 35,25 ± 42,13 µg/mg in the control group versus 15,75 ± 10,44 µg/mg in the decellularized one: in the cusps was 264,4 ± 126,16 µg/mg in control group versus 94,29 ± 27,05 µg/mg in decellularized group (P = 0,009). CONCLUSION: The decellularization with 0.1% SDS was effective as an anticalcification method in bovine pericardial grafts implanted in a sheep circulatory model for 180 days.

Descelularização como método anticalcificante em próteses valvares de pericárdio bovino sem suporte: estudo em ovinos / Decellularization as an anticalcification method in stentless bovine pericardium valve prosthesis: a study in sheep

OBJETIVO: Avaliar o processo de descelularização com dodecil sulfato de sódio (SDS) como método anticalcificante em próteses de pericárdio bovino fixadas em glutaraldeído, em modelo circulatório de ovinos. MÉTODOS: Tubos valvulados de pericárdio bovino foram implantados em posição pulmonar de ovinos por 180 dias. Os animais foram divididos em dois grupos com oito animais: grupo controle, com condutos de pericárdio fixado em glutaraldeído e grupo estudo, com pericárdio descelularizado com SDS 0,1% e posteriormente fixado em GDA. Os explantes foram submetidos à análise macroscópica, histológica com hematoxilina-eosina, alizarina-red e pentacrômico de Russel-Movatz, estudo radiológico e quantificação de cálcio com espectrometria de absorção atômica. RESULTADOS: Não houve mortalidade imediata, porém dois animais de cada grupo faleceram na evolução tardia. Os enxertos do grupo controle apresentavam intensa calcificação das cúspides e em algumas regiões dos condutos, enquanto que os enxertos descelularizados apresentavam-se preservados, sem calcificações macroscópicas evidentes. Esses resultados foram comprovados por análise histológica e radiográfica. Histologicamente, os enxertos descelularizados tiveram sua matriz melhor preservada e com diminuição acentuada da calcificação. O conteúdo de cálcio nos condutos foi de 35±42 µg/mg de tecido no grupo controle versus 15 ±10 µg/mg nos descelularizados. Nas cúspides valvares, esses valores foram de 264±126 µg/mg no grupo controle versus 94±27 µg/mg nos descelularizados (P=0,009). CONCLUSÃO: A descelularização com SDS 0,1% foi efetiva como método anticalcificante em condutos de pericárdio bovino implantados em modelo circulatório de ovinos por 180 dias.

OBJECTIVE: The objective was to analyze the decellularization process with SDS in glutaraldehyde-preserved bovine pericardium as an anticalcification method in a circulatory sheep model. METHODS: The valved tubs were implanted in pulmonary artery position in sheep by 180 days. The animals were divided in two groups of 8 animals: control group glutaraldehyde-preserved bovine pericardium and the study group - decellularized bovine pericardium with 0,1% SDS and glutaraldehyde-preserved. After explantation the tubs were analized by x-ray macroscopy, hematoxilin-eosin, alizarin-red and Russel-Movatz pentacromic histology. The calcium content was measured by flame atomic absorption spectrometry. RESULTS: There was no early mortality, but two animals in each group died during the study. All cusps in the control group were severely calcified and in some points in the conduits, while the decellularized group did not show macroscopic calcification. Data were proved by x-ray and histologycal exams. The matrix was preserved in histologycal analysis in decellularized group, without gross calcification. The wall conduits calcium content was 35,25±42,13 µg/mg in the control group versus 15,75±10,44 µg/mg in the decellularized one: in the cusps was 264,4±126,16 µg/mg in control group versus 94,29±27,05 µg/mg in decellularized group (P=0,009). CONCLUSION: The decellularization with 0.1% SDS was effective as an anticalcification method in bovine pericardial grafts implanted in a sheep circulatory model for 180 days.