Weissenstein C, Human P, Bezuidenhout D, Zilla P
Department of Cardiothoracic Surgery, Cape Heart Centre, University of Cape Town Medical School, South Africa.
J Heart Valve Dis. 2000 Mar;9(2):230-40.
Enhanced fixation of bioprosthetic tissue by both increased concentrations of glutaraldehyde (GA) and the introduction of additional cross-links with L-lysine significantly reduces calcification. We have previously reported that prolonged exposure to high-volume amino-compounds under warm, acidic conditions leads to thorough, non-rebounding GA detoxification. The aim of the present study was to prove that removal of excess GA can amplify the benefits of enhanced GA cross-linking with regard to bioprosthetic tissue calcification.
Porcine ascending aortas and leaflet tissue, and bovine pericardium were immediately fixed using three GA concentrations (0.2%, 1.0%, 3.0% (v/v)) for seven days at 4 degrees C. Samples were allocated to nine groups. Groups I to III received no further treatment (one at each GA concentration); groups IV to IX underwent an additional L-lysine interim step (48 h/37 degrees C/0.1 M) two days before completion of standard seven-day GA fixation; and groups VII to IX were additionally treated with a GA extraction process using high-volume urazole solution (acetic acid buffer, pH 4.5, 37 degrees C, one week) followed by NaBH4 reduction (2 days, 37 degrees C). Samples were implanted subcutaneously in rats (six per group) for six weeks. Tissue calcium was measured by atomic absorption spectrophotometry and examined histologically after von Kossa staining.
Calcification was reduced in all three tissue types by enhanced cross-linking and by extraction of excess GA. Increasing the GA concentration from 0.2% to 3.0% led to a reduction in calcification of 11.5% (p = 0.074; Student's t-test) in leaflets; 63.6% (p <0.0001) in pericardium; and 17.5% (p = 0.034) in aortic wall tissue. The introduction of additional cross-links with L-lysine resulted in a significant reduction of calcium in all tissues (maximally 42.5%, p = 0.0003 in leaflets; 79.3%, p = 0.005 in pericardium; and 49.6%, p <0.0001 in aortic wall; Student's t-test). Optimal reduction in calcification could be achieved with the combined effect of 3.0% GA fixation, L-lysine enhancement and urazole detoxification. When compared with 0.2% GA-fixed tissue, calcification could be reduced by 99.1% in leaflets, 95.9% in pericardium, and 90.8% in aortic wall tissue (p <0.0001 for all tissue types; Student's t-test).
Removal of excess GA from fixed bioprosthetic tissue was capable of markedly improving the anti-calcific effect of enhanced GA cross-linking.
通过提高戊二醛(GA)浓度以及引入与L - 赖氨酸的额外交联来增强生物假体组织的固定,可显著减少钙化。我们之前曾报道,在温暖、酸性条件下长时间暴露于高容量氨基化合物会导致彻底的、无反弹的GA解毒。本研究的目的是证明去除过量的GA可以增强GA交联在生物假体组织钙化方面的益处。
猪升主动脉和瓣叶组织以及牛心包立即用三种GA浓度(0.2%、1.0%、3.0%(v/v))在4℃下固定7天。样本分为九组。第一组至第三组未接受进一步处理(每种GA浓度一组);第四组至第九组在标准的7天GA固定完成前两天额外进行L - 赖氨酸中间步骤(48小时/37℃/0.1M);第七组至第九组还额外用高容量尿唑溶液(乙酸缓冲液,pH 4.5,37℃,一周)进行GA提取处理,随后用NaBH4还原(2天,37℃)。样本皮下植入大鼠(每组6只)六周。通过原子吸收分光光度法测量组织钙含量,并在冯·科萨染色后进行组织学检查。
通过增强交联和去除过量GA,所有三种组织类型的钙化均减少。将GA浓度从0.2%提高到3.0%导致瓣叶钙化减少11.5%(p = 0.074;学生t检验);心包钙化减少63.6%(p <0.0001);主动脉壁组织钙化减少17.5%(p = 0.034)。引入与L - 赖氨酸的额外交联导致所有组织中的钙显著减少(瓣叶最大减少42.5%,p = 0.0003;心包减少79.3%,p = 0.005;主动脉壁减少49.6%,p <0.0001;学生t检验)。通过3.0% GA固定、L - 赖氨酸增强和尿唑解毒的联合作用可实现钙化的最佳减少。与0.2% GA固定的组织相比,瓣叶钙化可减少99.1%,心包钙化可减少95.9%,主动脉壁组织钙化可减少90.8%(所有组织类型p <0.0001;学生t检验)。
从固定的生物假体组织中去除过量的GA能够显著提高增强GA交联的抗钙化效果。