Webb C L, Benedict J J, Schoen F J, Linden J A, Levy R J
Division of Pediatric Cardiology, C.S. Mott Children's Hospital, University of Michigan Medical Center, Ann Arbor 48109-0576.
Ann Thorac Surg. 1988 Sep;46(3):309-16. doi: 10.1016/s0003-4975(10)65932-2.
Calcification is the principal mode of failure of bioprosthetic heart valves (BPHV) fabricated from glutaraldehyde-pretreated porcine aortic valves or bovine pericardium. Covalent binding of aminopropanehydroxy-diphosphonate (APDP) to residual glutaraldehyde in pericardial BPHV tissue was studied as an approach for the inhibition of calcification. BPHV tissue was preincubated in 0.14 M APDP at pH 7.4, 9.0, and 11.0 for various durations (1 hour to 8 days). The need for NaBH4 stabilization of the tissue-bound APDP was also examined in vitro. The bound APDP was determined using 14C-labeled APDP. APDP uptake was dependent on incubation duration and pH. Calcification of APDP-pretreated BPHV was studied using 21-day rat subdermal implants. Calcification inhibition was directly related to the amount of tissue APDP incorporation. Inhibition of calcification to less than 15% of control was achieved with a concentration of bound APDP of greater than or equal to 30 nM/mg dry tissue with more than 1 hour of incubation at pH 11.0 (bound APDP, 33.55 nM/mg; BPHV calcium content = 3.1 +/- 0.9 micrograms/mg). No adverse effects such as rat growth inhibition or disruption of bone architecture were observed after any treatment. Additionally, in vitro, NaBH4 stabilized tissue-bound APDP. In conclusion, APDP covalently bound to residual aldehyde functions markedly inhibited calcification of BPHV tissue. This inhibition was dependent on the amount of APDP incorporated. NaBH4 stabilized APDP-glutaraldehyde covalent bonds.
钙化是由戊二醛预处理的猪主动脉瓣或牛心包制成的生物人工心脏瓣膜(BPHV)失效的主要方式。研究了氨基丙烷羟基二膦酸盐(APDP)与心包BPHV组织中残留戊二醛的共价结合,作为抑制钙化的一种方法。将BPHV组织在pH值为7.4、9.0和11.0的0.14 M APDP中预孵育不同时间(1小时至8天)。还在体外研究了用硼氢化钠稳定组织结合的APDP的必要性。使用14C标记的APDP测定结合的APDP。APDP的摄取取决于孵育时间和pH值。使用21天大鼠皮下植入物研究了APDP预处理的BPHV的钙化情况。钙化抑制与组织中APDP的掺入量直接相关。在pH值为11.0时孵育超过1小时,结合的APDP浓度大于或等于30 nM/mg干组织(结合的APDP,33.55 nM/mg;BPHV钙含量 = 3.1 +/- 0.9微克/mg),钙化抑制率达到对照的15%以下。任何处理后均未观察到诸如大鼠生长抑制或骨结构破坏等不良影响。此外,在体外,硼氢化钠稳定了组织结合的APDP。总之,与残留醛功能共价结合的APDP显著抑制了BPHV组织的钙化。这种抑制取决于APDP的掺入量。硼氢化钠稳定了APDP - 戊二醛共价键。