Levy R J, Schoen F J, Lund S A, Smith M S
Division of Pediatric Cardiology, C.S. Mott Children's Hospital, University of Michigan Medical Center, Ann Arbor 48109.
J Thorac Cardiovasc Surg. 1987 Oct;94(4):551-7.
Ethanehydroxydiphosphonate therapy was studied for prevention of calcification of bioprosthetic heart valve cusps (from glutaraldehyde-preserved porcine aortic valves) implanted subcutaneously in 3-week-old male rats. Animals received daily subcutaneous injections of the drug (1, 5, 10, 15, or 25 mg/kg/24 hr) for 21 days with maximal inhibition of bioprosthetic heart valve calcification at a dosage of 15 mg/kg/24 hr (calcium level of diphosphonate-treated bioprostheses 3.5 +/- 0.5 micrograms/ml; calcium level of control bioprostheses, 161.2 +/- 5.0 micrograms/mg), but with irreversibly diminished bone and somatic growth. A dosage optimum was observed at 10 mg/kg/24 hr with significant inhibition of bioprosthetic heart valve calcification (at 21 days, the calcium level was 16.4 +/- 3.6 micrograms/mg) and an absence of adverse effects on epiphyseal development and overall growth. Bioprosthetic heart valves retrieved from animal receiving ethanehydroxydiphosphonate (15 mg/kg/24 hr) for only the first week after implantation had significantly more calcification after 21 days than did bioprostheses from animals treated for 2 or 3 weeks. Bioprostheses explanted after 110 days from animals receiving the drug (15 mg/kg/24 hr) for the first 3 weeks had calcification equivalent to that of untreated control rats. Diphosphonate (15 mg/kg/24 hr) was most efficacious when initiated within 48 hours of bioprosthesis implantation, but was totally ineffective if administered after 1 week. It is concluded that ethanehydroxydiphosphonate optimally prevents bioprosthesis calcification without significant adverse effects on epiphyseal development and overall somatic growth at a dosage of 10 mg/kg/24 hr in rat subdermal implants, but it must be administered by continuous daily injections beginning within 48 hours of the implantation; this approach should be pursued in further long-term circulatory experimental studies because of its possible clinical relevance.
研究了乙烷羟基二膦酸盐疗法对预防皮下植入3周龄雄性大鼠体内的生物人工心脏瓣膜尖(来自戊二醛保存的猪主动脉瓣膜)钙化的作用。动物每天皮下注射该药物(1、5、10、15或25毫克/千克/24小时),持续21天,剂量为15毫克/千克/24小时时对生物人工心脏瓣膜钙化的抑制作用最大(二膦酸盐处理的生物人工瓣膜钙水平为3.5±0.5微克/毫升;对照生物人工瓣膜钙水平为161.2±5.0微克/毫克),但会使骨骼和身体生长不可逆地减少。在10毫克/千克/24小时的剂量下观察到最佳效果,对生物人工心脏瓣膜钙化有显著抑制作用(21天时,钙水平为16.4±3.6微克/毫克),且对骨骺发育和整体生长无不良影响。植入后仅在第一周接受乙烷羟基二膦酸盐(15毫克/千克/24小时)治疗的动物体内取出的生物人工心脏瓣膜,在21天后的钙化程度明显高于接受2或3周治疗的动物体内的生物人工瓣膜。在接受该药物(15毫克/千克/24小时)治疗3周的动物中,110天后取出的生物人工瓣膜钙化程度与未治疗的对照大鼠相当。二膦酸盐(15毫克/千克/24小时)在生物人工瓣膜植入后48小时内开始使用时效果最佳,但在1周后给药则完全无效。结论是,在大鼠皮下植入模型中,乙烷羟基二膦酸盐以10毫克/千克/24小时的剂量可最佳地预防生物人工瓣膜钙化,且对骨骺发育和整体身体生长无显著不良影响,但必须在植入后48小时内开始每日持续注射给药;鉴于其可能的临床相关性,应在进一步的长期循环实验研究中采用这种方法。