Lee Yeonju, Schmid Marian J, Marx David B, Beatty Mark W, Cullen Diane M, Collins Melissa E, Reinhardt Richard A
Department of Surgical Specialties and Oral Biology, University of Nebraska Medical Center, College of Dentistry, Lincoln, NE 68583, USA.
Biomaterials. 2008 Apr;29(12):1940-9. doi: 10.1016/j.biomaterials.2007.12.045. Epub 2008 Feb 5.
Systemic simvastatin is known to reduce cholesterol and stimulate modest bone formation, but local surgical placement in polylactic acid domes causes robust bone formation and local swelling. A less invasive and more flexible injection protocol was studied to evaluate the bone-inducing effects compared to surgical implantation. Bone formation rate, short- and long-term bone augmentation histology, and mechanical properties were evaluated to characterize the new bone in a rat bilateral mandible model (test and control sides in same animal). Results demonstrated that multiple (3) injections of 0.5 mg simvastatin effectively reduced soft tissue swelling while preserving bone growth (60% increase of bone width at 24 days) compared to simvastatin dome placement (43% increase at 24 days). Compared to controls, bone formation rate was significantly higher on the simvastatin side, especially in the dome. Three-point bending tests revealed higher maximum force to fracture and stiffness at 24 days with simvastatin injections. Long-term evaluation showed that 55% of maximum new bone formed 24 days post-injection was retained at 90 days.
已知全身性辛伐他汀可降低胆固醇并适度刺激骨形成,但将其局部手术放置于聚乳酸穹顶中会导致强劲的骨形成和局部肿胀。为了评估与手术植入相比的骨诱导效果,研究了一种侵入性较小且更灵活的注射方案。通过评估骨形成率、短期和长期骨增量组织学以及力学性能,以在大鼠双侧下颌骨模型(同一动物的测试侧和对照侧)中表征新骨。结果表明,与辛伐他汀穹顶放置相比(24天时增加43%),多次(3次)注射0.5mg辛伐他汀可有效减轻软组织肿胀,同时保持骨生长(24天时骨宽度增加60%)。与对照组相比,辛伐他汀侧的骨形成率显著更高,尤其是在穹顶处。三点弯曲试验显示,注射辛伐他汀后24天,骨折时的最大力和刚度更高。长期评估表明,注射后24天形成的最大新骨的55%在90天时得以保留。