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Enhancement of fracture healing in the rat, modulated by compounds that stimulate inducible nitric oxide synthase

骨愈合 一氧化氮合酶 老茧 一氧化氮 他达拉非 化学 截骨术 髓内棒 外科 医学 内科学 西地那非 生物 植物
作者
Rebecca Rajfer,A. Kılıç,Andrew S. Neviaser,Leah M. Schulte,Su M Hlaing,Jose Landeros,Mónica G. Ferrini,Edward Ebramzadeh,So Hyun Park
出处
期刊:Bone and Joint Research [British Editorial Society of Bone and Joint Surgery]
卷期号:6 (2): 90-97 被引量:15
标识
DOI:10.1302/2046-3758.62.bjr-2016-0164.r2
摘要

We investigated the effects on fracture healing of two up-regulators of inducible nitric oxide synthase (iNOS) in a rat model of an open femoral osteotomy: tadalafil, a phosphodiesterase inhibitor, and the recently reported nutraceutical, COMB-4 (consisting of L-citrulline, Paullinia cupana, ginger and muira puama), given orally for either 14 or 42 days.Unilateral femoral osteotomies were created in 58 male rats and fixed with an intramedullary compression nail. Rats were treated daily either with vehicle, tadalafil or COMB-4. Biomechanical testing of the healed fracture was performed on day 42. The volume, mineral content and bone density of the callus were measured by quantitative CT on days 14 and 42. Expression of iNOS was measured by immunohistochemistry.When compared with the control group, the COMB-4 group exhibited 46% higher maximum strength (t-test, p = 0.029) and 92% higher stiffness (t-test, p = 0.023), but no significant changes were observed in the tadalafil group. At days 14 and 42, there was no significant difference between the three groups with respect to callus volume, mineral content and bone density. Expression of iNOS at day 14 was significantly higher in the COMB-4 group which, as expected, had returned to baseline levels at day 42.This study demonstrates an enhancement in fracture healing by an oral natural product known to augment iNOS expression.Cite this article: R. A. Rajfer, A. Kilic, A. S. Neviaser, L. M. Schulte, S. M. Hlaing, J. Landeros, M. G. Ferrini, E. Ebramzadeh, S-H. Park. Enhancement of fracture healing in the rat, modulated by compounds that stimulate inducible nitric oxide synthase: Acceleration of fracture healing via inducible nitric oxide synthase. Bone Joint Res 2017:6:-97. DOI: 10.1302/2046-3758.62.BJR-2016-0164.R2.
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