Effect of Pentoxifylline Administration on an Experimental Rat Model of Femur Fracture Healing With Intramedullary Fixation

被引:6
作者
Farahani, Mohammad Mahdi Vashghani [1 ]
Farahani, Reza Masteri [2 ]
Mostafavinia, Ataroalsadat [2 ]
Abbasian, Mohammad Reza [3 ]
Pouriran, Ramin [4 ]
Noruzian, Mohammad [5 ]
Ghoreishi, Seyed Kamran [6 ]
Aryan, Arefe [2 ]
Bayat, Mohammad [2 ,7 ]
机构
[1] Shahid Beheshti Univ Med Sci, Paramed Sch, Basic Sci Dept, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Sch Med, Dept Anat Sci & Biol, Tehran, Iran
[3] Shahid Beheshti Univ Med Sci, Dept Orthoped Surg, Akhtar Hosp, Tehran, Iran
[4] Shahid Beheshti Univ Med Sci, Sch Med, Tehran, Iran
[5] Shahid Beheshti Univ Med Sci, Sch Dent, Tehran, Iran
[6] Univ Qom, Dept Stat, Qom, Iran
[7] Shahid Beheshti Univ Med Sci, Sch Med, Cellular & Mol Biol Res Ctr, Tehran, Iran
关键词
Pentoxifylline; Mechanical Phenomena; Biomechanics; Rats; Femoral Fractures; PARATHYROID-HORMONE; BONE-FORMATION; PHOSPHODIESTERASE; OSTEONECROSIS; EPIDEMIOLOGY; TOCOPHEROL; INHIBITOR; ROLIPRAM; THERAPY; TIBIA;
D O I
10.5812/ircmj.29513
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Globally, musculoskeletal injuries comprise a major public health problem that contributes to a large burden of disability and suffering. Pentoxifylline (FIX) has been originally used as a hemorheologic drug to treat intermittent claudication. Previous test tube and in vivo studies reported the beneficial effects of FIX on bony tissue. Objectives: This study aims to evaluate the effects of different dosages of PTX on biomechanical properties that occur during the late phase of the fracture healing process following a complete femoral osteotomy in a rat model. We applied intramedullary pin fixation as the treatment of choice. Materials and Methods: This experimental study was conducted at the Shahid Beheshti University of Medical Sciences, Tehran, Iran. We used the simple random technique to divide 35 female rats into five groups. Group I received intraperitoneal (i.p.) PTX (50 mg/kg, once daily) injections, starting 15 days before surgery, and group 2, group 3, and group 4 received 50 mg/kg, loo mg/kg, and 200 mg/kg i.p. PTX injections, respectively, once daily after surgery. All animals across groups received treatment for six weeks (until sacrificed). Complete surgical transverse osteotomy was performed in the right femur of all rats. At sixweeks after surgery, the femurs were subjected to a three-point bending test. Results: Daily administration of so mg/kg PTX (groups 1 and 2) decreased the high stress load in repairing osteotomized femurs when compared with the control group. The highest dose of PTX (200 mg/kg) significantly increased the high stress load when compared with the control group (P = 0.030), group 1(P = 0.023), group 2 (P = 0.008), and group 3 (P = 0.010), per the LSD findings. Conclusions: Treatment with 200 mg/kg PTX accelerated fracture healing when compared with the control group.
引用
收藏
页数:8
相关论文
共 31 条
[1]   Rapid protein kinase A-mediated activation of cyclic AMP-phosphodiesterase by parathyroid hormone in UMR-106 osteoblast-like cells [J].
Ahlstrom, M ;
Lamberg-Allardt, C .
JOURNAL OF BONE AND MINERAL RESEARCH, 1997, 12 (02) :172-178
[2]   Protective effect of pentoxifylline on growth plate in neonatal rats following long-term phototherapy [J].
Atabek, Mehmet Emre ;
Pirgon, Ozgur ;
Esen, H. Hasan .
PEDIATRIC RESEARCH, 2007, 62 (02) :163-166
[3]  
Aydin K, 2011, EKLEM HAST CERRAHISI, V22, P160
[4]  
BAYAT M, 2014, RECENT PAT REGEN MED, V4, P137, DOI DOI 10.2174/221029650466
[5]  
Bese Nuran Senel, 2003, Radiat Med, V21, P223
[6]  
Casanova Michele, 2014, Bonekey Rep, V3, P550, DOI 10.1038/bonekey.2014.45
[7]  
CIVITELLI R, 1994, J BONE MINER RES, V9, P1407
[8]   Epidemiology and outcomes of osteoporotic fractures [J].
Cummings, SR ;
Melton, LJ .
LANCET, 2002, 359 (9319) :1761-1767
[9]   SAMPLE-SIZE ESTIMATION FOR COMPARING 2 OR MORE TREATMENT GROUPS IN CLINICAL-TRIALS [J].
DAY, SJ ;
GRAHAM, DF .
STATISTICS IN MEDICINE, 1991, 10 (01) :33-43
[10]   Bone regeneration: current concepts and future directions [J].
Dimitriou, Rozalia ;
Jones, Elena ;
McGonagle, Dennis ;
Giannoudis, Peter V. .
BMC MEDICINE, 2011, 9