Journals / Eklem Hastalıkları ve Cerrahisi Dergisi (Eski Adı: Artroplasti Artroskopik Cerrahi Derg.) / 2015 / Cilt: 26 - Sayı: 3

Bir fosfodiesteraz 5 inhibitörü olan tadalafilin sıçan femurunda kırık iyileşmesi üzerindeki olumlu etkisi

Positive effect of tadalafil, a phosphodiesterase-5 inhibitor, on fracture healing in rat femur

Pages
137–144
Publication Date
2022-10-18
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Conclusion: This study demonstrated that tadalafil accelerates fracture healing by enhancing osseous tissue formation similar to sildenafil.

📌 3 Key Takeaways

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Objective & Hypothesis:Objectives: This study aims to investigate whether tadalafil accelerates fracture healing with an efficiency equal to that of sildenafil.
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Key Findings & Data:Forty-eight male Wistar albino rats (mean age 13 weeks; range 12 to 14 weeks) were divided into three groups: 16 received sildenafil (5 mg/kg/day per oral), 16 received tadalafil (1 mg/kg/day per oral), and 16 (control group) received saline daily.
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Conclusion & Impact:Conclusion: This study demonstrated that tadalafil accelerates fracture healing by enhancing osseous tissue formation similar to sildenafil.
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objectives: This study aims to investigate whether tadalafil accelerates fracture healing with an efficiency equal to that of sildenafil. Materials and methods: Fracture healing was studied using a rat closed femur fracture model. Forty-eight male Wistar albino rats (mean age 13 weeks; range 12 to 14 weeks) were divided into three groups: 16 received sildenafil (5 mg/kg/day per oral), 16 received tadalafil (1 mg/kg/day per oral), and 16 (control group) received saline daily. After two and five weeks, eight rats from each group were euthanized and bone healing was evaluated using radiographic, histologic, and histomorphometric analyses. Results: At second week, radiologic score of tadalafil group was higher than the sildenafil treated groups and the sildenafil and tadalafil groups both had higher radiographic scores than the control group, all groups had similar scores at fifth week. The sildenafil and tadalafil treated group exhibited smaller callus diameter at the second week comparing to control group but the difference was not statistically significant, while callus diameter was significantly smaller in tadalafil group when compared to the control group in fifth week. Compared with the control group, cartilage percentage of the callus was lower in the sildenafil group at two weeks and lower in both the tadalafil and sildenafil groups at five weeks. There were no differences between the tadalafil and sildenafil groups regarding the radiographic scores, callus size, cartilage and osseous callus percentage, and the qualitative bridging scores at second or fifth week. Conclusion: This study demonstrated that tadalafil accelerates fracture healing by enhancing osseous tissue formation similar to sildenafil.

Özet

Amaç: Bu çalışmada tadalafilin kırık iyileşmesini sildenafille eşit bir etkinlikte hızlandırıp hızlandırmadığı araştırıldı. Gereç ve yöntemler: Kırık iyileşmesi sıçan kapalı femur kırığı örneği kullanılarak incelendi. Kırk sekiz erkek Wistar albino sıçan (ort. yaş 13 hafta; dağılım 12-14 hafta) üç gruba ayrıldı: 16sına sildenafil (5 mg/kg/gün, oral), 16sına tadalafil (1 mg/kg/gün, oral) ve 16sına (kontrol grubu) her gün serum fizyolojik verildi. İki ve beş hafta sonra her gruptan sekiz sıçana ötanazi yapıldı ve kemik iyileşmesi radyolojik, histolojik ve histomorfometrik analizlerle değerlendirildi. Bulgular: İkinci haftanın sonunda tadalafil grubunun radyolojik skoru sildenafil grubundan yüksek ve her tadanafil hem sidenafil gruplarının skoru kontrol grubundan yüksekken, beşinci haftanın sonunda tüm grupların skorları benzerdi. Sildenafil ve tadalafil uygulanan gruplarda ikinci haftada kallus çapı kontrol grubuna göre daha küçük olarak saptanmış olsa da bu fark istatistiksel olarak anlamlı değildir. Beşinci haftadaki kallus çapı tadalafil grubunda kontrol grubuna göre anlamlı olarak küçüldü. Kontrol grubu ile karşılaştırıldığında, kallusun kıkırdak yüzdesi ikinci haftanın sonunda sildenafil grubunda daha düşük, beşinci haftanın sonunda hem tadalafil hem sildenafil grubunda daha düşüktü. Tadalafil ve sildenafil grupları arasında radyolojik skorlar, kallus çapı, kallusun kıkırdak ve kemik yüzdeleri ve köprüleşme skorları açısından ikinci ve beşinci haftanın sonunda farklılık yoktu. Sonuç: Bu çalışma; tadalafilin sildenafil ile benzer şekilde kemik doku oluşumunu artırarak kırık iyileşmesini hızlandırdığını göstermiştir.

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Cite This Article

KORKUSUZ, P., TOĞRAL, G., EKŞİOĞLU, M. F., ARIKAN, Ş. M., HESAR, R. H. (2022). Bir fosfodiesteraz 5 inhibitörü olan tadalafilin sıçan femurunda kırık iyileşmesi üzerindeki olumlu etkisi. Eklem Hastalıkları ve Cerrahisi Dergisi (Eski Adı: Artroplasti Artroskopik Cerrahi Derg.), Cilt: 26 - Sayı: 3, 137–144. https://ajindex.com/articles/498537

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References (14)

  1. Akkaya S, Nazalı M, Kılıç A, Bir F. Cefazolin-sodium has no adverse effect on fracture healing in an experimental rabbit model. Eklem Hastalik Cerrahisi 2012;23:44-8
  2. Halıcı M, Öner M, Güney A, Canöz Ö, Narin F, Halıcı C. Melatonin promotes fracture healing in the rat model. Eklem Hastalik Cerrahisi 2010;21:172-7
  3. Keramaris NC, Calori GM, Nikolaou VS, Schemitsch EH, Giannoudis PV. Fracture vascularity and bone healing: a systematic review of the role of VEGF. Injury 2008;39:45-57
  4. Hankenson KD, Zimmerman G, Marcucio R. Biological perspectives of delayed fracture healing. Injury 2014;45:8-15
  5. Histing T, Garcia P, Matthys R, Leidinger M, Holstein JH, Kristen A, et al. An internal locking plate to study intramembranous bone healing in a mouse femur fracture model. J Orthop Res 2010;28:397-402
  6. Oktaş B, Orhan Z, Erbil B, Değirmenci E, Ustündağ N. Effect of extracorporeal shock wave therapy on fracture healing in rat femural fractures with intact and excised periosteum. Eklem Hastalik Cerrahisi 2014;25:158-62
  7. Chaubey A, Grawe B, Meganck JA, Dyment N, Inzana J, Jiang X, et al. Structural and biomechanical responses of osseous healing: a novel murine nonunion model. J Orthop Traumatol 2013;14:247-57
  8. Lu CY, Chuang HY, Yu FJ, Sun LC, Shih YL, Chen FM, et al. Hypocaloric peripheral parenteral nutrition with lipid emulsion in postoperative gastrointestinal cancer patients. World J Gastrointest Oncol 2010;2:51-5
  9. Lienau J, Schell H, Epari DR, Schütze N, Jakob F, Duda GN, et al. CYR61 (CCN1) protein expression during fracture healing in an ovine tibial model and its relation to the mechanical fixation stability. J Orthop Res 2006;24:254-62
  10. Gur S, Kadowitz PJ, Serefoglu EC, Hellstrom WJ. PDE5 inhibitor treatment options for urologic and non-urologic indications: 2012 update. Curr Pharm Des 2012;18:5590-606
  11. Histing T, Marciniak K, Scheuer C, Garcia P, Holstein JH, Klein M, et al. Sildenafil accelerates fracture healing in mice. J Orthop Res 2011;29:867-73
  12. Yaman F, Atilgan S, Günes N, Agacayak S, Günay A, Ucan MC, et al. Phosphodiesterase-5 inhibitors may facilitate bone defect recovery. Eur Rev Med Pharmacol Sci 2011;15:1301-5
  13. Akgül T, Alemdaroğlu B. Phosphodiesterase 5 inhibitors may facilitate bone fracture recovery. Med Hypotheses 2008;70:461-2
  14. Smith WB, McCaslin IR, Gokce A, Mandava SH, Trost L, Hellstrom WJ. PDE5 inhibitors: considerations for preference and long-term adherence. Int J Clin Pract 2013;67:768-80. 1