Effects of local application of bovine amniotic fluid on fracture healing in rats (Rattus norvegicus)
Abstract
In this study, it was aim to examine the local application of bovine amniotic fluid on bone fracture healing in rats. Twenty female sprague dawley rats included in the study were divided into 2 groups of 10. The sham group (n=10): Bone fractures were created in the right tibia bones of the rats and fixed with kirschner wire. After a four–week recovery period, the subjects were sacrificed. Local bovine amniotic fluid group (n=10): Bone fractures were created in the right tibia bones of the rats and local bovine amniotic fuid was applied during fixation with kirschner wire. After a four–week recovery period, the subjects were sacrificed. Samples from all subjects were decalcified, stained with hematoxylin and eosin, and new bone formation and fibrosis were analyzed. When the groups were evaluated in terms of new bone regeneration, it was determined that the new bone regeneration in the subjects treated with local bovine amniotic fluid were statistically significantly higher than sham group (P<0.05). When the groups were evaluated in terms of fibrosis, the fibrosis value in the sham group was found to be statistically significantly higher when compared with the local bovine amniotic fluid group (P<0.05). It can be stated that local bovine amniotic fluid application may positively affect the healing of bone fractures.
Downloads
References
Acikan I, Dundar S. Biomechanical Examination of Osseointegration of Titanium Implants Placed Simultaneously With Allogeneic Bone Transfer. J. Craniofac. Surg. [Internet]. 2022; 33(1):350–353. doi: https://doi.org/gp5nmd
Padilla–Eguiluz NG, Gómez–Barrena E. Epidemiology of long bone non–unions in Spain. Injury. [Internet]. 2021; 52(Suppl4):S3–S7. doi: https://doi.org/mhsc
Wakefield SM, Giannoudis VP, Giannoudis PV. Reconstruction of a neglected hyperextension–bicondylar tibial plateau fracture 9 months after original injury and review of the literature. What outcomes can be expected? Trauma Case Rep. [Internet]. 2023; 45:e100823. doi: https://doi.org/mhss
Andrzejowski P, Giannoudis PV. The 'diamond concept' for long bone non–union management. J. Orthop Traumatol. [Internet]. 2019; 20(21):21–22. doi: https://doi.org/gh7zs5
Rodrigues M, Blattner C, Stuppia L. Amniotic Fluid Cells, Stem Cells, and p53: Can We Stereotype p53 Functions? Intern. J. Mol. Sci. [Internet]. 2019; 20(9):2236. doi: https://doi.org/mhsd
Fadhil E, Dosh RH, Wally ZJ, Haider J. Histological evaluation of the effects of bone morphogenetic protein 9 and angiopoietin 1 on bone healing. J. Taibah Univ. Med. Sci. [Internet]. 2023; 18(5):954–963. doi: https://doi.org/mhst
Mi J, Xu J, Yao H, Li X, Tong W, Li Y, Dai B, He X, Chow DHK, Li G, Lui KO, Zhao J, Qin L. Calcitonin Gene–Related Peptide Enhances Distraction Osteogenesis by Increasing Angiogenesis. Tissue Eng. Part A. [Internet]. 2021; 27(1–2):87–102. doi: https://doi.org/mhsf
Al Ruhaimi KA. Effect of calcium sulphate on the rate of osteogenesis in distracted bone, International J. Oral Maxillofacial Surgery. [Internet]. 2001; 30(3):228–233. doi: https://doi.org/fv8xnp
Akbulut Y, Gul M, Dundar S, Ozcan EC, Ozercan IH, Bozoglan A, Karasu N, Acikan I, Bingül MB. Evaluation of Effects of Systemic Zoledronic Acid Application on Bone Maturation in the Consolidation Period in Distraction Osteogenesis. J. Craniofac. Surg. [Internet]. 2021; 32(8):2901–2905. doi: https://doi.org/mhsg
Hagiwara T, Bell WH. Effect of electrical stimulation on mandibular distraction osteo–genesis. J. Craniomaxillofac. Surg. [Internet]. 2000; 28(1):12–19. doi: https://doi.org/cg9djh
Schortinghuis J, Bronckers AL, Gravendeel J, Stegenga B, Raghoebar GM. The effect of ultrasound on osteogenesis in the vertically distracted edentulous mandible: a double–blind trial. Intern. J. Oral Maxillofac. Surg. [Internet]. 2008; 37(11):1014–1021. doi: https://doi.org/cw8qsr
Hannouche D, Petite H, Sedel L. Current trends in the enhancement of fracture healing. J.Bone Joint Surg. Br. [Internet]. 2001; 83(2):15. doi: https://doi.org/bx48z8
Kerimoglu S, Livaoglu M, Sonmez B, Yulug E, Aynaci O, Topbas M, Yarar S. Effects of human amniotic fluid on fracture healing in rat tibia. J. Surg. Res. [Internet]. 2009; 152(2):281–287. doi: https://doi.org/dd5t62
Karaçal N, Koşucu P, Çobanoğlu Ü, Kutlu N. Effect of Human Amniotic Fluid on Bone Healing. J. Surg. Res. [Internet]. 2005; 129(2):283–287 doi: https://doi.org/bzr773
Gokce SM, Karacayli U, Nalcaci R, Avunduk MC, Özgöçmen M, Karasahin E, Gokce HS: The effect of human amniotic fluid on mandibular distraction osteogenesis. Intern. J. Oral Maxillofac. Surg. [Internet]. 2015; 44(3):404–411. doi: https://doi.org/f633kk
Dasari G, Prince I, Hearn MTW. Investigations into the rheological characteristics of bovine amniotic fluid. J. Biochem. Biophys. Meth. [Internet]. 1995; 30(4):217–225. doi: https://doi.org/dhbhbb
Ravelich SR, Breier BH, Reddy S,Keelan JA, Wells DN, Peterson AJ, Lee SF. Insulin–like growth factor–I and binding proteins 1, 2, and 3 in bovine nuclear transfer pregnancies. Biol. Reprod. [Internet]. 2004; 70(2):430–438. doi: https://doi.org/cdszx4
Decker M, Chiu ES, Dollbaum C, Moiin A, Hall J, Spendlove R, Longaker MT, Stern R. Hyaluronic acid–stimulating activity in sera from the bovine fetus and from breast cancer patients. Cancer Res. [Internet]. 1989; 49(13):3499–3505. Cited in PUBMED; PMID 2731171.
Tanrisever M, Eröksüz H, Bulut S. The comparison of the effects of intraarticular injections of bovine amniotic fluid and hyaluronic acid on cartilage tissue in an experimental osteoarthritic rabbit model: histopathological and immunohistochemical results. Turk. J. Vet. Anim. Sci. [Internet]. 2017; 41(2):273–281. doi: https://doi.org/mhsj
Lee HS,. Kim JC. Effect of amniotic fluid in corneal sensitivity and nerve regeneration after excimer laser ablation. Cornea. [Internet]. 1996; 15(5):517–524. Cited in PUBMED; PMID 8862929
Gunes N, Dundar S, Saybak A, Artas G, Acikan I, Ozercan I.H, Atilgan S, Yaman F. Systemic and local zoledronic acid treatment with hydroxyapatite bone graft: A histological and histomorphometric experimental study. Experim. Therap. Med. [Internet]. 2016;12(4):2417–2422. doi: https://doi.org/gbr3bs
Kim JS, Kim JC, Na BK, Jeong JM, Song CY. Amniotic membrane patching promotes healing and inhibits proteinase activity on wound healing following acute corneal alkali burn. Exp. Eye Res. [Internet]. 2000; 70(3):329–337. doi: https://doi.org/fwqnf3
Sato H, Shimazaki J, Shinozaki N, Tsuboto K. Role of growth factors for ocular surface reconstruction after amniotic membrane transplantation. Invest. Ophthalmol. Vis. Sci. 1998; 39:428.
Piamo A, García M, Romero D, Ferrer D. Healing of a chronic ulcer of the lower limb of venous origin with fresh human amniochorionic membrane allograft. Biomed. [Internet]. 2022; 42(Suppl 1):17–25. doi: https://doi.org/mhsk
Marangon FB, Alfonso EC, Miler D, Remonda NM, Mualem MS, Tseng SC. Incidence of microbial infection after amniotic membrane. Cornea. [Internet]. 2004; 23(3):264–269. doi: https://doi.org/fxf6zm
Dasari G, Prince I, Hearn MTW. Investigations into the rheological characteristics of bovine amniotic fluid. J. Biochem. Biophys. Meth. [Internet]. 1995; 30(4):217–225. doi: https://doi.org/dhbhbb
Ravelich SR, Breier BH, Reddy S, Keelan JA, Wells DN, Pteterson AJ, Lee RSF. Insulin–like growth factor–1 and binding proteins 1, 2, and 3 in bovine nuclear transfer pregnancies. Biol. Reprod. [Internet]. 2004; 70(2):430–438. doi: https://doi.org/cdszx4
Longaker MT, Adzick NS, Hall JL, Stair SE, Crombleholme TM, Duncan BW, Bradley SM, Harrison MR, Stern R. Studies in fetal wound healing, VII. Fetal wound healing may be modulated by hyaluronic acid stimulating activity in amniotic fluid. J. Pediatr. Surg. [internet]. 1990; 25(4):430–433. doi: https://doi.org/dhb9b5
Decker M, Chiu ES, Dolbaum C, Moiin A, Hall J, Longaker MT, Spendlove R, Stern R. Hyaluronic acid stimulating factor from the bovine fetus and from breast cancer patients. Cancer Res. [Internet]. 1989; 49(13):3499–3505. Cited in PUBMED; PMID 2731171.
Copyright (c) 2024 Murat Tanrısever, Ozmen Istek, Hatıce Eroksuz, Burak Karabulut, Erhan Cahıt Ozcan, Muhammet Bahattın Bıngul, Rıdvan Guler, Serkan Dundar
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.