The Radiological Analysis of The Effects Ofraloxifene, Nitric-Oxide and Estrogen on Scoliosis: Abipedal C57bl6 Mice Model

dc.contributor.author Demirkıran, H. Gökhan
dc.contributor.author Baş, Can Emre
dc.contributor.author Acaroğlu, Emre
dc.contributor.author Akel, İbrahim
dc.date.accessioned 2023-06-16T15:06:58Z
dc.date.available 2023-06-16T15:06:58Z
dc.date.issued 2020
dc.description.abstract Objective: Raloxifene (RLX), estrogen and nitric oxide (NO) medications were showed to be related to scoliosis, but the complex mechanism has not yet been elucidated. The prevention and non-surgical treatment of scoliosis may be achieved with these drugs since they are safe for use in humans. We aimed to investigate the effects of oestrogen, RLX and NO on scoliosis progression, bone mineral density and sagittal plan deformities.Materials and Methods: One hundred and fifty-two C57BL6 mice were grouped into bipedal Estrogen, bipedal RLX, bipedal NO, bipedal control and quadrupedal control groups. All of the animals’ forelimbs and tails were amputated, except for the quadrupedal group (n=28), and followedup for five weeks. Estrogen, NO and RLX groups received orally administered Estrogen, NO and RLX after the $5^th$ week for 35 weeks. Anteroposterior and lateral X-ray imaging were done at the$5^th$, $20^th$ and $40^th$ weeks and bone mineral density measurements were done at the $20^th$ and $40^th$ weeks.Results: There was no significant difference in mean Cobb angles between the groups at the fifth, $20^th$ and $40^th$ weeks (p=0.917, p=0.066, p=0.562, respectively). In contrast, a significant increase in mean Cobb angles was found in the quadrupedal group between the $20^th$ and $40^th$ weeks. In addition, no significant difference was found between the groups in terms of scoliosis incidence at the fifth and $20^th$ weeks (p=1.000, p=0.132, respectively). However, when the scoliosis progression was investigated, a decreasing tendency was found in the RLX group compared to the other groups. Although there was a decreasing tendency in terms of the thoracic kyphosis angles and pelvic incidence between the $20^th$ and $40^th$ weeks in all groups, no statistical difference was found. Spinosacral angles increased significantly between the $20^th$ and $40^th$ weeks in all groups, except the quadrupedal group. There was a significant increase of the bone mineral density in the RLX group (p=0.041). Conclusion: RLX may decrease scoliosis progression in a C57BL/6 mice model and increase the bone mineral density. Unlike previous studies, the quadrupedal mice group had a tendency to increase scoliosis progression between the $20^th$ and $40^th$weeks en_US
dc.identifier.doi 10.4274/jtss.galenos.2020.329
dc.identifier.issn 2147-5903
dc.identifier.issn 1301-0336
dc.identifier.uri https://doi.org/10.4274/jtss.galenos.2020.329
dc.identifier.uri https://search.trdizin.gov.tr/yayin/detay/410238
dc.identifier.uri https://hdl.handle.net/20.500.14365/4118
dc.language.iso en en_US
dc.relation.ispartof Journal of Turkish Spinal Surgery en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title The Radiological Analysis of The Effects Ofraloxifene, Nitric-Oxide and Estrogen on Scoliosis: Abipedal C57bl6 Mice Model en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.bip.impulseclass C5
gdc.bip.influenceclass C5
gdc.bip.popularityclass C5
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Ekonomi Üniversitesi en_US
gdc.description.departmenttemp Hacettepe Üniversitesi, Tıp Fakültesi, Ortopedi ve Travmatoloji Anabilim Dalı, Ankara, Türkiye Türkiye Sağlık Bilimleri Üniversitesi, Dışkapı Eğitim ve Araştırma Hastanesi, Ortopedi ve Travmatoloji Kliniği, Ankara, Türkiye Ankara Omurga Merkezi, Ortopedi ve Travmatoloji Anabilim Dalı, Ankara, Türkiye İzmir Ekonomi Üniversitesi, Tıp Fakültesi, İzmir, Türkiye en_US
gdc.description.endpage 206 en_US
gdc.description.issue 4 en_US
gdc.description.publicationcategory Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q4
gdc.description.startpage 201 en_US
gdc.description.volume 31 en_US
gdc.description.wosquality N/A
gdc.identifier.openalex W4238421384
gdc.identifier.trdizinid 410238
gdc.index.type TR-Dizin
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gdc.openalex.collaboration National
gdc.openalex.fwci 0.0
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gdc.opencitations.count 0
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gdc.virtual.author Akel, İbrahim
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