Dergiler / Acta Orthopaedica et Traumatologica Turcica / 2021 / Cilt: 55 - Sayı: 2

Effects of tamoxifen therapy on sciatic nerve crush injury: An experimental study in rats

Sayfa
87–93
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

In the immunohistochemical analysis, S100 immunoreactivitywas found significantly higher in group SNI than in the other 2 groups (p<0.05).Conclusion: The histomorphometric, histopathological, and immunohistochemical data obtained from this study have shown that tamoxifen has a beneficial effect on sciatic nerve crush injury in the experimental rat model.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Objective: This study aimed to determine the effects of tamoxifen on sciatic nerve crush injury in a rat model using histopathological,histomorphometric, and immunohistochemical approaches.Methods: In this study, 24 male Sprague-Dawley rats aged of 5 to 7 weeks and weighing between 300 g and 400g were used.
📊
Temel Bulgular & Veri:The ratswere randomly divided into 3 groups: control (group C), sciatic nerve injury (group SNI), and sciatic nerve injury with tamoxifen (groupSNT).
💡
Sonuç & Katkı:In the immunohistochemical analysis, S100 immunoreactivitywas found significantly higher in group SNI than in the other 2 groups (p<0.05).Conclusion: The histomorphometric, histopathological, and immunohistochemical data obtained from this study have shown that tamoxifen has a beneficial effect on sciatic nerve crush injury in the experimental rat model.
🔬Tür:Modelleme & Sayısal Simülasyon
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Objective: This study aimed to determine the effects of tamoxifen on sciatic nerve crush injury in a rat model using histopathological,histomorphometric, and immunohistochemical approaches.Methods: In this study, 24 male Sprague-Dawley rats aged of 5 to 7 weeks and weighing between 300 g and 400g were used. The ratswere randomly divided into 3 groups: control (group C), sciatic nerve injury (group SNI), and sciatic nerve injury with tamoxifen (groupSNT). The sciatic nerve crush injury model was performed using the De Koning’s crush force method. In group C, only a skin incisionwas made and then the skin was sutured. In group SNI, the injury model was performed but no treatment was applied. In group SNT, theinjury model was executed, and then 40 mg/kg/day tamoxifen was given for 4 weeks by intraperitoneal methods. At the end of 4 weeks,all animals were killed using high doses of an anesthetic. Approximately, 2-cm sciatic nerve samples were obtained for histopathological,histomorphometric, and immunohistochemical analyses using the old skin incision.Results: In the histopathological examination, vascular congestion and density of vacuolization were significantly lower in group SNTthan in group SNI (p<0.05). In the histomorphometric examination, the mean sciatic nerve diameter was 306±62 µm in group C, 510±42µm in group SNI, and 204±23 µm in group SNT. A significant difference was observed in the sciatic nerve diameter measurements amongthe 3 groups (p<0.05). In pairwise comparisons, the mean sciatic nerve diameter was significantly lower in group SNT than in group SNI(p=0.00002). Sciatic nerve diameter measurements of both groups were found to be significantly higher than group C (p<0.05). The meanepineurium thickness was 17±0.8 µm in group C, 32±2.5 µm in group SNI, and 17±0.8 µm in group SNT. A significant difference wasobserved in the epineurium thickness measurements among the 3 groups (p<0.05). In pairwise comparisons, the epineurium thicknesswas significantly higher in group SNI than in groups SNT and C (p<0.05). In the immunohistochemical analysis, S100 immunoreactivitywas found significantly higher in group SNI than in the other 2 groups (p<0.05).Conclusion: The histomorphometric, histopathological, and immunohistochemical data obtained from this study have shown that tamoxifen has a beneficial effect on sciatic nerve crush injury in the experimental rat model.

🔖

Bu Makaleye Atıf Yap

AKAR, E., EMON, S. T., EFENDİOĞLU, M., ERDOĞAN, B., ENGİN, T., aker, F. (2021). Effects of tamoxifen therapy on sciatic nerve crush injury: An experimental study in rats. Acta Orthopaedica et Traumatologica Turcica, Cilt: 55 - Sayı: 2, 87–93. https://ajindex.com/articles/353432

Kaynakça (13)

  1. Kalender AM, Doğan A, Bakan V, Yıldız H, Gökalp MA, Kalender M. Effect of Zofenopril on regeneration of sciatic nerve crush injury in a rat model. J Brachial Plex Peripher Nerve Inj 2009; 4: 6
  2. Wilgis EF, Murphy P. The significance of longitudinal excursion in peripheral nerves. Hand Clin 1986; 2: 761-6
  3. Ip WY, Shibata T, Tang FH, Mak AF, Chow SP. Adhesion formation after nerve repair: an experimental study of early protected mobilization in the rabbit. J Hand Surg Br 2000; 25: 582-4
  4. Soares-Lopes LR, Soares-Lopes IM, Filho LL, Alencar AP, da Silva BB. Morphological and morphometric analysis of the effects of intralesional tamoxifen on keloids. Exp Biol Med (Maywood) 2017; 242: 926-9
  5. Brandt AS, Kamper L, Kukuk S, Haage P, Roth S. Tamoxifen monotherapy in the treatment of retroperitoneal fibrosis. Urol Int 2014; 93: 320-5
  6. Karaca T, Gözalan AU, Yoldaş Ö, Bilgiç BÇ, Tezer A. Effects of tamoxifen citrate on postoperative intra-abdominal adhesion in a rat model. Int J Surg 2013; 11: 68-72
  7. De Koning P, Brakkee JH, Gispen WH. Methods for producing a reproducible crush in the sciatic and tibial nerve of the rat and rapid and precise testing of return of sensory function. Beneficial effects of melanocortins. J Neurol Sci 1986; 74: 237-46
  8. Byer SJ, Eckert JM, Brossier NM, et al. Tamoxifen inhibits malignant peripheral nerve sheath tumor growth in an estrogen receptor-independent manner. Neuro Oncol 2011; 13: 28-41
  9. Tsubaki M, Takeda T, Matsumoto M, et al. Tamoxifen suppresses paclitaxel-, vincristine-, and bortezomib-induced neuropathy via inhibition of the protein kinase C/extracellular signal-regulated kinase pathway. Tumour Biol 2018; 40: 1010428318808670
  10. Somay H, Emon ST, Uslu S, et al. The histological effects of ozone therapy on sciatic nerve crush injury in rats. World Neurosurg 2017; 105: 702-8
  11. Sezer A, Güçlü B, Kazancı B, Cakır M, Coban MK. Neuroprotective effects of agmatine in experimental peripheral nerve injury in rats: a prospective randomized and placebo-controlled trial. Turk Neurosurg 2014; 24: 196-201
  12. Göçmen S, Şirin S, Oysul K, Ulaş UH, Öztaş E. The effects of low-dose radiation in the treatment of sciatic nerve injury in rats. Turkish Neurosurg 2012; 22: 167- 73
  13. Renno WM, Al-Maghrebi M, Al-Banaw A. (-)-Epigallocatechin-3-gallate (EGCG) attenuates functional deficits and morphological alterations by diminishing apoptotic gene overexpression in skeletal muscles after sciatic nerve crush injury. Naun