Journals / Turkish Neurosurgery / 2016 / Cilt: 26 - Sayı: 3

Histopathological Evaluation of the Effects of CAPE in Experimental Spinal Cord Injury

Pages
437–444
DOI
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CONCLUSION: CAPE has a positive effect on spinal cord injuries by preventing apoptosis

📌 3 Key Takeaways

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Objective & Hypothesis:AIM: Spinal cord injuries negatively affect the individuals and the life quality of their families due to neurological deficits caused by trauma.
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Key Findings & Data:The prevalence of spinal cord injury is 15-45/1 million in the world.
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Conclusion & Impact:CONCLUSION: CAPE has a positive effect on spinal cord injuries by preventing apoptosis
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

AIM: Spinal cord injuries negatively affect the individuals and the life quality of their families due to neurological deficits caused by trauma. The prevalence of spinal cord injury is 15-45/1 million in the world. Caffeic acid phenethyl ester (CAPE) is the most active component of propolis and has neuroprotective, anti-oxidant and anti-apoptotic effects. Our aim was to determine the effects of CAPE on the prevention of secondary injury and to compare with methylprednisolone. MATERIAL and METHODS: Forty rats were divided into 4 groups. The control group did not undergo surgery (Group I), only trauma group (Group II), trauma+CAPE treatment group (Group III), and trauma+methylprednisolone treatment group (Group IV). Histopathological assessment was performed with two staining methods as hematoxylin-eosin (HE) and terminal deoxynucleotidyl Transferase Biotin - dUTP Nick End Labeling (TUNEL). The groups were statistically compared. RESULTS: The apoptotic cells decreased in treatment groups compared with the trauma. CAPE has more anti-apoptotic effect than methylprednisolone. The histological difference between the Group II, and Groups III and IV was statistically significant. CONCLUSION: CAPE has a positive effect on spinal cord injuries by preventing apoptosis

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Cite This Article

AYDIN, H. E., ÖZKARA, E., ÖZBEK, Z., VURAL, M., DÖNMEZ, D. B., ARSLANTAŞ, A., ATASOY, M. A. (2016). Histopathological Evaluation of the Effects of CAPE in Experimental Spinal Cord Injury. Turkish Neurosurgery, Cilt: 26 - Sayı: 3, 437–444. https://ajindex.com/articles/404681

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References (3)

  1. Aslan G, Okten A, Caylı S: Omurilik yaralanmasının patoloji ve fizyopatolojisi. Journal of CU Medical Faculty 28(2):73-78, 2006 (in Turkish
  2. Avcı CB, Baran Y, Sahin F, Yılmaz S, Dogan ZO, Saydam G: Caffeic acid phenethyl ester triggers apoptosis through induction of loss of mitochondrial membrane potential in CCRF-CEM cells. J Cancer Res Clin Oncol 137(1):41-47, 2011 3. Diener PS: Fetal spinal cord transplants support growth of supraspinal and segmental projections after cervical spinal cord hemisection in the neonatal rat. J Neurosci 18(2):778- 793, 1998 4. Dumont RJ, Okonkwo DO, Hurlbert RJ: Acute spinal cord injury, Part I: Contemporary pharmacotherapy. Clin Neuropharmocology 24(5):254-264, 2001 5. Gregory GJB: Spinal cord anatomy, localization, and overview of spinal cord syndromes. Lifelong Learning Neurol 14(3):11- 35, 2008 6. Guang C, Shouyu W, Decheng LV: Combined treatment with FK506 and nerve growth factor for spinal cord injury in rats. Exp Ther Med 6(4):868-872, 2013 7. Ho CH, Priebe MM, Chiodo AE, Scelza WM, Kirshblum SC: Spinal cord injury medicine
  3. Epidemiology and classification. Arch Phys Med Rehabil 88(3):49-54, 2007 8. Ilhan A, Gurel A, Armutcu F, Iraz M, Oztas E: Protective effects of caffeic acid phenethyl ester against experimental allergic encephalomyelitis-induced oxidative stress in rats. Free Radic Biol Med 37(3):386-394, 2004 9. Ilhan AKU, Ozen S, Uz E, Ciralik H, Akyol O: The effects of caffeic acid phenethyl ester (CAPE) on spinal cord ischemia/ reperfusion injury in rabbits. Eur J Cardiothorac Surg 16(1): 458-463, 1999 10. Is M, Ulu MO, Tanrıverdi T, Yildiz H, Akyuz F, Aksoy A, Gezen F, Uzan M: The use of methylprednisolone, vitamin E and their combination in acute spinal cord injury: An experimental study. Turk Neurosurg 16(1):2-8, 2006 11. Kaptanoglu E: Strategies for neuroprotection after spinal cord injury. Omurilik ve omurga cerrahisi 63:813-832, 2002 12. Kato H, Matsuo S, Wu YJ, Jacquin MF, Hsu CY, Kouchoukos NT, Choi DW: Neuronal apoptosis and necrosis following spinal cord ischemia in the rat. Exp Neurol 148(2):464-474, 1997 13. Kazanci A, Seckin H, Karadeniz U, Kazanci D, Turan S, Kazanci B, Yigitkali K, Bavbek M: Comparison of the effect of mexiletine and methylprednisolone on neural function and histopathological damage after transient spinal cord ischemia in rabbits. Turk Neurosurg 20(1):43-49, 2010 14. Kerr JFR, Currie AR: Apoptosis. A basic biological phenomenon with wide ranging implications in tissue k