Journals / Turkish Neurosurgery / 2017 / Cilt: 27 - Sayı: 4

Effects of Atorvastatin on Experimental Spinal Cord Ischemia-Reperfusion Injury in Rabbits

Pages
594–602
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

Further studies with larger cohorts and different time periods are also needed

📌 3 Key Takeaways

🎯
Objective & Hypothesis:AIm: Extent of secondary injury is the determinant of tissue destruction and functional worsening after primary spinal cord injury (SCI).
📊
Key Findings & Data:Treatment group received 5 mg/kg of atorvastatin via lavage for the preceding 14 days.
💡
Conclusion & Impact:Further studies with larger cohorts and different time periods are also needed
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

AIm: Extent of secondary injury is the determinant of tissue destruction and functional worsening after primary spinal cord injury (SCI). Data have accumulated on alleviation of secondary injury in SCI from many studies on the subject. Besides its cholesterol lowering effects, statins are known to have anti-inflammatory and anti-oxidant effects which are the main targets of spinal cord research. This study aims to evaluate the effects of atorvastatin on experimental spinal cord ischemia-reperfusion injury. mATERIAl and mEThODS: Thirty adult male New Zealand rabbits were allocated into control, ischemia-reperfusion (I/R) and treatment groups. Treatment group received 5 mg/kg of atorvastatin via lavage for the preceding 14 days. Other groups received placebo during the same time period. After two weeks, animals in the I/R and treatment groups underwent abdominal temporary aorta occlusion for 30 minutes. Neurological condition of the animals was recorded during the 48 hours of observation. Afterwards, animals were sacrificed and levels of malondialdehyde, glutathione and nitric oxide in spinal cord tissue and plasma and the histopathological tissue changes were determined. RESUlTS: Animals in the treatment groups demonstrated significantly better results than the I/R group regarding biochemical markers. Neurological evaluation using the Tarlov scale demonstrated significantly better results at the 48th hour in treatment group. Histopathological results were also better in the treatment groups. CONClUSION: Results of this study demonstrate the neuroprotective effects of atorvastatin. Atorvastatin has favorable effects on biochemical markers of oxidative stress in SCI. Further studies with larger cohorts and different time periods are also needed

🔖

Cite This Article

KARDEŞ, Ö., ÇİVİ, S., TUFAN, K., OYAR, E. Ö., ÖMEROĞLU, S., AYKOL, Ş. (2017). Effects of Atorvastatin on Experimental Spinal Cord Ischemia-Reperfusion Injury in Rabbits. Turkish Neurosurgery, Cilt: 27 - Sayı: 4, 594–602. https://ajindex.com/articles/404618

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (1)

  1. Aydemir S, Dogan D, Kocak A, Dilsiz N: The effect of melatonin on spinal cord after ischemia in rats. Spinal Cord 54(5):360- 363, 2016 2. Aykac G, Uysal M, Yalcin AS, Kocak-Toker N, Sivas A, Oz H: The effect of chronic ethanol ingestion on hepatic lipid peroxide, glutathione, glutathione peroxidase and glutathione transferase in rats. Toxicology 36:71–76, 1985 3. Azbill RD, Mu X, Bruce-Keller AJ, Mattson MP, Springer JE: Impaired mitochondrial function, oxidative stress and altered antioxidant enzyme activities following traumatic spinal cord injury. Brain Res 765:283-290, 1997 4. Baigent C, Keech A, Kearney PM, Blackwell L, Buck G, Pollicino C, Cholesterol Treatment Trialists’ (CTT) Collaborators: Efficacy and safety of cholesterol lowering treatment: Prospective metaanalysis of data from 90.056 participants in 14 randomized trials of statins. Lancet 366:1267-1278, 2005 5. Baptiste DC, Fehlings MG: Pharmacological approaches to repair the injured spinal cord. J Neurotrauma 23:318-334, 2006 6. Belboul A, Roberts D, Borjesson R, Johnsson J: Oxygen free radical generation in healthy blood donors and cardiac patients: The protective effect of allopurinol. Perfusion 16:59-65, 2001 7. Bosel J, Gandor F, Harms C, Synowitz M, Harms U, Djoufack PC, Megow D, Dirnagl U, Hortnagl H, Fink KB, Endres M: Neuroprotective effects of atorvastatin against glutamateinduced excitotoxicity in primary cortical neurones. J Neurochem 92:1386-1398, 2005 8. Carlson GD, Gorden C: Current developments in spinal cord injury research. Spine J 2:116-128, 2002 9. Casini A, Ferrali M, Pompelam A, Maellaro E, Comporti M: Lipid peroxidation and cellular damage in extrahepatic tissues of bromobenzene intoxicated mice. Am J Pathol 123:520– 531, 1986 10. Chan PH: Role of oxidants in ischemic brain damage. Stroke 27:1124-1129, 1996 11. Cheng MK, Robertson C, Grossman RG, Foltz R, Williams V: Neurological outcome correlated with spinal evoked potentials in a spinal cord ischemia model. J Neurosurg 60:786-795, 1984 12. Christie SD, Comeau B, Myers T, Sadi D, Purdy M, Mendez I: Duration of lipid peroxidation after acute spinal cord injury in rats and the effect of methylprednisolone. Neurosurg Focus 25:E5, 2008 13. Chu LW, Chen JY, Wu PC, Wu BN: Atorvastatin prevents neuroinflammation in chronic constriction injury rats through nuclear NFκB downregulation in the dorsal root ganglion and spinal cord. ACS Chem Neurosci 6:889-898, 2015 14. Conti A, Miscusi M, Cardali S, Germano A, Suzuki H, Cuzzoc