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Neuroprotective effect of atorvastatin in spinal cord ischemia-reperfusion injury
Nazli, Yunus; Colak, Necmettin; Alpay, Mehmet Fatih; Uysal, Sema; Uzunlar, Ali Kemal; Cakir, Omer.
  • Nazli, Yunus; University of Turgut Ozal. School of Medicine. Department of Cardiovascular Surgery. Ankara. TR
  • Colak, Necmettin; University of Turgut Ozal. School of Medicine. Department of Cardiovascular Surgery. Ankara. TR
  • Alpay, Mehmet Fatih; University of Turgut Ozal. School of Medicine. Department of Cardiovascular Surgery. Ankara. TR
  • Uysal, Sema; University of Turgut Ozal. School of Medicine. Department of Cardiovascular Surgery. Ankara. TR
  • Uzunlar, Ali Kemal; University of Turgut Ozal. School of Medicine. Department of Cardiovascular Surgery. Ankara. TR
  • Cakir, Omer; University of Turgut Ozal. School of Medicine. Department of Cardiovascular Surgery. Ankara. TR
Clinics ; 70(1): 52-60, 1/2015. tab, graf
Article in English | LILACS | ID: lil-735866
ABSTRACT

OBJECTIVES:

Prevention of the development of paraplegia during the repair of the damage caused by descending thoracic and thoracoabdominal aneurysms remains an important issue. Therefore, we investigated the protective effect of atorvastatin on ischemia-induced spinal cord injury in a rabbit model.

METHOD:

Thirty-two rabbits were divided into the following four equally sized groups group I (control), group II (ischemia-reperfusion), group III (atorvastatin treatment) and group IV (atorvastatin withdrawal). Spinal cord ischemia was induced by clamping the aorta both below the left renal artery and above the iliac bifurcation. Seventy-two hours postoperatively, the motor function of the lower limbs of each animal was evaluated according to the Tarlov score. Spinal cord and blood samples were obtained for histopathological and biochemical analyses.

RESULTS:

All of the rabbits in group II exhibited severe neurological deficits. Atorvastatin treatment (groups III and IV) significantly reduced the level of motor dysfunction. No significant differences were observed between the motor function scores of groups III and IV at the evaluated time points. Light microscopic examination of spinal cord tissue samples obtained at the 72nd hour of reperfusion indicated greater tissue preservation in groups III and IV than in group II.

CONCLUSION:

This study demonstrates the considerable neuroprotective effect of atorvastatin on the neurological, biochemical and histopathological status of rabbits with ischemia-induced spinal cord injury. Moreover, the acute withdrawal of atorvastatin therapy following the induction of spinal cord ischemia did not increase the neuronal damage in this rabbit model. .
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Paraplegia / Pyrroles / Reperfusion Injury / Neuroprotective Agents / Hydroxymethylglutaryl-CoA Reductase Inhibitors / Spinal Cord Ischemia / Heptanoic Acids Type of study: Prognostic study Limits: Animals Language: English Journal: Clinics Journal subject: Medicine Year: 2015 Type: Article Affiliation country: Turkey Institution/Affiliation country: University of Turgut Ozal/TR

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Full text: Available Index: LILACS (Americas) Main subject: Paraplegia / Pyrroles / Reperfusion Injury / Neuroprotective Agents / Hydroxymethylglutaryl-CoA Reductase Inhibitors / Spinal Cord Ischemia / Heptanoic Acids Type of study: Prognostic study Limits: Animals Language: English Journal: Clinics Journal subject: Medicine Year: 2015 Type: Article Affiliation country: Turkey Institution/Affiliation country: University of Turgut Ozal/TR