Effects of citicoline on experimental spinal cord injury

被引:22
作者
Cakir, E [1 ]
Usul, H
Peksoylu, B
Sayin, OC
Alver, A
Topbas, M
Baykal, S
Kuzeyli, K
机构
[1] Karadeniz Tech Univ, Sch Med, Dept Neurosurg, TR-61080 Trabzon, Turkey
[2] Karadeniz Tech Univ, Sch Med, Dept Biochem, TR-61080 Trabzon, Turkey
[3] Karadeniz Tech Univ, Sch Med, Dept Publ Hlth, TR-61080 Trabzon, Turkey
关键词
citicoline; malondialdehyde; spinal cord injury;
D O I
10.1016/j.jocn.2005.03.013
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To investigate the effects of citicoline on experimental spinal cord injury (SCI). Background Citicoline has been successfully used in clinical studies of head injury and cerebral infarction, but there is limited literature regarding its Use in experimental SCI. Study design: Twenty adult Wistar rats were divided into four groups: sham, trauma, vehicle, and citicoline-treated. SCI was produced using a weight drop technique. Citicoline 300 mg/kg was given intraperitoneally, 5 minutes after the induction of trauma. The animals were sacrificed and 1 cm long samples of injured spinal cord were obtained at 48 hours post-SCI. Lipid peroxidation was estimated try the thiobarbituric acid test. Neurological examinations were performed using a previously described grading scale. Results: Measures of lipid peroxidation and motor scores of the citicoline-treated group were significantly lower than those in the other injury groups. Conclusions: Citicoline attenuated lipid peroxidation after SCI and improved the motor scores. Further investigations will be required to determine the long-term effects of this drug on spinal cord injury. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:923 / 926
页数:4
相关论文
共 32 条
[1]  
Adibhatla RM, 2002, J NEUROCHEM, V80, P12
[2]   Impaired mitochondrial function, oxidative stress and altered antioxidant enzyme activities following traumatic spinal cord injury [J].
Azbill, RD ;
Mu, XJ ;
BruceKeller, AJ ;
Mattson, MP ;
Springer, JE .
BRAIN RESEARCH, 1997, 765 (02) :283-290
[3]   Neuroprotective effects of citicoline on brain edema and blood-brain barrier breakdown after traumatic brain injury [J].
Baskaya, MK ;
Dogan, A ;
Rao, AM ;
Dempsey, RJ .
JOURNAL OF NEUROSURGERY, 2000, 92 (03) :448-452
[4]   Acute phase effects of ATP-MgCl2 on experimental spinal cord injury [J].
Çakir, E ;
Baykal, S ;
Karahan, SC ;
Kuzeyli, K ;
Uydu, H .
NEUROSURGICAL REVIEW, 2003, 26 (01) :67-70
[5]   Acute inflammatory response in spinal cord following impact injury [J].
Carlson, SL ;
Parrish, ME ;
Springer, JE ;
Doty, K ;
Dossett, L .
EXPERIMENTAL NEUROLOGY, 1998, 151 (01) :77-88
[6]   BRAIN EDEMA - INDUCTION IN CORTICAL SLICES BY POLY-UNSATURATED FATTY-ACIDS [J].
CHAN, PH ;
FISHMAN, RA .
SCIENCE, 1978, 201 (4353) :358-360
[7]   Reactive oxygen radicals in signaling and damage in the ischemic brain [J].
Chan, PH .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2001, 21 (01) :2-14
[8]   A randomized dose-response trial of citicoline in acute ischemic stroke patients [J].
Clark, WM ;
Warach, SJ ;
Pettigrew, LC ;
Gammans, RE ;
Sabounjian, LA .
NEUROLOGY, 1997, 49 (03) :671-678
[9]   OXIDATIVE STRESS, GLUTAMATE, AND NEURODEGENERATIVE DISORDERS [J].
COYLE, JT ;
PUTTFARCKEN, P .
SCIENCE, 1993, 262 (5134) :689-695
[10]   CITICOLINE (CDP-CHOLINE) - MECHANISMS OF ACTION AND EFFECTS IN ISCHEMIC BRAIN INJURY [J].
DORLANDO, KJ ;
SANDAGE, BW .
NEUROLOGICAL RESEARCH, 1995, 17 (04) :281-284