Simvastatin impairs spatial memory in rats at a specific dose level

被引:24
作者
Baytan, Sukrucan H. [1 ]
Alkanat, Mehmet [1 ]
Okuyan, Mukadder [1 ]
Ekinci, Murat [2 ]
Gedikli, Eyup [2 ]
Ozeren, Mehmet [3 ]
Akgun, Ahmet [1 ]
机构
[1] Karadeniz Tech Univ, Sch Med, Dept Physiol, Trabzon, Turkey
[2] Karadeniz Tech Univ, Sch Engn, Dept Comp Engn, Trabzon, Turkey
[3] Karadeniz Tech Univ, Sch Med, Dept Obstet & Gynecol, Trabzon, Turkey
关键词
Barnes maze; behavior; statins; brain; locomotor;
D O I
10.1620/tjem.214.341
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Statins, inhibitors of cholesterol synthesis, are used to prevent cardiovascular complications. Moreover, statins have been shown to influence some cognitive functions. The modulating effects of simvastatin, one member of the statin family, on memory-related neurotransmitters and neuronal structures have also been reported. We aimed to investigate the behavioral effects of long-term simvastatin application on daily activity, psychomotor performance and spatial memory using Sprague-Dawley rats. Simvastatin (10 or 30 mg/kg/day) was administered orally to rats, in parallel with a vehicle-treated group. Daily activity test results of both simvastatin groups were found similar to the vehicle group after five weeks of simvastatin or vehicle application. Psychomotor performance was measured with the rotarod test. After 6 weeks of simvastatin or vehicle application, the vehicle-treated group stayed on the rotarod device for a shorter time compared with both simvastatin-treated groups. Spatial memory was evaluated by the Barnes maze test. Four weeks of 10 mg/kg/day simvastatin application led to poorer scores on spatial memory compared to the vehicle group, but surprisingly, this effect was not seen in the 30 mg/kg/day group. Our results revealed that simvastatin administration had no significant effect on daily activity. Psychomotor performance test results suggested that simvastatin alters psychomotor behavior at higher nervous system levels. Spatial memory test results indicate that long-term simvastatin usage impairs spatial memory only at 10 mg/kg/day dose.
引用
收藏
页码:341 / 349
页数:9
相关论文
共 45 条
[1]   Hind leg heat balance in obese Zucker rats during exercise [J].
Ardévol, A ;
Adán, C ;
Remesar, X ;
Fernández-López, JA ;
Alemany, M .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1998, 435 (04) :454-464
[2]   MEMORY DEFICITS ASSOCIATED WITH SENESCENCE - NEUROPHYSIOLOGICAL AND BEHAVIORAL-STUDY IN THE RAT [J].
BARNES, CA .
JOURNAL OF COMPARATIVE AND PHYSIOLOGICAL PSYCHOLOGY, 1979, 93 (01) :74-104
[3]   Fluvastatin alters psychomotor performance and daily activity but not the spatial memory in rats [J].
Baytan, Sukrucan H. ;
Alkanat, Mehmet ;
Ozeren, Mehmet ;
Ekinci, Murat ;
Akgun, Ahmet .
TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 209 (04) :311-320
[4]   EXERCISE-INDUCED GROWTH IN GOLDEN-HAMSTERS - EFFECTS OF AGE, WEIGHT, AND ACTIVITY LEVEL [J].
BORER, KT ;
KAPLAN, LR .
PHYSIOLOGY & BEHAVIOR, 1977, 18 (01) :29-34
[5]   Neuroprotective effects of atorvastatin against glutamate-induced excitotoxicity in primary cortical neurones [J].
Bösel, J ;
Gandor, F ;
Harms, C ;
Synowitz, M ;
Harms, U ;
Djoufack, PC ;
Megow, D ;
Dirnagl, U ;
Hörtnagl, H ;
Fink, KB ;
Endres, M .
JOURNAL OF NEUROCHEMISTRY, 2005, 92 (06) :1386-1398
[6]   Differential effects of statins and alendronate on cholinesterases in serum and brain of rats [J].
Cibickova, L. ;
Palicka, V. ;
Cibicek, N. ;
Cermakova, E. ;
Micuda, S. ;
Bartosova, L. ;
Jun, D. .
PHYSIOLOGICAL RESEARCH, 2007, 56 (06) :765-770
[7]   ACETYLCHOLINE MEDIATES A SLOW SYNAPTIC POTENTIAL IN HIPPOCAMPAL PYRAMIDAL CELLS [J].
COLE, AE ;
NICOLL, RA .
SCIENCE, 1983, 221 (4617) :1299-1301
[8]   Differential effects of lipid-lowering agents on human cholinesterases [J].
Darvesh, S ;
Martin, E ;
Walsh, R ;
Rockwood, K .
CLINICAL BIOCHEMISTRY, 2004, 37 (01) :42-49
[9]   Mechanism of action of statins and fibrates [J].
Duriez, P .
THERAPIE, 2003, 58 (01) :5-14
[10]   Dopamine D2 receptor plays a role in memory function:: implications of dopamine-acetylcholine interaction in the ventral hippocampus [J].
Fujishiro, H ;
Umegaki, H ;
Suzuki, Y ;
Oohara-Kurotani, S ;
Yamaguchi, Y ;
Iguchi, A .
PSYCHOPHARMACOLOGY, 2005, 182 (02) :253-261