l-deprenyl prevents lipid peroxidation and memory deficits produced by cerebral ischemia in rats

被引:19
作者
Maia, FD [1 ]
Pitombeira, BSS [1 ]
Araújo, DT [1 ]
Cunha, GMA [1 ]
Viana, GSB [1 ]
机构
[1] Univ Fed Ceara, Dept Physiol & Pharmacol, Neuropharmacol Lab, BR-60431970 Fortaleza, Ceara, Brazil
关键词
l-deprenyl; ischemia; memory; lipid peroxidation; nitrite;
D O I
10.1023/B:CEMN.0000012727.59502.c5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
1. The present work shows the results on behavior and on biochemical parameters of l-deprenyl (0.1, 5, and 10 mg/kg, p.o.) administered daily for 5 days to rats submitted to global cerebral ischemia. 2. The transient global ischemia was carried out by clamping the animals bilateral common carotid arteries for 20 min. The parameters studied were memory acquisition and memory retention, locomotor activity and thiobarbituric acid reactive substances, as an index of lipid peroxidation. 3. l-Deprenyl treatment significantly improved memory deficits as compared to the ischemic group as measured by the elevated T maze test. A similar result was observed on the passive avoidance test where l-deprenyl improved late but not early memory as compared to the ischemic group. Except for an increased locomotor activity observed in the group treated with 5 mg/kg, no other alteration was detected in this behavioral test. Rats submitted to transient global ischemia ( and without l-deprenyl) showed an increase in MDA levels in the hippocampus and the treatment with l-deprenyl ( 5 or 10 mg/kg) significantly reversed this effect bringing values close to those of the sham-operated controls. A similar profile was observed with nitrite levels. 4. In conclusion, the work showed a significant protective effect of l-deprenyl on memory deficits and lipid hyperperoxidation observed after cerebral ischemia. Possibly, the drug is acting at least in part through its antioxidant activity.
引用
收藏
页码:87 / 100
页数:14
相关论文
共 36 条
[1]   Impairment of working memory in the T-maze after transient global cerebral ischemia in the Mongolian gerbil [J].
Andersen, MB ;
Sams-Dodd, F .
BEHAVIOURAL BRAIN RESEARCH, 1998, 91 (1-2) :15-22
[2]   TESTS FOR EMOTIONALITY IN RATS AND MICE - REVIEW [J].
ARCHER, J .
ANIMAL BEHAVIOUR, 1973, 21 (MAY) :205-235
[3]  
Barbelivien A, 2001, PHARMACOL TOXICOL, V88, P304
[4]   EVALUATION OF 2, 3, 5-TRIPHENYLTETRAZOLIUM CHLORIDE AS A STAIN FOR DETECTION AND QUANTIFICATION OF EXPERIMENTAL CEREBRAL INFARCTION IN RATS [J].
BEDERSON, JB ;
PITTS, LH ;
GERMANO, SM ;
NISHIMURA, MC ;
DAVIS, RL ;
BARTKOWSKI, HM .
STROKE, 1986, 17 (06) :1304-1308
[5]  
Birks J, 2000, COCHRANE DB SYST REV
[6]   IMPROVEMENT OF COGNITIVE FUNCTION BY MAO-B INHIBITOR L-DEPRENYL IN AGED RATS [J].
BRANDEIS, R ;
SAPIR, M ;
KAPON, Y ;
BORELLI, G ;
CADEL, S ;
VALSECCHI, B .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1991, 39 (02) :297-304
[7]   Time course of oxidative damage in different brain regions following transient cerebral ischemia in gerbils [J].
Candelario-Jalil, E ;
Mhadu, NH ;
Al-Dalain, SM ;
Martínez, G ;
León, OS .
NEUROSCIENCE RESEARCH, 2001, 41 (03) :233-241
[8]   Protection from renal ischemia-reperfusion injury by the 2-methylaminochroman U83836E [J].
De Vecchi, E ;
Lubatti, L ;
Beretta, C ;
Ferrero, S ;
Rinaldi, P ;
Kienle, MG ;
Trazzi, R ;
Paroni, R .
KIDNEY INTERNATIONAL, 1998, 54 (03) :857-863
[9]   VINPOCETINE - NOOTROPIC EFFECTS ON SCOPOLAMINE-INDUCED AND HYPOXIA-INDUCED RETRIEVAL DEFICITS OF A STEP-THROUGH PASSIVE-AVOIDANCE RESPONSE IN RATS [J].
DENOBLE, VJ ;
REPETTI, SJ ;
GELPKE, LW ;
WOOD, LM ;
KEIM, KL .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1986, 24 (04) :1123-1128
[10]  
Dixit S N, 1999, J Assoc Physicians India, V47, P784