LONG-TERM EFFECT OF HU-211, A NOVEL NONCOMPETITIVE NMDA ANTAGONIST, ON MOTOR AND MEMORY FUNCTIONS AFTER CLOSED-HEAD INJURY IN THE RAT

被引:167
作者
SHOHAMI, E
NOVIKOV, M
BASS, R
机构
[1] Department of Pharmacology, The Hebrew University School of Pharmacy, Jerusalem
关键词
CLOSED-HEAD INJURY; EDEMA; MEMORY; HU-211; RAT;
D O I
10.1016/0006-8993(94)01433-I
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
HU-211 is a synthetic, non-psychotropic cannabinoid which acts as a non-competitive NMDA antagonist and antioxidant. We studied the drug's therapeutic window as well as its long-term effect on cognitive and motor functions in a model of closed head injury (CHI) in the rat. A weight-drop device was used to induce CHI in ether anesthetized male rats. HU-211 (5 mg/kg) was administered i.v. to the experimental groups. For the therapeutic window study, drug was injected at 4 or 6 h after CHI. Edema (water content) and clinical status (neurological severity score, NSS) were evaluated at 24 h. Reduction of edema was slight, whereas improvement of NSS was significant when the drug was administered at 4 or 6 h (P=0.0023 and 0.059, respectively). To determine the drug's long-term effect, it was administered 1 h after CHI and additional doses were later given. NSS was evaluated for a period of 30 d. A single dose of HU-211 given 1 h post-CHI improved the clinical outcome during the 30 d period (P<0.01). Repetitive doses of HU-211 injected during the post traumatic period had similar effects. Cognitive functions were evaluated in the Morris water maze, with rats trained either before or after CHI. CHI resulted in a highly significant impairment of these abilities, whereas HU-211 treatment 1 h after CHI improved performance. Our results indicate that HU-211 is a potent cerebroprotective agent, with a therapeutic window of about 4 h. The beneficial response obtained even after a single dose was long lasting, and ameliorated impairment of both motor and cognitive functions following CHI.
引用
收藏
页码:55 / 62
页数:8
相关论文
共 39 条
[1]   ELEVATION OF THE EXTRACELLULAR CONCENTRATIONS OF GLUTAMATE AND ASPARTATE IN RAT HIPPOCAMPUS DURING TRANSIENT CEREBRAL-ISCHEMIA MONITORED BY INTRACEREBRAL MICRODIALYSIS [J].
BENVENISTE, H ;
DREJER, J ;
SCHOUSBOE, A ;
DIEMER, NH .
JOURNAL OF NEUROCHEMISTRY, 1984, 43 (05) :1369-1374
[2]   ISCHEMIC DAMAGE IN HIPPOCAMPAL CA1 IS DEPENDENT ON GLUTAMATE RELEASE AND INTACT INNERVATION FROM CA3 [J].
BENVENISTE, H ;
JORGENSEN, MB ;
SANDBERG, M ;
CHRISTENSEN, T ;
HAGBERG, H ;
DIEMER, NH .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1989, 9 (05) :629-639
[3]  
BROOKS DN, 1972, J NERV MENT DIS, V155, P350
[4]  
BUCHAN AM, 1990, CEREBROVAS BRAIN MET, V2, P1
[5]  
CHOI DW, 1993, PROG BRAIN RES, V96, P137
[6]  
DIEMER NH, 1993, PROG BRAIN RES, V96, P105
[7]   HU-211, A NON-PSYCHOTROPIC CANNABINOID, RESCUES CORTICAL-NEURONS FROM EXCITATORY AMINO-ACID TOXICITY IN CULTURE [J].
ESHHAR, N ;
STRIEM, S ;
BIEGON, A .
NEUROREPORT, 1993, 5 (03) :237-240
[8]   NONPSYCHOTROPIC CANNABINOID ACTS AS A FUNCTIONAL N-METHYL-D-ASPARTATE RECEPTOR BLOCKER [J].
FEIGENBAUM, JJ ;
BERGMANN, F ;
RICHMOND, SA ;
MECHOULAM, R ;
NADLER, V ;
KLOOG, Y ;
SOKOLOVSKY, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (23) :9584-9587
[9]  
GASQUOINE P G, 1991, Brain Injury, V5, P169, DOI 10.3109/02699059109008087
[10]  
GILL R, 1987, J NEUROSCI, V7, P3343