The effects of lesions to thalamic lateral internal medullary lamina and posterior nuclei on learning, memory and habituation in the rat

被引:46
作者
Savage, LM
Sweet, AJ
Castillo, R
Langlais, PJ
机构
[1] VET AFFAIRS MED CTR, NEUROL RES SERV 127, SAN DIEGO, CA 92169 USA
[2] SAN DIEGO STATE UNIV, DEPT PSYCHOL, SAN DIEGO, CA 92182 USA
关键词
lesion; lateral internal medullary lamina; posterior nuclei; thalamus; learning; memory; habituation; rat;
D O I
10.1016/S0166-4328(97)80983-7
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The behavioral effects of radiofrequency lesions to the lateral internal medullary lamina region (IML) or the posterior region (Po: containing the parafascicular and posterior nuclei) of the thalamus were compared to sham operated controls. Subjects were pre-operatively trained and then tested for post-operative retention of a NMTP task. Whereas the Po-lesion group was impaired only on long delays (60, 90 s), the IML-lesion group was impaired on retention and re-acquisition and demonstrated lower performance at all delays (5-90 s) of the NMTP task. Post-operative training and testing was conducted on three additional tasks: Morris water maze, acoustic startle, and passive avoidance. The IML-lesion group was impaired in finding a hidden and visual platform in the Morris water maze, demonstrated a blunted response but normal habituation to an acoustic startle stimulus, and showed normal retention of a passive avoidance task. On those three tasks, the performance of the Po-lesion group was similar to controls. In the IML-lesion group, neuronal loss resulting from axotomy and/or transneuronal degeneration was observed within nuclei of the midline and anterior thalamus and the mammillary body. These results suggest that lesions to the IML region disrupt a range of cognitive functions and produce pathological destruction in distant brain regions; whereas damage to the posterior thalamus causes spatial delay-sensitive deficits.
引用
收藏
页码:133 / 147
页数:15
相关论文
共 85 条
[1]   BOTH FORNIX AND ANTERIOR THALAMIC, BUT NOT MAMMILLARY, LESIONS DISRUPT DELAYED NON-MATCHING-TO-POSITION MEMORY IN RATS [J].
AGGLETON, JP ;
KEITH, AB ;
SAHGAL, A .
BEHAVIOURAL BRAIN RESEARCH, 1991, 44 (02) :151-161
[2]   A COMPARISON OF THE EFFECTS OF ANTERIOR THALAMIC, MAMILLARY BODY AND FORNIX LESIONS ON REINFORCED SPATIAL ALTERNATION [J].
AGGLETON, JP ;
NEAVE, N ;
NAGLE, S ;
HUNT, PR .
BEHAVIOURAL BRAIN RESEARCH, 1995, 68 (01) :91-101
[3]   THE CONTRIBUTION OF THE ANTERIOR THALAMIC NUCLEI TO ANTEROGRADE AMNESIA [J].
AGGLETON, JP ;
SAHGAL, A .
NEUROPSYCHOLOGIA, 1993, 31 (10) :1001-1019
[4]   THE EFFECTS OF MAMMILLARY BODY AND COMBINED AMYGDALAR-FORNIX LESIONS ON TESTS OF DELAYED NON-MATCHING-TO-SAMPLE IN THE RAT [J].
AGGLETON, JP ;
HUNT, PR ;
SHAW, C .
BEHAVIOURAL BRAIN RESEARCH, 1990, 40 (02) :145-157
[5]   DORSAL RAPHE STIMULATION REDUCES RESPONSES OF PARAFASCICULAR NEURONS TO NOXIOUS-STIMULATION [J].
ANDERSEN, E ;
DAFNY, N .
PAIN, 1983, 15 (04) :323-331
[6]   EFFECTS OF CHRONIC ETHANOL-CONSUMPTION ASSOCIATED OR NOT WITH EXPERIMENTAL ANTERIOR THALAMIC LESIONS ON SPONTANEOUS SEQUENTIAL ALTERNATION IN MICE [J].
BERACOCHEA, D ;
JAFFARD, R .
NEUROSCIENCE LETTERS, 1991, 134 (01) :45-48
[7]   EFFECTS OF ANTERIOR OR DORSOMEDIAL THALAMIC IBOTENIC LESIONS ON LEARNING AND MEMORY IN RATS [J].
BERACOCHEA, DJ ;
JAFFARD, R ;
JARRARD, LE .
BEHAVIORAL AND NEURAL BIOLOGY, 1989, 51 (03) :364-376
[8]   IMPAIRMENT OF SPONTANEOUS-ALTERNATION BEHAVIOR IN SEQUENTIAL TEST PROCEDURES FOLLOWING MAMMILLARY BODY LESIONS IN MICE - EVIDENCE FOR TIME-DEPENDENT INTERFERENCE-RELATED MEMORY DEFICITS [J].
BERACOCHEA, DJ ;
JAFFARD, R .
BEHAVIORAL NEUROSCIENCE, 1987, 101 (02) :187-197
[9]   ORGANIZATION OF THE THALAMOSTRIATAL PROJECTIONS IN THE RAT, WITH SPECIAL EMPHASIS ON THE VENTRAL STRIATUM [J].
BERENDSE, HW ;
GROENEWEGEN, HJ .
JOURNAL OF COMPARATIVE NEUROLOGY, 1990, 299 (02) :187-228
[10]   T-MAZE ALTERNATION, RESPONSE PATTERNING, AND SEPTO-HIPPOCAMPAL CIRCUITRY IN RATS [J].
BRITO, GNO ;
THOMAS, GJ .
BEHAVIOURAL BRAIN RESEARCH, 1981, 3 (03) :319-340