Lesions of the rat nucleus basalis magnocellularis disrupt appetitive-to-aversive transfer learning

被引:15
作者
Butt, AE
Schultz, JA
Arnold, LL
Garman, EE
George, CL
Garraghty, PE
机构
[1] Calif State Univ San Bernardino, Dept Psychol, San Bernardino, CA 92407 USA
[2] Indiana Univ, Dept Psychol, Bloomington, IN 47405 USA
关键词
D O I
10.1007/BF02688857
中图分类号
B84 [心理学];
学科分类号
04 [教育学]; 0402 [心理学];
摘要
Rats with selective lesions of the nucleus basalis magnocellularis (NBM) and sham-lesion control animals were tested in an operant appetitive-to-aversive transfer task. We hypothesized that NBM lesions would not affect performance in the appetitive phase, but that performance would be impaired during subsequent transfer to the aversive phase of the task. Additional groups of NBM lesion and control rats were tested in the avoidance condition only, where we hypothesized that NBM lesions would not disrupt performance. These hypotheses were based on the argument that the NBM is not necessary for simple association learning that does not tax attention. Both the appetitive phase of the transfer task and the avoidance only task depend only on simple associative learning and are argued not to tax attention. Consequently, performance in these tasks was predicted to be spared following NBM lesions. Complex, attention-demanding associative learning, however, is argued to depend on the NBM. Performance in the aversive phase of the transfer task is both attentionally demanding and associatively more complex than in either the appetitive or aversive tasks alone; thus, avoidance performance in the NBM lesion group was predicted to be impaired following transfer from prior appetitive conditioning. Results supported our hypotheses, with the NBM lesion group acquiring the appetitive response normally, but showing impaired performance following transfer to the aversive conditioning phase of the transfer task. Impairments were not attributable to disrupted avoidance learning per se, as avoidance behavior was normal in the NBM lesion group tested in the avoidance condition only.
引用
收藏
页码:253 / 271
页数:19
相关论文
共 53 条
[1]
SOME PROPERTIES OF CONFIGURAL LEARNING - AN INVESTIGATION OF THE TRANSVERSE-PATTERNING PROBLEM [J].
ALVARADO, MC ;
RUDY, JW .
JOURNAL OF EXPERIMENTAL PSYCHOLOGY-ANIMAL BEHAVIOR PROCESSES, 1992, 18 (02) :145-153
[2]
The effects of nucleus basalis magnocellularis lesions in long-evans hooded rats on two learning set formation tasks, delayed matching-to-sample learning, and open-field activity [J].
Bailey, AM ;
Thomas, RK .
BEHAVIORAL NEUROSCIENCE, 2001, 115 (02) :328-340
[3]
The effects of carbamazepine on an appetitive-to-aversive transfer task: Comparison to untreated and phenytoin [J].
Banks, MK ;
Besheer, J ;
Szypczak, J ;
Goodpaster, LL ;
Phipps, EJ ;
Garraghty, PE .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2001, 25 (03) :551-572
[4]
The effects of phenytoin on instrumental appetitive-to-aversive transfer in rats [J].
Banks, MK ;
Mohr, NL ;
Besheer, J ;
Steinmetz, JE ;
Garraghty, PE .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1999, 63 (03) :465-472
[5]
THE CHOLINERGIC HYPOTHESIS OF GERIATRIC MEMORY DYSFUNCTION [J].
BARTUS, RT ;
DEAN, RL ;
BEER, B ;
LIPPA, AS .
SCIENCE, 1982, 217 (4558) :408-417
[6]
SELECTIVE IMMUNOTOXIC LESIONS OF BASAL FOREBRAIN CHOLINERGIC CELLS - EFFECTS ON LEARNING AND MEMORY IN RATS [J].
BAXTER, MG ;
BUCCI, DJ ;
WILEY, RG ;
GORMAN, LK ;
GALLAGHER, M .
BEHAVIORAL NEUROSCIENCE, 1995, 109 (04) :714-722
[7]
Intact spatial learning following lesions of basal forebrain cholinergic neurons [J].
Baxter, MG ;
Bucci, DJ ;
Sobel, TJ ;
Williams, MJ ;
Gorman, LK ;
Gallagher, M .
NEUROREPORT, 1996, 7 (08) :1417-1420
[8]
Cognitive functions of the basal forebrain [J].
Baxter, MG ;
Chiba, AA .
CURRENT OPINION IN NEUROBIOLOGY, 1999, 9 (02) :178-183
[9]
Bucci DJ, 1998, J NEUROSCI, V18, P8038
[10]
Impairments in negative patterning, but not simple discrimination learning, in rats with 192 IgG-saporin lesions of the nucleus basalis magnocellularis [J].
Butt, AE ;
Noble, MM ;
Rogers, JL ;
Rea, TE .
BEHAVIORAL NEUROSCIENCE, 2002, 116 (02) :241-255