Hypoinsulinemia may mediate the lowering of self-stimulation thresholds by food restriction and streptozotocin-induced diabetes

被引:42
作者
Carr, KD [1 ]
Kim, GY [1 ]
de Vaca, SC [1 ]
机构
[1] NYU, Sch Med, Dept Psychiat, Millhauser Labs, New York, NY 10016 USA
关键词
insulin; diabetes; reward; self-stimulation;
D O I
10.1016/S0006-8993(00)02143-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Streptozotocin (STZ)-induced diabetes and chronic food restriction have both been reported to lower thresholds for lateral hypothalamic self-stimulation (LHSS). In view of recent evidence that insulin regulates monoamine transporter gene expression in brain, it is possible that the hypoinsulinemia that is common to diabetes and food restriction mediates the enhancement of brain stimulation reward. Two experiments were conducted to test predictions of this hypothesis. In Experiment 1, the effect of STZ-induced diabetes on threshold for LHSS was monitored in rats maintained on either a high fat (HF; 64% fat/0% carbohydrate) or high carbohydrate (HC; 60% carbohydrate/4% fat) diet. Although HC rats were hyperphagic and lost weight at a faster rate than the normophagic HF rats, the two dietary groups displayed similar declines in LHSS threshold, consonant with their nearly identical plasma insulin levels of 25.1+/-2.1 and 24.8+/-0.9 mu IU/ml, respectively. In agreement with observations in food-restricted rats, the lowering of threshold in diabetic rats was preferentially associated with electrode placements adjacent or dorsal to the dorsolateral aspect of the fornix, In Experiment 2, the effect of subchronic intracerebroventricular (i.c.v.) insulin treatment on LHSS threshold was determined in ad libitum fed and food-restricted rats. A five day regimen of i.c.v. insulin (3 mU twice per day) produced a long-lasting (>7 days beyond cessation of insulin treatment) elevation of threshold in ad libitum fed rats and, more transiently, reversed the threshold-lowering effect of food restriction. Acute insulin treatment (3 mU, 15 min prior) also elevated threshold in food-restricted rats. These results rue consistent with the hypothesis that insulin modulates sensitivity of a brain reward system and that hypoinsulinemia may be the common factor in food restriction and diabetes that accounts for the enhancement of perifornical LHSS. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:160 / 168
页数:9
相关论文
共 63 条
[1]   Effect of adrenalectomy on cocaine facilitation of lateral hypothalamic self-stimulation [J].
Abrahamsen, GC ;
Carr, KD .
BRAIN RESEARCH, 1997, 755 (01) :156-161
[2]   CURVE-SHIFT ANALYSIS OF SELF-STIMULATION IN FOOD-RESTRICTED RATS - RELATIONSHIP BETWEEN DAILY MEAL, PLASMA-CORTICOSTERONE AND REWARD SENSITIZATION [J].
ABRAHAMSEN, GC ;
BERMAN, Y ;
CARR, KD .
BRAIN RESEARCH, 1995, 695 (02) :186-194
[3]   Effects of corticosteroid synthesis inhibitors on the sensitization of reward by food restriction [J].
Abrahamsen, GC ;
Carr, KD .
BRAIN RESEARCH, 1996, 726 (1-2) :39-48
[4]   Aminoglutethimide, a corticosteroid synthesis inhibitor, facilitates brain stimulation reward in food-restricted rats: an investigation of underlying mechanisms [J].
Abrahamsen, GC ;
Kandawire, MJ ;
Carr, KD .
PSYCHOPHARMACOLOGY, 1997, 133 (04) :405-412
[5]  
[Anonymous], RAT BRAIN STEREOTAXI
[6]   INSULIN IN THE BRAIN [J].
BASKIN, DG ;
FIGLEWICZ, DP ;
WOODS, SC ;
PORTE, D ;
DORSA, DM .
ANNUAL REVIEW OF PHYSIOLOGY, 1987, 49 :335-347
[7]   Food-deprivation increases cocaine-induced conditioned place preference and locomotor activity in rats [J].
Bell, SM ;
Stewart, RB ;
Thompson, SC ;
Meisch, RA .
PSYCHOPHARMACOLOGY, 1997, 131 (01) :1-8
[8]   Chronic food restriction and streptozotocin-induced diabetes differentially alter prodynorphin mRNA levels in rat brain regions [J].
Berman, Y ;
Devi, L ;
Spangler, R ;
Kreek, MJ ;
Carr, KD .
MOLECULAR BRAIN RESEARCH, 1997, 46 (1-2) :25-30
[9]   INSULIN STIMULATES SODIUM-POTASSIUM ACTIVATED ATPASE FROM RAT HIPPOCAMPUS [J].
BERNSTEIN, HG ;
POEGGEL, G ;
DORN, A ;
LUPPA, H ;
ZIEGLER, M .
EXPERIENTIA, 1981, 37 (04) :434-435
[10]   MODULATION OF TASTE AFFECT BY HUNGER, CALORIC SATIETY, AND SENSORY-SPECIFIC SATIETY IN THE RAT [J].
BERRIDGE, KC .
APPETITE, 1991, 16 (02) :103-120