Free-choice alcohol consumption in mice after application of the appetite regulating peptide leptin

被引:25
作者
Kiefer, F [1 ]
Jahn, H [1 ]
Wolf, K [1 ]
Kämpf, P [1 ]
Knaudt, K [1 ]
Wiedemann, K [1 ]
机构
[1] Univ Hamburg, Hosp Eppendorf, Dept Psychiat & Psychotherapy, D-20246 Hamburg, Germany
关键词
leptin; alcoholism craving; addiction; mice;
D O I
10.1097/00000374-200105000-00021
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Leptin has been shown to regulate food intake and energy expenditure. Very recently, associations of elevated leptin plasma levels during alcohol withdrawal with alcohol craving have been observed in humans. Therefore, we tested the hypothesis that the application of exogenous leptin modulates voluntary alcohol consumption in mice. Methods: Sixteen mice (129/Sv x C57BL/6J) were habituated to ethanol consumption over a time period of 3 months. After a basal 2-week free-choice drinking phase, mice were separated into two groups (n = 8) according to weight and alcohol consumption. They received recombinant leptin (1 mg/kg) versus saline intraperitoneally daily for 10 days. After 4 days of free-choice consumption of ethanol (16% v/v) versus water, ethanol was withdrawn at day 4 and replaced at day 6 to test the occurrence of an alcohol deprivation effects. Fluid intake was evaluated by controlling the weight of the drinking tubes daily. Results: Free-choice ethanol consumption after withdrawal was significantly elevated in mice after intraperitoneal injection of 1 mg/kg leptin (alcohol deprivation effect), but not during basal drinking. Conclusion: We suggest that leptin may enhance motivation for alcohol consumption in habituated mice after alcohol withdrawal.
引用
收藏
页码:787 / 789
页数:3
相关论文
共 18 条
[1]   RECOMBINANT MOUSE OB PROTEIN - EVIDENCE FOR A PERIPHERAL SIGNAL LINKING ADIPOSITY AND CENTRAL NEURAL NETWORKS [J].
CAMPFIELD, LA ;
SMITH, FJ ;
GUISEZ, Y ;
DEVOS, R ;
BURN, P .
SCIENCE, 1995, 269 (5223) :546-549
[2]   Modulation of brain reward circuitry by leptin [J].
Fulton, S ;
Woodside, B ;
Shizgal, P .
SCIENCE, 2000, 287 (5450) :125-128
[3]  
GRANT KA, 1990, ALCOHOL HEALTH RES W, V14, P187
[4]   WEIGHT-REDUCING EFFECTS OF THE PLASMA-PROTEIN ENCODED BY THE OBESE GENE [J].
HALAAS, JL ;
GAJIWALA, KS ;
MAFFEI, M ;
COHEN, SL ;
CHAIT, BT ;
RABINOWITZ, D ;
LALLONE, RL ;
BURLEY, SK ;
FRIEDMAN, JM .
SCIENCE, 1995, 269 (5223) :543-546
[5]   Feeding and body-weight regulation by hypothalamic neuropeptides - mediation of the actions of leptin [J].
Inui, A .
TRENDS IN NEUROSCIENCES, 1999, 22 (02) :62-67
[6]   Craving shift in chronic alcoholics [J].
Junghanns, K ;
Veltrup, C ;
Wetterling, T .
EUROPEAN ADDICTION RESEARCH, 2000, 6 (02) :64-70
[7]  
KIEFER F, 2001, IN PRESS ARCH GEN PS
[8]   LEPTIN LEVELS IN HUMAN AND RODENT - MEASUREMENT OF PLASMA LEPTIN AND OB RNA IN OBESE AND WEIGHT-REDUCED SUBJECTS [J].
MAFFEI, M ;
HALAAS, J ;
RAVUSSIN, E ;
PRATLEY, RE ;
LEE, GH ;
ZHANG, Y ;
FEI, H ;
KIM, S ;
LALLONE, R ;
RANGANATHAN, S ;
KERN, PA ;
FRIEDMAN, JM .
NATURE MEDICINE, 1995, 1 (11) :1155-1161
[9]   Leptin and the hypothalamus: neuroendocrine regulation of food intake [J].
Mantzoros, CS .
MOLECULAR PSYCHIATRY, 1999, 4 (01) :8-12
[10]   Hypothalamic pro-opiomelanocortin mRNA is reduced by fasting in ob/ob and db/db mice, but is stimulated by leptin [J].
Mizuno, TM ;
Kleopoulos, SP ;
Bergen, HT ;
Roberts, JL ;
Priest, CA ;
Mobbs, CV .
DIABETES, 1998, 47 (02) :294-297