Satiety threshold during maintained cocaine self-administration in outbred mice

被引:7
作者
Tsibulsky, VL
Norman, AB
机构
[1] Univ Cincinnati, Coll Med, Dept Psychiat, Div Neurosci, Cincinnati, OH 45267 USA
[2] Univ Cincinnati, Coll Med, Dept Pharmacol, Cincinnati, OH 45267 USA
[3] Univ Cincinnati, Coll Med, Dept Physiol, Cincinnati, OH 45267 USA
[4] Univ Cincinnati, Coll Med, Dept Cell Biol, Cincinnati, OH 45267 USA
关键词
addiction; cocaine; functional half-life; mice; satiety threshold; self-administration;
D O I
10.1097/00001756-200102120-00029
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Male Swiss Webster mice maintained cocaine self-administration in a regular and dose-dependent manner. These characteristics made it possible to apply the satiety threshold model of drug self-administration developed recently for cocaine self-administration in rats. Non-linear regression analysis revealed that cocaine satiety threshold was 1.3 +/- 0.6 mg/kg and the functional half-life of the cocaine was 8.1 +/- 2.2 min. Whether the self-administration of cocaine was maintained by lever presses or nose pokes did not influence the inter-injection intervals. The results are consistent with the pharmacological model of maintained cocaine self-administration. The ability to determine addiction-relevant phenotypes (the satiety threshold and functional half-rife of cocaine) in inbred strains of mice may help to identify the genetic determinants of cocaine self-administration behavior. NeuroReport 12:325-328 (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:325 / 328
页数:4
相关论文
共 17 条
[1]   Distribution and clearance of cocaine in brain is influenced by genetics [J].
Azar, MR ;
Acar, N ;
Erwin, VG ;
Barbato, GF ;
Morse, AC ;
Heist, CL ;
Jones, BC .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1998, 59 (03) :637-640
[2]  
BARR J E, 1979, Pharmacology Biochemistry and Behavior, V11, P115, DOI 10.1016/0091-3057(79)90307-1
[3]  
BENUCK M, 1987, J PHARMACOL EXP THER, V243, P144
[4]   Dose-response cocaine pharmacokinetics and metabolite profile following intravenous administration and arterial sampling in unanesthetized, freely moving male rats [J].
Booze, RM ;
Lehner, AF ;
Wallace, DR ;
Welch, MA ;
Mactutus, CF .
NEUROTOXICOLOGY AND TERATOLOGY, 1997, 19 (01) :7-15
[5]  
BOYER CS, 1992, DRUG METAB DISPOS, V20, P863
[6]   Method for training operant responding and evaluating cocaine self-administration behavior in mutant mice [J].
Caine, SB ;
Negus, SS ;
Mello, NK .
PSYCHOPHARMACOLOGY, 1999, 147 (01) :22-24
[7]   A SIMPLE METHODOLOGY FOR OPIATE SELF-ADMINISTRATION AND ELECTRICAL BRAIN-STIMULATION IN THE MOUSE [J].
CRISWELL, HE .
LIFE SCIENCES, 1982, 31 (20-2) :2391-2394
[8]   Differences in the liability to self-administer intravenous cocaine between C57BL/6xSJL and BALB/cByJ mice [J].
Deroche, V ;
Caine, SB ;
Heyser, CJ ;
Polis, I ;
Koob, GF ;
Gold, LH .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1997, 57 (03) :429-440
[9]   CALCIUM-ANTAGONISTS ISRADIPINE AND NIMODIPINE SUPPRESS COCAINE AND MORPHINE INTRAVENOUS SELF-ADMINISTRATION IN DRUG-NAIVE MICE [J].
KUZMIN, A ;
ZVARTAU, E ;
GESSA, GL ;
MARTELLOTTA, MC ;
FRATTA, W .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1992, 41 (03) :497-500
[10]   THE USE OF A BIOPSY PUNCH IN SURGICAL PREPARATION OF DRUG SELF-ADMINISTERING ANIMALS [J].
REYNOLDS, FA ;
DUVAUCHELLE, CL ;
KORNETSKY, C .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1994, 49 (01) :233-234