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A TRYPTAMINE-DERIVED CATECHOLAMINERGIC ENHANCER, (-)-1-(BENZOFURAN-2-YL)-2-PROPYLAMINOPENTANE [(-)-BPAP], ATTENUATES REINSTATEMENT OF METHAMPHETAMINE-SEEKING BEHAVIOR IN RATS
被引:5
作者:
Hiranita, T.
[2
]
Yamamoto, T.
[1
]
Nawata, Y.
[1
]
机构:
[1] Nagasaki Int Univ, Dept Pharmacol, Fac Pharmaceut Sci, Nagasaki 8593298, Japan
[2] Kyushu Univ, Dept Pharmacol, Grad Sch Pharmaceut Sci, Higashi Ku, Fukuoka 8128582, Japan
基金:
美国国家卫生研究院;
关键词:
craving;
dopamine;
methamphetamine;
reinstatement;
relapse;
self-administration;
COCAINE-INDUCED REINSTATEMENT;
PROPAGATION MEDIATED RELEASE;
DOPAMINE UPTAKE INHIBITORS;
RECEPTOR ANTAGONIST;
DRUG-SEEKING;
HYDROCHLORIDE (-)-BPAP;
SELECTIVE ENHANCER;
LIMBIC SELECTIVITY;
ANIMAL-MODELS;
D-3;
RECEPTORS;
D O I:
10.1016/j.neuroscience.2009.10.055
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Relapse to drug craving is problematic in treatment for drug abuse. Evidence suggests inactivation of dopaminergic neurotransmission during drug withdrawal. Meanwhile, a tryptamine analogue, (-)-1-(benzofuran-2-yl)-2-propylaminopentane [(-)-BPAP], has been reported to enhance electrical stimulation of monoamine release. This study examined the effect of (-)-BPAP on reinstatement of methamphetamine-seeking behavior in an animal model of relapse to drug abuse. Rats were trained to i.v. self-administer methamphetamine paired with a light and tone (methamphetamine-associated cues) under a fixed-ratio 1 schedule of reinforcement for 10 days. After extinction session under saline infusions without cues, a reinstatement test under saline infusions was begun. Reinstatement induced by methamphetamine-associated cues or methamphetamine-priming injections was attenuated by repeated administration of (-)BPAP during the extinction phase. Acute administration of (-)-BPAP on test day dose-dependently attenuated both reinstatements. Acute administration of (-)-BPAP neither reinstated methamphetamine-seeking behavior alone nor affected methamphetamine self-administration. Pretreatment with either R(+)-7-chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine (SCH-23390), a dopamine D-1-like receptor antagonist, or amisulpride, a dopamine D-1-like receptor antagonist, did not appreciably affected the acute effect of (-)BPAP on both reinstatements. Co-pretreatment with the dopamine receptor antagonists failed to alter the effects of (-)-BPAP. Meanwhile, pretreatment with a dopamine D-1-like receptor agonist, (+/-)-6-chloro-7,8-dihydroxy-1-phenyl-2,3, 4,5-tetrahydro-1H-3-benzazepine hydrobromide (SKF-81297), dose-dependently attenuated reinstatement induced by the cues or methamphetamine-priming injections. In contrast to (-)-BPAP, pretreatment with SCH-23390 reversed the effects of SKF-81297. Our findings suggest activation of dopamine D-1-like receptors results in attenuation of the reinstatement of methamphetamine-seeking behavior. Additionally, our findings provide evidence to develop (-)-BPAP and dopamine D-1-like receptor agonists as an anti-relapse medication for methamphetamine abusers. (C) 2010 IBRO. Published by Elsevier Ltd. All rights reserved.
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页码:300 / 312
页数:13
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