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.
引用
收藏
页码:300 / 312
页数:13
相关论文
共 61 条
[1]   D1-receptor drugs and cocaine-seeking behavior: investigation of receptor mediation and behavioral disruption in rats [J].
Alleweireldt, AT ;
Kirschner, KF ;
Blake, CB ;
Neisewander, JL .
PSYCHOPHARMACOLOGY, 2003, 168 (1-2) :109-117
[2]   Blockade or stimulation of D1 dopamine receptors attenuates cue reinstatement of extinguished cocaine-seeking behavior in rats [J].
Alleweireldt, AT ;
Weber, SM ;
Kirschner, KF ;
Bullock, BL ;
Neisewander, JL .
PSYCHOPHARMACOLOGY, 2002, 159 (03) :284-293
[3]   INTRAGASTRIC SELF-ADMINISTRATION OF PSYCHOACTIVE-DRUGS BY RHESUS-MONKEY [J].
ALTSHULER, H ;
WEAVER, S ;
PHILLIPS, P .
LIFE SCIENCES, 1975, 17 (06) :883-890
[4]   Naltrexone attenuates cue- but not drug-induced methamphetamine seeking: a possible mechanism for the dissociation of primary and secondary reward [J].
Anggadiredja, K ;
Sakimura, K ;
Hiranita, T ;
Yamamoto, T .
BRAIN RESEARCH, 2004, 1021 (02) :272-276
[5]   Endocannabinoid system modulates relapse to methamphetamine seeking: Possible mediation by the arachidonic acid cascade [J].
Anggadiredja, K ;
Nakamichi, M ;
Hiranita, T ;
Tanaka, H ;
Shoyama, Y ;
Watanabe, S ;
Yamamoto, T .
NEUROPSYCHOPHARMACOLOGY, 2004, 29 (08) :1470-1478
[6]   The binding sites for cocaine and dopamine in the dopamine transporter overlap [J].
Beuming, Thijs ;
Kniazeff, Julie ;
Bergmann, Marianne L. ;
Shi, Lei ;
Gracia, Luis ;
Raniszewska, Klaudia ;
Newman, Amy Hauck ;
Javitch, Jonathan A. ;
Weinstein, Harel ;
Gether, Ulrik ;
Loland, Claus J. .
NATURE NEUROSCIENCE, 2008, 11 (07) :780-789
[7]   Dual probes for the dopamine transporter and σ1 receptors:: novel piperazinyl alkyl-bis(4′-fluorophenyl)amine analogues as potential cocaine-abuse therapeutic agents [J].
Cao, JJ ;
Kulkarni, SS ;
Husbands, SM ;
Bowen, WD ;
Williams, W ;
Kopajtic, T ;
Katz, JL ;
George, C ;
Newman, AH .
JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (13) :2589-2598
[8]   Cocaine-seeking behavior in response to drug-associated stimuli in rats:: Involvement receptors of D3 and D2 dopamine receptors [J].
Cervo, L ;
Carnovali, F ;
Stark, JA ;
Mennini, T .
NEUROPSYCHOPHARMACOLOGY, 2003, 28 (06) :1150-1159
[9]   Selective antagonism at dopamine D3 receptors attenuates cocaine-seeking behaviour in the rat [J].
Cervo, Luigi ;
Cocco, Arianna ;
Petrella, Cinzia ;
Heidbreder, Christian A. .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2007, 10 (02) :167-181
[10]   Identification of a dopamine transporter ligand that blocks the stimulant effects of cocaine [J].
Desai, RI ;
Kopajtic, TA ;
Koffarnus, M ;
Newman, AH ;
Katz, JL .
JOURNAL OF NEUROSCIENCE, 2005, 25 (08) :1889-1893