Critical role of cholinergic transmission from the laterodorsal tegmental nucleus to the ventral tegmental area in cocaine-induced place preference

被引:35
作者
Shinohara, Fumiya [1 ]
Kihara, Yukari [1 ]
Ide, Soichiro [1 ]
Minami, Masabumi [1 ]
Kaneda, Katsuyuki [1 ]
机构
[1] Hokkaido Univ, Grad Sch Pharmaceut Sci, Dept Pharmacol, Sapporo, Hokkaido 0600812, Japan
关键词
Laterodorsal tegmental nucleus; Ventral tegmental area; Conditioned place preference; Addiction; Acetylcholine; Mesocorticolimbic system; DOPAMINE EFFLUX; SUBSTANTIA-NIGRA; MEASURING REWARD; NMDA-RECEPTORS; NEURONS; ACTIVATION; PEDUNCULOPONTINE; STIMULATION; RAT; ACETYLCHOLINE;
D O I
10.1016/j.neuropharm.2014.01.019
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Conditioned place preference (CPP) is widely used to investigate the rewarding properties of cocaine. Various brain regions and neurotransmitters are involved in developing cocaine CPP. However, the contribution of cholinergic transmission in the ventral tegmental area (VTA) to cocaine CPP remains largely unexplored. Here, we examined the role of cholinergic input arising from the laterodorsal tegmental nucleus (LDT) to the VTA in the acquisition and expression of cocaine CPP in rats. Intra-LDT injection of carbachol, which hyperpolarizes LDT neurons, and of NMDA and AMPA receptor antagonists before cocaine conditioning blocked and attenuated cocaine CPP, respectively, indicating the necessity of LDT activity for acquiring the CPP. Additionally, intra-VTA injection of scopolamine or mecamylamine before cocaine conditioning also attenuated cocaine CPP, demonstrating the contribution of cholinergic transmission via muscarinic and nicotinic acetylcholine receptors in CPP acquisition. Furthermore, intra-VTA injection of scopolamine or mecamylamine immediately before the test. attenuated cocaine CPP, indicating that cholinergic signaling is also associated with the expression of CPP. These results suggest that cholinergic transmission from the LDT to the VTA is critically involved in both acquiring and retrieving cocaine-associated memories in cocaine CPP. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:573 / 579
页数:7
相关论文
共 47 条
[1]   Mammalian Nicotinic Acetylcholine Receptors: From Structure to Function [J].
Albuquerque, Edson X. ;
Pereira, Edna F. R. ;
Alkondon, Manickavasagom ;
Rogers, Scott W. .
PHYSIOLOGICAL REVIEWS, 2009, 89 (01) :73-120
[2]  
Blaha CD, 1996, J NEUROSCI, V16, P714
[3]   EFFECTS OF DOPAMINERGIC AND GLUTAMATERGIC RECEPTOR ANTAGONISTS ON THE ACQUISITION AND EXPRESSION OF COCAINE CONDITIONING PLACE PREFERENCE [J].
CERVO, L ;
SAMANIN, R .
BRAIN RESEARCH, 1995, 673 (02) :242-250
[4]  
Chapman CA, 1997, NEUROSCIENCE, V76, P177
[5]   Cocaine but not natural reward self-administration nor passive cocaine infusion produces persistent LTP in the VTA [J].
Chen, Billy T. ;
Bowers, M. Scott ;
Martin, Miquel ;
Hopf, F. Woodward ;
Guillory, Anitra M. ;
Carelli, Regina M. ;
Chou, Jonathan K. ;
Bonci, Antonello .
NEURON, 2008, 59 (02) :288-297
[6]   Roles of pedunculopontine tegmental cholinergic receptors in brain stimulation reward in the rat [J].
Chen, J ;
Nakamura, M ;
Kawamura, T ;
Takahashi, T ;
Nakahara, D .
PSYCHOPHARMACOLOGY, 2006, 184 (3-4) :514-522
[7]   TONIC ACTIVATION OF NMDA RECEPTORS CAUSES SPONTANEOUS BURST DISCHARGE OF RAT MIDBRAIN DOPAMINE NEURONS INVIVO [J].
CHERGUI, K ;
CHARLETY, PJ ;
AKAOKA, H ;
SAUNIER, CF ;
BRUNET, JL ;
BUDA, M ;
SVENSSON, TH ;
CHOUVET, G .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1993, 5 (02) :137-144
[8]  
EINHORN LC, 1988, J NEUROSCI, V8, P100
[9]   Laterodorsal tegmental stimulation elicits dopamine efflux in the rat nucleus accumbens by activation of acetylcholine and glutamate receptors in the ventral tegmental area [J].
Forster, GL ;
Blaha, CD .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2000, 12 (10) :3596-3604
[10]   Prominent activation of brainstem and pallidal afferents of the ventral tegmental area by cocaine [J].
Geisler, Stefanie ;
Marinelli, Michela ;
DeGarmo, Beth ;
Becker, Mary L. ;
Freiman, Alexander J. ;
Beales, Mitch ;
Meredith, Gloria E. ;
Zahm, Daniel S. .
NEUROPSYCHOPHARMACOLOGY, 2008, 33 (11) :2688-2700