Cholinergic Interneurons Control Local Circuit Activity and Cocaine Conditioning

被引:354
作者
Witten, Ilana B. [1 ]
Lin, Shih-Chun [1 ,2 ]
Brodsky, Matthew [1 ]
Prakash, Rohit [1 ]
Diester, Ilka [1 ]
Anikeeva, Polina [1 ]
Gradinaru, Viviana [1 ]
Ramakrishnan, Charu [1 ]
Deisseroth, Karl [1 ,3 ,4 ,5 ]
机构
[1] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Neurosurg, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
[4] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
[5] Stanford Univ, CNC Program, Stanford, CA 94305 USA
关键词
NUCLEUS-ACCUMBENS CORE; ACETYLCHOLINE-RECEPTORS; RAT NEOSTRIATUM; FIRING PATTERNS; NEURONS; ADDICTION; STRIATUM; NICOTINE; SYSTEMS; REINFORCEMENT;
D O I
10.1126/science.1193771
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cholinergic neurons are widespread, and pharmacological modulation of acetylcholine receptors affects numerous brain processes, but such modulation entails side effects due to limitations in specificity for receptor type and target cell. As a result, causal roles of cholinergic neurons in circuits have been unclear. We integrated optogenetics, freely moving mammalian behavior, in vivo electrophysiology, and slice physiology to probe the cholinergic interneurons of the nucleus accumbens by direct excitation or inhibition. Despite representing less than 1% of local neurons, these cholinergic cells have dominant control roles, exerting powerful modulation of circuit activity. Furthermore, these neurons could be activated by cocaine, and silencing this drug-induced activity during cocaine exposure (despite the fact that the manipulation of the cholinergic interneurons was not aversive by itself) blocked cocaine conditioning in freely moving mammals.
引用
收藏
页码:1677 / 1681
页数:5
相关论文
共 39 条
[1]   Selective cognitive dysfunction in acetylcholine M1 muscarinic receptor mutant mice [J].
Anagnostaras, SG ;
Murphy, GG ;
Hamilton, SE ;
Mitchell, SL ;
Rahnama, NP ;
Nathanson, NM ;
Silva, AJ .
NATURE NEUROSCIENCE, 2003, 6 (01) :51-58
[2]  
AOSAKI T, 1994, J NEUROSCI, V14, P3969
[3]   A FLEX switch targets channelrhodopsin-2 to multiple cell types for imaging and long-range circuit mapping [J].
Atasoy, Deniz ;
Aponte, Yexica ;
Su, Helen Hong ;
Sternson, Scott M. .
JOURNAL OF NEUROSCIENCE, 2008, 28 (28) :7025-7030
[4]   Induction of a physiological memory in the cerebral cortex by stimulation of the nucleus basalis [J].
Bakin, JS ;
Weinberger, NM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) :11219-11224
[5]   Millisecond-timescale, genetically targeted optical control of neural activity [J].
Boyden, ES ;
Zhang, F ;
Bamberg, E ;
Nagel, G ;
Deisseroth, K .
NATURE NEUROSCIENCE, 2005, 8 (09) :1263-1268
[6]  
CARELLI RM, 1994, J NEUROSCI, V14, P7735
[7]   Biological substrates of reward and aversion: A nucleus accumbens activity hypothesis [J].
Carlezon, William A., Jr. ;
Thomas, Mark J. .
NEUROPHARMACOLOGY, 2009, 56 :122-132
[8]   Nicotinic receptors and nicotine addiction [J].
Changeux, Jean-Pierre .
COMPTES RENDUS BIOLOGIES, 2009, 332 (05) :421-425
[9]   Synaptic plasticity in the mesolimbic system Therapeutic implications for substance abuse [J].
Chen, Billy T. ;
Hopf, F. Woodward ;
Bonci, Antonello .
ADDICTION REVIEWS 2, 2010, 1187 :129-139
[10]   Activation of muscarinic and nicotinic acetylcholine receptors in the nucleus accumbens core is necessary for the acquisition of drug reinforcement [J].
Crespo, Jose A. ;
Sturm, Katja ;
Saria, Alois ;
Zernig, Gerald .
JOURNAL OF NEUROSCIENCE, 2006, 26 (22) :6004-6010