References
- Adamantidis, A.R., Tsai, H.C., Boutrel, B., Zhang, F., Stuber, G.D., Budygin, E.A., Tourino, C., Bonci, A., Deisseroth, K., and de Lecea, L. (2011). Optogenetic interrogation of dopaminergic modulation of the multiple phases of reward-seeking behavior. J. Neurosci. 31, 10829-10835. https://doi.org/10.1523/JNEUROSCI.2246-11.2011
- Alcantara, A.A., Chen, V., Herring, B.E., Mendenhall, J.M., and Berlanga, M.L. (2003). Localization of dopamine D2 receptors on cholinergic interneurons of the dorsal striatum and nucleus accumbens of the rat. Brain Res. 986, 22-29. https://doi.org/10.1016/S0006-8993(03)03165-2
- Alexander, G.E., DeLong, M.R., and Strick P.L. (1986). Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Annu. Rev. Neurosci. 9, 357-381. https://doi.org/10.1146/annurev.ne.09.030186.002041
- Amalric, M., and Koob, G.F. (1993). Functionally selective neurochemical afferents and efferents of the mesocorticolimbic and nigrostriatal dopamine system. Prog. Brain Res. 99, 209-226.
- Bock, R., Shin, J.H., Kaplan, A.R., Dobi, A., Markey, E., Kramer, P.F., Gremel, C.M., Christensen, C.H., Adrover, M.F., and Alvarez, V.A. (2013). Strengthening the accumbal indirect pathway promotes resilience to compulsive cocaine use. Nat. Neurosci. 16, 632-638. https://doi.org/10.1038/nn.3369
- Bolam, J.P., Hanley, J.J., Booth, P.A.C., and Bevan, M.D. (2000). Synaptic organisation of the basal ganglia. J. Anat. 196, 527-542. https://doi.org/10.1046/j.1469-7580.2000.19640527.x
- Borgland, S.L., Malenka, R.C., and Bonci, A. (2004). Acute and chronic cocaine-induced potentiation of synaptic strength in the ventral tegmental area: electrophysiological and behavioral correlates in individual rats. J. Neurosci. 24, 7482-7490. https://doi.org/10.1523/JNEUROSCI.1312-04.2004
- Bossert, J.M., Stern, A.L., Theberge, F.R., Cifani, C., Koya, E., Hope, B.T., and Shaham, Y. (2011). Ventral medial prefrontal cortex neuronal ensembles mediate context-induced relapse to heroin. Nat. Neurosci. 14, 420-422. https://doi.org/10.1038/nn.2758
- Britt, J.P., Benaliouad, F., McDevitt, R.A., Stuber, G.D., Wise, R.A., and Bonci, A. (2012). Synaptic and behavioral profile of multiple glutamatergic inputs to the nucleus accumbens. Neuron 76, 790-803. https://doi.org/10.1016/j.neuron.2012.09.040
- Brown, M.T., Tan, K.R., O'Connor, E.C., Nikonenko, I., Muller, D., and Lüscher, C. (2012). Ventral tegmental area GABA projections pause accumbal cholinergic interneurons to enhance associative learning. Nature 492, 452-456. https://doi.org/10.1038/nature11657
- Brown, T.E., Lee, B.R., Mu, P., Ferguson, D., Dietz, D., Ohnishi, Y.N., Lin, Y., Suska, A., Ishikawa, M., Huang, Y.H., et al. (2011). A silent synapse-based mechanism for cocaine-Induced locomotor sensitization. J. Neurosci. 31, 8163-8174. https://doi.org/10.1523/JNEUROSCI.0016-11.2011
- Cachope, R., Mateo, Y., Mathur, B.N., Irving, J., Wang, H.L., Morales, M., Lovinger, D.M., and Cheer, J.F. (2012). Selective activation of cholinergic interneurons enhances accumbal phasic dopamine release: setting the tone for reward processing. Cell Rep. 2, 33-41. https://doi.org/10.1016/j.celrep.2012.05.011
- Caine, S.B., Humby, T., Robbins, T.W., and Everitt, B.J. (2001). Behavioral effects of psychomotor stimulants in rats with dorsal or ventral subiculum lesions : locomotion , cocaine self administration, and prepulse inhibition of startle. Behav. Neurosci. 115, 880-894. https://doi.org/10.1037/0735-7044.115.4.880
- Caine, S.B., Negus, S.S., Mello, N.K., Patel, S., Bristow, L., Kulagowski, J., Vallone, D., Saiardi, A., and Borrelli, E. (2002). Role of dopamine D2-like receptors in cocaine self-administration: studies with D2 receptor mutant mice and novel D2 receptor antagonists. J. Neurosci. 22, 2977-2988. https://doi.org/10.1523/JNEUROSCI.22-07-02977.2002
- Caine, S.B., Thomsen, M., Gabriel, K.I., Berkowitz, J.S., Gold, L.H., Koob, G.F., Tonegawa, S., Zhang, J., and Xu, M. (2007). Lack of selfadministration of cocaine in dopamine D1 receptor knock-out mice. J. Neurosci. 27, 13140-13150. https://doi.org/10.1523/JNEUROSCI.2284-07.2007
- Creed, M., Ntamati, N.R., Chandra, R., Lobo, M.K., and Luscher, C. (2016). Convergence of reinforcing and anhedonic cocaine effects in the ventral pallidum. Neuron 92, 214-226. https://doi.org/10.1016/j.neuron.2016.09.001
- Crittenden, J.R., and Graybiel, A.M. (2011). Basal ganglia disorders associated with imbalances in the striatal striosome and matrix compartments. Front. Neuroanat. 5, 1-25.
- Dalley, J.W., Cardinal, R.N., and Robbins, T.W. (2004). Prefrontal executive and cognitive functions in rodents: Neural and neurochemical substrates. Neurosci. Biobehav. Rev. 28, 771-784. https://doi.org/10.1016/j.neubiorev.2004.09.006
- Dobbs, L.K., Kaplan, A.R., Lemos, J.C., Matsui, A., Rubinstein, M., and Alvarez, V.A. (2016). Dopamine regulation of lateral inhibition between striatal neurons gates the stimulant actions of cocaine. Neuron 90, 1100-1113. https://doi.org/10.1016/j.neuron.2016.04.031
- Durieux, P.F., Bearzatto, B., Guiducci, S., Buch, T., Waisman, A., Zoli, M., Schiffmann, S.N., and de Kerchove d'Exaerde, A. (2009). D2R striatopallidal neurons inhibit both locomotor and drug reward processes. Nat. Neurosci. 12, 393-395. https://doi.org/10.1038/nn.2286
- Everitt, B.J., and Robbins, T.W. (2005). Neural systems of reinforcement for drug addiction: from actions to habits to compulsion. Nat. Neurosci. 8, 1481-1489. https://doi.org/10.1038/nn1579
- Farrell, M.S., Pei, Y., Wan, Y., Yadav, P.N., Daigle, T.L., Urban, D.J., Lee, H.M., Sciaky, N., Simmons, A., Nonneman, R.J., et al. (2013). A Gas DREADD mouse for selective modulation of cAMP production in striatopallidal neurons. Neuropsychopharmacology 38, 854-862. https://doi.org/10.1038/npp.2012.251
- Ferguson, S.M., and Neumaier, J.F. (2015). Using DREADDs to investigate addiction behaviors. Curr. Opin. Behav. Sci. 2, 69-72. https://doi.org/10.1016/j.cobeha.2014.09.004
- Ferguson, S.M., Eskenazi, D., Ishikawa, M., Wanat, M.J., Phillips, P.E., Dong, Y., Roth, B.L., and Neumaier, J.F. (2011). Transient neuronal inhibition reveals opposing roles of indirect and direct pathways in sensitization. Nat. Neurosci. 14, 22-24. https://doi.org/10.1038/nn.2703
- Freund, T.F., Powell, J.F., and Smith, A.D. (1984). Freund Tyrosine hydroxylase immunoreactive boutons in synaptic contact with identified striatonigral neurons with particular reference to dendritic spines. Neuroscience. 13, 1189-1215. https://doi.org/10.1016/0306-4522(84)90294-X
- Fuchs, R.A., Weber, S.M., Rice, H.J., and Neisewander, J.L. (2002). Effects of excitotoxic lesions of the basolateral amygdala on cocaineseeking behavior and cocaine conditioned place preference in rats. Brain Res. 929, 15-25. https://doi.org/10.1016/S0006-8993(01)03366-2
- Fuchs, R.A., Eaddy, J.L., Su, Z.I., and Bell, G.H. (2007). Interactions of the basolateral amygdala with the dorsal hippocampus and dorsomedial prefrontal cortex regulate drug context-induced reinstatement of cocaine-seeking in rats. Eur. J. Neurosci. 26, 487-498. https://doi.org/10.1111/j.1460-9568.2007.05674.x
- Gerfen, C.R., and Surmeier, D.J. (2011). Modulation of striatal projection systems by dopamine. Annu. Rev. Neurosci. 34, 441-466. https://doi.org/10.1146/annurev-neuro-061010-113641
- Gerfen, C.R., Engber, T.M., Mahan, L.C., Susel, Z., Chase, T.N, Monsma, F.J.Jr., and Sibley, D.R.(1990). D1 and D2 dopamine receptor-regulated gene expression of striatonigral and striatopallidal neurons. Science 250, 1429-1432. https://doi.org/10.1126/science.2147780
- Giorgetti, M., Hotsenpiller, G., Ward, P., Teppen, T., and Wolf, M.E. (2001). Amphetamine-induced plasticity of AMPA receptors in the ventral tegmental area: effects on extracellular levels of dopamine and glutamate in freely moving rats. J. Neurosci. 21, 6362-6369. https://doi.org/10.1523/JNEUROSCI.21-16-06362.2001
- Haber, S.N. (2003). The primate basal ganglia: parallel and integrative networks. J. Chem. Neuroanat. 26, 317-330. https://doi.org/10.1016/j.jchemneu.2003.10.003
- Hyman, S.E., Malenka, R.C., and Nestler, E.J. (2006). NEURAL MECHANISMS OF ADDICTION: The Role of Reward-Related Learning and Memory. Annu. Rev. Neurosci. 29, 565-598. https://doi.org/10.1146/annurev.neuro.29.051605.113009
- Ishikawa, M., Otaka, M., Huang, Y.H., Neumann, P.A., Winters, B.D., Grace, A.A., Schlu, O.M., and Dong, Y. (2013). Dopamine Triggers Heterosynaptic Plasticity. J. Neurosci. 33, 6759-6765. https://doi.org/10.1523/JNEUROSCI.4694-12.2013
- Kalivas, P.W. (2009). The glutamate homeostasis hypothesis of addiction. Nat. Rev. Neurosci. 10, 561-572. https://doi.org/10.1038/nrn2515
- Kalivas, P.W., and Duffy, P. (1993). Time course of extracellular dopamine and behavioral sensitization to cocaine. I. Dopamine axon terminals. J. Neurosci. 13, 266-275. https://doi.org/10.1523/JNEUROSCI.13-01-00266.1993
- Kalivas, P.W., and McFarland, K. (2003). Brain circuitry and the reinstatement of cocaine-seeking behavior. Psychopharmacology (Berl) 168, 44-56. https://doi.org/10.1007/s00213-003-1393-2
- Killcross, S., and Coutureau, E. (2003). Coordination of actions and habits in the medial prefrontal cortex of rats. Cereb. Cortex 13, 400-408. https://doi.org/10.1093/cercor/13.4.400
- Kim, J., Pignatelli, M., Xu, S., Itohara, S., and Tonegawa, S. (2016). Antagonistic negative and positive neurons of the basolateral amygdala. Nat. Neurosci. 19, 1636-1646. https://doi.org/10.1038/nn.4414
- Kincaid, A.E., Zheng, T., and Wilson, C.J. (1998). Connectivity and convergence of single corticostriatal axons. J. Neurosci. 18, 4722-4731. https://doi.org/10.1523/JNEUROSCI.18-12-04722.1998
- Koya, E., Uejima, J.L., Wihbey, K.A., Bossert, J.M., Hope, B.T., and Shaham, Y. (2009). Role of ventral medial prefrontal cortex in incubation of cocaine craving. Neuropharmacology 56, 177-185. https://doi.org/10.1016/j.neuropharm.2008.04.022
- Koya, E., Cruz, F.C., Ator, R., Golden, S.A., Hoffman, A.F., Lupica, C.R., and Hope, B.T. (2012). Silent synapses in selectively activated nucleus accumbens neurons following cocaine sensitization. Nat. Neurosci. 15, 1556-1562. https://doi.org/10.1038/nn.3232
- Kravitz, A.V., Tye, L.D., and Kreitzer, A.C. (2012). Distinct roles for direct and indirect pathway striatal neurons in reinforcement. Nat. Neurosci. 15, 816-818. https://doi.org/10.1038/nn.3100
- Lee, B.R., Ma, Y.Y., Huang, Y.H., Wang, X., Otaka, M., Ishikawa, M., Neumann, P.A., Graziane, N. M., Brown, T.E., Suska, A., et al. (2013). Maturation of silent synapses in amygdala-accumbens projection contributes to incubation of cocaine craving. Nat. Neurosci. 16, 1644-1651. https://doi.org/10.1038/nn.3533
- Lobo, M.K., Covington, H.E. 3rd., Chaudhury, D, Friedman, A.K., Sun, H., Damez-Werno, D., Dietz, D.M., Zaman, S., Koo, J.W., Kennedy P.J., et al. (2010). Cell type-specific loss of BDNF signaling mimics optogenetic control of cocaine reward. Science 330, 385-390. https://doi.org/10.1126/science.1188472
- Luscher, C., Pascoli, V., and Creed, M. (2015). Optogenetic dissection of neural circuitry: From synaptic causalities to blue prints for novel treatments of behavioral diseases. Curr. Opin. Neurobiol. 35, 95-100. https://doi.org/10.1016/j.conb.2015.07.005
- Ma, Y.Y., Lee, B.R., Wang, X., Guo, C., Liu, L., Cui, R., Lan, Y., Balcita-Pedicino, J.J., Wolf, M.E., Sesack, S.R., et al. (2014). Bidirectional modulation of incubation of cocaine craving by silent synapse-based remodeling of prefrontal cortex to accumbens projections. Neuron 83, 1453-1467. https://doi.org/10.1016/j.neuron.2014.08.023
- MacAskill, A.F., Cassel, J.M., and Carter, A.G. (2014). Cocaine exposure reorganizes cell type- and input-specific connectivity in the nucleus accumbens. Nat. Neurosci. 17, 1198-1207. https://doi.org/10.1038/nn.3783
- Neve, K.A., Seamans, J.K., and Trantham-Davidson, H. (2004). Dopamine Receptor Signaling. J. Recept. Signal Transduct. 24, 165-205. https://doi.org/10.1081/RRS-200029981
- Ostlund, S.B., and Balleine, B.W. (2005). Lesions of Medial Prefrontal Cortex disrupt the acquisition but not the expression of goal-directed learning. J. Neurosci. 25, 7763-7770. https://doi.org/10.1523/JNEUROSCI.1921-05.2005
- Pascoli, V., Terrier, J., Espallergues, J., Valjent, E., O'Connor, E.C., and Luscher, C. (2014). Contrasting forms of cocaine-evoked plasticity control components of relapse. Nature 509, 459-464. https://doi.org/10.1038/nature13257
- Pascoli, V., Terrier, J., Hiver, A., and Lu, C. (2015). Sufficiency of mesolimbic dopamine neuron stimulation for the progression to addiction. Neuron 88, 1054-1066. https://doi.org/10.1016/j.neuron.2015.10.017
- Paton, J.J., Belova, M.A., Morrison, S.E., and Salzman, C.D. (2006). The primate amygdala represents the positive and negative value of visual stimuli during learning. Nature 439, 865-870. https://doi.org/10.1038/nature04490
- Peters, J., Vallone, J., Laurendi, K., and Kalivas, P.W. (2008). Opposing roles for the ventral prefrontal cortex and the basolateral amygdala on the spontaneous recovery of cocaine-seeking in rats. Psychopharmacology (Berl) 197, 319-326. https://doi.org/10.1007/s00213-007-1034-2
- Rogers, J.L., and See, R.E. (2007). Selective inactivation of the ventral hippocampus attenuates cue-induced and cocaine-primed reinstatement of drug-seeking in rats. Neurobiol. Learn. Mem. 87, 688-692. https://doi.org/10.1016/j.nlm.2007.01.003
- Saal, D., Dong, Y., Bonci, A., and Malenka, R.C. (2003). Drugs of abuse and stress trigger a common synaptic adaptation in dopamine neurons. Neuron 37, 577-582. https://doi.org/10.1016/S0896-6273(03)00021-7
- Shaham, Y., Erb, S., and Stewart, J. (2000). Stress-induced relapse to heroin and cocaine seeking in rats: a review. Brain Res. Rev. 33, 13-33. https://doi.org/10.1016/S0165-0173(00)00024-2
- Shukla, A., Beroun, A., Panopoulou, M., Neumann, P.A., Grant, S.G., Olive, M.F., Dong, Y., and Schluter, O.M. (2017). Calcium-permeable AMPA receptors and silent synapses in cocaine-conditioned place preference. EMBO J. 36, 458-474. https://doi.org/10.15252/embj.201695465
- Smith, Y., Bennett, B.D., Bolam, J.P., Parent, A., and Sadikot, A.F. (1994). Synaptic relationships between dopaminergic afferents and cortical or thalamic input in the sensorimotor territory of the striatum in monkey. J. Comp. Neurol. 344, 1-19. https://doi.org/10.1002/cne.903440102
- Stefanik, M.T., Moussawi, K., Kupchik, Y.M., Smith, K.C., Miller, R.L., Huff, M.L., Deisseroth, K., Kalivas, P.W., and Lalumiere, R.T. (2013). Optogenetic inhibition of cocaine seeking in rats. Addict. Biol. 18, 50-53. https://doi.org/10.1111/j.1369-1600.2012.00479.x
- Steinberg, E.E., Boivin, J.R., Saunders, B.T., Witten, I.B., Deisseroth, K., and Janak, P.H. (2014). Positive reinforcement mediated by midbrain dopamine neurons requires D1 and D2 receptor activation in the nucleus accumbens. PLoS One 9, e94771. https://doi.org/10.1371/journal.pone.0094771
- Stuber, G.D., Sparta, D.R., Stamatakis, A.M., van Leeuwen, W.A., Hardjoprajitno, J.E., Cho, S., Tye, K.M., Kempadoo, K.A., Zhang, F., Deisseroth, K., et al. (2011). Excitatory transmission from the amygdala to nucleus accumbens facilitates reward seeking. Nature 475, 377-380. https://doi.org/10.1038/nature10194
- Tsai, H.C., Zhang, F., Adamantidis, A., Stuber, G.D., Bonci, A., de Lecea L., Deisseroth, K. (2009). Phasic Firing in dopaminergic neurons is sufficient for behavioral conditioning. Science 324, 1080-1084. https://doi.org/10.1126/science.1168878
- Tye, K.M., and Deisseroth, K. (2012). Optogenetic investigation of neural circuits underlying brain disease in animal models. Nat. Rev. Neurosci. 13, 251-266. https://doi.org/10.1038/nrn3171
- Tzschentke, T.M. (1998). Measuring reward with the conditioned place preference paradigm: a comprehensive review of drug effects, recent progress and new issues. Prog. Neurobiol. 56, 613-672. https://doi.org/10.1016/S0301-0082(98)00060-4
- Ungless, M.A., Whistler, J.L., Malenka, R.C., and Bonci, A. (2001). Single cocaine exposure in vivo induces long-term potentiation in dopamine neurons. Nature 411, 583-587. https://doi.org/10.1038/35079077
- Walsh, J.J., Friedman, A.K., Sun, H., Heller, E.A., Ku, S.M., Juarez, B., Burnham, V.L., Mazei-Robison, M.S., Ferguson, D., Golden, S.A., et al. (2014). Stress and CRF gate neural activation of BDNF in the mesolimbic reward pathway. Nat. Neurosci. 17, 27-29. https://doi.org/10.1038/nn.3591
- Warner-Schmidt, J.L., Schmidt, E.F., Marshall, J.J., Rubin, A.J., Arango-Lievano, M., Kaplitt, M.G., Ibanez-Tallon, I., Heintz, N., Greengard, P. (2012). Cholinergic interneurons in the nucleus accumbens regulate depression-like behavior. Proc. Natl. Acad. Sci. USA 109, 11360-11365. https://doi.org/10.1073/pnas.1209293109
- Whitelaw, R.B., Markou, A., Robbins, T.W., Everitt, B.J. (1996). Excitotoxic lesions of the basolateral amygdala impair the acquisition of cocaine-seeking behaviour under a second-order schedule of reinforcememt. Psychopharmacology 127, 213-224. https://doi.org/10.1007/BF02805996
- Wise, R.A. (1998). Drug-activation of brain reward pathways. Drug Alcohol Depend. 51, 13-22. https://doi.org/10.1016/S0376-8716(98)00063-5
- Wise, R.A., and Koob, G.F. (2014). The development and maintenance of drug addiction. Neuropsychopharmacology 39, 254-262. https://doi.org/10.1038/npp.2013.261
- Witten, I.B., Steinberg, E.E., Lee, S.Y., Davidson, T.J., Zalocusky, K.A., Brodsky, M., Yizhar, O., Cho, S.L., Gong, S., Ramakrishnan, C., et al. (2011). Recombinase-driver rat lines: tools, techniques, and optogenetic application to dopamine-mediated reinforcement. Neuron 72, 721-733. https://doi.org/10.1016/j.neuron.2011.10.028
- Yin, H.H., and Knowlton, B.J. (2006). The role of the basal ganglia in habit formation. Nat. Rev. Neurosci. 7, 464-476. https://doi.org/10.1038/nrn1919
- Yorgason, J.T., Zeppenfeld, D.M., and Williams, J.T. (2017). Cholinergic interneurons underlie spontaneous dopamine release in nucleus accumbens. J. Neurosci. 37, 2086-2096. https://doi.org/10.1523/JNEUROSCI.3064-16.2017
- Zhu, Y., Wienecke, C.F., Nachtrab, G., and Chen, X. (2016). A thalamic input to the nucleus accumbens mediates opiate dependence. Nature 530, 219-222. https://doi.org/10.1038/nature16954
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