Granular insular cortex inactivation as a novel therapeutic strategy for nicotine addiction
Open accessAbstract
Background Nicotine is the principal component of tobacco smoke, resulting in addiction, and recent evidence suggests that damage to the insular cortex (insula) disrupts tobacco addiction in human smokers. However, the effect of an inactivation of this structure in an animal model of nicotine addiction has yet to be evaluated. Methods To study this question, we investigated the effects of reversible inactivation of the granular insula by local injection of a gamma-aminobutyric acid agonists mixture (baclofen/muscimol) on nicotine self-administration (SA) under fixed and progressive ratio and on reinstatement of nicotine seeking induced by nicotine priming or nicotine-associated cues in rats. We also evaluated the effects of granular insula inactivation on food SA and relapse as a control. Results The inactivation of the granular insula decreased nicotine SA under both fixed and progressive ratios without affecting the SA of food under the same schedules of reinforcement. This inactivation also prevented the reinstatement, after extinction, of nicotine seeking induced by nicotine-associated cues or nicotine priming without modifying the reinstatement of food seeking. Conclusions Our study indicates that the integrity of the granular insula is necessary for exhibiting motivation to take nicotine and to relapse to nicotine seeking but not for consuming food pellets or to relapse for food seeking. Indeed, it might be interesting to study the effect of methods that are able to modulate the activity of the insula--such as repetitive transcranial magnetic stimulation or deep brain stimulation--on tobacco addiction and relapse in humans.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
aAgIC or pGIC chemical inactivation attenuates nicotine taking under various ratio schedules of reinforcement.
“Our own laboratory demonstrated that aAgIC or pGIC chemical inactivation attenuates nicotine taking, under various ratio schedules of reinforcement”
From The Insula: A Brain Stimulation Target for the Treatment of Addiction (2019) · cites this paper as Forget et al., 2010
aAgIC or pGIC inactivation demonstrated no effect on food taking in rats under a moderately restricted diet.
“These methods of inactivation demonstrated no effect on food taking in rats under a moderately restricted diet.”
From The Insula: A Brain Stimulation Target for the Treatment of Addiction (2019) · cites this paper as Forget et al., 2010
aAgIC or pGIC inactivation attenuates nicotine seeking.
“Our own laboratory demonstrated that aAgIC or pGIC inactivation attenuates nicotine seeking”
From The Insula: A Brain Stimulation Target for the Treatment of Addiction (2019) · cites this paper as Forget et al., 2010
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The rat brain in stereotaxic coordinates
Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959 · see citing works
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works
How do you feel? Interoception: The sense of the physiological condition of the body
Craig, A. D. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn894 · Cited by 6,006 · see citing works
Subcortical and cortical brain activity during the feeling of self-generated emotions
Damasio, A. R., Grabowski, T. J., Bechara, A., Damasio, H., Ponto, L. L. B., Parvizi, J., & Hichwa, R. D. (2000) · Nature Neuroscience · doi:10.1038/79871 · Cited by 2,117 · see citing works
The reinstatement model of drug relapse: history, methodology and major findings
Shaham, Y., Shalev, U., Lu, L., de Wit, H., & Stewart, J. (2003) · Psychopharmacology · doi:10.1007/s00213-002-1224-x · Cited by 1,615 · see citing works
Paulus, M. P., & Stein, M. B. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.03.042 · Cited by 1,325 · see citing works
A role for lateral hypothalamic orexin neurons in reward seeking
Harris, G. C., Wimmer, M., & Aston-Jones, G. (2005) · Nature · doi:10.1038/nature04071 · Cited by 1,311 · see citing works
Damage to the insula disrupts addiction to cigarette smoking
Naqvi, N. H., Rudrauf, D., Damasio, H., & Bechara, A. (2007) · Science · doi:10.1126/science.1135926 · Cited by 1,245 · see citing works
The circuitry mediating cocaine-induced reinstatement of drug-seeking behavior
McFarland, K., & Kalivas, P. W. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-21-08655.2001 · Cited by 905 · see citing works
The hidden island of addiction: the insula
Naqvi, N. H., & Bechara, A. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2008.09.009 · Cited by 833 · see citing works
Evidence for a viscerotopic sensory representation in the cortex and thalamus in the rat
Cechetto, D. F., & Saper, C. B. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902620104 · Cited by 703 · see citing works
Brain circuitry and the reinstatement of cocaine-seeking behavior
Kalivas, P., & McFarland, K. (2003) · Psychopharmacology · doi:10.1007/s00213-003-1393-2 · Cited by 613 · see citing works
Nicotine maintains robust self-administration in rats on a limited-access schedule
Corrigall, W. A., & Coen, K. M. (1989) · Psychopharmacology · doi:10.1007/bf00589894 · Cited by 578 · see citing works
Markou, A., Weiss, F., Gold, L. H., Caine, S. B., Schulteis, G., & Koob, G. F. (1993) · Psychopharmacology · doi:10.1007/bf02244907 · Cited by 551 · see citing works
Infralimbic Prefrontal Cortex Is Responsible for Inhibiting Cocaine Seeking in Extinguished Rats
Peters, J., LaLumiere, R. T., & Kalivas, P. W. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1045-08.2008 · Cited by 537 · see citing works
Role for hypocretin in mediating stress-induced reinstatement of cocaine-seeking behavior
Boutrel, B., Kenny, P. J., Specio, S. E., Martin-Fardon, R., Markou, A., Koob, G. F., & de Lecea, L. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507480102 · Cited by 520 · see citing works
Neural systems and cue-induced cocaine craving
Bonson, K. (2002) · Neuropsychopharmacology · doi:10.1016/s0893-133x(01)00371-2 · Cited by 507 · see citing works
Organization of visceral and limbic connections in the insular cortex of the rat
Allen, G. V., Saper, C. B., Hurley, K. M., & Cechetto, D. F. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903110102 · Cited by 501 · see citing works
Microstimulation-Induced Inhibition of Neuronal Firing in Human Globus Pallidus
Dostrovsky, J. O., Levy, R., Wu, J. P., Hutchison, W. D., Tasker, R. R., & Lozano, A. M. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.1.570 · Cited by 470 · see citing works
Brain metabolic changes during cigarette craving
Brody, A. L., Mandelkern, M. A., London, E. D., Childress, A. R., Lee, G. S., Bota, R. G., Ho, M. L., Saxena, S., Baxter, L. R., Madsen, D., et al. (2002) · Archives of General Psychiatry · doi:10.1001/archpsyc.59.12.1162 · Cited by 425 · see citing works
The Cortical Dopamine System: Role in Memory and Cognition
Goldman, P. S. (1997) · Advances in pharmacology · doi:10.1016/s1054-3589(08)60846-7 · Cited by 393 · see citing works
The orexin system regulates alcohol-seeking in rats
Lawrence, A. J., Cowen, M. S., Yang, H., Chen, F., & Oldfield, B. (2006) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706789 · Cited by 392 · see citing works
Arnold, J. M., & Roberts, D. C. S. (1997) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(96)00445-5 · Cited by 390 · see citing works
Franklin, T. R., wang, Z., Wang, J., Sciortino, N., Harper, D., Li, Y., Ehrman, R., Kampman, K. M., O’Brien, C. P., Detre, J. A., et al. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301371 · Cited by 359 · see citing works
Persistent Behavior at High Rates Maintained by Intravenous Self-Administration of Nicotine
Goldberg, S. R., Spealman, R. D., & Goldberg, D. M. (1981) · Science · doi:10.1126/science.7291998 · Cited by 343 · see citing works
Regional brain metabolic activation during craving elicited by recall of previous drug experiences
Wang, G.-J., Volkow, N. D., Fowler, J. S., Cervany, P., Hitzemann, R. J., Pappas, N. R., Wong, C. T., & Felder, C. (1999) · Life Sciences · doi:10.1016/s0024-3205(98)00619-5 · Cited by 336 · see citing works
McBride, D., Barrett, S. P., Kelly, J. T., Aw, A., & Dagher, A. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301075 · Cited by 323 · see citing works
Inactivation of the Interoceptive Insula Disrupts Drug Craving and Malaise Induced by Lithium
Contreras, M., Ceric, F., & Torrealba, F. (2007) · Science · doi:10.1126/science.1145590 · Cited by 297 · see citing works
Insular hypocretin transmission regulates nicotine reward
Hollander, J. A., Lu, Q., Cameron, M. D., Kamenecka, T. M., & Kenny, P. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808023105 · Cited by 296 · see citing works
Nicotine self-administration in animals and humans: similarities and differences
Rose, J. E., & Corrigall, W. A. (1997) · Psychopharmacology · doi:10.1007/s002130050209 · Cited by 262 · see citing works
Pharmacological inactivation in the analysis of the central control of movement
Martin, J. H., & Ghez, C. P. (1999) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(98)00163-0 · Cited by 245 · see citing works
Increase of Extracellular Dopamine in Primate Prefrontal Cortex During a Working Memory Task
Watanabe, M., Kodama, T., & Hikosaka, K. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.5.2795 · Cited by 236 · see citing works
Richards, J. K., Simms, J. A., Steensland, P., Taha, S. A., Borgland, S. L., Bonci, A., & Bartlett, S. E. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1136-5 · Cited by 234 · see citing works
Nicotine self-administration in rats
Donny, E. C., Caggiula, A. R., Knopf, S., & Brown, C. (1995) · Psychopharmacology · doi:10.1007/bf02246272 · Cited by 227 · see citing works
Daskalakis, Z. J., Möller, B., Christensen, B. K., Fitzgerald, P. B., Gunraj, C. A., & Chen, R. E. (2006) · Experimental Brain Research · doi:10.1007/s00221-006-0472-0 · Cited by 224 · see citing works
McClernon, F. J., Hiott, F. B., Huettel, S. A., & Rose, J. E. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300780 · Cited by 216 · see citing works
Magariños-Ascone, C. M., Pazo, J. H., Macadar, O., & Buño, W. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00538-9 · Cited by 169 · see citing works
D1 dopamine receptor binding in mood disorders measured by positron emission tomography
Suhara, T., Nakayama, K., Inoue, O., Fukuda, H., Shimizu, M., Mori, A., & Tateno, Y. (1992) · Psychopharmacology · doi:10.1007/bf02253582 · Cited by 163 · see citing works
Paterson, N. E., & Markou, A. (2004) · Psychopharmacology · doi:10.1007/s00213-004-2070-9 · Cited by 155 · see citing works
Markou, A., & Paterson, N. E. (2001) · Nicotine & Tobacco Research · doi:10.1080/14622200110073380 · Cited by 155 · see citing works
Lee, J.-H., Lim, Y., Wiederhold, B. K., & Graham, S. J. (2005) · Applied Psychophysiology and Biofeedback · doi:10.1007/s10484-005-6377-z · Cited by 153 · see citing works
Morrisj, J. S. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(02)01946-0 · Cited by 142 · see citing works
Analgesia elicited by prefrontal stimulation
Patrick Hardy, S. G. (1985) · Brain Research · doi:10.1016/0006-8993(85)90093-9 · Cited by 133 · see citing works
Nicotine as a typical drug of abuse in experimental animals and humans
Foll, B. L., & Goldberg, S. R. (2005) · Psychopharmacology · doi:10.1007/s00213-005-0155-8 · Cited by 131 · see citing works
Forget, B., Coen, K. M., & Foll, B. L. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1569-5 · Cited by 118 · see citing works
Self-citationThe Global Smoking Epidemic: A History and Status Report
Proctor, R. N. (2004) · Clinical Lung Cancer · doi:10.3816/clc.2004.n.016 · Cited by 111 · see citing works
Corrigall, W. A., Coen, K. M., Zhang, J., & Adamson, L. K. (2001) · Psychopharmacology · doi:10.1007/s002130100869 · Cited by 96 · see citing works
Activation of orexin neurons by acute nicotine
Pasumarthi, R. K., Reznikov, L. R., & Fadel, J. R. (2006) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2006.02.021 · Cited by 90 · see citing works
Kiss, Z. H. T., Mooney, D., Renaud, L. P., & Hu, B. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00122-7 · Cited by 82 · see citing works
Ciano, P. D., & Everitt, B. J. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03232.x · Cited by 79 · see citing works
van Duuren, E., Plasse, G., van der Blom, R., Joosten, R. N. J. M. A., Mulder, A. B., Pennartz, C. M. A., & Feenstra, M. G. P. (2007) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.124784 · Cited by 78 · see citing works
Mecamylamine Attenuates Cue-Induced Reinstatement of Nicotine-Seeking Behavior in Rats
Liu, X., Caggiula, A. R., Yee, S. K., Nobuta, H., Sved, A. F., Pechnick, R. N., & Poland, R. E. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301129 · Cited by 69 · see citing works
High Reinforcing Efficacy of Nicotine in Non-Human Primates
Foll, B. L., Wertheim, C. E., & Goldberg, S. R. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000230 · Cited by 66 · see citing works
Self-Administration of Intravenous Nicotine in Male and Female Cigarette Smokers
Sofuoglu, M., Yoo, S., Hill, K. P., & Mooney, M. E. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301460 · Cited by 63 · see citing works
Changing cortical excitability with low-frequency magnetic stimulation
Chen, R., & Seitz, R. (2001) · Neurology · doi:10.1212/wnl.57.3.379 · Cited by 62 · see citing works
Self-administration of stimulants and serotonergic systems.
Roberts, D. (1992) · PubMed · Cited by 8 · see citing works
Flagged first, then by citations
1 of the 58 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Bossert, J. M., Marchant, N. J., Calu, D. J., & Shaham, Y. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3120-y · Cited by 453 · see citing works
Neural substrates of smoking cue reactivity: A meta-analysis of fMRI studies
Engelmann, J. M., Versace, F., Robinson, J. D., Minnix, J. A., Lam, C. Y., Cui, Y., Brown, V. L., & Cinciripini, P. M. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.024 · Cited by 394 · see citing works
The insula: a critical neural substrate for craving and drug seeking under conflict and risk
Naqvi, N. H., Gaznick, N., Tranel, D., & Bechara, A. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12415 · Cited by 336 · see citing works
Animal models of drug relapse and craving
Vènniro, M., Caprioli, D., & Shaham, Y. (2015) · Progress in brain research · doi:10.1016/bs.pbr.2015.08.004 · Cited by 322 · see citing works
Revisiting the role of the insula in addiction
Droutman, V., Read, S. J., & Bechara, A. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.05.005 · Cited by 317 · see citing works
Neural Primacy of the Salience Processing System in Schizophrenia
Palaniyappan, L. K., Simmonite, M., White, T. P., Liddle, E. B., & Liddle, P. F. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.027 · Cited by 297 · see citing works
Neural systems underlying approach and avoidance in anxiety disorders
Robin L., A., & Martin, P. P. (2010) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2010.12.4/raupperle · Cited by 227 · see citing works
Deep brain stimulation in addiction: a review of potential brain targets
Luigjes, J., van den Brink, W., Feenstra, M. G. P., van den Munckhof, P., Schuurman, P. R., Schippers, R., Mazaheri, A., Vries, T. J. D., & Denys, D. A. J. P. (2011) · Molecular Psychiatry · doi:10.1038/mp.2011.114 · Cited by 222 · see citing works
Regulation of nausea and vomiting by cannabinoids and the endocannabinoid system
Sharkey, K. A., Darmani, N. A., & Parker, L. A. (2013) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2013.09.068 · Cited by 195 · see citing works
Conditioned flavor avoidance and conditioned gaping: Rat models of conditioned nausea
Parker, L. A. (2013) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2013.09.070 · Cited by 140 · see citing works
The Insula: A Brain Stimulation Target for the Treatment of Addiction
Ibrahim, C., Rubin-Kahana, D. S., Pushparaj, A., Musiol, M., Blumberger, D. M., Daskalakis, Z. J., Zangen, A., & Le Foll, B. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00720 · Cited by 133 · see citing works
Self-citationThe hypocretin (orexin) system: from a neural circuitry perspective
Li, S., & de Lecea, L. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.107993 · Cited by 130 · see citing works
Deep brain stimulation of the nucleus accumbens for the treatment of addiction
Müller, U., Voges, J., Steiner, J. H., Galazky, I., Heinze, H., Möller, M., Pisapia, J. M., Halpern, C. H., Caplan, A. L., Bogerts, B., et al. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06834.x · Cited by 120 · see citing works
Central role for the insular cortex in mediating conditioned responses to anticipatory cues
Kusumoto‐Yoshida, I., Liu, H., Chen, B. T., Fontanini, A., & Bonci, A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1416573112 · Cited by 119 · see citing works
Better living through understanding the insula: Why subregions can make all the difference
Centanni, S. W., Janes, A. C., Haggerty, D. L., Atwood, B. K., & Hopf, F. W. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108765 · Cited by 108 · see citing works
Ouzir, M., & Errami, M. (2016) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2016.06.005 · Cited by 110 · see citing works
Cannabinoid receptor stimulation increases motivation for nicotine and nicotine seeking
Gamaleddin, I., Wertheim, C. E., Zhu, A. Z. X., Coen, K. M., Vemuri, K. V., Makryannis, A., Goldberg, S. R., & Foll, B. L. (2011) · Addiction Biology · doi:10.1111/j.1369-1600.2011.00314.x · Cited by 92 · see citing works
Janes, A. C., Farmer, S. L., Peechatka, A. L., Frederick, B. B., & Lukas, S. E. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.9 · Cited by 90 · see citing works
Brain Stimulation Methods to Treat Tobacco Addiction
Wing, V. C., Barr, M. S., Wass, C., Lipsman, N., Lozano, A. M., Daskalakis, Z. J., & George, T. P. (2012) · Brain stimulation · doi:10.1016/j.brs.2012.06.008 · Cited by 88 · see citing works
A Role for the Insular Cortex in Long-Term Memory for Context-Evoked Drug Craving in Rats
Contreras, M., Billeke, P. B., Vicencio, S., Madrid, C., Perdomo, G., González, M., & Torrealba, F. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.59 · Cited by 81 · see citing works
A genetically defined insula-brainstem circuit selectively controls motivational vigor
Deng, H., Xiao, X., Yang, T., Ritola, K., Hantman, A., Li, Y., Huang, Z. J., & Li, B. (2021) · Cell · doi:10.1016/j.cell.2021.11.019 · Cited by 75 · see citing works
Functional role for cortical-striatal circuitry in modulating alcohol self-administration
Jaramillo, A. A., Randall, P. A., Stewart, S., Fortino, B., Voorhies, K. V., & Besheer, J. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.11.035 · Cited by 76 · see citing works
Gueye, A. B., Pryslawsky, Y., Trigo, J. M., Poulia, N., Delis, F., Antoniou, K., Loureiro, M., Laviolette, S. R., Vemuri, K., Makriyannis, A., et al. (2016) · International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyw068 · Cited by 74 · see citing works
Gaznick, N., Tranel, D., McNutt, A., & Bechara, A. (2014) · Nicotine & Tobacco Research · doi:10.1093/ntr/ntt172 · Cited by 72 · see citing works
Pushparaj, A. P., Hamani, C., Yu, W., Shin, D. S.-H., Kang, B., Nóbrega, J. N., & Foll, B. L. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.235 · Cited by 73 · see citing works
Self-citationTuerke, K. J., Limebeer, C. L., Fletcher, P. J., & Parker, L. A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.2042-12.2012 · Cited by 71 · see citing works
Yan, Y., Pushparaj, A. P., Strat, Y. L., Gamaleddin, I., Barnes, C., Justinová, Z., Goldberg, S. R., & Foll, B. L. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.245 · Cited by 67 · see citing works
Self-citationTurel, O., & Bechara, A. (2016) · Frontiers in Psychology · doi:10.3389/fpsyg.2016.00455 · Cited by 68 · see citing works
Gamaleddin, I., Zvonok, A. M., Makriyannis, A., Goldberg, S. R., & Foll, B. L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029900 · Cited by 66 · see citing works
Foll, B. L., Ciano, P. D., Panlilio, L. V., Goldberg, S. R., & Ciccocioppo, R. (2013) · Current Drug Targets · doi:10.2174/1389450111314070006 · Cited by 66 · see citing works
Damage to the insula leads to decreased nicotine withdrawal during abstinence
Abdolahi, A., Williams, G. C., Benesch, C. G., Wang, H. Z., Spitzer, E. M., Scott, B. E., Block, R., & van Wijngaarden, E. (2015) · Addiction · doi:10.1111/add.13061 · Cited by 65 · see citing works
Cosme, C. V., Gutman, A. L., & LaLumiere, R. T. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.92 · Cited by 64 · see citing works
Deconstructing Craving: Dissociable Cortical Control of Cue Reactivity in Nicotine Addiction
Scott, D., & Hiroi, N. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.01.023 · Cited by 63 · see citing works
Foll, B. L., Chatterjee‐Chakraborty, M., Lev‐Ran, S., Barnes, C., Pushparaj, A. P., Gamaleddin, I., Yan, Y., Khaled, M. A. T. M., & Goldberg, S. R. (2011) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145711001398 · Cited by 61 · see citing works
Self-citationBotticelli, L., Bonaventura, E. M. D., Bello, F. D., Giorgioni, G., Piergentili, A., Romano, A., Quaglia, W., Cifani, C., & Bonaventura, M. V. M. D. (2020) · Nutrients · doi:10.3390/nu12082288 · Cited by 61 · see citing works
Malik, S., Jacobs, M., Cho, S.-S., Boileau, I., Blumberger, D., Heilig, M., Wilson, A., Daskalakis, Z. J., Strafella, A. P., Zangen, A., et al. (2018) · Brain Imaging and Behavior · doi:10.1007/s11682-017-9800-1 · Cited by 58 · see citing works
Cocker, P. J., Foll, B. L., Rogers, R. D., & Winstanley, C. A. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.08.026 · Cited by 55 · see citing works
Gamaleddin, I., Guranda, M., Goldberg, S. R., & Foll, B. L. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01440.x · Cited by 53 · see citing works
Involvement of the rostral agranular insular cortex in nicotine self-administration in rats
Pushparaj, A. P., Kim, A. S., Musiol, M., Trigo, J. M., & Foll, B. L. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.04.039 · Cited by 50 · see citing works
Self-citationThe role of alpha-7 nicotinic receptors in food intake behaviors
Legget, K. T., Cornier, M., & Tregellas, J. R. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.00553 · Cited by 49 · see citing works
N-Oleoyl-glycine reduces nicotine reward and withdrawal in mice
Donvito, G., Piscitelli, F., Muldoon, P. P., Jackson, A. B., Vitale, R. M., D’Aniello, E., Giordano, C., Ignatowska-Jankowska, B. M., Mustafa, M. A., Guida, F., et al. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.03.020 · Cited by 49 · see citing works
McClernon, F. J., Conklin, C. A., Kozink, R. V., Adcock, R. A., Sweitzer, M. M., Addicott, M. A., Chou, Y., Chen, N., Hallyburton, M. B., & DeVito, A. M. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.214 · Cited by 49 · see citing works
Namba, M. D., Tomek, S. E., Olive, M. F., Beckmann, J. S., & Gipson, C. D. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00017 · Cited by 47 · see citing works
Gil-Lievana, E., Balderas, I., Moreno‐Castilla, P., Luis-Islas, J., McDevitt, R. A., Tecuapetla, F., Gutiérrez, R., Bonci, A., & Bermúdez‐Rattoni, F. (2020) · Communications Biology · doi:10.1038/s42003-020-0862-z · Cited by 43 · see citing works
Janes, A. C., Gilman, J. M., Radoman, M., Pachas, G. N., D, M. F. M., & Evins, A. E. (2017) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2017.06.012 · Cited by 46 · see citing works
Li, C.-L., Zhu, N., Meng, X., Li, Y., & Sui, N. (2013) · Journal of Psychopharmacology · doi:10.1177/0269881113492028 · Cited by 45 · see citing works
The implication of salience network abnormalities in young male adult smokers
Li, Y., Yuan, K., Guan, Y., Cheng, J., Bi, Y., Shi, S., Xue, T., Lu, X., Qin, W., Yu, D., et al. (2016) · Brain Imaging and Behavior · doi:10.1007/s11682-016-9568-8 · Cited by 42 · see citing works
A Human Polymorphism in CHRNA5 Is Linked to Relapse to Nicotine Seeking in Transgenic Rats
Forget, B., Scholze, P., Vives, F. L., Morel, C., Pons, S., Mondoloni, S., Besson, M., Cuttoli, R. D.-D., Hay, Y. A., Tricoire, L., et al. (2018) · Current Biology · doi:10.1016/j.cub.2018.08.044 · Cited by 41 · see citing works
Self-citationJanes, A. C., Krantz, N. L., Nickerson, L. D. H., Frederick, B. B., & Lukas, S. E. (2019) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2019.09.005 · Cited by 40 · see citing works
Role of insular cortex D1 and D2 dopamine receptors in nicotine self-administration in rats
Kutlu, M. G., Burke, D., Slade, S., Hall, B. J., Rose, J. E., & Levin, E. D. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.08.005 · Cited by 41 · see citing works
Ibrahim, C., Tang, V. M., Blumberger, D. M., Malik, S., Tyndale, R. F., Trevizol, A. P., Barr, M. S., Daskalakis, Z. J., Zangen, A., & Foll, B. L. (2023) · Brain stimulation · doi:10.1016/j.brs.2023.10.002 · Cited by 37 · see citing works
Zelle, S. L., Gates, K. M., Fiez, J. A., Sayette, M. A., & Wilson, S. J. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.03.015 · Cited by 40 · see citing works
Reward loss and addiction: Opportunities for cross-pollination
Ortega, L. A., Solano, J. L., Torres, C., & Papini, M. R. (2017) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2017.02.001 · Cited by 38 · see citing works
Development of Novel Pharmacotherapeutics for Tobacco Dependence: Progress and Future Directions
Harmey, D., Griffin, P. R., & Kenny, P. J. (2012) · Nicotine & Tobacco Research · doi:10.1093/ntr/nts201 · Cited by 37 · see citing works
How the Brain Wants What the Body Needs: The Neural Basis of Positive Alliesthesia
Avery, J. A., Burrows, K., Kerr, K. L., Bodurka, J., Khalsa, S. S., Paulus, M. P., & Simmons, W. K. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2016.128 · Cited by 35 · see citing works
Wei, Z., Yang, N., Liu, Y., Yang, L., Wang, Y., Han, L., Zha, R., Huang, R., Zhang, P., Zhou, Y., et al. (2016) · Scientific Reports · doi:10.1038/srep21778 · Cited by 34 · see citing works
Belief about Nicotine Modulates Subjective Craving and Insula Activity in Deprived Smokers
Gu, X., Lohrenz, T. M., Salas, R., Baldwin, P. R., Soltani, A., Kirk, U., Cinciripini, P. M., & Montague, P. R. (2016) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2016.00126 · Cited by 34 · see citing works
The insula in nicotine use disorder: Functional neuroimaging and implications for neuromodulation
Regner, M. F., Tregellas, J. R., Kluger, B. M., Wylie, K. P., Gowin, J. L., & Tanabe, J. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.06.002 · Cited by 34 · see citing works
Forget, B., Guranda, M., Gamaleddin, I., Goldberg, S. R., & Foll, B. L. (2016) · Psychopharmacology · doi:10.1007/s00213-016-4232-y · Cited by 34 · see citing works
Self-citationInvolvement of the caudal granular insular cortex in alcohol self-administration in rats
Pushparaj, A. P., & Foll, B. L. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.07.044 · Cited by 34 · see citing works
Self-citationPushparaj, A. P., Kim, A. S., Musiol, M., Zangen, A., Daskalakis, Z. J., Zack, M. H., Winstanley, C. A., & Foll, B. L. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.133 · Cited by 33 · see citing works
Self-citationXu, X., Wang, J., Aron, A. P., Lei, W., Westmaas, J. L., & Weng, X. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042235 · Cited by 32 · see citing works
Deep brain stimulation in addiction due to psychoactive substance use
Kuhn, J., Bührle, C., Lenartz, D., & Sturm, V. (2013) · Handbook of clinical neurology · doi:10.1016/b978-0-444-53497-2.00021-8 · Cited by 32 · see citing works
Smoking cessation behaviors three months following acute insular damage from stroke
Abdolahi, A., Williams, G. C., Benesch, C. G., Wang, H. Z., Spitzer, E. M., Scott, B. E., Block, R., & van Wijngaarden, E. (2015) · Addictive Behaviors · doi:10.1016/j.addbeh.2015.07.001 · Cited by 32 · see citing works
Do brain responses to emotional images and cigarette cues differ? An fMRI study in smokers
Versace, F., Engelmann, J. M., Jackson, E. F., Costa, V. D., Robinson, J. D., Lam, C. Y., Minnix, J. A., Brown, V., Wetter, D. W., & Cinciripini, P. M. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07915.x · Cited by 31 · see citing works
Transcriptomic Characterization of the Human Insular Cortex and Claustrum
Ibrahim, C., Foll, B. L., & French, L. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2019.00094 · Cited by 30 · see citing works
Dopaminergic modulation of impulsive decision making in the rat insular cortex
Pattij, T., Schetters, D., & Schoffelmeer, A. N. M. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.05.010 · Cited by 29 · see citing works
Kushnir, V., Menon, M., Balducci, X. L., Selby, P. L., Busto, U. E., & Zawertailo, L. A. (2010) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145710000696 · Cited by 29 · see citing works
Janes, A. C., Ross, R. S., Farmer, S., Frederick, B. B., Nickerson, L. D., Lukas, S. E., & Stern, C. E. (2015) · Addiction Biology · doi:10.1111/adb.12112 · Cited by 28 · see citing works
Immediate and Sustained Decrease in Smoking Urges After Acute Insular Cortex Damage
Abdolahi, A., Williams, G. C., Benesch, C. G., Wang, H. Z., Spitzer, E. M., Scott, B. E., Block, R., & van Wijngaarden, E. (2017) · Nicotine & Tobacco Research · doi:10.1093/ntr/ntx046 · Cited by 28 · see citing works
Maldonado, R. J., Calvé, P., García‐Blanco, A., Domingo‐Rodriguez, L., Senabre, E., & Martín‐García, E. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108466 · Cited by 28 · see citing works
Loney, G. C., King, C. P., & Meyer, P. (2021) · Scientific Reports · doi:10.1038/s41598-021-81955-5 · Cited by 24 · see citing works
Cocker, P. J., Lin, M.-Y., Barrus, M. M., Foll, B. L., & Winstanley, C. A. (2016) · Psychopharmacology · doi:10.1007/s00213-016-4355-1 · Cited by 24 · see citing works
Janes, A. C., Gilman, J. M., Frederick, B. B., Radoman, M., Pachas, G. N., D, M. F. M., & Evins, A. E. (2017) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2017.11.005 · Cited by 23 · see citing works
Harris, N. A., & Winder, D. G. (2018) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.8b00169 · Cited by 22 · see citing works
FDA cigarette warning labels lower craving and elicit frontoinsular activation in adolescent smokers
Do, K. T., & Galván, A. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv038 · Cited by 22 · see citing works
Role of anterior insula cortex in context-induced relapse of nicotine-seeking
Ghareh, H., Alonso-Lozares, I., Schetters, D., Herman, R. J., Heistek, T. S., van Mourik, Y., Jean-Richard-dit-Bressel, P., Zernig, G., Mansvelder, H. D., Vries, T. J. D., et al. (2022) · eLife · doi:10.7554/elife.75609 · Cited by 22 · see citing works
Yu, G., & Sharp, B. M. (2015) · Psychopharmacology · doi:10.1007/s00213-015-3911-4 · Cited by 21 · see citing works
Foll, B. L., Pushparaj, A. P., Pryslawsky, Y., Forget, B., Vemuri, K. V., Makriyannis, A., & Trigo, J. M. (2013) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2013.10.009 · Cited by 20 · see citing works
Self-citationNicotine-induced dendritic remodeling in the insular cortex
Ehlinger, D. G., Bergstrom, H. C., McDonald, C. G., & Smith, R. F. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.03.064 · Cited by 20 · see citing works
Stoker, A. K., & Markou, A. (2015) · Current topics in behavioral neurosciences · doi:10.1007/978-3-319-13482-6_5 · Cited by 21 · see citing works
Alcohol sensory processing and its relevance for ingestion
Brasser, S. M., Castro, N., & Feretic, B. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.09.004 · Cited by 21 · see citing works
Ma, H., Wang, N., Wang, X., Jia, M., Li, Y., & Cui, C. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.10.032 · Cited by 19 · see citing works
Pribut, H. J., Vázquez, D., Brockett, A. T., Wei, A. D., Tennyson, S. S., & Roesch, M. R. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.3025-20.2021 · Cited by 19 · see citing works
Sato, H., Kawano, T., Yin, D. X., Kato, T., & Toyoda, H. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.06.031 · Cited by 16 · see citing works
Duehlmeyer, L., & Hester, R. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.101819 · Cited by 16 · see citing works
Role of the orbitofrontal cortex and the dorsal striatum in incentive motivation for cocaine
Minogianis, E.-A., Servonnet, A., Filion, M.-P., & Samaha, A. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112026 · Cited by 14 · see citing works
GABAB Receptor: Structure, Biological Functions, and Therapy for Diseases
Xie, W., Li, Y., Wang, X., Blokhina, E. A., Krupitsky, E. M., Vetrova, M., Hu, J., Yuan, T., Chen, J., Wang, H., et al. (2025) · MedComm · doi:10.1002/mco2.70163 · Cited by 14 · see citing works
Interoceptive Stimulus Effects of Drugs of Abuse
Thompson, B. M., Bevins, R. A., & Murray, J. E. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812202-0.00007-5 · Cited by 14 · see citing works
Wang, F., JING, X., Yang, J., Wang, H., Xiang, R., Han, W., Liu, X., & WU, C. (2016) · Physiological Research · doi:10.33549/physiolres.933106 · Cited by 14 · see citing works
Nicotine facilitates synaptic depression in layer V pyramidal neurons of the mouse insular cortex
Toyoda, H. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.02.046 · Cited by 14 · see citing works
Tang, V. M., Goud, R., Zawertailo, L. A., Selby, P. L., Coroiu, A., Sloan, M. E., Chenoweth, M. J., Buchman, D. Z., Ibrahim, C., Blumberger, D. M., et al. (2023) · Psychiatry Research · doi:10.1016/j.psychres.2023.115340 · Cited by 13 · see citing works
McGregor, M. S., Cosme, C. V., & LaLumiere, R. T. (2024) · Neuropsychopharmacology · doi:10.1038/s41386-024-01846-x · Cited by 12 · see citing works
Ma, P., Liu, H., Li, H., Huang, X., Chen, L., & Zhai, H. (2014) · Neuroreport · doi:10.1097/wnr.0000000000000146 · Cited by 12 · see citing works
Cue-Elicited Brain Activity and Treatment Outcomes in Substance Use Disorders
Evohr, B., Wenzel, S., Chen, N., Wade, C., Ekhtiari, H., Ketron, A. C., Janes, A. C., & Gilman, J. M. (2025) · JAMA Network Open · doi:10.1001/jamanetworkopen.2025.48809 · Cited by 11 · see citing works
Nicotinic activity layer specifically modulates synaptic potentiation in the mouse insular cortex
Toyoda, H. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13857 · Cited by 11 · see citing works
Bozinoff, N., & Foll, B. L. (2018) · Expert Review of Respiratory Medicine · doi:10.1080/17476348.2018.1507736 · Cited by 11 · see citing works
Forget, B., Icick, R., Robert, J., Correia, C., Prevost, M. S., Gielen, M. C., Corringer, P., Bellivier, F., Vorspan, F., Besson, M., et al. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101898 · Cited by 11 · see citing works
Self-citationYan, Y., Pushparaj, A. P., Gamaleddin, I., Steiner, R. C., Picciotto, M. R., Roder, J., & Foll, B. L. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.01.042 · Cited by 11 · see citing works
Self-citationExercise Modulates Brain Glucose Utilization Response to Acute Cocaine
Hanna, C., Hamilton, J., Blum, K., Badgaiyan, R. D., & Thanos, P. K. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12121976 · Cited by 10 · see citing works
- Authors
- Forget, B., Pushparaj, A., & Le Foll, B.
- Affiliations
- University of Toronto (CA)
- ORCID
- Pushparaj, Abhiram
- Venue
- Biological Psychiatry
- Publisher
- Elsevier BV
- Published
- 2010-08
- Volume
- 68
- Issue
- 3
- Pages
- 265-271
- ISSN
- 0006-3223 (ISSN-L)
- OpenAlex
- W2035027501
- Cited by
- 153
- References
- 58
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 7 · 2023: 6 · 2022: 6 · 2021: 9 · 2020: 10 · 2019: 9 · 2018: 12 · 2017: 11 · 2016: 13 · 2015: 17 · 2014: 7 · 2013: 14 · 2012: 13
- FWCI
- 8.45
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Biological Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ontario Ministry of Research, Innovation and Science
- Topics
- Health Sciences › Medicine › Physiology › Smoking Behavior and Cessation
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Keywords
- nicotine dependence, insula, neural inactivation, nicotine self-administration, relapse, food self-administration, motivation
- MeSH terms
- Analysis of Variance, Animals, Association Learning, Baclofen, Behavior, Animal, Cerebral Cortex, Conditioning, Classical, Disease Models, Animal, Drug Combinations, Extinction, Psychological, Male, Microinjections, Motivation, Muscimol, Nicotine, Reinforcement Schedule, Self Administration, Tobacco Use Disorder, Behavior, Addictive, Nicotinic Agonists, GABA Agonists, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review