The DOI matches its Crossref record; 70 of the 70 references it cites were found in a registry or an index.
Basolateral to Central Amygdala Neural Circuits for Appetitive Behaviors
Open accessAbstract
Summary Basolateral amygdala (BLA) principle cells are capable of driving and antagonizing behaviors of opposing valence. BLA neurons project to the central amygdala (CeA), which also participates in negative and positive behaviors. However, the CeA has primarily been studied as the site for negative behaviors and the causal role for CeA circuits underlying appetitive behaviors is poorly understood. Here we identified several genetically distinct populations of CeA neurons that mediate appetitive behaviors and dissected the BLA to CeA circuit for appetitive behaviors. Protein phosphatase 1 regulatory subunit 1B+ BLA pyramidal neurons to dopamine receptor 1+ CeA neurons define a pathway for promoting appetitive behaviors, while R-spondin 2+ BLA pyramidal neurons to dopamine receptor 2+ CeA neurons define a pathway for suppressing appetitive behaviors. These data reveal genetically defined neural circuits in the amygdala that promote and suppress appetitive behaviors analogous to the direct and indirect pathway of the basal ganglia.
Overview
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
Verification
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.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
D 1 and D 2 Dopamine Receptor-regulated Gene Expression of Striatonigral and Striatopallidal Neurons
Gerfen, C. R., Engber, T. M., Mahan, L. C., Susel, Z., Chase, T. N., Monsma, F. J., & Sibley, D. R. (1990) · Science · doi:10.1126/science.2147780 · Cited by 2,967
The role of the amygdala in fear and anxiety
Davis, M. (1992) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.15.030192.002033 · Cited by 2,357
Berridge, K. C., & Robinson, T. E. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00233-9 · Cited by 1,869
LeDoux, J., Iwata, J., Cicchetti, P., & Reis, D. (1988) · The Journal of Neuroscience · doi:10.1523/jneurosci.08-07-02517.1988 · Cited by 1,580
Swanson, L. W., & Petrovich, G. D. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01265-x · Cited by 1,351
Monosynaptic Restriction of Transsynaptic Tracing from Single, Genetically Targeted Neurons
Wickersham, I. R., Lyon, D. C., Barnard, R. J. O., Mori, T., Finke, S., Conzelmann, K.-K., Young, J. A. T., & Callaway, E. M. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.033 · Cited by 1,187
Pitkänen, A., Savander, V., & LeDoux, J. E. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01125-9 · Cited by 980
(1998) · Neuroscience · doi:10.1016/s0306-4522(98)00004-9 · Cited by 941
Activity-dependent neuronal plasticity following tissue injury and inflammation
Dubner, R., & Ruda, M. A. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90019-5 · Cited by 926
Encoding of conditioned fear in central amygdala inhibitory circuits
Ciocchi, S., Herry, C., Grenier, F., Wolff, S. B. E., Letzkus, J. J., Vlachos, I., Ehrlich, I., Sprengel, R., Deisseroth, K., Stadler, M. B., et al. (2010) · Nature · doi:10.1038/nature09559 · Cited by 924
Amygdala inhibitory circuits and the control of fear memory
Ehrlich, I., Humeau, Y., Grenier, F., Ciocchi, S., Herry, C., & Lüthi, A. (2009) · Neuron · doi:10.1016/j.neuron.2009.05.026 · Cited by 878
Genetic dissection of an amygdala microcircuit that gates conditioned fear
Haubensak, W., Kunwar, P. S., Cai, H., Ciocchi, S., Wall, N. R., Ponnusamy, R., Biag, J., Dong, H.-W., Deisseroth, K., Callaway, E. M., et al. (2010) · Nature · doi:10.1038/nature09553 · Cited by 840 · cited 11×
“Cell-type-specific studies have shown evidence for the involvement of several genetically defined CeA neurons in aversive behaviors such as defensive responses and anxiogenesis (Andero et al., 2014; Han et al., 2015; Haubensak et al., 2010; Isosaka et al., 2015; Li et al., 2013;McCall et al., 2015; Pomrenze et al., 20…”
BackgroundResultInfluentialCorticostriatal connectivity and its role in disease
Shepherd, G. M. G. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3469 · Cited by 824
Amygdala Microcircuits Controlling Learned Fear
Duvarci, S., & Pare, D. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.042 · Cited by 751
Midbrain circuits for defensive behaviour
Tovote, P., Esposito, M. S., Botta, P., Chaudun, F., Fadok, J. P., Markovic, M., Wolff, S. B. E., Ramakrishnan, C., Fenno, L., Deisseroth, K., et al. (2016) · Nature · doi:10.1038/nature17996 · Cited by 732
CRH Engagement of the Locus Coeruleus Noradrenergic System Mediates Stress-Induced Anxiety
McCall, J. G., Al-Hasani, R., Siuda, E. R., Hong, D. Y., Norris, A. J., Ford, C. P., & Bruchas, M. R. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.002 · Cited by 666
Different types of fear-conditioned behaviour mediated by separate nuclei within amygdala
Killcross, S., Robbins, T. W., & Everitt, B. J. (1997) · Nature · doi:10.1038/41097 · Cited by 644
Kim, J. J., Rison, R. A., & Fanselow, M. S. (1993) · Behavioral Neuroscience · doi:10.1037/0735-7044.107.6.1093 · Cited by 615
Self-citationHemmings, H. C., Greengard, P., Tung, H. Y. L., & Cohen, P. (1984) · Nature · doi:10.1038/310503a0 · Cited by 614
Genetic identification of a neural circuit that suppresses appetite
Carter, M. E., Soden, M. E., Zweifel, L. S., & Palmiter, R. D. (2013) · Nature · doi:10.1038/nature12596 · Cited by 587
Histology of the nervous system of man and vertebrates
y Cajal, S. R. (1995) · Cited by 553
Hitchcock, J., & Davis, M. (1986) · Behavioral Neuroscience · doi:10.1037/0735-7044.100.1.11 · Cited by 541
Cell type–specific genetic and optogenetic tools reveal hippocampal CA2 circuits
Kohara, K., Pignatelli, M., Rivest, A. J., Jung, H.-Y., Kitamura, T., Suh, J., Frank, D., Kajikawa, K., Mise, N., Obata, Y., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3614 · Cited by 528
Self-citationExperience-dependent modification of a central amygdala fear circuit
Li, H., Penzo, M. A., Taniguchi, H., Kopec, C. D., Huang, Z. J., & Li, B. (2013) · Nature Neuroscience · doi:10.1038/nn.3322 · Cited by 497 · cited 10×
“A previous study has demonstrated that CeL Sst+ neurons elicit and are required for defensive behaviors (Li et al., 2013).”
BackgroundResultInfluentialEncoding of fear learning and memory in distributed neuronal circuits
Herry, C., & Johansen, J. P. (2014) · Nature Neuroscience · doi:10.1038/nn.3869 · Cited by 474
Elucidating an Affective Pain Circuit that Creates a Threat Memory
Han, S., Soleiman, M. T., Soden, M. E., Zweifel, L. S., & Palmiter, R. D. (2015) · Cell · doi:10.1016/j.cell.2015.05.057 · Cited by 454
Goosens, K. A., & Maren, S. (2001) · Learning & Memory · doi:10.1101/lm.37601 · Cited by 451
Antagonistic negative and positive neurons of the basolateral amygdala
Kim, J., Pignatelli, M., Xu, S., Itohara, S., & Tonegawa, S. (2016) · Nature Neuroscience · doi:10.1038/nn.4414 · Cited by 445
Self-citationSkofitsch, G., & Jacobowitz, D. M. (1985) · Peptides · doi:10.1016/0196-9781(85)90178-0 · Cited by 426
Gallagher, M., & Chiba, A. A. (1996) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(96)80076-6 · Cited by 410 · cited 6×
“Nevertheless, the involvement of several distinct CeA projection neurons as positive mediators of appetitive behavior validates the integral role of the CeA in reward-related function (Badrinarayan et al., 2012; Gallagher and Chiba, 1996; Gallagher et al., 1990; Knapska et al., 2006; Parkinson et al., 2000; Ron and Ba…”
BackgroundInfluentialThe Midbrain Periaqueductal Gray as a Coordinator of Action in Response to Fear and Anxiety
Fanselow, M. S. (1991) · The Midbrain Periaqueductal Gray Matter · doi:10.1007/978-1-4615-3302-3_10 · Cited by 391
Central amygdala PKC-δ+ neurons mediate the influence of multiple anorexigenic signals
Cai, H., Haubensak, W., Anthony, T. E., & Anderson, D. J. (2014) · Nature Neuroscience · doi:10.1038/nn.3767 · Cited by 376
Mcdonald, A. J. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90248-m · Cited by 372
Gallagher, M., Graham, P., & Holland, P. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-06-01906.1990 · Cited by 359
Warden, M. K., & Young, W. S. (1988) · Journal of Comparative Neurology · doi:10.1002/cne.902720107 · Cited by 315
Moga, M. M., & Gray, T. S. (1985) · Journal of Comparative Neurology · doi:10.1002/cne.902410304 · Cited by 315
Dissociable roles of the central and basolateral amygdala in appetitive emotional learning
Parkinson, J. A., Robbins, T. W., & Everitt, B. J. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00960.x · Cited by 268
Merali, Z., McIntosh, J., Kent, P., Michaud, D., & Anisman, H. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-12-04758.1998 · Cited by 268
Ethanol Augments GABAergic Transmission in the Central Amygdala via CRF1 Receptors
Nie, Z., Schweitzer, P., Roberts, A. J., Madamba, S. G., Moore, S. D., & Siggins, G. R. (2004) · Science · doi:10.1126/science.1092550 · Cited by 266
Parabrachial CGRP Neurons Control Meal Termination
Campos, C. A., Bowen, A. J., Schwartz, M. W., & Palmiter, R. D. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.04.006 · Cited by 262
Histology of the Nervous System of Man and Vertebrates
Freemon, F. R. (1996) · JAMA: The Journal of the American Medical Association · doi:10.1001/jama.1996.03530300077050 · Cited by 252
Reiner, A., Jiao, Y., Del Mar, N., Laverghetta, A. V., & Lei, W. L. (2003) · Journal of Comparative Neurology · doi:10.1002/cne.10541 · Cited by 241
Corticostriatal projection neurons – dichotomous types and dichotomous functions
Reiner, A. (2010) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2010.00142 · Cited by 201
A Central Amygdala CRF Circuit Facilitates Learning about Weak Threats
Sanford, C. A., Soden, M. E., Baird, M. A., Miller, S. M., Schulkin, J., Palmiter, R. D., Clark, M., & Zweifel, L. S. (2017) · Neuron · doi:10.1016/j.neuron.2016.11.034 · Cited by 198
Penzo, M. A., Robert, V., & Li, B. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4166-13.2014 · Cited by 187
Robinson, M. J. F., Warlow, S. M., & Berridge, K. C. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.2013-14.2014 · Cited by 183
Koo, J. W., Han, J.-S., & Kim, J. J. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1644-04.2004 · Cited by 179
Self-citationHtr2a-Expressing Cells in the Central Amygdala Control the Hierarchy between Innate and Learned Fear
Isosaka, T., Matsuo, T., Yamaguchi, T., Funabiki, K., Nakanishi, S., Kobayakawa, R., & Kobayakawa, K. (2015) · Cell · doi:10.1016/j.cell.2015.10.047 · Cited by 179
Molecular mechanisms underlying alcohol-drinking behaviours
Ron, D., & Barak, S. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.85 · Cited by 165
Neuronal organization of the lateral and basolateral amygdaloid nuclei in the rat
McDonald, A. J. (1984) · Journal of Comparative Neurology · doi:10.1002/cne.902220410 · Cited by 160
Zirlinger, M., Kreiman, G., & Anderson, D. J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.091094698 · Cited by 159
The basolateral amygdaloid complex as a cortical-like structure
Carlsen, J., & Heimer, L. (1988) · Brain Research · doi:10.1016/0006-8993(88)91418-7 · Cited by 151
The one-two punch of alcoholism: role of central amygdala dynorphins/kappa-opioid receptors
Kissler, J. L., Sirohi, S., Reis, D. J., Jansen, H. T., Quock, R. M., Smith, D. G., & Walker, B. M. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.03.014 · Cited by 145
Pomrenze, M. B., Millan, E. Z., Hopf, F. W., Keiflin, R., Maiya, R., Blasio, A., Dadgar, J., Kharazia, V., de Guglielmo, G., Crawford, E. F., et al. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00487 · Cited by 130
Galaverna, O., Seeley, R. J., Berridge, K. C., Grill, H. J., Epstein, A. N., & Schulkin, J. A. (1993) · Behavioural Brain Research · doi:10.1016/0166-4328(93)90146-h · Cited by 122
Differential involvement of the central amygdala in appetitive versus aversive learningPreprint
Knapska, E., Walasek, G., Nikolaev, E., Neuhäusser-Wespy, F., Lipp, H., Kaczmarek, L., & Werka, T. (2006) · Learning & Memory · doi:10.1101/lm.54706 · Cited by 121
A Role for Tac2 , NkB, and Nk3 Receptor in Normal and Dysregulated Fear Memory Consolidation
Andero, R., Dias, B. G., & Ressler, K. J. (2014) · Neuron · doi:10.1016/j.neuron.2014.05.028 · Cited by 104
Bandler, R. J., & Depaulis, A. (1988) · Neuroscience Letters · doi:10.1016/0304-3940(88)90226-1 · Cited by 96
Seo, D.-O., Funderburk, S. C., Bhatti, D. L., Motard, L. E., Newbold, D. J., Girven, K. S., McCall, J. G., Krashes, M. J., Sparta, D. R., & Bruchas, M. R. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1164-16.2016 · Cited by 67
D’Hanis, W., Linke, R., & Yilmazer‐Hanke, D. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21495 · Cited by 61
Dynorphins Regulate Fear Memory: from Mice to Men
Bilkei‐Gorzó, A., Erk, S., Schurmann, B., Mauer, D., Michel, K., Boecker, H., Scheef, L., Walter, H., & Zimmer, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1034-12.2012 · Cited by 59
Rosén, A., Zhang, Y., Lund, I., Lundeberg, T., & Yu, L. (2004) · Brain Research · doi:10.1016/j.brainres.2003.11.060 · Cited by 55
Mercaptoacetate-induced feeding is impaired by central nucleus of the amygdala lesions
RITTER, S. (1995) · Physiology & Behavior · doi:10.1016/0031-9384(95)02050-0 · Cited by 52
Hwang, B. H., Stewart, R. B., Zhang, J. K., Lumeng, L., & Li, T. (2004) · Brain Research · doi:10.1016/j.brainres.2004.08.042 · Cited by 49
Cui, X.-Y., Lundeberg, T., & Yu, L. (2003) · Brain Research · doi:10.1016/j.brainres.2003.09.050 · Cited by 38
Helmchen, C., Fu, Q., & Sandkühler, J. (1995) · Neuroscience Letters · doi:10.1016/0304-3940(95)11345-2 · Cited by 35
Pereira, D. T. B., Vendramini, R. C., Menani, J. V., et al. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00359.2009 · Cited by 21
Dalmasso, C., Antunes‐Rodrigues, J., Vivas, L., & Junior, L. A. D. L. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.08.020 · Cited by 12
The Role of the Central Amygdala in Selecting Circuits and Responses
Badrinarayan, A., Prater, K. E., & Orsini, C. A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1820-12.2012 · Cited by 12
Cornea-Hébert (1999) · doi:10.1002/(sici)1096-9861(19990628)409:2<187::aid-cne2>3.0.co;2-p
Cited by
Initiative, A. N. G., Watson, H. J., Eating Disorders Working Group of the Psychiatric Genomics Consortium, Yilmaz, Z., Thornton, L. M., Hübel, C., Coleman, J. R. I., Gaspar, H. A., Bryois, J., Hinney, A., et al. (2019) · Nature Genetics · doi:10.1038/s41588-019-0439-2 · Cited by 1,109
Brain circuit dysfunction in post-traumatic stress disorder: from mouse to man
Fenster, R. J., Lebois, L. A. M., Ressler, K. J., & Suh, J. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0039-7 · Cited by 456
Overlapping Brain Circuits for Homeostatic and Hedonic Feeding
Rossi, M. A., & Stuber, G. D. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2017.09.021 · Cited by 415
Neuromodulation by the immune system: a focus on cytokines
Salvador, A. F., de Lima, K. A., & Kipnis, J. (2021) · Nature Reviews Immunology · doi:10.1038/s41577-021-00508-z · Cited by 389
“Liking” and “wanting” in eating and food reward: Brain mechanisms and clinical implications
Morales, I., & Berridge, K. C. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.113152 · Cited by 346
Metadata
- Authors
- Kim, J., Zhang, X., Muralidhar, S., LeBlanc, S. A., & Tonegawa, S.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2017-03
- Volume
- 93
- Issue
- 6
- Pages
- 1464-1479.e5
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2602799162
- Cited by
- 458
- References
- 70
- FWCI
- 24.19
- Type
- journal article
- Language
- en
- Open access
- bronze
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.