Differential efferent projections of GABAergic neurons in the basolateral and central nucleus of amygdala in mice
Abstract
The Basolateral amygdala (BLA) and central nucleus of the amygdala (CEA) have been proved to play a key role in the control of anxiety, stress and fear-related behaviors. BLA is a cortex-like complex consisting of both γ-aminobutyric acidergic (GABAergic) interneurons and glutamatergic neurons. The CEA is a striatum-like output of the amygdala, consisting almost exclusively of GABAergic medium spiny neurons. In this study, we explored the morphology and axonal projections of the GABAergic neurons in BLA and CEA, using conditional anterograde axonal tracing, immunohistochemistry, and VGAT-Cre transgenic mice to further understand their functional roles. We found that the axonal projections of GABAergic neurons from the BLA mainly distributed to the forebrain, whilst GABAergic neurons from the CEA distributed to the forebrain, midbrain and brainstem. In the forebrain, the axonal projections of GABAergic neurons from the BLA projected to the anterior olfactory nucleus, the cerebral cortex, the septum, the striatum, the thalamus, the amygdala and the hippocampus. The axonal projections of GABAergic neurons from the CEA distributed to the nuclei of the prefrontal cortex, the bed nucleus of the stria terminalis, the hypothalamus and the thalamus. In the midbrain and brainstem, the axonal projections of GABAergic neurons from the CEA were found in the periaqueductal gray, the substantia nigra, and the locus coeruleus. These data reveal the neuroanatomical basis for exploring the function of GABAergic neurons in the BLA and CEA, particularly during the processing of fear-related behavior.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
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?
The CeA can work indirectly via the midbrain with the dorsolateral striatum to regulate habit formation.
“The CeA can also work indirectly, likely via the midbrain67,68, with the dorsolateral striatum to regulate habit formation32,66.”
From A dual-pathway architecture for stress to disrupt agency and promote habit (2025) · cites this paper as [67]
Cites
The mouse brain in stereotaxic coordinates
Konsman, J. (2003) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(03)00088-x · Cited by 16,796 · see citing works
The Mouse Brain in Stereotaxic Coordinates
Paxinos, G. (2001) · Cited by 12,859 · see citing works
From circuits to behaviour in the amygdala
Janak, P. H., & Tye, K. M. (2015) · Nature · doi:10.1038/nature14188 · Cited by 2,011 · see citing works
Neuronal circuits for fear and anxiety
Tovote, P., Fadok, J. P., & Lüthi, A. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3945 · Cited by 1,786 · see citing works
The Amygdaloid Complex: Anatomy and Physiology
SAH, P., FABER, E. S. L., LOPEZ DE ARMENTIA, M., & POWER, J. (2003) · Physiological Reviews · doi:10.1152/physrev.00002.2003 · Cited by 1,745 · see citing works
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 · see citing works
Amygdala Microcircuits Controlling Learned Fear
Duvarci, S., & Pare, D. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.042 · Cited by 751 · see citing works
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 · see citing works
BLA to vHPC inputs modulate anxiety-related behaviors
Felix-Ortiz, A. C., Beyeler, A., Seo, C., Leppla, C. A., Wildes, C. P., & Tye, K. M. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.016 · Cited by 592 · see citing works
Experience-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 · see citing works
Anxiety disorders and GABA neurotransmission: a disturbance of modulation
Nuss, P. (2015) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s58841 · Cited by 482 · see citing works
Amygdala inputs to the ventral hippocampus bidirectionally modulate social behavior
Felix-Ortiz, A. C., & Tye, K. M. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4257-13.2014 · Cited by 473 · see citing works
The Central Amygdala as an Integrative Hub for Anxiety and Alcohol Use Disorders
Gilpin, N. W., Herman, M. A., & Roberto, M. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.09.008 · Cited by 457 · see citing works
Bzdok, D., Laird, A. R., Zilles, K., Fox, P. T., & Eickhoff, S. B. (2012) · Human Brain Mapping · doi:10.1002/hbm.22138 · Cited by 430 · see citing works
Arousal Effect of Caffeine Depends on Adenosine A2A Receptors in the Shell of the Nucleus Accumbens
Lazarus, M., Shen, H.-Y., Cherasse, Y., Qu, W.-M., Huang, Z.-L., Bass, C. E., Winsky-Sommerer, R., Semba, K., Fredholm, B. B., Boison, D., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6730-10.2011 · Cited by 327 · see citing works
Inhibition in the amygdala anxiety circuitry
Babaev, O., Chatain, C. P., & Krueger‐Burg, D. (2018) · Experimental & Molecular Medicine · doi:10.1038/s12276-018-0063-8 · Cited by 312 · see citing works
Amygdala Inhibitory Circuits Regulate Associative Fear Conditioning
Krabbe, S., Gründemann, J., & Lüthi, A. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.10.006 · Cited by 255 · see citing works
New perspectives on central amygdala function
Fadok, J. P., Marković, M., Tovote, P., & Lüthi, A. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.02.009 · Cited by 255 · see citing works
Thompson, J. M., & Neugebauer, V. (2017) · Pain Research and Management · doi:10.1155/2017/8296501 · Cited by 231 · see citing works
Functional neuroanatomy of anxiety: a neural circuit perspective
Etkin, A. (2009) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2009_5 · Cited by 227 · see citing works
Chhatwal, J. P., Myers, K. M., Ressler, K. J., & Davis, M. E. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3301-04.2005 · Cited by 214 · see citing works
Generalization of amygdala LTP and conditioned fear in the absence of presynaptic inhibition
Shaban, H., Humeau, Y., Herry, C., Casassus, G., Shigemoto, R., Ciocchi, S., Barbieri, S., van der Putten, H., Kaupmann, K., Bettler, B., et al. (2006) · Nature Neuroscience · doi:10.1038/nn1732 · Cited by 208 · see citing works
Durieux, P. F., Schiffmann, S. N., & d’Exaerde, A. D. K. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.400 · Cited by 206 · see citing works
A Central Amygdala CRF Circuit Facilitates Learning about Weak Threats
Sanford, C. A., Soden, M. E., Baird, M. A., Miller, S. M., Schulkin, J. A., Palmiter, R. D., Clark, M., & Zweifel, L. S. (2016) · Neuron · doi:10.1016/j.neuron.2016.11.034 · Cited by 199 · see citing works
Penzo, M. A., Robert, V., & Li, B. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4166-13.2014 · Cited by 187 · see citing works
The basolateral amygdala γ‐aminobutyric acidergic system in health and disease
Prager, E. M., Bergstrom, H. C., Wynn, G. H., & Braga, M. F. M. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23690 · Cited by 179 · see citing works
Distribution of GABA immunoreactivity in the amygdaloid complex of the cat
Paré, D., & Smith, Y. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90049-l · Cited by 152 · see citing works
Stress in Regulation of GABA Amygdala System and Relevance to Neuropsychiatric Diseases
Jie, F., Yin, G., Yang, W., Yang, M., Gao, S., Lv, J., & Li, B. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00562 · Cited by 139 · see citing works
Andrewes, D., & Jenkins, L. (2019) · Neuropsychology Review · doi:10.1007/s11065-019-09398-4 · Cited by 138 · see citing works
The developing amygdala: a student of the world and a teacher of the cortex
Tottenham, N., & Gabard-Durnam, L. J. (2017) · Current Opinion in Psychology · doi:10.1016/j.copsyc.2017.06.012 · Cited by 130 · see citing works
A feedback neural circuit for calibrating aversive memory strength
Ozawa, T., Ycu, E. A., Kumar, A., Yeh, L.-F., Ahmed, T., Koivumaa, J., & Johansen, J. P. (2016) · Nature Neuroscience · doi:10.1038/nn.4439 · Cited by 123 · see citing works
Almeida-Suhett, C. P., Prager, E. M., Pidoplichko, V. I., Figueiredo, T. H., Marini, A. M., Li, Z., Eiden, L. E., & Braga, M. F. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102627 · Cited by 117 · see citing works
Considerations When Using Cre-Driver Rodent Lines for Studying Ventral Tegmental Area Circuitry
Stuber, G. D., Stamatakis, A. M., & Kantak, P. A. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.034 · Cited by 105 · see citing works
Aroniadou‐Anderjaska, V., Qashu, F. M., & Braga, M. F. M. (2006) · Amino Acids · doi:10.1007/s00726-006-0415-x · Cited by 92 · see citing works
Gautron, L., Lazarus, M., Scott, M. M., Saper, C. B., & Elmquist, J. K. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22323 · Cited by 82 · see citing works
McDonald, A. J., Mascagni, F., & Zaric, V. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00046 · Cited by 78 · see citing works
Superior Colliculus GABAergic Neurons Are Essential for Acute Dark Induction of Wakefulness in Mice
Zhang, Z., Liu, W., Diao, Y., Xu, W., Zhong, Y.-H., Zhang, J., Lazarus, M., Liu, Y., Qu, W., & Huang, Z. (2019) · Current Biology · doi:10.1016/j.cub.2018.12.031 · Cited by 73 · see citing works
Amygdala Circuits for Fear Memory: A Key Role for Dopamine Regulation
Lee, J. H., Lee, S. H., & Kim, J. (2016) · The Neuroscientist · doi:10.1177/1073858416679936 · Cited by 63 · see citing works
Zhang, J., Xu, Q., Yuan, X.-S., Chérasse, Y., Schiffmann, S. N., d’Exaerde, A. D. K., Qu, W., Urade, Y., Lazarus, M., Huang, Z., et al. (2013) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2013.00043 · Cited by 55 · see citing works
Self-citationKlumpp, H., & Fitzgerald, J. M. (2018) · Current Psychiatry Reports · doi:10.1007/s11920-018-0948-1 · Cited by 53 · see citing works
Stefanits, H., Milenković, I., Mahr, N., Pataraia, E., Hainfellner, J. A., Kovács, G. G., Sieghart, W., Yilmazer‐Hanke, D., & Czech, T. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24337 · Cited by 48 · see citing works
GABAergic somatostatin-immunoreactive neurons in the amygdala project to the entorhinal cortex
McDonald, A. J., & Zaric, V. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.01.028 · Cited by 45 · see citing works
Li, R., Nishijo, H., Wang, Q.-X., Uwano, T., Tamura, R., Ohtani, O., & Ono, T. (2001) · The Journal of comparative neurology · doi:10.1002/cne.1359 · Cited by 38 · see citing works
Self-citationLi, Y., Ge, J., Luo, Y., Xu, W., Wang, J., Lazarus, M., Hong, Z., Qu, W., & Huang, Z. (2019) · Pain · doi:10.1097/j.pain.0000000000001725 · Cited by 36 · see citing works
Liu, J., Zhang, M., Wu, X., Lazarus, M., Chérasse, Y., Yuan, M.-Y., Huang, Z., & Li, R. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.10.013 · Cited by 32 · see citing works
Self-citationLi, R., Nishijo, H., Ono, T., Ohtani, Y., & Ohtani, O. (2001) · Synapse · doi:10.1002/syn.10017 · Cited by 30 · see citing works
Self-citationAmygdala GABA Neurons Project To vlPAG And mPFC
Sun, Y., Blanco‐Centurion, C., Zou, B., Bendell, E., Shiromani, P. J., & Liu, M. (2019) · IBRO Reports · doi:10.1016/j.ibror.2019.03.001 · Cited by 25 · see citing works
Lesion of intergeniculate leaflet GABAergic neurons attenuates sleep in mice exposed to light
Shi, H., Xu, W., Guo, H., Dong, H., Qu, W., & Huang, Z. (2019) · SLEEP · doi:10.1093/sleep/zsz212 · Cited by 14 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
The integrated brain network that controls respiration
Krohn, F., Novello, M., van der Giessen, R. S., Zeeuw, C. I. D., Pel, J. J. M., & Bosman, L. W. J. (2023) · eLife · doi:10.7554/elife.83654 · Cited by 155 · see citing works
Kim, J., Kang, S., Choi, T.-Y., Chang, K., & Koo, J. W. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.01.006 · Cited by 55 · see citing works
Amygdala-driven apnea and the chemoreceptive origin of anxiety
Feinstein, J. S., Gould, D. A., & Khalsa, S. S. (2022) · Biological Psychology · doi:10.1016/j.biopsycho.2022.108305 · Cited by 53 · see citing works
Sex Differences in CGRP Regulation and Function in the Amygdala in a Rat Model of Neuropathic Pain
Presto, P., & Neugebauer, V. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.928587 · Cited by 36 · see citing works
The hippocampus associated GABAergic neural network impairment in early-stage of Alzheimer's disease
Tang, Y., Yan, Y., Mao, J., Ni, J., & Qing, H. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101865 · Cited by 34 · see citing works
A dual-pathway architecture for stress to disrupt agency and promote habit
Giovanniello, J. R., Paredes, N., Wiener, A., Ramírez-Armenta, K., Oragwam, C., Uwadia, H. O., Yu, A. L., Lim, K., Pimenta, J. S., Vilchez, G. E., et al. (2025) · Nature · doi:10.1038/s41586-024-08580-w · Cited by 30 · see citing works
Lee, I. B., Lee, E., Han, N.-E., Slavuj, M., Hwang, J., Lee, A., Sun, T., Jeong, Y., Baik, J.-H., Park, J.-Y., et al. (2024) · Nature Communications · doi:10.1038/s41467-023-44322-8 · Cited by 17 · see citing works
Gomes-de-Souza, L., Costa-Ferreira, W., Mendonça, M. M., Xavier, C. H., & Crestani, C. C. (2021) · Scientific Reports · doi:10.1038/s41598-021-95401-z · Cited by 23 · see citing works
Wang, X., Bi, S., Yue, Z., Chen, X., Liu, Y., Deng, T., Shao, L., Jing, X., Wang, C., Wang, Y., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-58791-6 · Cited by 24 · see citing works
Organisation of enkephalin inputs and outputs of the central nucleus of the amygdala in mice
Viden, A., Ch’ng, S. S., Walker, L. C., Shesham, A., Hamilton, S. M., Smith, C. M., & Lawrence, A. J. (2022) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2022.102167 · Cited by 17 · see citing works
Hmgb1 Silencing in the Amygdala Inhibits Pain-Related Behaviors in a Rat Model of Neuropathic Pain
Presto, P., Ji, G., Ponomareva, O., Ponomarev, I., & Neugebauer, V. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241511944 · Cited by 14 · see citing works
Kirouac, G. J., Li, S., & Li, S. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02534-6 · Cited by 11 · see citing works
Exercise therapy for chronic pain: How does exercise change the limbic brain function?
Senba, E., & Kami, K. (2023) · Neurobiology of Pain · doi:10.1016/j.ynpai.2023.100143 · Cited by 11 · see citing works
Jin, S., Maddern, X. J., Campbell, E. J., & Lawrence, A. J. (2022) · Neuroscience Letters · doi:10.1016/j.neulet.2022.136858 · Cited by 9 · see citing works
Subregional Differences in Alcohol Modulation of Central Amygdala Neurocircuitry
Melkumyan, M., & Silberman, Y. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.888345 · Cited by 9 · see citing works
Domi, A., Domi, E., Lagström, O., Gobbo, F., Jerlhag, E., & Adermark, L. (2023) · eNeuro · doi:10.1523/eneuro.0468-22.2023 · Cited by 9 · see citing works
Neurexin 3α in the Central Amygdala has a Role in Orofacial Varicella Zoster Pain
Kramer, P. R., Umorin, M., Hornung, R. S., & Kinchington, P. R. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.06.003 · Cited by 8 · see citing works
GABAergic Neurons in the Central Amygdala Promote Emergence from Isoflurane Anesthesia in Mice
Zhang, J., Yao, W., Zhang, L., Li, Z.-S., Gong, X.-T., Duan, L.-L., Huang, Z.-X., Chen, T., Huang, J.-C., Yang, S.-X., et al. (2024) · Anesthesiology · doi:10.1097/aln.0000000000005279 · Cited by 8 · see citing works
Central amygdala somatostatin neurons modulate stress-induced sleep-onset insomnia
Yao, W., Huang, S., Zhang, L., Li, Z.-S., Huang, D.-Y., Huang, K.-Q., Huang, Z.-X., Nian, L., Li, J.-L., Chen, L., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-07679-8 · Cited by 10 · see citing works
He, X., Ji, P., Guo, R., Ming, X., Zhang, H., Yu, L., Chen, Z., Gao, S., & Guo, F. (2022) · Neurogastroenterology & Motility · doi:10.1111/nmo.14498 · Cited by 8 · see citing works
Wang, H., Liu, W.-J., Wang, X., Chen, X., Cai, R.-L., Zhang, M.-T., Wang, H., He, G., Zhang, Z., & Shen, G.-M. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1074979 · Cited by 8 · see citing works
Self-citationAnxiety and ultrastructural consequences of chronic mild stress in rats
Zhvania, M. G., Japaridze, N. J., Tizabi, Y., Sharikadze, I., Pochkhidze, N., & Cheishvili, L. A. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136390 · Cited by 8 · see citing works
Involvement of brain cell phenotypes in stress-vulnerability and resilience
Favoretto, C. A., Pagliusi, M., & Morais‐Silva, G. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1175514 · Cited by 8 · see citing works
Projections from thalamic nucleus reuniens to medial septum enable extinction of remote fear memory
Tomaszewski, K. F., Gajewska‐Woźniak, O., Ziółkowska, M., Łukasiewicz, K., Cały, A., Sotoudeh, N., Puchalska, M., Salamian, A., & Radwańska, K. (2026) · Acta Neurobiologiae Experimentalis · doi:10.55782/zd27ss41 · Cited by 7 · see citing works
Ji, G., Presto, P., Kiritoshi, T., Chen, Y., Navratilova, E., Porreca, F., & Neugebauer, V. (2024) · Cells · doi:10.3390/cells13080705 · Cited by 7 · see citing works
Hypothalamic GABAergic neurocircuitry in the regulation of energy homeostasis and sleep/wake control
Jiang, H. (2022) · Medical Review · doi:10.1515/mr-2022-0022 · Cited by 7 · see citing works
A dual-pathway architecture enables chronic stress to disrupt agency and promote habit formationPreprint
Giovanniello, J. R., Paredes, N., Wiener, A. J., Ramírez-Armenta, K., Oragwam, C., Uwadia, H. O., Yu, A. L., Lim, K. Y., Pimenta, J. S., Vilchez, G. E., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.03.560731 · Cited by 7 · see citing works
Activation of Centromedial Amygdala GABAergic Neurons Produces Hypotension in Mice
Wang, X., Yue, Z., Shi, L., He, W., Shao, L., Liu, Y., Zhang, J., Bi, S., Deng, T., Yuan, F., et al. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01317-9 · Cited by 6 · see citing works
Neural Correlates of Perceptual Plasticity in the Auditory Midbrain and Thalamus
Ying, R., Stolzberg, D. J., & Caras, M. L. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0691-24.2024 · Cited by 6 · see citing works
Stanley, S. A. (2025) · Diabetes · doi:10.2337/dbi24-0051 · Cited by 6 · see citing works
Vestin, E., Lagström, O., Domi, A., Ericson, M., Söderpalm, B., & Adermark, L. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109041 · Cited by 6 · see citing works
Deciphering the role of brainstem glycinergic neurons during startle and prepulse inhibition
Huang, W., Cano, J. C., & Fénelon, K. (2023) · Brain Research · doi:10.1016/j.brainres.2024.148938 · Cited by 5 · see citing works
Kramer, P. R., Hornung, R. S., Umorin, M., Benson, M. D., & Kinchington, P. R. (2024) · Journal of Pain Research · doi:10.2147/jpr.s441706 · Cited by 5 · see citing works
Liu, J., Chen, D.-H., Li, X., Xu, C., & Hu, T. (2022) · Brain Research · doi:10.1016/j.brainres.2022.148174 · Cited by 5 · see citing works
Self-citationZhang, Y., Shi, S.-J., Mao, E., Wang, X., Zhou, Y.-H., Chen, Y., Chen, J., Tian, M., Huang, F.-S., Cai, Z., et al. (2025) · Brain Research · doi:10.1016/j.brainres.2025.149492 · Cited by 4 · see citing works
Fan, W., Engborg, C. B., & Sciolino, N. R. (2024) · eNeuro · doi:10.1523/eneuro.0535-23.2024 · Cited by 3 · see citing works
Seizures and breathing: lessons from peri-ictal respiratory disturbances
Micalizzi, E., Ballerini, A., Lacuey, N., Giunta, L., Villani, F. S., Meletti, S., & Vaudano, A. E. (2025) · Clinical Neurophysiology · doi:10.1016/j.clinph.2025.2110962 · Cited by 3 · see citing works
Granget, J., Nierat, M., Lehongre, K., Lambrecq, V., Frazzini, V., Navarro, V., Buonviso, N., & Similowski, T. (2024) · The Journal of Physiology · doi:10.1113/jp287045 · Cited by 3 · see citing works
Calcium imaging of central amygdala activity after escalation of fentanyl self-administration
Malone, S. G., Tavakoli, N. S., Keller, P. S., Bardo, M. T., & Ortinski, P. I. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110370 · Cited by 3 · see citing works
Díez, G. G., Cuesta, P., Lazar, S. W., Rotaeche, L. S., Bruña, R., Maestú, F., Anitua, E., & Castellanos, N. P. (2025) · Cerebral Cortex · doi:10.1093/cercor/bhaf313 · Cited by 2 · see citing works
Nrxn3 reduces myofascial nociceptive pain
Nguyen, L. A., Umorin, M., & Kramer, P. R. (2025) · Neurobiology of Pain · doi:10.1016/j.ynpai.2025.100197 · Cited by 2 · see citing works
Kraeuter, K., Reith, C., Kolber, B. J., & Neilan, R. M. (2024) · Spora A Journal of Biomathematics · doi:10.61403/2473-5493.1094 · Cited by 1 · see citing works
Estrogens produced within the central amygdala inhibit varicella zoster‐induced orofacial pain
Kramer, P. R., Nguyen, L. A., & Kinchington, P. R. (2025) · Journal of Neuroendocrinology · doi:10.1111/jne.70012 · Cited by 1 · see citing works
Amphetamine produces sex- and subregion-selective neuroplasticity in the amygdala of Wistar rats
Cadeddu, D., Lucente, E., Ericson, M., & Adermark, L. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.178302 · Cited by 1 · see citing works
Lucente, E., Domi, A., Ericson, M., & Adermark, L. (2026) · Neuropharmacology · doi:10.1016/j.neuropharm.2026.110879 · Cited by 1 · see citing works
Neural correlates of flexible sound perception in the auditory midbrain and thalamusPreprint
Ying, R., Stolzberg, D. J., & Caras, M. L. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.12.589266 · Cited by 1 · see citing works
Carrette, L. L. G., Sneddon, E. A., & George, O. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-823453-2.00003-5
Zhang, J., & Li, R. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4569416
Self-citationProjections from Thalamic Nucleus Reuniens to Medial Septum Enable Extinction of Remote Fear MemoryPreprint
Tomaszewski, K. F., Ziółkowska, M., Łukasiewicz, K., Cały, A., Sotoudeh, N., Puchalska, M., Salamian, A., & Radwańska, K. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4778213
Regulation of Fear Behavior by Microcircuits within the Mouse Amygdala
Wei, C., & Yao, W. (2025) · Journal of Neuroscience and Neurological Disorders · doi:10.29328/journal.jnnd.1001105
Holmes, N. M., Talaron, M. M., Killcross, A. S., Laurent, V., Lingawi, N. W., & Westbrook, F. R. (2026) · Neuroscience and Biobehavioral Reviews · doi:10.1016/j.neubiorev.2026.106705 · Cited by 1 · see citing works
Amygdala: Function and neural basis
Chen, G.-D. (2026) · Hearing Research · doi:10.1016/j.heares.2026.109839
- Authors
- Liu, J., Hu, T., Zhang, M.-Q., Xu, C.-Y., Yuan, M.-Y., & Li, R.-X.
- Affiliations
- Xuzhou Medical College (CN)
- Shanghai Medical College of Fudan University (CN)
- Corresponding author
- Liu, Jing
- Venue
- Neuroscience Letters
- Publisher
- Elsevier BV
- Published
- 2021-02
- Volume
- 745
- Pages
- 135621
- ISSN
- 0304-3940 (ISSN-L)
- OpenAlex
- W3119584880
- Cited by
- 52
- References
- 48
- Citations by year
- 2026: 4 · 2025: 13 · 2024: 10 · 2023: 11 · 2022: 12 · 2021: 2
- FWCI
- 4.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Neuroscience Letters (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Natural Science Foundation of Jiangsu Province
- National Natural Science Foundation of China
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- GABAergic neurons, basolateral amygdala, central amygdala, axonal projections, efferent projections, neuroanatomy, fear processing, anxiety, stress, anterior olfactory nucleus, periaqueductal gray, substantia nigra, locus coeruleus, bed nucleus of the stria terminalis, thalamus, hippocampus, striatum, septum
- MeSH terms
- Animals, Efferent Pathways, Humans, Mice, Transgenic, Mice, HEK293 Cells, GABAergic Neurons, Basolateral Nuclear Complex, Central Amygdaloid Nucleus
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