Control of locomotor speed, arousal, and hippocampal theta rhythms by the nucleus incertus
Open accessAbstract
Navigation requires not only the execution of locomotor programs but also high arousal and real-time retrieval of spatial memory that is often associated with hippocampal theta oscillations. However, the neural circuits for coordinately controlling these important processes remain to be fully dissected. Here we show that the activity of the neuromedin B (NMB) neurons in the nucleus incertus (NI) is tightly correlated with mouse locomotor speed, arousal level, and hippocampal theta power. These processes are reversibly suppressed by optogenetic inhibition and rapidly promoted by optogenetic stimulation of NI NMB neurons. These neurons form reciprocal connections with several subcortical areas associated with arousal, theta oscillation, and premotor processing. Their projections to multiple downstream stations regulate locomotion and hippocampal theta, with the projection to the medial septum being particularly important for promoting arousal. Therefore, NI NMB neurons functionally impact the neural circuit for navigation control according to particular brains states.
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Locomotion is a homogeneous behavioral state tightly coupled to arousal.
“This is because locomotion—where place cell activity has been classically characterized—is a homogeneous behavioral state, tightly coupled to arousal32–35.”
From Place and behavioral modulation of hippocampal neurons during immobility (2026) · cites this paper as [32]
The Introduction says locomotion and arousal are often linked, supporting an association. But it also says they can be separately controlled, and the Results report increased arousal without locomotion. The paper does not characterize locomotion as a homogeneous behavioral state, and 'tightly coupled' omits the paper's qualification. (LLM, conf=0.87)
Experimental — accuracy not yet measuredThe onset of locomotion, as well as vestibular activation, are correlated with pupil dilations and brain state transitions.
“Indeed, the onset of locomotion, as well as vestibular activation, are correlated with pupil dilations and brain state transitions32,34,36.”
From Place and behavioral modulation of hippocampal neurons during immobility (2026) · cites this paper as [32]
The Results section ('NI NMB neurons encode locomotion, arousal, and theta rhythms'; page unavailable) links locomotion with pupil-measured arousal and hippocampal theta activity, supporting the locomotion portion of the claim. The copy does not address vestibular activation or show that it correlates with pupil dilation and brain-state transitions (searched: 'vestibular'). (LLM, conf=0.87)
Experimental — accuracy not yet measured
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Cites
The Mouse Brain in Stereotaxic Coordinates
Paxinos, G. (2001) · Cited by 12,859 · see citing works
Genome-wide atlas of gene expression in the adult mouse brain
Lein, E. S., Hawrylycz, M. J., Ao, N., Ayres, M., Bensinger, A., Bernard, A., Boe, A. F., Boguski, M. S., Brockway, K. S., Byrnes, E. J., et al. (2007) · Nature · doi:10.1038/nature05453 · Cited by 5,572 · see citing works
Self-citationMemory, navigation and theta rhythm in the hippocampal-entorhinal system
Buzsáki, G., & Moser, E. I. (2013) · Nature Neuroscience · doi:10.1038/nn.3304 · Cited by 1,847 · see citing works
Descending Pathways in Motor Control
Lemon, R. N. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125547 · Cited by 1,599 · see citing works
Yang, H., Wang, H., Shivalila, C. S., Cheng, A. W., Shi, L., & Jaenisch, R. (2013) · Cell · doi:10.1016/j.cell.2013.08.022 · Cited by 1,596 · see citing works
Neural substrates of awakening probed with optogenetic control of hypocretin neurons
Adamantidis, A. R., Zhang, F., Aravanis, A. M., Deisseroth, K., & de Lecea, L. (2007) · Nature · doi:10.1038/nature06310 · Cited by 1,341 · see citing works
AGRP neurons are sufficient to orchestrate feeding behavior rapidly and without training
Aponte, Y., Atasoy, D., & Sternson, S. M. (2011) · Nature Neuroscience · doi:10.1038/nn.2739 · Cited by 1,157 · see citing works
The subcellular organization of neocortical excitatory connections
Petreanu, L., Mao, T., Sternson, S. M., & Svoboda, K. (2009) · Nature · doi:10.1038/nature07709 · Cited by 1,047 · see citing works
Tuning arousal with optogenetic modulation of locus coeruleus neurons
Carter, M. E., Yizhar, O., Chikahisa, S., Nguyen, H., Adamantidis, A., Nishino, S., Deisseroth, K., & de Lecea, L. (2010) · Nature Neuroscience · doi:10.1038/nn.2682 · Cited by 993 · see citing works
Pupil fluctuations track rapid changes in adrenergic and cholinergic activity in cortex
Reimer, J., McGinley, M. J., Liu, Y., Rodenkirch, C., Wang, Q., McCormick, D. A., & Tolias, A. S. (2016) · Nature Communications · doi:10.1038/ncomms13289 · Cited by 926 · see citing works
Self-citationLoss of Hippocampal Theta Rhythm Results in Spatial Memory Deficit in the Rat
Winson, J. (1978) · Science · doi:10.1126/science.663646 · Cited by 857 · see citing works
Arousal and Locomotion Make Distinct Contributions to Cortical Activity Patterns and Visual Encoding
Vinck, M., Batista-Brito, R., Knoblich, U., & Cardin, J. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.028 · Cited by 819 · see citing works
Midbrain circuits for defensive behaviour
Tovote, P., Esposito, M. S., Botta, P., Chaudun, F., Fadok, J. P., Marković, M., Wolff, S. B. E., Ramakrishnan, C., Fenno, L. E., Deisseroth, K. A., et al. (2016) · Nature · doi:10.1038/nature17996 · Cited by 739 · see citing works
Cortical membrane potential signature of optimal states for sensory signal detection
McGinley, M. J., David, S. V., & McCormick, D. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.038 · Cited by 728 · see citing works
Pupil fluctuations track fast switching of cortical states during quiet wakefulness
Reimer, J., Froudarakis, E., Cadwell, C. R., Yatsenko, D., Denfield, G. H., & Tolias, A. S. (2014) · Neuron · doi:10.1016/j.neuron.2014.09.033 · Cited by 717 · see citing works
Natural light-gated anion channels: A family of microbial rhodopsins for advanced optogenetics
Govorunova, E. G., Sineshchekov, O. A., Janz, R., Liu, X., & Spudich, J. L. (2015) · Science · doi:10.1126/science.aaa7484 · Cited by 694 · see citing works
Representation of negative motivational value in the primate lateral habenula
Matsumoto, M., & Hikosaka, O. (2009) · Nature Neuroscience · doi:10.1038/nn.2233 · Cited by 547 · see citing works
Potter, E., Sutton, S., Donaldson, C., Chen, R., Perrin, M., Lewis, K., Sawchenko, P. E., & Vale, W. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.19.8777 · Cited by 514 · see citing works
Human hippocampal theta oscillations and the formation of episodic memories
Lega, B. C., Jacobs, J., & Kahana, M. (2012) · Hippocampus · doi:10.1002/hipo.20937 · Cited by 485 · see citing works
Dorsal raphe neurons signal reward through 5-HT and glutamate
Liu, Z., Zhou, J., Li, Y., Hu, F., Lu, Y., Ma, M., Feng, Q., Zhang, J.-E., Wang, D., Zeng, J., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.010 · Cited by 469 · see citing works
Self-citationMidbrain circuits that set locomotor speed and gait selection
Caggiano, V., Leiras, R., Goñi-Erro, H., Masini, D., Bellardita, C., Bouvier, J., Caldeira, V., Fisone, G., & Kiehn, O. (2018) · Nature · doi:10.1038/nature25448 · Cited by 447 · see citing works
Serotonin neurons in the dorsal raphe nucleus encode reward signals
Li, Y., Zhong, W., Wang, D., Feng, Q., Liu, Z., Zhou, J., Jia, C., Hu, F., Zeng, J., Guo, Q., et al. (2016) · Nature Communications · doi:10.1038/ncomms10503 · Cited by 420 · see citing works
Self-citationVandecasteele, M., Varga, V., Berényi, A., Papp, E., Barthó, P., Venance, L., Freund, T. F., & Buzsáki, G. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1411233111 · Cited by 409 · see citing works
Cell-Type-Specific Control of Brainstem Locomotor Circuits by Basal Ganglia
Roseberry, T. K., Lee, A. M., Lalive, A. L., Wilbrecht, L., Bonci, A., & Kreitzer, A. C. (2016) · Cell · doi:10.1016/j.cell.2015.12.037 · Cited by 390 · see citing works
Ford, B., Holmes, C. J., Mainville, L., & Jones, B. E. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903630203 · Cited by 350 · see citing works
Fuhrmann, F., Justus, D., Sosulina, L., Kaneko, H., Beutel, T., Friedrichs, D., Schoch, S., Schwarz, M. K., Fuhrmann, M., & Remy, S. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.001 · Cited by 347 · see citing works
GABAergic Neurons of the Medial Septum Lead the Hippocampal Network during Theta Activity
Hangya, B., Borhegyi, Z., Szilágyi, N., Freund, T. F., & Varga, V. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5665-08.2009 · Cited by 331 · see citing works
Identification of preoptic sleep neurons using retrograde labelling and gene profiling
Chung, S., Weber, F., Zhong, P., Tan, C. L., Nguyen, T. N., Beier, K. T., Hörmann, N., Chang, W.-C., Zhang, Z., Do, J. P., et al. (2017) · Nature · doi:10.1038/nature22350 · Cited by 317 · see citing works
Locomotor speed control circuits in the caudal brainstem
Capelli, P., Pivetta, C., Soledad Esposito, M., & Arber, S. (2017) · Nature · doi:10.1038/nature24064 · Cited by 288 · see citing works
Identification of a brainstem circuit regulating visual cortical state in parallel with locomotion
Lee, A. M., Hoy, J. L., Bonci, A., Wilbrecht, L., Stryker, M. P., & Niell, C. M. (2014) · Neuron · doi:10.1016/j.neuron.2014.06.031 · Cited by 282 · see citing works
Brainstem nucleus MdV mediates skilled forelimb motor tasks
Esposito, M. S., Capelli, P., & Arber, S. (2014) · Nature · doi:10.1038/nature13023 · Cited by 279 · see citing works
Dorsal Raphe Dopamine Neurons Modulate Arousal and Promote Wakefulness by Salient Stimuli
Cho, J. R., Treweek, J. B., Robinson, J. E., Xiao, C., Bremner, L. R., Greenbaum, A., & Gradinaru, V. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.020 · Cited by 276 · see citing works
Neurons expressing relaxin 3/INSL 7 in the nucleus incertus respond to stress
Tanaka, M., Iijima, N., Miyamoto, Y., Fukusumi, S., Itoh, Y., Ozawa, H., & Ibata, Y. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03980.x · Cited by 234 · see citing works
Connections of the nucleus incertus
Goto, M., Swanson, L. W., & Canteras, N. S. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1303 · Cited by 219 · see citing works
Theta oscillations regulate the speed of locomotion via a hippocampus to lateral septum pathway
Bender, F., Gorbati, M., Carús-Cadavieco, M., Denisova, N. P., Gao, X., Holman, C., Korotkova, T. M., & Ponomarenko, A. A. (2015) · Nature Communications · doi:10.1038/ncomms9521 · Cited by 206 · see citing works
Role of the Lateral Mammillary Nucleus in the Rat Head Direction Circuit
Blair, H. T., Cho, J., & Sharp, P. E. (1998) · Neuron · doi:10.1016/s0896-6273(00)80657-1 · Cited by 199 · see citing works
Behavior-Dependent Coordination of Multiple Theta Dipoles in the Hippocampus
Montgomery, S. M., Betancur, M. I., & Buzsáki, G. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4339-08.2009 · Cited by 190 · see citing works
Zhao, Z., Chen, Z., Xiang, X., Hu, M., Xie, H., Jia, X., Cai, F., Cui, Y., Chen, Z., Qian, L., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0404-5 · Cited by 184 · see citing works
Neural Correlates for Angular Head Velocity in the Rat Dorsal Tegmental Nucleus
Bassett, J. P., & Taube, J. S. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-15-05740.2001 · Cited by 173 · see citing works
Proopiomelanocortin Expression in both GABA and Glutamate Neurons
Hentges, S. T., Otero-Corchón, V., Pennock, R. L., King, C. M., & Low, M. J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3770-09.2009 · Cited by 171 · see citing works
Zhang, J.-E., Tan, L., Ren, Y., Liang, J., Lin, R., Feng, Q., Zhou, J., Hu, F., Ren, J., Wei, C., et al. (2016) · Cell · doi:10.1016/j.cell.2016.06.026 · Cited by 162 · see citing works
Self-citationRapid, biphasic CRF neuronal responses encode positive and negative valence
Kim, J., Lee, S., Fang, Y., Shin, A., Park, S., Hashikawa, K., Bhat, S., Kim, D., Sohn, J., Lin, D., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0342-2 · Cited by 152 · see citing works
Berridge, C. W., & Foote, S. L. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-21-06999.1996 · Cited by 151 · see citing works
Calcium imaging of sleep-wake related neuronal activity in the dorsal pons
Cox, J., Pinto, L., & Dan, Y. (2016) · Nature Communications · doi:10.1038/ncomms10763 · Cited by 133 · see citing works
Banerjee, A., Shen, P., Ma, S., Bathgate, R. A. D., & Gundlach, A. L. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.06.019 · Cited by 132 · see citing works
Vitalis, T., Cases, O., Callebert, J., Launay, J., Price, D. J., Seif, I., & Gaspar, P. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980406)393:2 · Cited by 129 · see citing works
Pan, W. X., & McNaughton, N. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02267.x · Cited by 112 · see citing works
Brainstem nucleus incertus controls contextual memory formation
Szőnyi, A., Sos, K. E., Nyilas, R., Schlingloff, D., Domonkos, A., Takács, V. T., Pósfai, B., Hegedüs, P., Priestley, J. B., Gundlach, A. L., et al. (2019) · Science · doi:10.1126/science.aaw0445 · Cited by 108 · see citing works
Nucleus incertus contribution to hippocampal theta rhythm generation
Núñez, Á., Cervera‐Ferri, A., Olucha-Bordonau, F. E., Ruiz‐Torner, A., & Teruel‐Martí, V. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04797.x · Cited by 105 · see citing works
Ma, S., Błasiak, A., Olucha-Bordonau, F. E., Verberne, A. J. M., & Gundlach, A. L. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2013.254300 · Cited by 95 · see citing works
Transforming Sensory Cues into Aversive Emotion via Septal-Habenular Pathway
Zhang, G., Shen, L., Zhong, W., Xiong, Y., Zhang, L. I., & Tao, H. W. (2018) · Neuron · doi:10.1016/j.neuron.2018.07.023 · Cited by 89 · see citing works
Effects of Treadmill Running on Brain Activation and the Corticotropin-Releasing Hormone System
Timofeeva, E., Huang, Q., & Richard, D. (2003) · Neuroendocrinology · doi:10.1159/000071311 · Cited by 78 · see citing works
Nucleus incertus promotes cortical desynchronization and behavioral arousal
Ma, S., Allocca, G., Ong-Pålsson, E., Singleton, C. E., Hawkes, D. J., McDougall, S. J., Williams, S. J., Bathgate, R. A. D., & Gundlach, A. L. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1230-0 · Cited by 54 · see citing works
Assessment of antinociceptive drug effects in the presence of impaired motor performance
Plummer, J. L., Cmielewski, P., Gourlay, G. K., Owen, H., & Cousins, M. J. (1991) · Journal of Pharmacological Methods · doi:10.1016/0160-5402(91)90057-c · Cited by 45 · see citing works
Szabó, B., Hedler, L., & Starke, K. (1989) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/bf00717740 · Cited by 45 · see citing works
Błasiak, A., Siwiec, M., Grabowiecka, A., Błasiak, T., Guguła, A., Błasiak, E., Kania, A., Rajfur, Z., Lewandowski, M. H., & Gundlach, A. L. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.08.014 · Cited by 40 · see citing works
Reversal of clonidine induced miosis by the alpha 2‐adrenoreceptor antagonist RX 781094.
Clifford, J., Day, M., & Orwin, J. (1982) · British Journal of Clinical Pharmacology · doi:10.1111/j.1365-2125.1982.tb04941.x · Cited by 35 · see citing works
Nucleus incertus inactivation impairs spatial learning and memory in rats
Nategh, M., Nikseresht, S., Khodagholi, F., & Motamedi, F. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.11.014 · Cited by 35 · see citing works
Theta synchronization between the hippocampus and the nucleus incertus in urethane-anesthetized rats
Cervera‐Ferri, A., Guerrero, J., Bataller‐Mompeán, M., Taberner-Cortés, A., Martínez‐Ricós, J., Ruiz‐Torner, A., & Teruel‐Martí, V. (2011) · Experimental Brain Research · doi:10.1007/s00221-011-2666-3 · Cited by 27 · see citing works
Glutamatergic projection from the nucleus incertus to the septohippocampal system
Cervera‐Ferri, A., Rahmani, Y., Martínez‐Bellver, S., Teruel‐Martí, V., & Martínez‐Ricós, J. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.04.014 · Cited by 27 · see citing works
Bland, B. H., Bland, C. E., & MacIver, M. B. (2015) · Hippocampus · doi:10.1002/hipo.22521 · Cited by 25 · see citing works
Regular theta‐firing neurons in the nucleus incertus during sustained hippocampal activation
Martínez‐Bellver, S., Cervera‐Ferri, A., Martínez‐Ricós, J., Ruiz‐Torner, A., Luque‐García, A., Blasco‐Serra, A., Guerrero, J., Bataller‐Mompeán, M., & Teruel‐Martí, V. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12884 · Cited by 25 · see citing works
Electrical microstimulation of the nucleus incertus induces forward locomotion and rotation in rats
Farooq, U., Kumar, J. R., Rajkumar, R., & Dawe, G. S. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.03.033 · Cited by 21 · see citing works
The interpeduncular nucleus regulates nicotineʼs effects on free-field activity
Hentall, I. D., & Gollapudi, L. A. (1995) · Neuroreport · doi:10.1097/00001756-199512150-00008 · Cited by 19 · see citing works
Evidence of D2 receptor expression in the nucleus incertus of the rat
Kumar, J. R., Rajkumar, R., Farooq, U., Lee, L. C., Tan, F. C. K., & Dawe, G. S. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.08.024 · Cited by 17 · see citing works
The inferior olive is essential for long-term maintenance of a simple motor skill
Chen, X. Y., Wang, Y., Chen, Y., Chen, L., & Wolpaw, J. R. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00085.2016 · Cited by 12 · see citing works
Asakura, W., Matsumoto, K., Ohta, H., & Watanabe, H. (1994) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(94)90459-6 · Cited by 10 · see citing works
Protein-calorie malnutrition in young Sinclair(S-1) miniature swine.
Badger, T. M., Tumbleson, M. E., & Hutcheson, D. P. (1972) · PubMed · Cited by 10 · see citing works
[Apparatus for recording of verbal instructions in electroencephalography].
Venturini, R., & Pascalis, V. D. (1974) · PubMed · Cited by 3 · see citing works
Flagged first, then by citations
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Sorted by citations
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Rudolph, S., Badura, A., Lutzu, S., Pathak, S. S., Thieme, A. G., Verpeut, J. L., Wagner, M. J., Yang, Y., & Fioravante, D. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1451-23.2023 · Cited by 196 · see citing works
The Theta Rhythm of the Hippocampus: From Neuronal and Circuit Mechanisms to Behavior
Núñez, Á., & Buño, W. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.649262 · Cited by 169 · see citing works
Neurobehavioral meaning of pupil size
Grujic, N., Polanía, R. H., & Burdakov, D. (2024) · Neuron · doi:10.1016/j.neuron.2024.05.029 · Cited by 93 · see citing works
Li, L., Lu, L., Ren, Y., Tang, G. Y., Zhao, Y., Cai, X., Shi, Z. H., Ding, H., Liu, C., Cheng, D., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-28539-7 · Cited by 87 · see citing works
Self-citationThe Medial Septum as a Potential Target for Treating Brain Disorders Associated With Oscillopathies
Takeuchi, Y., Nagy, A. J., Barcsai, L., Li, Q., Ohsawa, M., Mizuseki, K., & Berényi, A. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.701080 · Cited by 66 · see citing works
A spatially-resolved transcriptional atlas of the murine dorsal pons at single-cell resolution
Nardone, S., Luca, R. D., Zito, A., Klymko, N., Nicoloutsopoulos, D., Amsalem, O., Brannigan, C., Resch, J. M., Jacobs, C. L., Pant, D. B., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-45907-7 · Cited by 64 · see citing works
The role of hippocampal mossy cells in novelty detection
Fredes, F., & Shigemoto, R. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107486 · Cited by 50 · see citing works
Xiao, C., Wei, J., Zhang, G., Tao, C., Huang, J., Shen, L., Wickersham, I. R., Tao, H. W., & Zhang, L. I. (2023) · Neuron · doi:10.1016/j.neuron.2023.02.012 · Cited by 58 · see citing works
Medial Septum Glutamatergic Neurons Control Wakefulness Through a Septo-Hypothalamic Circuit
An, S., Sun, H., Wu, M., Xie, D., Hu, S.-W., Ding, H., & Cao, J. (2020) · Current Biology · doi:10.1016/j.cub.2021.01.019 · Cited by 47 · see citing works
Pupil-linked arousal with very light exercise: pattern of pupil dilation during graded exercise
Kuwamizu, R., Yamazaki, Y., Aoike, N., Ochi, G., Suwabe, K., & Soya, H. (2022) · The Journal of Physiological Sciences · doi:10.1186/s12576-022-00849-x · Cited by 43 · see citing works
The medial septum controls hippocampal supra-theta oscillations
Király, B., Domonkos, A., Jelitai, M., Lopes‐dos‐Santos, V., Martínez‐Bellver, S., Kocsis, B., Schlingloff, D., Joshi, A., Salib, M., Fiáth, R., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-41746-0 · Cited by 40 · see citing works
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Kuwamizu, R., Yamazaki, Y., Aoike, N., Hiraga, T., Hata, T., Yassa, M. A., & Soya, H. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120244 · Cited by 39 · see citing works
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EEG, MEG and neuromodulatory approaches to explore cognition: Current status and future directions
Beppi, C., Violante, I. R., Scott, G., & Sandrone, S. (2021) · Brain and Cognition · doi:10.1016/j.bandc.2020.105677 · Cited by 31 · see citing works
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Nasirova, N., Quina, L. A., Morton, G., Walker, A. W., & Turner, E. E. (2020) · eNeuro · doi:10.1523/eneuro.0272-20.2020 · Cited by 28 · see citing works
Zhang, J., Jiang, H., Ma, Y.-S., Shi, Y., Zhang, D., Yang, X., Jia, C., Yin, Y., Jiang, G.-X., Fu, D., et al. (2021) · Disease Markers · doi:10.1155/2021/6696198 · Cited by 26 · see citing works
A brainstem circuit amplifies aversion.
Liang, J., Zhou, Y., Feng, Q., Zhou, Y., Jiang, T., Ren, M., Jia, X.-Y., Gong, H., Di, R., Jiao, P., et al. (2024) · Neuron · doi:10.1016/j.neuron.2024.08.010 · Cited by 19 · see citing works
Self-citationGil‐Miravet, I., Mañas-Ojeda, A., Ros‐Bernal, F., Castillo-Gómez, E., Albert‐Gascó, H., Gundlach, A. L., & Olucha-Bordonau, F. E. (2021) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.637922 · Cited by 23 · see citing works
Ganea, D. A., Bexter, A., Günther, M., Gardères, P.-M., Kampa, B. M., & Haiss, F. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.00159 · Cited by 20 · see citing works
Neuropeptide S (NPS) neurons: Parabrachial identity and novel distributions
Huang, D., Zhang, R., Gasparini, S., McDonough, M. C., Paradee, W. J., & Geerling, J. C. (2022) · The Journal of Comparative Neurology · doi:10.1002/cne.25400 · Cited by 19 · see citing works
Wei, J., Xiao, C., Zhang, G., Shen, L., Tao, H. W., & Zhang, L. I. (2024) · Current Biology · doi:10.1016/j.cub.2024.08.020 · Cited by 20 · see citing works
Skovbjerg, G., Roostalu, U., Hansen, H. H., Lutz, T. A., Foll, C. L., Salinas, C. G., Skytte, J. L., Jelsing, J., Vrang, N., & Hecksher‐Sørensen, J. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15254 · Cited by 19 · see citing works
KCTD8 and KCTD12 Facilitate Axonal Expression of GABABReceptors in Habenula Cholinergic Neurons
Ren, Y., Liu, Y., Zheng, S., & Luo, M. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1676-21.2021 · Cited by 18 · see citing works
Self-citationBehavioral and physiological monitoring for awake neurovascular coupling experiments: a how-to guide
Zhang, Q., Turner, K. L., Gheres, K. W., Hossain, M. S., & Drew, P. J. (2022) · Neurophotonics · doi:10.1117/1.nph.9.2.021905 · Cited by 18 · see citing works
Lu, L., Wang, R., & Luo, M. (2020) · Science China Life Sciences · doi:10.1007/s11427-020-1675-x · Cited by 17 · see citing works
Self-citationSzlaga, A., Sambak, P., Trenk, A., Guguła, A., Singleton, C. E., Drwiȩga, G., Błasiak, T., Ma, S., Gundlach, A. L., & Błasiak, A. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.836116 · Cited by 14 · see citing works
Trenk, A., Walczak, M., Szlaga, A., Pradel, K., Błasiak, A., & Błasiak, T. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0230-21.2022 · Cited by 13 · see citing works
Genetically defined nucleus incertus neurons differ in connectivity and function
Spikol, E. D., Cheng, J., Macurak, M., Subedi, A., & Halpern, M. E. (2023) · eLife · doi:10.7554/elife.89516 · Cited by 13 · see citing works
León-Moreno, L., Castañeda-Arellano, R., Aguilar-García, I., Desentis-Desentis, M. F., Torres-Anguiano, E., Gutiérrez-Almeida, C. E., Najar-Acosta, L. J., Mendizabal-Ruiz, G., Ascencio-Piña, C., Dueñas-Jiménez, J. M., et al. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.579162 · Cited by 12 · see citing works
Relaxin-3 Innervation From the Nucleus Incertus to the Parahippocampal Cortex of the Rat
Díaz, C. G., Gil‐Miravet, I., Albert‐Gascó, H., Mañas-Ojeda, A., Ros‐Bernal, F., Castillo-Gómez, E., Gundlach, A. L., & Olucha-Bordonau, F. E. (2021) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.674649 · Cited by 12 · see citing works
Sleep fragmentation reduces explorative behaviors and impairs motor coordination in male mice
Xiong, Y., Zhu, J. H., He, Y., Qu, W., Huang, Z., & Ding, F. (2023) · Journal of Neuroscience Research · doi:10.1002/jnr.25268 · Cited by 11 · see citing works
Wong, W. L. E., Dawe, G. S., & Young, A. H. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.09.028 · Cited by 11 · see citing works
Recent advances in the biology of bombesin-like peptides and their receptors
Qin, X., & Qu, X. (2020) · Current Opinion in Endocrinology Diabetes and Obesity · doi:10.1097/med.0000000000000606 · Cited by 10 · see citing works
Gil‐Miravet, I., Núñez, Á., Navarro-Sánchez, M., Castillo-Gómez, E., Ros‐Bernal, F., Gundlach, A. L., & Olucha-Bordonau, F. E. (2023) · Brain Structure and Function · doi:10.1007/s00429-023-02650-x · Cited by 9 · see citing works
Chernykh, M., Vodianyk, B., Seleznov, I., Harmatiuk, D., Zyma, I. G., Popov, A. O., & Kiyono, K. (2022) · Applied Sciences · doi:10.3390/app12157849 · Cited by 9 · see citing works
Błasiak, A., Guguła, A., Gundlach, A. L., Olucha-Bordonau, F. E., Aniello, F., & Donizetti, A. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.984524 · Cited by 8 · see citing works
Ni, H., Guo, Z., Wang, J., Zhu, Z., Xia, C., Xu, M., Zhang, G., & Wang, D. (2025) · Scientific Reports · doi:10.1038/s41598-025-95585-8 · Cited by 6 · see citing works
Zhuang, Y., Liao, X., Niu, F., Li, M., Yu, Y., He, C., Wu, X., Tian, R., & Gao, G. (2025) · Nature Communications · doi:10.1038/s41467-025-59856-2 · Cited by 6 · see citing works
The anterior cingulate cortex modulates pupil-linked arousal
Chintalacheruvu, N., Kalelkar, A., Alatriste-León, H., Boutin, J., Breton‐Provencher, V., & Huda, R. (2026) · Science Advances · doi:10.1126/sciadv.adv5652 · Cited by 9 · see citing works
Szlaga, A., Sambak, P., Guguła, A., Trenk, A., Gundlach, A. L., & Błasiak, A. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109216 · Cited by 4 · see citing works
de Ávila, C., Guguła, A., Trenk, A., Intorcia, A. J., Suazo, C., Nolz, J., Plamondon, J., Khatri, D., Tallant, L., Caron, A., et al. (2024) · Biological Research · doi:10.1186/s40659-024-00523-z · Cited by 4 · see citing works
Silkis, I. G. (2022) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-022-01330-3 · Cited by 4 · see citing works
Guguła, A., Sambak, P., Trenk, A., Drabik, S., Nogaj, A., Sołtys, Z., Gundlach, A. L., & Błasiak, A. (2025) · Neuropsychopharmacology · doi:10.1038/s41386-025-02089-0 · Cited by 3 · see citing works
Mori, R., Mae, M., Yamanaka, H., Kato, S., & Masuyama, R. (2023) · Nutrition · doi:10.1016/j.nut.2023.112117 · Cited by 3 · see citing works
Neuroanatomical distribution of fluorophores within adult RXFP3 Cre-tdTomato/YFP mouse brain
Eraslan, I. M., Egberts-Brugman, M., Read, J. L., Voglsanger, L. M., Samarasinghe, R. M., Hamilton, D. L., Dhar, P., Williams, R. J., Walker, L. C., Ch’ng, S. S., et al. (2024) · Biochemical Pharmacology · doi:10.1016/j.bcp.2024.116265 · Cited by 3 · see citing works
Kania, A., Błasiak, A., & Gundlach, A. L. (2021) · Masterclass in neuroendocrinology · doi:10.1007/978-3-030-86630-3_16 · Cited by 3 · see citing works
Pupil Dynamics Predict Exercise Brain Stimulation: An Overview of Exercise Pupillometry
Kuwamizu, R., Yamazaki, Y., Suwabe, K., Suzuki, K., Sankai, Y., & Soya, H. (2025) · Advances in neurobiology · doi:10.1007/978-981-95-0066-6_6 · Cited by 2 · see citing works
Cheron, G. A., Ris, L., & Cebolla, A. M. (2023) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2023.1180627 · Cited by 2 · see citing works
Williams, E., Snively, L., O'Meara, B. R., Jacobs, H., Kolb, M., Zhao-Shea, R., Pavchinskiy, R. G., Keppler, E., Baratta, M. V., Tapper, A. R., et al. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03131-9 · Cited by 2 · see citing works
Genetically defined nucleus incertus neurons differ in connectivity and function
Spikol, E. D., Cheng, J., Macurak, M., Subedi, A., & Halpern, M. E. (2024) · eLife · doi:10.7554/elife.89516.3 · Cited by 1 · see citing works
Rapid Spectral Dynamics in Hippocampal Oscillons
Zobaer, M. S., Domenico, C., Perotti, L., Ji, D.-Y., & Dabaghian, Y. (2022) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2022.880742 · Cited by 1 · see citing works
Alpirez, J., León-Moreno, L. C., Aguilar-García, I. G., Castañeda‐Arellano, R., Dueñas-Jiménez, J. M., Ascencio-Piña, C. R., & Dueñas-Jiménez, S. H. (2023) · Brain Sciences · doi:10.3390/brainsci13111545 · Cited by 1 · see citing works
Tesmer, A. L., Viskaitis, P., Donegan, D., Bracey, E. F., Grujic, N., Patriarchi, T., Peleg‐Raibstein, D., & Burdakov, D. (2025) · eLife · doi:10.7554/elife.103738.3 · Cited by 1 · see citing works
Hippocampal Physiology in the Behaving Animal
Krupic, J., & O'Keefe, J. M. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780190065324.003.0011 · Cited by 1 · see citing works
Espinosa, N., Caneo, M., Alonso, A., Moran, C., & Fuentealba, P. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.30.510330 · Cited by 1 · see citing works
Neural Dynamic Underlying Coordination Process between Habitual and Goal-Directed BehaviorPreprint
He, M., Wen, W., & Qi, C. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.16.533062 · Cited by 1 · see citing works
Genetically defined nucleus incertus neurons differ in connectivity and functionPreprint
Spikol, E. D., Cheng, J., Macurak, M., Subedi, A., & Halpern, M. E. (2023) · eLife · doi:10.7554/elife.89516.1 · Cited by 1 · see citing works
Tesmer, A. L., Viskaitis, P., Donegan, D., Bracey, E. F., Grujic, N., Patriarchi, T., Peleg‐Raibstein, D., & Burdakov, D. (2025) · eLife · doi:10.7554/elife.103738 · Cited by 1 · see citing works
Interplay of pupil-linked arousal and cortical decision computations in micePreprint
Maheu, M., Copeland, J. B., Cantón, A. C., de la Rocha, J., Wiegert, J. S., & Donner, T. H. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.05.730199 · Cited by 1 · see citing works
Place and behavioral modulation of hippocampal neurons during immobility
Sartorato, N., Zouridis, I. S., Narantsatsralt, U.-U., Blanco-Hernández, E., & Burgalossi, A. (2026) · Nature Communications · doi:10.1038/s41467-026-75492-w · Cited by 1 · see citing works
“This is because locomotion — where place cell activity has been classically characterized — is a homogeneous behavioral state, tightly coupled to arousal 32 – 35 .”
Genetically defined nucleus incertus neurons differ in connectivity and functionPreprint
Spikol, E. D., Cheng, J., Macurak, M., Subedi, A., & Halpern, M. E. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.07.487414
Ohki‐Hamazaki, H. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820649-2.00087-5
de Ávila, C., Guguła, A., Trenk, A., Intorcia, A. J., Suazo, C., Nolz, J., Plamondon, J., Khatri, D., Tallant, L., Caron, A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.08.556922
Genetically defined nucleus incertus neurons differ in connectivity and functionPreprint
Spikol, E. D., Cheng, J., Macurak, M., Subedi, A., & Halpern, M. E. (2024) · eLife · doi:10.7554/elife.89516.2
Ni, H., Guo, Z., Wang, J., Zhu, Z., Xia, C., Xu, M., Zhang, G., & Wang, D. (2024) · Research Square · doi:10.21203/rs.3.rs-4531158/v1
Molas, S., Williams, E., Snively, L., O'Meara, B. R., Jacobs, H., Kolb, M., Zhao-Shea, R., Baratta, M. V., & Tapper, A. R. (2024) · Research Square · doi:10.21203/rs.3.rs-4661779/v1
Tesmer, A. L., Viskaitis, P., Donegan, D., Bracey, E. F., Grujic, N., Patriarchi, T., Peleg‐Raibstein, D., & Burdakov, D. (2025) · eLife · doi:10.7554/elife.103738.1
Nagai, T., & Takahashi, A. (2025) · Psychopharmacology · doi:10.1007/s00213-025-06824-9
The brain's ‘Allow, Restrain, Amplify, Respond’ (ARAR) architecture
Rappoport, A. (2025) · Elsevier eBooks · doi:10.1016/b978-0-44-345008-2.00019-9
Tesmer, A. L., Viskaitis, P., Donegan, D., Bracey, E. F., Grujic, N., Patriarchi, T., Peleg‐Raibstein, D., & Burdakov, D. (2025) · eLife · doi:10.7554/elife.103738.2
Vellus Hair-Inspired Triboelectric Antenna for Approach and Pressure Sensing
Shen, L., Jiang, J., Lei, H., Lu, B., Zhang, P., Miao, D., Sun, X., & Wen, Z. (2025) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.5c12911
Liu, X., Huang, H., Feng, X., Li, X., Ye, J., Yang, H. M., Liu, J., Liang, Z., Guo, Z., Cai, R., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.23.677968
de Ávila, C., Guguła, A., Trenk, A., Intorcia, A. J., Suazo, C., Nolz, J., Plamondon, J., Khatri, D., Tallant, L., Caron, A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26315492
de Ávila, C., Guguła, A., Trenk, A., Intorcia, A. J., Suazo, C., Nolz, J., Plamondon, J., Khatri, D., Tallant, L., Caron, A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26315692
Fernández, A. M. M. M., Netherton, S., Niladhuri, S. B., Brown, A. C., Rivera, P., Tseng, K. Y., & Peters, C. J. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107240
Wu, J., Cui, C., Dai, X.-Y., Wang, W., Liu, D.-Q., Wu, H., Gao, S., Zhang, L.-Q., Liu, L., Song, W., et al. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.1383-25.2026
A disynaptic pathway linking the cerebellum to the hippocampus
Zenelaj, X. (2024) · theses.fr (ABES) · doi:10.70675/94d94e26z34bez4c6bz880az1e3421294c0a
A dorsal pontine tegmentum syndrome
Shuleshova, N. V., Panchenko, N. I., & Kiryanov, Y. M. (2026) · The Scientific Notes of the Pavlov University · doi:10.24884/1607-4181-2026-33-1-48-57
Genc, M., Sevinc, C., Yuksel, B., & Ünal, G. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.0146-26.2026
de Ávila, C., Chakraborti, A., Gundlach, A. L., & Maeng, L. Y. (2026) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2026.1852733
Liao, X., Shi, L. M., Niu, F., Zhao, Z., Hong, J., Deng, Y., Yan, Y., He, C., Liao, Y., Li, R., et al. (2026) · Annals of Medicine · doi:10.1080/07853890.2026.2735720
Xiao, T., Chen, Y., & Kimbrough, A. (2026) · Neuropharmacology · doi:10.1016/j.neuropharm.2026.111236
- Authors
- Lu, L., Ren, Y., Yu, T., Liu, Z., Wang, S., Tan, L., Zeng, J., Feng, Q., Lin, R., Liu, Y., Guo, Q., & Luo, M.
- Affiliations
- National Institute of Biological Sciences, Beijing (CN)
- Peking University (CN)
- Chinese Institute for Brain Research (CN)
- Corresponding author
- Luo, Minmin
- Venue
- Nature Communications
- Published
- 2020-01-14
- Volume
- 11
- Issue
- 1
- Pages
- 262-262
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC6959274
- OpenAlex
- W3000107610
- Cited by
- 84
- References
- 69
- Citations by year
- 2026: 9 · 2025: 15 · 2024: 13 · 2023: 14 · 2022: 15 · 2021: 12 · 2020: 6
- FWCI
- 6.32
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- Ministry of Science and Technology of the People's Republic of China (2015BAI08B02)
- National Natural Science Foundation of China (91632302)
- The Beijing Municipal Government
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- nucleus incertus, locomotion speed, arousal, hippocampal theta oscillations, navigation, medial septum, optogenetic manipulation, spatial memory retrieval, brain states
- MeSH terms
- Animals, Arousal, Female, Hippocampus, Locomotion, Male, Neural Pathways, Neurons, Raphe Nuclei, Theta Rhythm, Neurokinin B, Septum of Brain, Mice, Optogenetics, Spatial Navigation
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