The DOI matches its Crossref record; 282 of the 283 references it cites were found in a registry or an index.
Brain areas that influence general anesthesia
Abstract
This document reviews the literature on local brain manipulation of general anesthesia in animals, focusing on behavioral and electrographic effects related to hypnosis or loss of consciousness. Local inactivation or lesion of wake-active areas, such as locus coeruleus, dorsal raphe, pedunculopontine tegmental nucleus, perifornical area, tuberomammillary nucleus, ventral tegmental area and basal forebrain, enhanced general anesthesia. Anesthesia enhancement was shown as a delayed emergence (recovery of righting reflex) from anesthesia or a decrease in the minimal alveolar concentration that induced loss of righting. Local activation of various wake-active areas, including pontis oralis and centromedial thalamus, promoted behavioral or electrographic arousal during maintained anesthesia and facilitated emergence. Lesion of the sleep-active ventrolateral preoptic area resulted in increased wakefulness and decreased isoflurane sensitivity, but only for 6 days after lesion. Inactivation of any structure within limbic circuits involving the medial septum, hippocampus, nucleus accumbens, ventral pallidum, and ventral tegmental area, amygdala, entorhinal and piriform cortex delayed emergence from anesthesia, and often reduced anesthetic-induced behavioral excitation. In summary, the concept that anesthesia works on the sleep-wake system has received strong support from studies that inactivated/lesioned or activated wake-active areas, and weak support from studies that lesioned sleep-active areas. In addition to the conventional wake-sleep areas, limbic structures such as the medial septum, hippocampus and prefrontal cortex are also involved in the behavioral response to general anesthesia. We suggest that hypnosis during general anesthesia may result from disrupting the wake-active neuronal activities in multiple areas and suppressing an atropine-resistant cortical activation associated with movements.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
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?
In the citing paper
“Many of these nuclei have been explored as targets of the inhibitory effects of general anesthetics [113]”
From The Biology of General Anesthesia from Paramecium to Primate (2019) · cites this paper as [113]
Citations
Cites
Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging
Fox, M. D., & Raichle, M. E. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2201 · Cited by 6,700
Brain stem reticular formation and activation of the EEG
Moruzzi, G., & Magoun, H. W. (1949) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(49)90219-9 · Cited by 4,307
Neurons containing hypocretin (orexin) project to multiple neuronal systems
Peyron, C., Tighe, D. K., van den Pol, A. N., de Lecea, L., Heller, H. C., Sutcliffe, J. G., & Kilduff, T. S. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-23-09996.1998 · Cited by 3,466
Theta oscillations in the hippocampus
Buzsáki, G. (2002) · Neuron · doi:10.1016/s0896-6273(02)00586-x · Cited by 3,332
Krystal, J. H. (1994) · Archives of General Psychiatry · doi:10.1001/archpsyc.1994.03950030035004 · Cited by 3,330
Endogenous Pain Control Systems: Brainstem Spinal Pathways and Endorphin Circuitry
Basbaum, A. I., & Fields, H. L. (1984) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.07.030184.001521 · Cited by 2,687
Excitatory actions of gaba during development: the nature of the nurture
Ben-Ari, Y. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn920 · Cited by 2,448
Central cholinergic pathways in the rat: An overview based on an alternative nomenclature (Ch1–Ch6)
Mesulam, M. M., Mufson, E. J., Wainer, B. H., & Levey, A. I. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90108-2 · Cited by 2,329
Aston-Jones, G., & Bloom, F. (1981) · The Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00876.1981 · Cited by 1,960
Zăgrean, L. (2014) · Acta Endocrinologica (Bucharest) · doi:10.4183/aeb.2014.529 · Cited by 1,922
Research works printed but not linked: 3
- Ma, 2003, Forebrain structures that participate in general anesthesia, Soc. Neurosci. Abstr., 29, 384.7
- Mogenson, 1993, From motivation to action: a review of dopaminergic regulation of limbic–nucleus accumbens–ventral pallidum–pedunculopontine nucleus circuits involved in limbic–motor integration, 193
- Vertes, 1997, Brainstem-diencephalo-septohippocampal systems controlling the theta rhythm of the hippocampus, Neuroscience, 81, 893
Cited by
Sorted by citations
Clinical pharmacokinetics and pharmacodynamics of propofol
Sahinovic, M. M., Struys, M. M. R. F., & Absalom, A. R. (2018) · Clinical Pharmacokinetics · doi:10.1007/s40262-018-0672-3 · Cited by 809
Towards a comprehensive understanding of anesthetic mechanisms of action: a decade of discovery
Hemmings, H. C., Riegelhaupt, P. M., Kelz, M. B., Solt, K., Eckenhoff, R. G., Orser, B. A., & Goldstein, P. A. (2019) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2019.05.001 · Cited by 244
Etomidate and its Analogs: A Review of Pharmacokinetics and Pharmacodynamics
Valk, B. I., & Struys, M. M. R. F. (2021) · Clinical Pharmacokinetics · doi:10.1007/s40262-021-01038-6 · Cited by 200
Challenges and opportunities for brainstem neuroimaging with ultrahigh field MRI
Sclocco, R., Beißner, F., Bianciardi, M., Polimeni, J. R., & Napadow, V. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.02.052 · Cited by 163
The Biology of General Anesthesia from Paramecium to Primate
Kelz, M. B., & Mashour, G. A. (2019) · Current Biology · doi:10.1016/j.cub.2019.09.071 · Cited by 151
Mashour, G. A., & Hudetz, A. G. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00044 · Cited by 133
Bao, W., Xu, W., Pan, G.-J., Wang, T., Han, Y., Qu, W., Li, W., & Huang, Z. (2021) · Current Biology · doi:10.1016/j.cub.2021.02.011 · Cited by 91
Parabrachial Neurons Promote Behavior and Electroencephalographic Arousal From General Anesthesia
Luo, T., Yu, S., Cai, S., Zhang, Y., Jiao, Y., Yu, T., & Yu, W. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00420 · Cited by 79
Self-citationReimann, H. M., & Niendorf, T. (2020) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2020.00008 · Cited by 75
Escape From Oblivion: Neural Mechanisms of Emergence From General Anesthesia
Kelz, M. B., García, P. S., Mashour, G. A., & Solt, K. (2019) · Anesthesia & Analgesia · doi:10.1213/ane.0000000000004006 · Cited by 75
Bettinardi, R. G., Tort-Colet, N., Ruiz-Mejias, M., Sanchez-Vives, M. V., & Deco, G. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.03.037 · Cited by 68
Du, W., Zhang, R., Li, J. X., Zhang, B., Peng, X., Cao, S., Yuan, J., Yuan, C.-D., Yu, T., & Du, J. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.08.046 · Cited by 57
Basal Forebrain Cholinergic Activity Modulates Isoflurane and Propofol Anesthesia
Luo, T., Cai, S., Qin, Z.-X., Yang, S., Shu, Y. L., Liu, C., Zhang, Y., Zhang, L., Zhou, L., Yu, T., et al. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.559077 · Cited by 53
Self-citationHe, E., Xu, S., Dai, Y., Wang, Y., Xiao, G., Xie, J., Xu, S., Fan, P., Mo, F., Wang, M., et al. (2021) · ACS Sensors · doi:10.1021/acssensors.1c01241 · Cited by 52
Endocannabinoid signaling in hypothalamic circuits regulates arousal from general anesthesia in mice
Zhong, H., Li, T., Gu, N., Gao, F., Lu, Y.-C., Xie, R., Liu, J., Li, X., Bergeron, R., Pomeranz, L. E., et al. (2017) · Journal of Clinical Investigation · doi:10.1172/jci91038 · Cited by 51
Chaos analysis of EEG during isoflurane-induced loss of righting in rats
MacIver, M. B., & Bland, B. H. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00203 · Cited by 50
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 53
Gui, H., Liu, C., He, H., Zhang, J., Chen, H., & Zhang, Y. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.671473 · Cited by 50
The General Anesthetic Isoflurane Bilaterally Modulates Neuronal Excitability
Ou, M., Zhao, W., Liu, J., Liang, P., Huang, H., Yu, H., Zhu, T., & Zhou, C. (2019) · iScience · doi:10.1016/j.isci.2019.100760 · Cited by 47
Resting state functional network disruptions in a kainic acid model of temporal lobe epilepsy
Gill, R. S., Mirsattari, S. M., & Leung, L.-W. S. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.11.002 · Cited by 43
Self-citationZhang, Y., Fu, B., Liu, C., Yu, S., Luo, T., Zhang, L., Zhou, W., & Yu, T. (2019) · The FASEB Journal · doi:10.1096/fj.201802164rr · Cited by 41
Self-citationBrainstem node for loss of consciousness due to GABAA receptor-active anesthetics
Minert, A., & Devor, M. G. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.10.001 · Cited by 41
Pradier, B., Wachsmuth, L., Nagelmann, N., Segelcke, D., Kreitz, S., Heß, A., Pogatzki-Zahn, E. M., & Faber, C. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118626 · Cited by 38
Voss, L. J., García, P. S., Hentschke, H., & Banks, M. I. (2019) · Anesthesiology · doi:10.1097/aln.0000000000002554 · Cited by 38
Pullon, R. M., Yan, L., SLEIGH, J. W., & Warnaby, C. E. (2020) · Anesthesiology · doi:10.1097/aln.0000000000003398 · Cited by 38
Feng, Z.-X., Dong, H., Qu, W., & Zhang, W. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.01196 · Cited by 37
Hu, Y., Du, W., Qi, J., Luo, H., Zhang, Z., Luo, M., & Wang, Y. (2023) · eLife · doi:10.7554/elife.88420 · Cited by 33
Renal effects of general anesthesia from old to recent studies
Alizadeh, R. F., & fard, Z. A. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28407 · Cited by 29
Lv, P., Xiao, Y., Liu, B., Wang, Y., Zhang, X., Sun, H., Li, F. Y., Li, Y., Zhang, W., Liu, L., et al. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.11.037 · Cited by 28
The hippocampus participates in a pharmacological rat model of absence seizures
Arcaro, J. A., Ma, J., Chu, L.-W., Kuo, M., Mirsattari, S. M., & Leung, L.-W. S. (2015) · Epilepsy Research · doi:10.1016/j.eplepsyres.2015.12.007 · Cited by 26
Self-citationNeuroimaging in the Kleine-Levin Syndrome
Engström, M., Latini, F., & Landtblom, A. (2018) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-018-0866-y · Cited by 25
Mesopontine Switch for the Induction of General Anesthesia by Dedicated Neural Pathways
Sukhotinsky, I., Minert, A., Soja, P. J., & Devor, M. G. (2016) · Anesthesia & Analgesia · doi:10.1213/ane.0000000000001489 · Cited by 24
Brain state identification and neuromodulation to promote recovery of consciousness
van der Lande, G., Casas-Torremocha, D., Manasanch, A., Porta, L. D., Gosseries, O., Alnagger, N., Barra, A., Mejías, J. F., Panda, R., Riefolo, F., et al. (2024) · Brain Communications · doi:10.1093/braincomms/fcae362 · Cited by 26
Yu, W., Gao, Y., Wang, H., Li, P., Xu, N., Zhu, L., & Cai, M. (2016) · Medical Gas Research · doi:10.4103/2045-9912.196901 · Cited by 23
Leung, L.-W. S., & Ma, J. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.07.053 · Cited by 24
Self-citationLanir-Azaria, S., Meiri, G., Avigdor, T., Minert, A., & Devor, M. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.12.035 · Cited by 20
Zhou, F., Wang, D., Li, H., Wang, S., Zhang, X., Li, A., Tong, T., Zhong, H., Yang, Q., & Dong, H. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14106 · Cited by 18
Effects of isoflurane and ethanol administration on c-Fos immunoreactivity in mice
Smith, M. L., Li, J., Cote, D. M., & Ryabinin, A. E. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.12.047 · Cited by 21
Minert, A., Baron, M. S., & Devor, M. G. (2019) · Anesthesiology · doi:10.1097/aln.0000000000003087 · Cited by 21
Wang, D., Huang, Y., Wang, X., Chen, X., Li, J., Zhang, S., Wu, J., Liu, D.-Q., Ma, D., & Mei, W. (2020) · British Journal of Anaesthesia · doi:10.1016/j.bja.2020.07.012 · Cited by 21
He, J., Zhu, Y., Wu, C., Wu, J., Chen, Y., Yuan, M., Cheng, Z., Zeng, L., & Ji, X. (2023) · Ultrasonics · doi:10.1016/j.ultras.2023.107132 · Cited by 20
Model of anaesthetic induction by unilateral intracerebral microinjection of GABA ergic agonists
Devor, M. G., Zalkind, V. I., Fishman, Y., & Minert, A. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13186 · Cited by 20
Xie, J.-F., Fan, K., Wang, C., Xie, P., Hou, M., Xin, L., Cui, G.-F., Wang, L., Shao, Y.-F., & Hou, Y.-P. (2017) · Neurochemical Research · doi:10.1007/s11064-017-2247-3 · Cited by 20
Nutritional ketosis delays the onset of isoflurane induced anesthesia
Ari, C., Kovács, Z., Murdun, C., Koutnik, A. P., Goldhagen, C. R., Rogers, C. Q., Diamond, D. M., & D’Agostino, D. P. (2018) · BMC Anesthesiology · doi:10.1186/s12871-018-0554-0 · Cited by 19
Zhang, D., Liu, J., Zhu, T., & Zhou, C. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666210909150200 · Cited by 19
Forebrain Acetylcholine Modulates Isoflurane and Ketamine Anesthesia in Adult Mice
Leung, L.-W. S., Chu, L.-W., Prado, M. A. M., & Prado, V. F. (2021) · Anesthesiology · doi:10.1097/aln.0000000000003713 · Cited by 23
Self-citationFontana, B. D., Alnassar, N., & Parker, M. O. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.686102 · Cited by 17
Claustrum modulates behavioral sensitivity and EEG activity of propofol anesthesia
Luo, T., Li, L., Li, J., Cai, S., Wang, Y., Zhang, L., Yu, S., & Yu, T. (2022) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14012 · Cited by 16
Self-citationGABAergic Neurons in the Nucleus Accumbens are Involved in the General Anesthesia Effect of Propofol
Yan, J., Hang, B.-N., Ma, L., Lin, J.-T., Zhou, Y. X., Jiao, X., Yuan, Y.-X., Shao, K.-J., Zhang, L., Xue, Q., et al. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03445-1 · Cited by 16
Midline thalamic inputs to the amygdala: Ultrastructure and synaptic targets
Amir, A., Paré, J., Smith, Y., & Paré, D. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24557 · Cited by 16
Matsumoto, Y., Fujino, Y., & Furue, H. (2021) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2021.07.065 · Cited by 16
Xia, J.-M., Fan, B., Yi, X., Ni, W., Zhou, Y., Chen, D., Yi, W.-J., Feng, L., Xia, Y., Li, S., et al. (2023) · Anesthesiology · doi:10.1097/aln.0000000000004798 · Cited by 15
Liu, Y., Chen, B., Cai, Y., Han, Y., Xia, Y., Li, N., Fan, B., Yuan, T., Jiang, J., Gao, P., et al. (2021) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmab056 · Cited by 15
Avigdor, T., Minert, A., Baron, M. S., & Devor, M. G. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113760 · Cited by 15
Samanta, S., Joncour, V. L., Wegrzyniak, O., Rangasami, V. K., Ali‐Löytty, H., Hong, T., Selvaraju, R. K., Åberg, O., Hilborn, J. G., Laakkonen, P. M., et al. (2022) · Advanced Therapeutics · doi:10.1002/adtp.202200001 · Cited by 15
Dopaminergic System in Promoting Recovery from General Anesthesia
Wang, J., Miao, X., Sun, Y., Li, S., Wu, A., & Wei, C. (2023) · Brain Sciences · doi:10.3390/brainsci13040538 · Cited by 14
A Comparison of Brain-State Dynamics across Common Anesthetic Agents in Male Sprague-Dawley Rats
Ward-Flanagan, R., Lo, A. S., Clement, E., & Dickson, C. T. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073608 · Cited by 14
Electroresponsive properties of rat central medial thalamic neurons
Jhangiani-Jashanmal, I. T., Yamamoto, R., Güngör, N. Z., & Paré, D. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00982.2015 · Cited by 16
Esketamine Anesthetizes Mice With a Similar Potency to Racemic Ketamine
Ma, X., Peng, J., Chen, Y., Wang, Z., Zhou, Q., Yan, J., & Jiang, H. (2023) · Dose-Response · doi:10.1177/15593258231157563 · Cited by 11
Yi, R., Chen, S., Zhong, F., Luo, D., You, Y., Yu, T., Wang, H., Zhou, L., & Zhang, Y. (2024) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14782 · Cited by 8
Vu, P. A., McNamara, E. H., Liu, J., Tucker, L. B., Fu, A. H., & McCabe, J. (2020) · Brain Research · doi:10.1016/j.brainres.2020.147147 · Cited by 8
Disruption of Hippocampal Multisynaptic Networks by General Anesthetics
Kuo, M., & Leung, L.-W. S. (2017) · Anesthesiology · doi:10.1097/aln.0000000000001861 · Cited by 9
Self-citationKovács, Z., D’Agostino, D. P., & Ari, C. (2023) · BMC Anesthesiology · doi:10.1186/s12871-023-02000-8 · Cited by 12
Zhang, J., Peng, Y., Liu, C., Zhang, Y., Liang, X., Yuan, C., Shi, W., & Zhang, Y. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14267 · Cited by 9
No cognitive processing in the unconscious, anesthetic‐like , state of sleep
Vertes, R. P., & Linley, S. B. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24963 · Cited by 10
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 9
Brain areas modulation in consciousness during sevoflurane anesthesia
Jie, L., Cai, H., Chen, Y., & Chen, G. (2022) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2022.1031613 · Cited by 8
Lammers‐Lietz, F., Borchers, F., Feinkohl, I., Hetzer, S., Kanar, Ç., Konietschke, F., Lachmann, G., Chien, C., Spies, C., Winterer, G., et al. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16282 · Cited by 8
Baron, M., Vaso, K., Ibraheem, A., Minert, A., & Devor, M. G. (2024) · Pain · doi:10.1097/j.pain.0000000000003504 · Cited by 7
Xu, X., Xiao, Y., Liu, X., Huang, Y., Ji, Y., Ji, Y., Gao, Y., Liu, S., Yang, J., Cao, J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-59857-1 · Cited by 7
Hu, R., Fan, P., Wang, Y., Shan, J., Jing, L., Xu, W., Mo, F., Wang, M., Luo, Y., Wang, Y., et al. (2023) · Fundamental Research · doi:10.1016/j.fmre.2023.05.015 · Cited by 7
Leung, L.-W. S., & Ma, J. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.895000 · Cited by 9
Self-citationAnesthetic loss of consciousness induced by chemogenetic excitation of mesopontine effector neurons.
Baron, M. S., Vaso, K., Avigdor, T., Charit, Y., Minert, A., & Devor, M. G. (2022) · Experimental Neurology · doi:10.1016/j.expneurol.2022.114169 · Cited by 8
Zhao, S., Han, L., Zhou, R., Huang, S., Wang, Y., Xu, F., Shu, S., Xia, L., & Chen, X. (2021) · Frontiers in Medicine · doi:10.3389/fmed.2021.678185 · Cited by 6
Zhai, X., Yuan, Y., Xu, L., Jiang, J., Li, Y., Yan, Y., & Zhang, L. (2022) · Brain Research · doi:10.1016/j.brainres.2022.148168 · Cited by 7
Adapa, R. (2017) · Springer eBooks · doi:10.1007/978-3-319-47609-4_4 · Cited by 6
Kurita, T., Kawashima, S., Morita, K., & Nakajima, Y. (2018) · Journal of Neurosurgical Anesthesiology · doi:10.1097/ana.0000000000000503 · Cited by 6
Yin, J., Fu, B., Wang, Y., & Yu, T. (2019) · Neuroreport · doi:10.1097/wnr.0000000000001344 · Cited by 6
Dopaminergic D1 receptors in the nucleus basalis modulate recovery from propofol anesthesia in rats.
Li, K., Zhou, Y., & Fu, B. (2020) · PubMed · doi:10.22038/ijbms.2019.37716.8962 · Cited by 6
Jia, L., Yin, J., Liu, T., Qi, W., Du, T., Li, Q., Ma, K., Yin, J., Yin, J., & Li, Y. (2024) · Neurochemical Research · doi:10.1007/s11064-024-04169-x · Cited by 5
Consciousness, Anesthesia, and Acetylcholine
Pal, D., & Mashour, G. A. (2021) · Anesthesiology · doi:10.1097/aln.0000000000003696 · Cited by 5
Dopamine D2-receptor neurons in nucleus accumbens regulate sevoflurane anesthesia in mice
Niu, L., Hao, M., Wang, Y., Wu, K., Yuan, C., Zhang, Y., Zhang, J., Liang, X., & Zhang, Y. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1287160 · Cited by 5
Raud, S., Reimets, R., Loomets, M., Sütt, S., Altpere, A., Visnapuu, T., Innos, J., Luuk, H., Plaas, M., Volke, V., et al. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.02.019 · Cited by 8
Aberrant slow waves in the hippocampus during activation in mice with low cholinergic tone
Leung, L.-W. S., & Chu, L.-W. (2021) · Hippocampus · doi:10.1002/hipo.23387 · Cited by 5
Self-citationPrice, C. C., Pereira, D. B., Andre, R., GARVAN, C. W., Nguyen, P., Herman, M. A. R., & Seubert, C. N. (2014) · International Journal of Behavioral Medicine · doi:10.1007/s12529-014-9451-1 · Cited by 6
Suzuki, T., Nagasaka, K., Otsuki, T., Otsuru, N., & Onishi, H. (2025) · European Journal of Neuroscience · doi:10.1111/ejn.70020 · Cited by 4
Glutamatergic neurons of piriform cortex delay induction of inhalational general anesthesia
Zhou, L., Ran, Q., Yi, R., Tang, H., Zhang, Y., & Yu, T. (2023) · Fundamental Research · doi:10.1016/j.fmre.2022.12.014 · Cited by 5
Meso-scale reorganization of local–global brain networks under mild sedation of propofol anesthesia
Dong, K., Zhang, L., Zhong, Y., Xu, T., Zhao, Y., Chen, S., Mahmoud, S. S., & Fang, Q. (2024) · NeuroImage · doi:10.1016/j.neuroimage.2024.120744 · Cited by 6
Two Cases of Crimean-Congo Hemorrhagic Fever Detected in a Non-endemic Feast of Sacrifice
Gümüş, A., Sayar, M. S., & Aşan, A. (2022) · Turkish Journal of Parasitology · doi:10.4274/tpd.galenos.2022.03016 · Cited by 4
Ajaz, R., Mousavi, S. R., Mirsattari, S. M., & Leung, L.-W. S. (2023) · Epilepsy Research · doi:10.1016/j.eplepsyres.2023.107103 · Cited by 4
Self-citationRauch, E., Ari, C., D’Agostino, D. P., & Kovács, Z. (2024) · Nutrients · doi:10.3390/nu16101477 · Cited by 4
Baron, M., & Devor, M. G. (2024) · Neuroscience Letters · doi:10.1016/j.neulet.2024.138030 · Cited by 4
Neurobiological Parallels, Overlaps, and Divergences of Sleep and Anesthesia
Ward-Flanagan, R., & Dickson, C. T. (2019) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-813743-7.00015-3 · Cited by 4
Leng, Y., Yang, Y., Li, Q., Wu, Y., Huang, H., Liang, P., Zhang, D., Zhou, C., & Hemmings, H. C. (2025) · British Journal of Anaesthesia · doi:10.1016/j.bja.2025.07.046 · Cited by 3
Wang, S., Li, Z., Wang, X., Xu, M., Fan, S., Liu, X., Qin, L., & Zhao, P. (2026) · British Journal of Anaesthesia · doi:10.1016/j.bja.2026.01.050 · Cited by 3
Berger, T. A., Xu, T., & Opitz, A. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00243 · Cited by 4
Comparison of anaesthetic- and seizure-induced states of unconsciousness: a narrative review
Gruenbaum, B. F. (2020) · British Journal of Anaesthesia · doi:10.1016/j.bja.2020.07.056 · Cited by 3
Dopamine in the ventral tegmental area facilitates emergence from general anesthesia
Leung, L.-W. S. (2017) · Annals of Translational Medicine · doi:10.21037/atm.2017.01.61 · Cited by 2
Self-citationPropofol: farmacodinámica y uso práctico
Haberer, J. P. (2021) · EMC - Anestesia-Reanimación · doi:10.1016/s1280-4703(20)44593-1 · Cited by 5
Comparative Brain-Wide Mapping of Isoflurane and Ketamine-Activated Nuclei and Functional NetworksPreprint
Hu, Y., Qi, J., Zhang, Z., Luo, M., & Wang, Y. (2024) · eLife · doi:10.7554/elife.88420.3 · Cited by 3
Metadata
- Authors
- Leung, L. S., Luo, T., Ma, J., & Herrick, I.
- Affiliations
- Peking University Shenzhen Hospital (CN)
- Western University (CA)
- ORCID
- Venue
- Progress in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2014-11
- Volume
- 122
- Pages
- 24-44
- ISSN
- 0301-0082 (ISSN-L)
- OpenAlex
- W2001908985
- Cited by
- 126
- References
- 283
- Citations by year
- 2026: 7 · 2025: 7 · 2024: 15 · 2023: 19 · 2022: 9 · 2021: 16 · 2020: 9 · 2019: 13 · 2018: 8 · 2017: 9 · 2016: 5 · 2015: 7 · 2014: 2
- FWCI
- 0.74
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Progress in Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Scholarship@Western (Western University) (submittedVersion)
- Funders
- Canadian Institutes of Health
- Natural Sciences and Engineering Research Council of Canada
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Health Sciences › Medicine › Anesthesiology and Pain Medicine › Anesthesia and Sedative Agents
- Life Sciences › Neuroscience › Developmental Neuroscience › Anesthesia and Neurotoxicity Research
- Keywords
- general anesthesia, emergence from anesthesia, locus coeruleus, dorsal raphe nucleus, pedunculopontine nucleus, perifornical area, tuberomammillary nucleus, ventral tegmental area, basal forebrain, ventrolateral preoptic area, limbic system, medial septum, hippocampus, nucleus accumbens, ventral pallidum, amygdala, prefrontal cortex, anesthetic sensitivity, isoflurane, loss of consciousness, hypnosis, righting reflex, lesion studies, brain activation
- MeSH terms
- Anesthesia, General, Animals, Brain, Humans, Sleep, Wakefulness, Anesthetics, General
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