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Motor, cognitive, and affective areas of the cerebral cortex influence the adrenal medulla
Open accessAbstract
Significance: How does the “mind” (brain) influence the “body” (internal organs)? We identified key areas in the primate cerebral cortex that are linked through multisynaptic connections to the adrenal medulla. The most substantial influence originates from a broad network of motor areas that are involved in all aspects of skeletomotor control from response selection to motor preparation and movement execution. A smaller influence originates from a network in medial prefrontal cortex that is involved in the regulation of cognition and emotion. Thus, cortical areas involved in the control of movement, cognition, and affect are potential sources of central commands to influence sympathetic arousal. These results provide an anatomical basis for psychosomatic illness where mental states can alter organ function.
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“A complementary set of regions involved in visceromotor actions represents key efferent processing regions, including the anterior insula, anterior cingulate, subgenual cingulate, orbitofrontal, ventromedial prefrontal, supplementary motor, and premotor areas (44–46).”
From Interoception and Mental Health: A Roadmap. (2018) · cites this paper as [46]
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Cognitive and emotional influences in anterior cingulate cortex
Bush, G., Luu, P., & Posner, M. I. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01483-2 · Cited by 6,259
The integration of negative affect, pain and cognitive control in the cingulate cortex
Shackman, A. J., Salomons, T. V., Slagter, H. A., Fox, A. S., Winter, J. J., & Davidson, R. J. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2994 · Cited by 2,082
Bodily Changes in Pain, Hunger, Fear, and Rage.
Washburn, M. F., & Cannon, W. B. (1917) · The Journal of Philosophy Psychology and Scientific Methods · doi:10.2307/2013624 · Cited by 1,912
Motor Areas of the Medial Wall: A Review of Their Location and Functional Activation
Picard, N., & Strick, P. L. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.3.342 · Cited by 1,712
Self-citationCerebellar loops with motor cortex and prefrontal cortex of a nonhuman primate
Kelly, R. M., & Strick, P. L. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-23-08432.2003 · Cited by 1,595
Self-citationThe origin of corticospinal projections from the premotor areas in the frontal lobe
Dum, R., & Strick, P. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-03-00667.1991 · Cited by 1,447
Self-citationLaBar, K. S., Gatenby, J. C., Gore, J. C., LeDoux, J. E., & Phelps, E. A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80475-4 · Cited by 1,402
Bodily Changes in Pain, Hunger, Fear and Rage
Cannon, W. B. (1929) · Southern Medical Journal · doi:10.1097/00007611-192909000-00037 · Cited by 1,359
Neural mechanisms of autonomic, affective, and cognitive integration
Critchley, H. D. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20749 · Cited by 1,214
Human cingulate cortex and autonomic control: converging neuroimaging and clinical evidence
Critchley, H. D., Mathias, C. J., Josephs, O., O’Doherty, J., Zanini, S., Dewar, B., Cipolotti, L., Shallice, T., & Dolan, R. J. (2003) · Brain · doi:10.1093/brain/awg216 · Cited by 1,201
Cited by
Sorted by citations
Interoception and Mental Health: A Roadmap.
Khalsa, S. S., Adolphs, R., Cameron, O. G., Critchley, H. D., Davenport, P. W., Feinstein, J. S., Feusner, J. D., Garfinkel, S. N., Lane, R. D., Mehling, W. E., et al. (2018) · Biological psychiatry. Cognitive neuroscience and neuroimaging · doi:10.1016/j.bpsc.2017.12.004 · Cited by 1,453
Evidence for a large-scale brain system supporting allostasis and interoception in humans
Kleckner, I. R., Zhang, J., Touroutoglou, A., Chanes, L., Xia, C., Simmons, W. K., Quigley, K. S., Dickerson, B. C., & Feldman Barrett, L. (2017) · Nature Human Behaviour · doi:10.1038/s41562-017-0069 · Cited by 641
A somato-cognitive action network alternates with effector regions in motor cortex
Gordon, E. M., Chauvin, R. J., Van, A. N., Rajesh, A., Nielsen, A. N., Newbold, D. J., Lynch, C. J., Seider, N. A., Krimmel, S. R., Scheidter, K. M., et al. (2023) · Nature · doi:10.1038/s41586-023-05964-2 · Cited by 687
The hierarchical basis of neurovisceral integration
Smith, R., Thayer, J. F., Khalsa, S. S., & Lane, R. D. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.02.003 · Cited by 523
Neural circuits of interoception
Berntson, G. G., & Khalsa, S. S. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.09.011 · Cited by 419
Allostasis: A brain-centered, predictive mode of physiological regulation
Schulkin, J., & Sterling, P. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2019.07.010 · Cited by 265
The self in context: brain systems linking mental and physical health
Koban, L., Gianaros, P. J., Hedy Kober, A., & Wager, T. D. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00446-8 · Cited by 258
The brain’s action-mode network
Dosenbach, N. U. F., Raichle, M. E., & Gordon, E. M. (2025) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00895-x · Cited by 224
Ginty, A. T., Kraynak, T. E., Fisher, J. P., & Gianaros, P. J. (2017) · Autonomic Neuroscience · doi:10.1016/j.autneu.2017.03.003 · Cited by 180
The Cognitive Neuroscience of Placebo Effects: Concepts, Predictions, and Physiology
Geuter, S., Koban, L., & Wager, T. D. (2017) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031132 · Cited by 174
Placebo Effects on the Neurologic Pain Signature
Zunhammer, M., Bingel, U., & Wager, T. D. (2018) · JAMA Neurology · doi:10.1001/jamaneurol.2018.2017 · Cited by 167
Kraynak, T. E., Marsland, A. L., Wager, T. D., & Gianaros, P. J. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.07.013 · Cited by 165
Cardiac sympathetic-vagal activity initiates a functional brain–body response to emotional arousal
Candia‐Rivera, D., Catrambone, V., Thayer, J. F., Gentili, C., & Valenza, G. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2119599119 · Cited by 176
The extended autonomic system, dyshomeostasis, and COVID-19
Goldstein, D. S. (2020) · Clinical Autonomic Research · doi:10.1007/s10286-020-00714-0 · Cited by 150
Systemic inflammation and resting state connectivity of the default mode network
Marsland, A. L., Kuan, D. C.-H., Sheu, L. K., Krajina, K., Kraynak, T. E., Manuck, S. B., & Gianaros, P. J. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.01.013 · Cited by 135
Karrer, T. M., Kim, J. Z., Stiso, J., Kahn, A. E., Pasqualetti, F., Habel, U., & Bassett, D. S. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/ab6e8b · Cited by 124
Multivariate Brain Prediction of Heart Rate and Skin Conductance Responses to Social Threat
Eisenbarth, H., Chang, L. J., & Wager, T. D. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3672-15.2016 · Cited by 118
The Cortical Motor Areas and the Emergence of Motor Skills: A Neuroanatomical Perspective
Strick, P. L., Dum, R. P., & Rathelot, J.-A. (2021) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070918-050216 · Cited by 114
Self-citationMultiple areas of the cerebral cortex influence the stomach
Levinthal, D. J., & Strick, P. L. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2002737117 · Cited by 103
Self-citationBrydges, C. R., Fiehn, O., Mayberg, H. S., Schreiber, H. L., Dehkordi, S. M., Bhattacharyya, S., Cha, J., Choi, K. S., Craighead, W. E., Krishnan, R. R., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-99845-1 · Cited by 104
Goldstein, D. S. (2019) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00396.2018 · Cited by 96
Corticolimbic regulation of cardiovascular responses to stress
Myers, B. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.10.015 · Cited by 98
Gianaros, P. J., & Jennings, J. R. (2018) · American Psychologist · doi:10.1037/amp0000232 · Cited by 93
Tiemann, L., Hohn, V. D., Dinh, S. T., May, E. S., Nickel, M. M., Groß, J., & Ploner, M. (2018) · Nature Communications · doi:10.1038/s41467-018-06875-x · Cited by 96
The Peripersonal Space in a social world
Bogdanova, O. V., Bogdanov, V. B., Dureux, A., Farnè, A., & Hadj-Bouziane, F. (2021) · Cortex · doi:10.1016/j.cortex.2021.05.005 · Cited by 86
“One possible pathway through which PPS coding could be modulated is via the adrenal medulla that has direct links with the motor cortex (Dum et al., 2016).”
BackgroundMiroschnikow, A., Schlegel, P., Schoofs, A., Hueckesfeld, S., Li, F., Schneider-Mizell, C. M., Fetter, R. D., Truman, J. W., Cardona, A., & Pankratz, M. J. (2018) · eLife · doi:10.7554/elife.40247 · Cited by 84
Wood, M., Adil, O., Wallace, T., Fourman, S. M., Wilson, S. P., Herman, J. P., & Myers, B. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1762-6 · Cited by 90
Ludyga, S., Gerber, M., Mücke, M., Brand, S., Weber, P., Brotzmann, M., & Pühse, U. (2018) · Journal of Attention Disorders · doi:10.1177/1087054718757647 · Cited by 89
Kozlowska, K., Chudleigh, C., Cruz, C., Lim, M., McClure, G., Savage, B., Shah, U. H., Cook, A., Scher, S., Carrive, P., et al. (2017) · Clinical Child Psychology and Psychiatry · doi:10.1177/1359104517730116 · Cited by 77
Brain activity in mindfulness depends on experience: a meta-analysis of fMRI studies
Falcone, G., & Jerram, M. (2018) · Mindfulness · doi:10.1007/s12671-018-0884-5 · Cited by 71
Mir, H.-D., Milman, A., Monnoye, M., Douard, V., Philippe, C., Aubert, A., Castanon, N., Vancassel, S., Guérineau, N. C., Naudon, L., et al. (2020) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2020.104750 · Cited by 72
Neural Mechanisms Linking Emotion with Cardiovascular Disease
Kraynak, T. E., Marsland, A. L., & Gianaros, P. J. (2018) · Current Cardiology Reports · doi:10.1007/s11886-018-1071-y · Cited by 70
Goel, M., Mittal, A., Jain, V. R., Bharadwaj, A., Modi, S., Ahuja, G., Jain, A., & Kumar, K. (2024) · Annals of Neurosciences · doi:10.1177/09727531241255492 · Cited by 68
The mind–body problem: Circuits that link the cerebral cortex to the adrenal medulla
Dum, R. P., Levinthal, D. J., & Strick, P. L. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1902297116 · Cited by 71
Self-citationPrefrontal cortex interactions with the amygdala in primates
Murray, E. A., & Fellows, L. K. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01128-w · Cited by 66
Affective symptoms in patients with oropharyngeal dysphagia: A systematic review
Verdonschot, R. J. C. G., Baijens, L. W. J., Vanbelle, S., van de Kolk, I., Kremer, B., & Leue, C. (2017) · Journal of Psychosomatic Research · doi:10.1016/j.jpsychores.2017.04.006 · Cited by 64
A Focus on the Functions of Area 25
Alexander, L., Clarke, H. F., & Roberts, A. (2019) · Brain Science · doi:10.3390/brainsci9060129 · Cited by 54
Motor system dysfunction in the schizophrenia diathesis: Neural systems to neurotransmitters
Abboud, R., Noronha, C., & Diwadkar, V. A. (2017) · European Psychiatry · doi:10.1016/j.eurpsy.2017.04.004 · Cited by 65
Nickel, M. M., May, E. S., Tiemann, L., Postorino, M., Dinh, S. T., & Ploner, M. (2017) · Pain · doi:10.1097/j.pain.0000000000001010 · Cited by 66
Psychogenic non-epileptic seizures in children and adolescents: Part I – Diagnostic formulations
Kozlowska, K., Chudleigh, C., Cruz, C., Lim, M., McClure, G., Savage, B., Shah, U. H., Cook, A., Scher, S., Carrive, P., et al. (2017) · Clinical Child Psychology and Psychiatry · doi:10.1177/1359104517732118 · Cited by 63
Functional Involvement of Human Periaqueductal Gray and Other Midbrain Nuclei in Cognitive Control
Kragel, P. A., Bianciardi, M., Hartley, L., Matthewson, G., Choi, J., Quigley, K. S., Wald, L. L., Wager, T. D., Barrett, L. F., & Satpute, A. B. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2043-18.2019 · Cited by 61
Stodden, D. F., Pesce, C., Zarrett, N. R., Tomporowski, P. D., Ben‐Soussan, T. D., Brian, A., Abrams, T. C., & Weist, M. D. (2023) · Clinical Child and Family Psychology Review · doi:10.1007/s10567-023-00428-5 · Cited by 72
Homeostatic systems, biocybernetics, and autonomic neuroscience
Goldstein, D. S., & Kopin, I. J. (2017) · Autonomic Neuroscience · doi:10.1016/j.autneu.2017.09.001 · Cited by 63
Dempsey, B., Le, S., Turner, A. J., Bokiniec, P., Ramadas, R., Bjaalie, J. G., Menuet, C., Neve, R. L., Allen, A. M., Goodchild, A. K., et al. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00009 · Cited by 55
Structural Covariance of the Prefrontal-Amygdala Pathways Associated with Heart Rate Variability
Wei, L., Chen, H., & Wu, G. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00002 · Cited by 58
Osteopathy and Mental Health: An Embodied, Predictive, and Interoceptive Framework
Bohlen, L., Shaw, R., Cerritelli, F., & Esteves, J. E. (2021) · Frontiers in Psychology · doi:10.3389/fpsyg.2021.767005 · Cited by 56
A vocalization-processing network in marmosets
Jafari, A., Dureux, A., Zanini, A., Menon, R. S., Gilbert, K. M., & Everling, S. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112526 · Cited by 51
Kozlowska, K., Rampersad, R., Cruz, C., Shah, U., Chudleigh, C., Soe, S., Gill, D., Scher, S., & Carrive, P. (2017) · European Child & Adolescent Psychiatry · doi:10.1007/s00787-017-0976-0 · Cited by 48
Kozlowska, K., Spooner, C. J., Palmer, D. M., Harris, A., Korgaonkar, M. S., Scher, S., & Williams, L. M. (2018) · NeuroImage: Clinical · doi:10.1016/j.nicl.2018.02.003 · Cited by 47
Rebollo, I., & Tallon-Baudry, C. (2022) · The Journal of Neuroscience · doi:10.1523/jneurosci.1285-21.2021 · Cited by 46
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Teckentrup, V., & Kroemer, N. B. (2023) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2023.11.001 · Cited by 42
A meta-analytic study of experimental and chronic orofacial pain excluding headache disorders
Ayoub, L. J., Seminowicz, D. A., & Moayedi, M. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.09.018 · Cited by 40
Population-based body–brain mapping links brain morphology with anthropometrics and body composition
Gurholt, T. P., Kaufmann, T., Frei, O., Alnæs, D., Haukvik, U. K., van der Meer, D., Moberget, T., O’Connell, K. S., Leinhard, O. D., Linge, J., et al. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01414-7 · Cited by 38
First-Hand Accounts of Interoceptive Difficulties in Autistic Adults
Trevisan, D. A., Parker, T., & McPartland, J. C. (2021) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-020-04811-x · Cited by 44
Cortical basis for skilled vocalization
Cerkevich, C. M., Rathelot, J.-A., & Strick, P. L. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2122345119 · Cited by 37
Self-citationMitz, A. R., Chacko, R. V., Putnam, P. T., Rudebeck, P. H., & Murray, E. A. (2017) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2017.01.004 · Cited by 36
From ideas to action: The prefrontal–premotor connections that shape motor behavior
Grafton, S. T., & Volz, L. J. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-12-804281-6.00013-6 · Cited by 35
Signal processing in the vagus nerve: Hypotheses based on new genetic and anatomical evidence
Shaffer, C., Barrett, L. F., & Quigley, K. S. (2023) · Biological Psychology · doi:10.1016/j.biopsycho.2023.108626 · Cited by 34
Ethical Challenges in Digital Psychology and Cyberpsychology
Parsons, T. D. (2019) · Cambridge University Press eBooks · doi:10.1017/9781108553384 · Cited by 33
Association between dysphagia and symptoms of depression and anxiety after ischemic stroke
Karisik, A., Dejakum, B., Moelgg, K., Komarek, S., Toell, T., Mayer‐Suess, L., Pechlaner, R., Kostner, S., Sollereder, S., Zollner-Kiechl, S., et al. (2024) · European Journal of Neurology · doi:10.1111/ene.16224 · Cited by 32
Ventromedial prefrontal cortex connectivity during and after psychological stress in women
Ginty, A. T., Kraynak, T. E., Kuan, D. C.-H., & Gianaros, P. J. (2019) · Psychophysiology · doi:10.1111/psyp.13445 · Cited by 35
Ping, S., Qiu, X., Kyle, M. M., Hughes, K., Longo, J. A., & Zhao, L. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104561 · Cited by 32
Cunningham, N. R., Kashikar‐Zuck, S., & Coghill, R. C. (2019) · PAIN Reports · doi:10.1097/pr9.0000000000000767 · Cited by 30
Lee, C. Y., Hyun, S., Ko, M. Y., Kim, H. R., Rho, J., Kim, K. K., Kim, W.-Y., & Ka, M. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab183 · Cited by 29
Distinct neural networks subserve placebo analgesia and nocebo hyperalgesia
Fu, J., Wu, S., Liu, C., Camilleri, J. A., Eickhoff, S. B., & Yu, R. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117833 · Cited by 30
Norcliffe‐Kaufmann, L. (2022) · Autonomic Neuroscience · doi:10.1016/j.autneu.2022.102946 · Cited by 27
Voluntary modulation of mental effort investment: an fMRI study
Khachouf, O. T., Chen, G., Duzzi, D., Porro, C. A., & Pagnoni, G. (2017) · Scientific Reports · doi:10.1038/s41598-017-17519-3 · Cited by 30
Rengasamy, M. L., Marsland, A. L., Spada, M. L., Hsiung, K. S., Kovats, T., & Price, R. B. (2021) · Journal of Affective Disorders Reports · doi:10.1016/j.jadr.2021.100177 · Cited by 29
Jennings, J. R., Muldoon, M. F., Ryan, C. M., Gach, H. M., Heim, A. F., Sheu, L. K., & Gianaros, P. J. (2017) · Journal of the American Heart Association · doi:10.1161/jaha.116.004856 · Cited by 26
Patients with Head-and-Neck Cancer: Dysphagia and Affective Symptoms
Krebbers, I., Simon, S. R., Pilz, W., Kremer, B., Winkens, B., & Baijens, L. W. J. (2020) · Folia Phoniatrica et Logopaedica · doi:10.1159/000508367 · Cited by 25
Hindbrain Adrenergic/Noradrenergic Control of Integrated Endocrine and Autonomic Stress Responses
Pace, S. A., & Myers, B. (2023) · Endocrinology · doi:10.1210/endocr/bqad178 · Cited by 26
Midcingulate somatomotor and autonomic functions
Amiez, C., & Procyk, E. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64196-0.00004-2 · Cited by 28
Potential Mechanisms of the Alexander Technique: Toward a Comprehensive Neurophysiological Model
Cacciatore, T. W., Johnson, P. M., & Cohen, R. G. (2020) · Kinesiology Review · doi:10.1123/kr.2020-0026 · Cited by 29
Cortisol effects on brain functional connectivity during emotion processing in women with depression
Rivera-Bonet, C. N., Birn, R. M., Ladd, C. O., Meyerand, M. E., & Abercrombie, H. C. (2021) · Journal of Affective Disorders · doi:10.1016/j.jad.2021.03.034 · Cited by 23
Neural Signaling of Cortisol, Childhood Emotional Abuse, and Depression-Related Memory Bias
Abercrombie, H. C., Frost, C. P., Walsh, E. C., Hoks, R. M., Cornejo, M. D., Sampe, M., Gaffey, A. E., Plante, D. T., Ladd, C. O., & Birn, R. M. (2017) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2017.11.005 · Cited by 26
Zheng, H., Ford, B. N., Kuplicki, R., Burrows, K., Hunt, P. W., Bodurka, J., Teague, T. K., Irwin, M. R., Yolken, R. H., Paulus, M. P., et al. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01558-6 · Cited by 23
Writing's Potential to Heal: Women Writing from Their Bodies
Vieira, K. (2019) · Community Literacy Journal · doi:10.1353/clj.2019.0016 · Cited by 23
White matter connections within the central sulcus subserving the somato-cognitive action network
Skandalakis, G. P., Viganò, L., Neudorfer, C., Rossi, M., Fornia, L., Cerri, G., KINSMAN, K., Bajouri, Z., Tavakkoli, A. D., Koutsarnakis, C., et al. (2025) · Brain · doi:10.1093/brain/awaf022 · Cited by 21
Li, Y., Yu, Z., Zhou, X., Wu, P., & Chen, J. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.996621 · Cited by 20
Stimulant medications affect arousal and reward, not attention networks
Kay, B. P., Wheelock, M. D., Siegel, J. S., Raut, R. V., Chauvin, R. J., Metoki, A., Rajesh, A., Eck, A., Pollaro, J., Wang, A., et al. (2025) · Cell · doi:10.1016/j.cell.2025.11.039 · Cited by 25
Rodrigues, B., Barboza, C. D. A., Moura, E. G., Ministro, G., Ferreira‐Melo, S. E., Castaño, J. B., Nunes, W. M. S., Mostarda, C. T., Coca, A., Vianna, L. C., et al. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.853427 · Cited by 19
Xia, L., Ou, J., Li, K., Guo, H., Hu, Z., Bai, T., Zhao, J., Xia, K., & Zhang, F. (2019) · Autism Research · doi:10.1002/aur.2229 · Cited by 19
Nature, Mind, and Medicine: A Model for Mind–Body Healing
Kaufman, J. A. (2018) · EXPLORE · doi:10.1016/j.explore.2018.01.001 · Cited by 19
Verdonschot, R. J. C. G., Baijens, L. W. J., Vanbelle, S., Florie, M. G. M. H., Dijkman, R., Leeters, I. P. M., Kremer, B., & Leue, C. (2018) · Dysphagia · doi:10.1007/s00455-018-9912-9 · Cited by 18
Impact of stress, immunity, and signals from endocrine and nervous system on fascia
Barsotti, N., Chiera, M., Lanaro, D., & Fioranelli, M. (2020) · Frontiers in Bioscience-Elite · doi:10.2741/870 · Cited by 18
Qiu, X., Ping, S., Kyle, M. M., Chin, L. S., & Zhao, L. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113335 · Cited by 15
Sympathetic involvement in time-constrained sequential foraging
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Ugolini, G. (2020) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2020.108917 · Cited by 16
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Metadata
- Authors
- Dum, R. P., Levinthal, D. J., & Strick, P. L.
- Affiliations
- University of Pittsburgh (US)
- Corresponding author
- Strick, Peter L.
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2016-08-15
- Volume
- 113
- Issue
- 35
- Pages
- 9922-9927
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC5024624
- OpenAlex
- W2512266290
- Cited by
- 188
- References
- 84
- Citations by year
- 2026: 12 · 2025: 14 · 2024: 8 · 2023: 12 · 2022: 16 · 2021: 28 · 2020: 18 · 2019: 34 · 2018: 20 · 2017: 22 · 2016: 4
- FWCI
- 17.03
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- HHS | NIH | National Institute of Neurological Disorders and Stroke (R01 NS24328, P40 OD010996, P30 NS076405)
- HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (T32 DK063922, K08 DK101756)
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- adrenal medulla, cerebral cortex, supplementary motor area, anterior cingulate cortex, medial prefrontal cortex, motor cortex, somatosensory cortex, sympathetic nervous system, autonomic regulation, psychosomatic disorders, chronic stress, depression, neural circuits
- MeSH terms
- Adrenal Medulla, Animals, Biological Transport, Cebus, Cerebral Cortex, Cognition, Female, Gyrus Cinguli, Humans, Male, Motor Cortex, Movement, Nerve Net, Neural Pathways, Rabies, Rabies virus, Prefrontal Cortex
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