Neuroimmune stress responses: reciprocal connections between the hypothalamus and the brainstem
Open accessAbstract
Hypothalamic nuclei, particularly the paraventricular nuclei (PVN), are important brain sites responsible for eliciting stress responses following a systemic immune challenge. The activation of PVN cells by a systemic immune challenge is critically dependent on the integrity of inputs from brainstem cells situated in the nucleus tractus solitarius (NTS) and ventrolateral medulla (VLM). Interestingly, a descending pathway from the PVN to the brainstem, recruited by systemic immune challenge, might also exist. It is well documented that PVN neurons innervate the NTS and VLM and recent evidence from our laboratory shows that lesions of the PVN reduce brainstem cell responses elicited by a systemic bolus of the proinflammatory cytokine interleukin-1beta (IL-1beta). Although a number of different PVN divisions are candidates for the source of inputs to the brainstem, we have demonstrated that the majority of descending PVN projections recruited by systemic IL-1beta arise from cell bodies localized in the medial and lateral parvocellular PVN. These findings suggest that central nervous system responses to an immune challenge are likely to involve complex reciprocal connections between the PVN and the brainstem, whereby brainstem cell populations could essentially act as integratory sites for descending and ascending immune signals. For instance, these brainstem pathways may have significant implications not only for the regulation of central hypothalamic and extra-hypothalamic targets but also the autonomic nervous system.
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When a threat signal is recognized, the central nervous system components amygdala, hypothalamus, and parts of brainstem such as the locus coeruleus are activated.
“When a threat signal is recognized, the central nervous system (CNS): amygdala (84), hypothalamus (85), and parts of brainstem such as the locus coeruleus, (86–88), which are regarded as the central components of the stress response, will be activated.”
From Epigenetic Modifications in Stress Response Genes Associated With Childhood Trauma (2019) · cites this paper as [86]
The ‘Ascending Pathways That Contribute to PVN Cell Recruitment’ section reports activation of brainstem NTS and VLM cell groups and hypothalamic PVN cells after a systemic immune challenge. It does not identify the locus coeruleus as an activated region or establish the same response to a general threat signal; the amygdala is mentioned in relation to systemic IL-1β in ‘Putative Significance of Descending PVN Pathways.’ Page numbers were not available in our copy. (LLM, conf=0.84)
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Cites
Morgan, J., & Curran, T. (1991) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.14.030191.002225 · Cited by 2,689 · see citing works
Excitatory Amino Acid Transmitters
Watkins, J. C., & Evans, R. H. (1981) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.21.040181.001121 · Cited by 2,497 · see citing works
Expression of c- <i>fos</i> Protein in Brain: Metabolic Mapping at the Cellular Level
Sagar, S. M., Sharp, F. R., & Curran, T. (1988) · Science · doi:10.1126/science.3131879 · Cited by 1,925 · see citing works
Immune-neuro-endocrine interactions: facts and hypotheses.
BESEDOVSKY, H. O., & REY, A. D. (1996) · Endocrine Reviews · doi:10.1210/edrv-17-1-64 · Cited by 1,564 · see citing works
Interleukin-1 stimulates the secretion of hypothalamic corticotropin-releasing factor
Sapolsky, R., Rivier, C., Yamamoto, G., Plotsky, P., & Vale, W. (1987) · Science · doi:10.1126/science.2821621 · Cited by 1,504 · see citing works
THE PHENOMENON OF THE ACUTE PHASE RESPONSE*
Kushner, I. (1982) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1982.tb22124.x · Cited by 1,494 · see citing works
The use of c-fos as a metabolic marker in neuronal pathway tracing
Dragunow, M., & Faull, R. (1989) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(89)90150-7 · Cited by 1,416 · see citing works
Swanson, L. W., & Kuypers, H. G. J. M. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901940306 · Cited by 1,413 · see citing works
Fever: Role of Pyrogens and Cryogens
Kluger, M. J. (1991) · Physiological Reviews · doi:10.1152/physrev.1991.71.1.93 · Cited by 1,220 · see citing works
Corticotropin-releasing factor-producing neurons in the rat activated by interleukin-1
Berkenbosch, F., van Oers, J., del Rey, A., Tilders, F., & Besedovsky, H. (1987) · Science · doi:10.1126/science.2443979 · Cited by 1,151 · see citing works
Sawchenko, P. E., & Swanson, L. W. (1982) · Journal of Comparative Neurology · doi:10.1002/cne.902050306 · Cited by 1,150 · see citing works
Sawchenko, P. E., & Swanson, L. W. (1982) · Brain Research Reviews · doi:10.1016/0165-0173(82)90010-8 · Cited by 1,141 · see citing works
Paraventricular Nucleus:A Site for the Integration of Neuroendocrine and Autonomic Mechanisms
Swanson, L. W., & Sawchenko, P. E. (2008) · Neuroendocrinology · doi:10.1159/000123111 · Cited by 1,001 · see citing works
Cytokines and the nervous system II: actions and mechanisms of action
Rothwell, N. J., & Hopkins, S. J. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93890-a · Cited by 922 · see citing works
Cytokines and the nervous system I: expression and recognition
Hopkins, S. J., & Rothwell, N. J. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)80029-2 · Cited by 793 · see citing works
van der Kooy, D., Koda, L. Y., McGinty, J. F., Gerfen, C. R., & Bloom, F. E. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902240102 · Cited by 733 · see citing works
Ericsson, A. B., Kovacs, K., & Sawchenko, P. E. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-02-00897.1994 · Cited by 684 · see citing works
Ross, C. A., Ruggiero, D. A., JOH, T. H., Park, D. H., & Reis, D. J. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902280204 · Cited by 545 · see citing works
Projections from the nucleus tractus solitarii to the rostral ventrolateral medulla
Ross, C. A., Ruggiero, D. A., & Reis, D. J. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902420405 · Cited by 518 · see citing works
Luiten, P. G. M., Horst, G. J. T., Karst, H., & Steffens, A. B. (1985) · Brain Research · doi:10.1016/0006-8993(85)90554-2 · Cited by 480 · see citing works
Banks, W. A., Ortiz, L., Plotkin, S. R., & Kastin, A. J. (1991) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)20576-6 · Cited by 474 · cited 1× · see citing works
“We do know that because of its hydrophilic nature and size limitations, IL-1b is unlikely to cross the blood–brain barrier in any significant amount whether by simple diffusion or saturable carrier-mediated transport mechanisms (Banks et al., 1989; 1991).”
BackgroundEricsson, A., Liu, C., Hart, R. P., & Sawchenko, P. E. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903610410 · Cited by 471 · see citing works
Ek, M., Kurosawa, M., Lundeberg, T., & Ericsson, A. B. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-22-09471.1998 · Cited by 370 · see citing works
Uehara, A., Gottschall, P. E., Dahl, R. R., & Arimura, A. (1987) · Endocrinology · doi:10.1210/endo-121-4-1580 · Cited by 337 · see citing works
Goehler, L. E., Relton, J. K., Dripps, D. J., Kiechle, R., Tartaglia, N. R., Maier, S. F., & Watkins, L. R. (1997) · Brain Research Bulletin · doi:10.1016/s0361-9230(97)00020-8 · Cited by 326 · see citing works
Bidirectional transport of interleukin-1 alpha across the blood-brain barrier
Banks, W. A., Kastin, A. J., & Durham, D. A. (1989) · Brain Research Bulletin · doi:10.1016/0361-9230(89)90185-8 · Cited by 325 · see citing works
Cao, C., Matsumura, K., Yamagata, K., & Watanabe, Y. (1996) · Brain Research · doi:10.1016/0006-8993(96)00575-6 · Cited by 308 · see citing works
DLX-1, DLX-2, and DLX-5 expression define distinct stages of basal forebrain differentiation
Eisenstat, D. D., Liu, J. K., Mione, M., Zhong, W., Yu, G. K., Anderson, S. A., Ghattas, I. R., Puelles, L., & Rubenstein, J. L. R. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19991115)414:2 · Cited by 286 · see citing works
Pyner, S., & Coote, J. H. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00283-9 · Cited by 284 · see citing works
Elmquist, J. K., Breder, C. D., Sherin, J. E., Scammell, T. E., Hickey, W. F., DeWitt, D. L., & Saper, C. B. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970505)381:2 · Cited by 282 · see citing works
Ericsson, A. B., Arias, C., & Sawchenko, P. E. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-18-07166.1997 · Cited by 281 · see citing works
Shafton, A. D., Ryan, A., & Badoer, E. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00587-3 · Cited by 268 · see citing works
Comparison of ibotenate and kainate neurotoxicity in rat brain: A histological study
Köhler, C., & Schwarcz, R. M. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90013-1 · Cited by 236 · see citing works
Gaykema, R. P. A., Dijkstra, I., & Tilders, F. J. H. (1995) · Endocrinology · doi:10.1210/endo.136.10.7664696 · Cited by 212 · see citing works
Breder, C. D., & Saper, C. B. (1996) · Brain Research · doi:10.1016/0006-8993(95)01474-8 · Cited by 198 · see citing works
Rivest, S. (2001) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(01)00064-6 · Cited by 195 · see citing works
Interleukin-1β induced corticosterone elevation and hypothalamic NE depletion is vagally mediated
Fleshner, M., Goehler, L. E., Hermann, J., Relton, J. K., Maier, S. F., & Watkins, L. R. (1995) · Brain Research Bulletin · doi:10.1016/0361-9230(95)00051-f · Cited by 192 · see citing works
Localization of type I interleukin-1 receptor mRNA in the rat brain
Yabuuchi, K., Minami, M., Katsumata, S., & Satoh, M. (1994) · Molecular Brain Research · doi:10.1016/0169-328x(94)90180-5 · Cited by 186 · see citing works
Mechanisms of sickness-induced decreases in food-motivated behavior
Kent, S., Bret-Dibat, J. L., Kelley, K. W., & Dantzer, R. (1996) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(95)00037-f · Cited by 183 · see citing works
Herbert, H., & Saper, C. B. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902930405 · Cited by 181 · see citing works
Neuroendocrine, Sympathetic and Metabolic Responses Induced by Interleukin-1
Berkenbosch, F., de Goeij, D. E. C., del Rey, A., & Besedovsky, H. O. (2008) · Neuroendocrinology · doi:10.1159/000125283 · Cited by 162 · see citing works
Niijima, A., Hori, T., Aou, S., & Oomura, Y. (1991) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(91)90042-2 · Cited by 141 · see citing works
Interleukin‐1 receptors on rat brain endothelial cells: a role in neuroimmune interaction?
van Dam, A., de Vries, H. E., Kuipeb, J., Zijlstra, F. J., de Boer, A. G., Tilders, F. J. H., & BERKENBOSCH, F. (1996) · The FASEB Journal · doi:10.1096/fasebj.10.2.8641570 · Cited by 136 · see citing works
Day, H. E. W., & Akil, H. (2008) · Neuroendocrinology · doi:10.1159/000126959 · Cited by 136 · see citing works
Zhang, Y.-H., Lu, J., Elmquist, J. K., & Saper, C. B. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-17-06578.2000 · Cited by 135 · see citing works
Sawchenko, P. E., Arias, C. M., & Bittencourt, J. C. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902910209 · Cited by 128 · see citing works
Zagon, A., & Smith, A. D. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90243-9 · Cited by 128 · see citing works
Pyner, S., & Coote, J. H. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00255-3 · Cited by 120 · see citing works
Localization of Interleukin 1 Type I Receptor mRNA in Rat Brain
Wong, M., & Licinio, J. (2006) · NeuroImmunoModulation · doi:10.1159/000097143 · Cited by 118 · see citing works
Voorn, P., & Buijs, R. M. (1983) · Brain Research · doi:10.1016/0006-8993(83)90809-0 · Cited by 112 · see citing works
Sgambato, V., Abó, V., Rogard, M., Besson, M., & Deniau, J. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00179-6 · Cited by 111 · see citing works
Schwanzel‐Fukuda, M., Morrell, J. I., & Pfaff, D. W. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902260102 · Cited by 103 · see citing works
Chapter 28 Endogenous pyrogens in the CNS: role in the febrile response
Saper, C. B., & Breder, C. D. (1992) · Progress in brain research · doi:10.1016/s0079-6123(08)64587-2 · Cited by 92 · see citing works
Kapcala, L. P., He, J., Gao, Y., Pieper, J. O., & DeTolla, L. J. (1996) · Brain Research · doi:10.1016/0006-8993(96)00511-2 · Cited by 83 · see citing works
Activation of sympathetic outflow by recombinant human interleukin-1 beta in conscious rats
Kannan, H., Tanaka, Y., Kunitake, T., Ueta, Y., Hayashida, Y., & Yamashita, H. (1996) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1996.270.2.r479 · Cited by 77 · see citing works
Buller, K. M., Xu, & Day (1998) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1998.00231.x · Cited by 75 · see citing works
Self-citationZhang, J., & Rivest, S. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0742134.x · Cited by 73 · see citing works
Systemic administration of interleukin‐1β activates select populations of central amygdala afferents
Buller, K. M., & Day, T. A. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10389 · Cited by 51 · see citing works
Self-citationKrukoff, T. L., Vu, T., Harris, K., Aippersbach, S. E., & Jhamandas, J. H. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90130-t · Cited by 51 · see citing works
Buller, K. M., Dayas, C. V., & Day, T. A. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00808-4 · Cited by 51 · see citing works
Self-citationIshizuka, Y., Ishida, Y., Kunitake, T., Kato, K., Hanamori, T., Mitsuyama, Y., & Kannan, H. (1997) · Neuroscience Letters · doi:10.1016/s0304-3940(97)13388-2 · Cited by 49 · see citing works
Chan, R. K. W., Peto, C. A., & Sawchenko, P. E. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903510107 · Cited by 49 · see citing works
Coexpression of neurocalcin with other calcium-binding proteins in the rat main olfactory bulb
Bri��n, J. G., Martinez-Guijarro, F. J., Bravo, I. G., Ar�valo, R., Crespo, C., Okazaki, K., Hidaka, H., Aij�n, J., & Alonso, J. R. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990510)407:3 · Cited by 47 · see citing works
Portillo, F., Carrasco, M., & Vallo, J. J. (1998) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(97)10022-9 · Cited by 41 · see citing works
Systemic endotoxin induces Fos-like immunoreactivity in rat spinal sympathetic regions
Tkacs, N. C., & Strack, A. M. (1995) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(95)80001-q · Cited by 33 · see citing works
Tseng, C., Lin, H., Wang, S., & Tung, C. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903340210 · Cited by 33 · see citing works
Salomé, N., Viltart, O., Leman, S., & Sequeira, H. (2001) · Brain Research · doi:10.1016/s0006-8993(00)03178-4 · Cited by 30 · see citing works
Effect of cervical vagotomy on sympathetic nerve responses to peripheral interleukin-1β
Saindon, C. S., Blecha, F., Musch, T. I., Morgan, D. A., Fels, R. J., & Kenney, M. (2001) · Autonomic Neuroscience · doi:10.1016/s1566-0702(00)00280-0 · Cited by 29 · see citing works
Buijs, R. M., van der Beek, E. M., Renaud, L. P., Day, T. A., & Jhamandas, J. H. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90255-3 · Cited by 29 · see citing works
Sakata, Y., Morimoto, A., & Murakami, N. (1994) · The Japanese Journal of Physiology · doi:10.2170/jjphysiol.44.693 · Cited by 22 · see citing works
Acuna, C., Fuentealba, P., & Torrealba, F. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02845-6 · Cited by 12 · see citing works
Harbuz, M. S., Chover-González, A. J., Condé, G. L., Renshaw, D. W., Lightman, S. L., & Jessop, D. S. (1997) · NeuroImmunoModulation · doi:10.1159/000097296 · Cited by 10 · see citing works
Sympathoexcitation to intravenous interleukin-1β is dependent on forebrain neural circuits
Kenney, M., Blecha, F., Wang, Y., McMurphy, R. M., & Fels, R. J. (2002) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00181.2002 · Cited by 10 · see citing works
Kawano, H., & Masuko, S. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00171-6 · Cited by 9 · see citing works
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Epigenetic Modifications in Stress Response Genes Associated With Childhood Trauma
Jiang, S., Postovit, L., Cattaneo, A., Binder, E. B., & Aitchison, K. J. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00808 · Cited by 288 · see citing works
Neural Acupuncture Unit: A New Concept for Interpreting Effects and Mechanisms of Acupuncture
Zhang, Z., Wang, X.-M., & McAlonan, G. M. (2012) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2012/429412 · Cited by 277 · see citing works
The overtraining syndrome in athletes: A stress-related disorder
Angeli, A., Minetto, M., Dovio, A., & Paccotti, P. (2004) · Journal of Endocrinological Investigation · doi:10.1007/bf03347487 · Cited by 169 · see citing works
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May, A., & Burstein, R. (2019) · Cephalalgia · doi:10.1177/0333102419867280 · Cited by 166 · see citing works
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Swain, M. G. (2006) · Canadian Journal of Gastroenterology · doi:10.1155/2006/624832 · Cited by 148 · see citing works
Leukocyte Coping Capacity: A Novel Technique for Measuring the Stress Response in Vertebrates
McLaren, G. W., Macdonald, D. W., Georgiou, C., Mathews, F., Newman, C., & Mian, R. (2003) · Experimental Physiology · doi:10.1113/eph8802571 · Cited by 103 · see citing works
Understanding migraine as a cycling brain syndrome: reviewing the evidence from functional imaging
May, A. (2017) · Neurological Sciences · doi:10.1007/s10072-017-2866-0 · Cited by 101 · see citing works
The microbiota influences cell death and microglial colonization in the perinatal mouse brain
Castillo-Ruiz, A., Mosley, M., George, A. J., Mussaji, L. F., Fullerton, E. F., Ruszkowski, E. M., Jacobs, A. J., Gewirtz, A. T., Chassaing, B., & Forger, N. G. (2018) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2017.08.027 · Cited by 91 · see citing works
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Lomax, L. B., Spencer, S. J., Mouihate, A., Vergnolle, N., & Pittman, Q. J. (2005) · Pain · doi:10.1016/j.pain.2005.09.022 · Cited by 83 · see citing works
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Sominsky, L., Hodgson, D. M., McLaughlin, E. A., Smith, R., Wall, H. M., & Spencer, S. J. (2017) · Endocrine Reviews · doi:10.1210/er.2016-1133 · Cited by 77 · see citing works
Moreno-Rius, J. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100774 · Cited by 75 · see citing works
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Balasubramanian, P., Jagannathan, L., Mahaley, R. E., Subramanian, M., Gilbreath, E., MohanKumar, P. S., & MohanKumar, S. M. J. (2011) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2011.02276.x · Cited by 75 · see citing works
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Fekete, C., Wittmann, G., Liposits, Z., & Lechan, R. M. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.10999 · Cited by 66 · see citing works
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Kiss, D. S., Tóth, I., Jócsák, G., Bárány, Z. B., Bartha, T., Frenyó, L. V., Horváth, T. L., & Zsarnovszky, A. (2020) · Brain Sciences · doi:10.3390/brainsci10060389 · Cited by 31 · see citing works
Franco‐Pérez, J., Montes, S., Sánchez-Hernández, J., & Ballesteros‐Zebadúa, P. (2020) · Radiation Oncology · doi:10.1186/s13014-020-01716-y · Cited by 27 · see citing works
Banihashemi, L., & Rinaman, L. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.09.081 · Cited by 27 · see citing works
Reyes, B. A. S., Glaser, J. D., Magtoto, R. L., & Bockstaele, E. J. V. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04744.x · Cited by 26 · see citing works
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Pickel, V. M., Chan, J., Linden, J. M., & Rosin, D. L. (2006) · Synapse · doi:10.1002/syn.20326 · Cited by 23 · see citing works
Glass, M. J., Huang, J., Speth, R. C., Iadecola, C., & Pickel, V. M. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.08.057 · Cited by 19 · see citing works
Li, C., Li, Y., Zhang, W., Ma, Z., Xiao, S., Xie, W., Miao, S., Li, B., Lu, G., Liu, Y., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242316876 · Cited by 18 · see citing works
Cortical stimulation in conscious rats controls joint inflammation
Bassi, G. S., Ulloa, L., Santos, V. R., Vecchio, F. D., Delfino-Pereira, P., Rodrigues, G. J., Castania, J. A., Cunha, F. Q., Salgado, H. C., Cunha, T. M., et al. (2018) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2018.02.013 · Cited by 15 · see citing works
Inflammatory disorders of the central nervous system
Giovannoni, G., & Baker, D. (2003) · Current Opinion in Neurology · doi:10.1097/00019052-200306000-00015 · Cited by 14 · see citing works
Cárnio, E. C., Branco, L. G. S., Brognara, F., Passaglia, P., Foresti, R., & Motterlini, R. (2025) · British Journal of Pharmacology · doi:10.1111/bph.70093 · Cited by 9 · see citing works
Ventrolateral periaqueductal grey matter neurotransmission modulates cardiac baroreflex activity
Lagatta, D. C., Ferreira‐Junior, N. C., Deolindo, M. V., Corrêa, F. M. D. A., & Resstel, L. B. M. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13407 · Cited by 8 · see citing works
Austin, P., & Henderson, S. E. (2010) · Pain Medicine · doi:10.1111/j.1526-4637.2010.01025.x · Cited by 6 · see citing works
Bringing Forth the Next Generation … and the Next
Russell, J. A., & Brunton, P. J. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-374285-8.00013-5 · Cited by 5 · see citing works
Neveu, P. J. (2003) · Stress · doi:10.1080/1025389031000096517 · Cited by 5 · see citing works
Achievements of Recent Decades in the Diagnosis and Study of Migraine Pathogenesis
Belopasova, A. V., Добрынина, Л. А., Gubanova, M. V., & Suslina, A. D. (2020) · Human Physiology · doi:10.1134/s0362119720080034 · Cited by 3 · see citing works
Carbon Monoxide: A Context-Dependent Regulator of the Stress Axis
Mancuso, C., & Santangelo, R. (2026) · Biomolecules · doi:10.3390/biom16060898 · Cited by 2 · see citing works
Kleine-Levin syndrome: report of a case with marked dysautonomic features
Fiamingo, G., Esposto, R., Fabbro, B. D., & Terzaghi, M. (2022) · Journal of Clinical Sleep Medicine · doi:10.5664/jcsm.9988 · Cited by 2 · see citing works
Actions of appetite regulating peptides on supraoptic nucleus (SON) oxytocin neurones
Velmurugan, S. (2009) · ERA · Cited by 1 · see citing works
Anatomical Networks: Structure and Function of the Nervous System
Masliah, E. (2008) · Springer eBooks · doi:10.1007/978-0-387-72573-4_3
Hernández, M. E., Becerril‐Villanueva, E., Alvarez, L., Pavón, L., Anti-Inflama, V. C., & Anti-Inflamatoria, V. C. (2008)
Anatomical Networks: Structure and Function of the Nervous System
Masliah, E. (2016) · Springer eBooks · doi:10.1007/978-3-319-44022-4_7
- Authors
- Buller, K. M.
- Affiliations
- The University of Queensland (AU)
- Corresponding author
- Buller, Kathryn M.
- ORCID
- Buller, Kathryn M.
- Venue
- Stress
- Publisher
- Informa UK Limited
- Published
- 2003-01
- Volume
- 6
- Issue
- 1
- Pages
- 11-17
- ISSN
- 1025-3890 (ISSN-L)
- 1607-8888
- OpenAlex
- W2095976919
- Cited by
- 41
- References
- 74
- Citations by year
- 2026: 1 · 2025: 1 · 2023: 1 · 2022: 1 · 2021: 2 · 2020: 3 · 2019: 3 · 2018: 1 · 2017: 3 · 2016: 2 · 2012: 1
- FWCI
- 1.77
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Stress (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Medical Research Council
- National Health and Medical Research Council
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroscience of respiration and sleep
- Life Sciences › Neuroscience › Neurology › Vagus Nerve Stimulation Research
- Keywords
- neuroimmune interactions, hypothalamus, paraventricular nucleus, brainstem, nucleus tractus solitarius, ventrolateral medulla, IL-1β, descending projections, reciprocal connections, autonomic nervous system, stress response
- MeSH terms
- Animals, Brain Stem, Hypothalamus, Medulla Oblongata, Neural Pathways, Paraventricular Hypothalamic Nucleus, Recruitment, Neurophysiological, Stress, Physiological, Neuroimmunomodulation, Solitary Nucleus
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