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State-dependent opioid control of pain
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“The high concentration of opioid receptors expressed in rACC (Vogt et al., 1993; Fields, 2004) has been hypothesized to relate to attentional mechanisms that can suppress pain processing (Petrovic et al., 2002), a suggestion that has received experimental support (Zubieta et al., 2005; Wager et al., 2007; Eippert et al., 2009).”
From Top-Down Dysregulation—From ADHD to Emotional Instability (2016) · cites this paper as Fields, 2004
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Molecular mechanisms of nociception
Julius, D., & Basbaum, A. I. (2001) · Nature · doi:10.1038/35093019 · Cited by 2,685 · cited 1×
“We now know a great deal about the molecular mechanisms of transduction and the relationship of the firing of these neurons to stimulus intensity and to the psychophysics of perceived pain intensit”
BackgroundTHE MECHANISM OF PLACEBO ANALGESIA
Levine, J., Gordon, N., & Fields, H. (1978) · The Lancet · doi:10.1016/s0140-6736(78)92762-9 · Cited by 1,094
Self-citationOrganization of endogenous opiate and nonopiate pain control systems
Watkins, L. R., & Mayer, D. J. (1982) · Science · doi:10.1126/science.6281891 · Cited by 791
Response expectancies in placebo analgesia and their clinical relevance
Pollo, A., Amanzio, M., Arslanian, A., Casadio, C., Maggi, G., & Benedetti, F. (2001) · Pain · doi:10.1016/s0304-3959(01)00296-2 · Cited by 442
Liebeskind, J. C., Guilbaud, G., Besson, J.-M., & Oliveras, J.-L. (1973) · Brain Research · doi:10.1016/0006-8993(73)90748-8 · Cited by 439
The role of conditioning and verbal expectancy in the placebo response
Voudouris, N. J., Peck, C. L., & Coleman, G. (1990) · Pain · doi:10.1016/0304-3959(90)90057-k · Cited by 369
Sucrose ingestion causes opioid analgesia.
Segato, F. N., Castro-Souza, C., Segato, E. N., Morato, S., & Coimbra, N. C. (1997) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x1997000800011 · Cited by 72
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“There is also thought to be state-dependent and bidirectional control of pain modulation through serotonergic projections from the RVM to the TCC that is distinct to “ON” and “OFF” cells (269).”
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“Descending opioid-dependent pain modulation pathways are also engaged by other behavioural and motivational states, including vigilance and fea”
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“…example, ascending interoceptive signals bring sensory prediction errors from the internal milieu to the brain via lamina I and vagal afferent pathways, and they are anatomically positioned to be modulated by descending visceromotor predictions that control the internal milieu (e.g. Fields, 2004).”
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“They also have found that these reductions are accompanied by increases in neural activity within brain areas known to be involved in emotional regulation (Fields 2004, Petrovic et al. 2005, Zubieta et al. 2001).”
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“…example, ascending interoceptive signals bring sensory prediction errors from the internal milieu to the brain via lamina I and vagal afferent pathways, and they are anatomically positioned to be modulated by descending visceromotor predictions that control the internal milieu (e.g. Fields, 2004).”
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“The gate control theory posits and much subsequent work on central regulation of pain has shown that the periaqueductal gray (PAG) exerts central control over spinal pain pathways (Melzack and Wall, 1965; Fields, 2004).”
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“opioid receptors on the presynaptic terminals of primary nociceptive neurons and spinal cord resident neurons [38].”
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“In addition to its tissue-protective role, pain provides a teaching signal that enables individuals to avoid future harm (Apkarian et al., 2009; Johansen and Fields, 2004).”
Self-citationUnmasking the tonic-aversive state in neuropathic pain
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“The RVM (as well as the PAG) is characterized by distinctive cells (Fields et al., 1983; Heinricher et al., 1987) that show a pause of firing (Off cells) or a burst of firing (On cells) just before a nociceptive withdrawal reflex occurs in the anesthetized animal (Fields, 2004; but see Mason, 2012).”
Cortical excitation and chronic pain
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“Indeed, endogenous opioids play a central role in analgesia and the perception of painful stimuli (Fields, 2004).”
BackgroundBad news from the brain: descending 5-HT pathways that control spinal pain processing
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Individual differences in reward responding explain placebo-induced expectations and effects
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Reward and motivation in pain and pain relief
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Self-citationOpponent appetitive-aversive neural processes underlie predictive learning of pain relief
Seymour, B., O'Doherty, J. P., Koltzenburg, M., Wiech, K., Frackowiak, R., Friston, K., & Dolan, R. (2005) · Nature Neuroscience · doi:10.1038/nn1527 · Cited by 439
“This illustrates a critical issue in our understanding of pain relief as an affective and motivational stat”
BackgroundCancer pain and its impact on diagnosis, survival and quality of life
Mantyh, P. W. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1914 · Cited by 443
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Brain mediators of predictive cue effects on perceived pain
Atlas, L. Y., Bolger, N., Lindquist, M. A., & Wager, T. D. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.0057-10.2010 · Cited by 389
“This may explain why we did not observe cue effects on the PAG, a PPN region critical for endogenous opioid-based analgesia (Fields, 2004) that is modulated by placebo (Wager et al.”
BackgroundKucyi, A., Moayedi, M., Weissman-Fogel, I., Goldberg, M. B., Freeman, B. V., Tenenbaum, H. C., & Davis, K. D. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.5055-13.2014 · Cited by 396
“Notably, although a role of the PAG in descending pain inhibition is well established (Millan, 2002), there is also evidence from animal studies for pronociceptive effects of the PAG under certain contexts such as stress (Fields, 2004; Lovick, 2008).”
BackgroundPetrovic, P., Dietrich, T., Fransson, P., Andersson, J., Carlsson, K., & Ingvar, M. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.023 · Cited by 437
Keltner, J. R., Furst, A., Fan, C., Redfern, R., Inglis, B., & Fields, H. L. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4463-05.2006 · Cited by 346
“One possible mechanism for the modulatory effect of expectancy on pain is that it activates descending modulatory systems (Fields, 2004; Fields et al., 2006).”
BackgroundSelf-citationGeorge, O., & Koob, G. F. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.05.002 · Cited by 322
“For instance, under great emotion or intense concentration, people often report few signs of pain despite severe injuries (Fields, 2004).”
BackgroundThe role of sleep in pain and fibromyalgia
Choy, E. H. S. (2015) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2015.56 · Cited by 333
Younger, J., Aron, A., Parke, S., Chatterjee, N., & Mackey, S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013309 · Cited by 314
Common brain mechanisms of chronic pain and addiction
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Motor cortex stimulation for pain control induces changes in the endogenous opioid system
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Epigenetic suppression of GAD65 expression mediates persistent pain
Zhang, Z., Cai, Y.-Q., Zou, F., Bie, B., & Pan, Z. Z. (2011) · Nature Medicine · doi:10.1038/nm.2442 · Cited by 281
“Whereas spinal adaptive mechanisms are important in chronic pain, our study focused on the brainstem nucleus raphe magnus (NRM), a crucial supraspinal site for maintenance of pain hypersensitivity in behavioral states of chronic pai”
BackgroundWhen pain gets stuck: the evolution of pain chronification and treatment resistance
Borsook, D., Youssef, A. M., Simons, L., Elman, I., & Eccleston, C. (2018) · Pain · doi:10.1097/j.pain.0000000000001401 · Cited by 281
Neuroimaging Acupuncture Effects in the Human Brain
Dhond, R. P., Kettner, N. W., & Napadow, V. (2007) · The Journal of Alternative and Complementary Medicine · doi:10.1089/acm.2007.7040 · Cited by 261
“Bottom image: shows activation in right anterior insula (46, 20, 4), and C shows activation in bilateral rostral anterior cingulate cortex (2, 44, 10).”
BackgroundGarland, E. L., Froeliger, B., Zeidan, F., Partin, K., & Howard, M. O. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.08.006 · Cited by 277
What is reinforced by phasic dopamine signals?
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“The reinforcing consequences of terminating an aversive event are widely appreciated (Craig, 2003; Fields, 2004; Kim et al., 2006; Seymour et al., 2005).”
BackgroundJensen, K. B., Loitoile, R., Kosek, E., Petzke, F. W., Carville, S. F., Fransson, P., Marcus, H. E., Williams, S., Choy, E., Mainguy, Y., et al. (2012) · Molecular Pain · doi:10.1186/1744-8069-8-32 · Cited by 276
“Using the same region as seed for the present connectivity fMRI analysis, we found that healthy controls displayed higher rACC connectivity than FM patients to the hippocampus, a cluster that extended into the PAG area of the brainstem.”
BackgroundResultInfluentialTrigeminal Nociceptive Transmission in Migraineurs Predicts Migraine Attacks
Stankewitz, A., Aderjan, D., Eippert, F., & May, A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4496-10.2011 · Cited by 260
“Mean values of pain ratings and SEMs were as follows: interictal patients, 6.7 2.3; preictal patients, 6.2 3.4; ictal patients, 6.5 2.3; controls, 6.5 2.4 (Table 1).”
BackgroundInfluentialThe anatomy of pain and suffering in the brain and its clinical implications
Ridder, D. D., Adhia, D. B., & Vanneste, S. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.08.013 · Cited by 298
“…descending pain inhibitory pathway (Fields, 2004; Kong et al., 2010a), involving the rostral and pregenual anterior cingulate cortex (pgACC), the periaqueductal gray, the parahippocampal area, hypothalamus, and rostral ventromedial brainstem (Fields, 2004; Kong et al., 2010a; Eippert et al., 2009).”
BackgroundMesolimbic dopamine signaling in acute and chronic pain
Taylor, A. M. W., Becker, S., Schweinhardt, P., & Cahill, C. M. (2016) · Pain · doi:10.1097/j.pain.0000000000000494 · Cited by 248
“Copyright (cid:1) 2016 by the International Association for the Study of Pain.”
BackgroundInfluentialNon-suicidal self-injurious behavior, endogenous opioids and monoamine neurotransmitters
Stanley, B., Sher, L., Wilson, S., Ekman, R., Huang, Y., & Mann, J. J. (2009) · Journal of Affective Disorders · doi:10.1016/j.jad.2009.10.028 · Cited by 249
“There is a well-established relationship between pain perception and endogenous opioids (Urban and Gebhart, 1999; Fields, 2004; Przewlocki and Przewlocka 2001).”
BackgroundRütgen, M., Seidel, E.-M., Silani, G., Riečanský, I., Hummer, A., Windischberger, C., Petrovic, P., & Lamm, C. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1511269112 · Cited by 208
“This finding implies that these areas play an important role in opioidergically mediated pain regulation (20).”
BackgroundHemispheric Lateralization of Pain Processing by Amygdala Neurons
Ji, G., & Neugebauer, V. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00166.2009 · Cited by 214
Thomsen, K. R., Whybrow, P. C., & Kringelbach, M. L. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00049 · Cited by 256
“The study by Pessiglione et al. showed that even when participants are unable to report how much money is at stake, they still use more effort in terms of force for higher amounts of money.”
BackgroundDisrupted functional connectivity of the periaqueductal gray in chronic low back pain
Yu, R., Gollub, R. L., Spaeth, R. B., Napadow, V., Wasan, A. D., & Kong, J. (2014) · NeuroImage Clinical · doi:10.1016/j.nicl.2014.08.019 · Cited by 224
“These nuisance signals are typically adjusted for in resting-state FC studies because they reflect signal fluctuations of nonneuronal origin (e.g., physiological artifacts associated with variables such as cardiac and respiratory cycles, CSF motion, and scanner drift) (Fox and Raichle, 2007).”
BackgroundJensen, K. B., Srinivasan, P., Spaeth, R. B., Tan, Y. H. V., Kosek, E., Petzke, F. W., Carville, S. F., Fransson, P., Marcus, H. E., Williams, S., et al. (2013) · Arthritis & Rheumatism · doi:10.1002/art.38170 · Cited by 225
“Since the rACC is a key region for descending inhibition of pain (43, 44), the lower rACC coherence in FM patients provides support for the hypothesis that the FM pathology may be associated with dysfunction of descending pain modulation (36, 45, 46).”
ResultBenarroch, E. E. (2012) · Neurology · doi:10.1212/wnl.0b013e31823fcdee · Cited by 223
Spinal cord stimulation in chronic pain: evidence and theory for mechanisms of action
Caylor, J. R., Reddy, R. D., Yin, S., Cui, C. L., Huang, M., Huang, C. W., Rao, R., Baker, D. G., Simmons, A. N., Souza, D., et al. (2019) · Bioelectronic Medicine · doi:10.1186/s42234-019-0023-1 · Cited by 251
“While neutral cells and 5-HT like cells have only been partially characterized, more is understood about the firing patterns of ON and OFF cells (Fields, 2004).”
BackgroundChen, T., Taniguchi, W., Chen, Q.-Y., Tozaki‐Saitoh, H., Song, Q., Liu, R.-H., Koga, K., Matsuda, T., Kaito-Sugimura, Y., Wang, J., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-04309-2 · Cited by 254
“Subsequently, all sections were processed according to the following steps: (1) post-fixation with glutaraldehyde, (2) silver enhancement using the HQ Silver Kit (Nanoprobes, Stony Brook, NY, USA), (3) incubation with the ABC kit (Vector), (4) reaction with DAB tetrahydrochloride and H2O2, (5) osmification, and (6) co…”
Pain imaging in health and disease — how far have we come?
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Interactions between brain and spinal cord mediate value effects in nocebo hyperalgesia
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Attention modulates spinal cord responses to pain
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“This phylogenetically highly conserved network is anatomically well-suited to mediate between higher-order brain processes and the spinal cord level through dorsal horn facilitation or inhibition [28, 29].”
Neuroendocrinology of social information processing in rats and mice
Choleris, E., Clipperton-Allen, A. E., Phan, A., & Kavaliers, M. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.05.003 · Cited by 205
“a direct response to noxious stimuli might otherwise disrupt other adaptive responses [89].”
A Systems Neuroscience Approach to Migraine
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“In RVM, ON and OFF cells fire on nociceptive stimulus onset and offset, and are thought to be associated with pain facilitation and suppression, respectively(Fields, 2004).”
Brain circuits for pain and its treatment
Lindsay, N. M., Chen, C., Gilam, G., Mackey, S., & Scherrer, G. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.abj7360 · Cited by 246
Pain and Poppies: The Good, the Bad, and the Ugly of Opioid Analgesics
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“…medulla, and locus ceruleus) from which descending pain-modulating pathways originate and in the dorsal horn region of the spinal cord, an area important for the relay of nociceptive input to the brain and a primary site of action for the analgesic effects of opioids (Fields, 2004; Fig.”
Tinnitus: perspectives from human neuroimaging
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“Similarly, the utility and consequently the hedonic experience of interpersonal touch largely depends on the context and internal needs and motivational goals.”
BackgroundIntrinsic functional connectivity of the periaqueductal gray, a resting fMRI study
Kong, J., Tu, P., Zyloney, C. E., & Su, T. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.03.042 · Cited by 207
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BackgroundPsychological Risk Factors in Headache
Nicholson, R. A., Houle, T. T., Rhudy, J. L., & Norton, P. J. (2007) · Headache The Journal of Head and Face Pain · doi:10.1111/j.1526-4610.2006.00716.x · Cited by 203
Burst and Tonic Spinal Cord Stimulation: Different and Common Brain Mechanisms
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“The pgACC is part of the descending pain-modulating antinociceptive system, which also involves other areas such as the periaqueductal gray, the parahippocampal area, anterior insula, hypothalamus and rostral ventromedial brainstem (6,11,69).”
BackgroundPeripheral and central mechanisms of visceral sensitization in man
Anand, P., Aziz, Q., Willert, R. P., & Oudenhove, L. V. (2007) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2006.00873.x · Cited by 190
Functional connectivity of the frontoparietal network predicts cognitive modulation of pain
Kong, J., Jensen, K. B., Loiotile, R. E., Cheetham, A., Wey, H., Tan, Y. H. V., Rosen, B. R., Smoller, J. W., Kaptchuk, T. J., & Gollub, R. L. (2012) · Pain · doi:10.1016/j.pain.2012.12.004 · Cited by 191
“The brainstem/medulla [17,21] is another important region in the descending pain modulatory network, which sends direct projections to dorsal horn laminae to modulate pain transmission.”
BackgroundSprenger, C., Bingel, U., & Büchel, C. (2011) · Pain · doi:10.1016/j.pain.2010.11.018 · Cited by 192
“modulation [25,50,65,68] and is anatomically substantiated by a thoroughly described descending pain-modulating pathway [26].”
BackgroundA prefrontal non-opioid mechanism in placebo analgesia
Petrovic, P., Kalso, E., Petersson, K. M., Andersson, J., Fransson, P., & Ingvar, M. (2010) · Pain · doi:10.1016/j.pain.2010.03.011 · Cited by 182
“Similar cognitive processes are involved in the placebo mechanism [14].”
Inhibiting the breakdown of endogenous opioids and cannabinoids to alleviate pain
Roques, B. P., Fournié‐Zaluski, M., & Wurm, M. (2012) · Nature Reviews Drug Discovery · doi:10.1038/nrd3673 · Cited by 198
“All three of these factors vary according to the neuronal pathways involved and the type of stimulatio”
BackgroundReward, motivation, and emotion of pain and its relief
Porreca, F., & Navratilova, E. (2017) · Pain · doi:10.1097/j.pain.0000000000000798 · Cited by 210
“medulla where OFF and ON cells that respectively mediate descending inhibition and facilitation have been identified.(29) The motivation-decision model of Fields has suggested a contextdependent activation of these cells that guide the behavioral outcome of a nociceptive stimulus.”
BackgroundThe role of psychosocial factors and psychiatric disorders in functional dyspepsia
Oudenhove, L. V., & Aziz, Q. (2013) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2013.10 · Cited by 195
Zaki, J., Ochsner, K. N., Hanelin, J., Wager, T. D., & Mackey, S. (2007) · Social Neuroscience · doi:10.1080/17470910701401973 · Cited by 193
“The PAG is a key region in the top-down control of pain transmission in the spinal cord through influences on the medulla (Fields, 2004; Wager, 2005a).”
BackgroundInfluentialTop-Down Dysregulation—From ADHD to Emotional Instability
Petrovic, P., & Castellanos, F. X. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00070 · Cited by 179
“The high concentration of opioid receptors expressed in rACC (Vogt et al., 1993; Fields, 2004) has been hypothesized to relate to attentional mechanisms that can suppress pain processing (Petrovic et al., 2002), a suggestion that has received experimental support (Zubieta et al., 2005; Wager et…”
ResultThe Mechanisms Involved in Morphine Addiction: An Overview
Listos, J., Łupina, M., Talarek, S., Mazur, A., Orzelska‐Górka, J., & Kotlinska, J. H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20174302 · Cited by 201
“These receptors are localized in subcortical regions of the brain, as previously mentioned, from which the descending pain pathways originate, such as in the thalamus, the PAG and the RVM, as well as in the spinal cord’s dorsal horn [85].”
BackgroundMaione, S., Piscitelli, F., Gatta, L., Vita, D. D., PETROCELLIS, L. D., Palazzo, E., de Novellis, V., & Marzo, V. D. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2010.01063.x · Cited by 186
“and adenosine A1 receptor agonists, have been found to reduce ON cell and stimulate OFF cell activity after intra-PAG injections (Fields et al., 1983; Heinricher and Tortorici, 1994; Meng et al., 1998; Fields, 2004; de Novellis et al., 2005; Maione et al., 2007).”
BackgroundInfluentialPlacebo and Nocebo Effects: An Introduction to Psychological and Biological Mechanisms
Kong, J., & Benedetti, F. (2014) · Handbook of experimental pharmacology · doi:10.1007/978-3-662-44519-8_1 · Cited by 34
How expectations influence pain
Fields, H. L. (2018) · Pain · doi:10.1097/j.pain.0000000000001272 · Cited by 175
“either facilitate (ON cells) or inhibit (OFF cells) dorsal horn responses to noxious stimulation.(15) Although prediction-based facilitation of nociceptive transmission has not been extensively studied in human subjects, we demonstrated using functional magnetic resonance imaging that there is relative activation in t…”
BackgroundSelf-citationStarowicz, K., Maione, S., Cristino, L., Palazzo, E., Marabese, I., Rossi, F., de Novellis, V., & Marzo, V. D. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3258-07.2007 · Cited by 168
“Of these, the RVM is the principal relay in the integration of ascending nociceptive inputs with descending outputs from rostral sites (Fields, 2004; Fields et al., 2005), as well as the major source of bulbospinal projections that terminate in laminas I, II and V of the dorsal horn, mostly via OFF…”
BackgroundInfluentialThe importance of context: When relative relief renders pain pleasant
Leknes, S., Berna, C., Lee, M., Snyder, G. D., Biele, G., & Tracey, I. (2012) · Pain · doi:10.1016/j.pain.2012.11.018 · Cited by 187
“Since the function of the DPMS is state dependent, we hypothesised that this state change would be reflected in alterations in the connectivity pattern of the DPMS, specifically the periacqueductal grey (PAG) [18,19].”
BackgroundOptoactivation of Locus Ceruleus Neurons Evokes Bidirectional Changes in Thermal Nociception in Rats
Hickey, L., Li, Y., Fyson, S. J., Watson, T. C., Perrins, R., Hewinson, J., Teschemacher, A. G., Furue, H., Lumb, B. M., & Pickering, A. E. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4835-13.2014 · Cited by 169
“Since the original report that electrical stimulation of the midbrain produces profound analgesia (Reynolds, 1969), much attention has been focused on descending control systems, which can influence the spinal transmission of noxious inputs (Millan, 2002; Fields, 2004).”
BackgroundPain, affective symptoms, and cognitive deficits in patients with cerebral dopamine dysfunction
Jarcho, J. M., Mayer, E. A., Jiang, Z. K., Feier, N. A., & London, E. D. (2012) · Pain · doi:10.1016/j.pain.2012.01.002 · Cited by 160
“While it is well established that endogenous opioids play a key role in modulating these systems [44,175], emerging research implicates central dopamine (DA) signaling as another important”
BackgroundDifferential brain opioid receptor availability in central and peripheral neuropathic pain
Maarrawi, J., Peyron, R., Mertens, P., Costes, N., Magnin, M., Sindou, M., Laurent, B., & Garcı́a-Larrea, L. (2006) · Pain · doi:10.1016/j.pain.2006.10.013 · Cited by 156
“Indeed, endogenous opioid secretion is considered as part of a defensive reaction to inescapable stress conditions, including pain (Vaccarino et al., 1999; Fields, 2004) that depends on pain intensity independent of its aetiology or lesion site, and should therefore have occurred in both peripheral and central pain (a…”
BackgroundInfluentialUnderstanding how opioids contribute to reward and analgesia
Fields, H. L. (2007) · Regional Anesthesia and Pain Medicine · doi:10.1097/00115550-200705000-00012 · Cited by 166
Self-citationAdvances in Achieving Opioid Analgesia Without Side Effects
Machelska, H., & Celik, M. Ö. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.01388 · Cited by 191
“Opioid peptides, including β-endorphin, enkephalins and dynorphins are expressed in neurons in pain-relevant regions of the central or peripheral nervous system as well as in immune cells accumulating in peripheral painful tissue (Fields, 2004; Stein and Machelska, 2011).”
BackgroundGavériaux‐Ruff, C., Nozaki, C., Nadal, X., Hever, X. C., Weibel, R., Matifas, A., Reiss, D. J., Filliol, D., Nassar, M. A., Wood, J. N., et al. (2011) · Pain · doi:10.1016/j.pain.2010.12.031 · Cited by 161
“first-order primary afferent neurons, second-order neurons in the spinal cord, and brain where pain messages are integrated, and descending inhibitory pain pathways recruiting periaqueductal gray and rostral ventral medulla systems [16,17].”
BackgroundPain and the Triple Network Model
Ridder, D. D., Vanneste, S., Smith, M. L., & Adhia, D. B. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.757241 · Cited by 189
“A third pathway, namely the descending pain inhibitory pathway, balances the two ascending pain pathways (25, 26, 56, 57).”
BackgroundSamineni, V. K., Grajales‐Reyes, J. G., Copits, B. A., O’Brien, D. E., Trigg, S. L., Gomez, A. M., Bruchas, M. R., & Gereau, R. W. (2017) · eNeuro · doi:10.1523/eneuro.0129-16.2017 · Cited by 188
“The cellular mechanisms underlying the analgesic and hyperalgesic effects of manipulating inhibitory and excitatory neurotransmission in the vlPAG have not been directly evaluated (Moreau and Fields, 1986; Carstens et al., 1988; Jacquet, 1988; Sandkühler et al., 1989; Vaughan et al., 1997; Budai and Fields, 1998; Fiel…”
BackgroundMethodInfluentialTsuda, M., Koga, K., Chen, T., & Zhuo, M. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14001 · Cited by 171
FMRI Connectivity Analysis of Acupuncture Effects on an Amygdala-Associated Brain Network
Qin, W., Tian, J., Bai, L., Pan, X., Yang, L., Chen, P., Dai, J., Ai, L., Zhao, B., Gong, Q., et al. (2008) · Molecular Pain · doi:10.1186/1744-8069-4-55 · Cited by 142
“The ACC contains a high concentration of opioid receptors [48], and has been regarded as a functional region in opioid analgesia and in other forms of pain modulation [49,50], which may suggest a similar involvement of higher order control of opioid-dependent placebo analgesia.”
BackgroundRaehal, K. M., & Bohn, L. M. (2014) · Handbook of Experimental Pharmacology · doi:10.1007/978-3-642-41199-1_22 · Cited by 154
“The decrease in GABA release promotes disinhibition of the OFF nociceptive neurons and direct inhibition of ON cells, resulting in antinociception (for reviews, see Fields 2004; Rea et al. 2007; Palazzo et al. 2010; Fig.”
BackgroundPreclinical and early clinical investigations related to monoaminergic pain modulation
Bannister, K., Bee, L., & Dickenson, A. (2009) · Neurotherapeutics · doi:10.1016/j.nurt.2009.07.009 · Cited by 153
Facilitation of Pain in the Human Spinal Cord by Nocebo Treatment
Geuter, S., & Büchel, C. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2191-13.2013 · Cited by 152
“, 2009a), and given its bidirectional control of pain modulation (Fields, 2004), it is probably also engaged in nocebo hyperalgesia.”
BackgroundInfluentialKoshi, E. B., & Short, C. (2007) · Pain Practice · doi:10.1111/j.1533-2500.2007.00104.x · Cited by 146
“with rostral ventromedial medulla and the dorsal horn of spinal cord.(69) This pathway can exert both inhibitory and facilitatory control through off-cells and on-cells.”
Background
Metadata
- Authors
- Fields, H.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Fields, Howard
- ORCID
- Fields, Howard
- Venue
- Nature Reviews Neuroscience
- Published
- 2004-07
- Volume
- 5
- Issue
- 7
- Pages
- 565-575
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- OpenAlex
- W2030751218
- Cited by
- 946
- References
- 0
- Citations by year
- 2026: 46 · 2025: 43 · 2024: 36 · 2023: 42 · 2022: 54 · 2021: 52 · 2020: 38 · 2019: 43 · 2018: 49 · 2017: 66 · 2016: 45 · 2015: 39 · 2014: 48 · 2013: 47 · 2012: 56
- FWCI
- 3.38
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Pain Mechanisms and Treatments
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- opioid analgesia, mu-opioid receptor, delta opioid receptor, kappa opioid receptor, motivational states, aversive motivation, appetitive motivation, pain transmission, pain modulation, opioid use disorder, choice behavior
- MeSH terms
- Analgesics, Opioid, Animals, Behavior, Animal, Humans, Medulla Oblongata, Models, Neurological, Motivation, Opioid-Related Disorders, Neural Pathways, Neurons, Nociceptors, Pain, Receptors, Opioid, Reinforcement, Psychology, Serotonin, Synapses, Neural Networks, Computer
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