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      Top-down descending facilitation of spinal sensory excitatory transmission from the anterior cingulate cortex

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          Abstract

          Spinal sensory transmission is under descending biphasic modulation, and descending facilitation is believed to contribute to chronic pain. Descending modulation from the brainstem rostral ventromedial medulla (RVM) has been the most studied, whereas little is known about direct corticospinal modulation. Here, we found that stimulation in the anterior cingulate cortex (ACC) potentiated spinal excitatory synaptic transmission and this modulation is independent of the RVM. Peripheral nerve injury enhanced the spinal synaptic transmission and occluded the ACC-spinal cord facilitation. Inhibition of ACC reduced the enhanced spinal synaptic transmission caused by nerve injury. Finally, using optogenetics, we showed that selective activation of ACC-spinal cord projecting neurons caused behavioral pain sensitization, while inhibiting the projection induced analgesic effects. Our results provide strong evidence that ACC stimulation facilitates spinal sensory excitatory transmission by a RVM-independent manner, and that such top-down facilitation may contribute to the process of chronic neuropathic pain.

          Abstract

          It is known that descending facilitation of spinal responses may contribute to chronic pain, however many studies have focussed on brainstem mechanisms. Here the authors show that stimulation of the anterior cingulate cortex increases excitatory transmission in the dorsal horn, and that this may be via a direct pathway independent of the brainstem.

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          Most cited references49

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          Descending control of pain.

          Upon receipt in the dorsal horn (DH) of the spinal cord, nociceptive (pain-signalling) information from the viscera, skin and other organs is subject to extensive processing by a diversity of mechanisms, certain of which enhance, and certain of which inhibit, its transfer to higher centres. In this regard, a network of descending pathways projecting from cerebral structures to the DH plays a complex and crucial role. Specific centrifugal pathways either suppress (descending inhibition) or potentiate (descending facilitation) passage of nociceptive messages to the brain. Engagement of descending inhibition by the opioid analgesic, morphine, fulfils an important role in its pain-relieving properties, while induction of analgesia by the adrenergic agonist, clonidine, reflects actions at alpha(2)-adrenoceptors (alpha(2)-ARs) in the DH normally recruited by descending pathways. However, opioids and adrenergic agents exploit but a tiny fraction of the vast panoply of mechanisms now known to be involved in the induction and/or expression of descending controls. For example, no drug interfering with descending facilitation is currently available for clinical use. The present review focuses on: (1) the organisation of descending pathways and their pathophysiological significance; (2) the role of individual transmitters and specific receptor types in the modulation and expression of mechanisms of descending inhibition and facilitation and (3) the advantages and limitations of established and innovative analgesic strategies which act by manipulation of descending controls. Knowledge of descending pathways has increased exponentially in recent years, so this is an opportune moment to survey their operation and therapeutic relevance to the improved management of pain.
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            Pain and emotion interactions in subregions of the cingulate gyrus.

            Brent Vogt (2005)
            Acute pain and emotion are processed in two forebrain networks, and the cingulate cortex is involved in both. Although Brodmann's cingulate gyrus had two divisions and was not based on any functional criteria, functional imaging studies still use this model. However, recent cytoarchitectural studies of the cingulate gyrus support a four-region model, with subregions, that is based on connections and qualitatively unique functions. Although the activity evoked by pain and emotion has been widely reported, some view them as emergent products of the brain rather than of small aggregates of neurons. Here, we assess pain and emotion in each cingulate subregion, and assess whether pain is co-localized with negative affect. Amazingly, these activation patterns do not simply overlap.
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              Synaptic plasticity in the anterior cingulate cortex in acute and chronic pain.

              The anterior cingulate cortex (ACC) is activated in both acute and chronic pain. In this Review, we discuss increasing evidence from rodent studies that ACC activation contributes to chronic pain states and describe several forms of synaptic plasticity that may underlie this effect. In particular, one form of long-term potentiation (LTP) in the ACC, which is triggered by the activation of NMDA receptors and expressed by an increase in AMPA-receptor function, sustains the affective component of the pain state. Another form of LTP in the ACC, which is triggered by the activation of kainate receptors and expressed by an increase in glutamate release, may contribute to pain-related anxiety.
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                Author and article information

                Contributors
                deptanat@fmmu.edu.cn
                nakatsuka@kansai.ac.jp
                minzhuo@utoronto.ca
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                14 May 2018
                14 May 2018
                2018
                : 9
                : 1886
                Affiliations
                [1 ]ISNI 0000 0001 0599 1243, GRID grid.43169.39, Center for Neuron and Disease, Frontier Institute of Science and Technology, , Xi’an Jiaotong University, ; Xi’an, 710054 China
                [2 ]ISNI 0000 0004 1761 4404, GRID grid.233520.5, Department of Anatomy, Histology and Embryology and K.K. Leung Brain Research Centre, , The Fourth Military Medical University, ; 710032 Xi’an, China
                [3 ]ISNI 0000 0001 2185 3035, GRID grid.412013.5, Pain Research Center, , Kansai University of Health Sciences, Kumatori, ; Osaka, 590-0482 Japan
                [4 ]ISNI 0000 0001 2242 4849, GRID grid.177174.3, Department of Life Innovation, Graduate School of Pharmaceutical Sciences, , Kyushu University, ; Fukuoka, 812-8582 Japan
                [5 ]ISNI 0000 0001 2242 4849, GRID grid.177174.3, Department of Molecular and System Pharmacology, Graduate School of Pharmaceutical Sciences, , Kyushu University, ; Fukuoka, 812-8582 Japan
                [6 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Department of Physiology, Faculty of Medicine, Center for the Study of Pain, , University of Toronto, ; 1 King’s College Circle, Toronto, ON M5S 1A8 Canada
                [7 ]ISNI 0000 0004 1763 1087, GRID grid.412857.d, Department of Orthopaedic Surgery, , Wakayama Medical University, ; Wakayama, 641-8510 Japan
                Author information
                http://orcid.org/0000-0003-0423-2143
                Article
                4309
                10.1038/s41467-018-04309-2
                5951839
                29760484
                abc79269-6688-4c9d-8604-c99944a715e6
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 26 January 2016
                : 20 April 2018
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