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      Multiple modulatory roles of serotonin in chronic pain and injury-related anxiety

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          Abstract

          Chronic pain is long-lasting pain that often persists during chronic diseases or after recovery from disease or injury. It often causes serious side effects, such as insomnia, anxiety, or depression which negatively impacts the patient’s overall quality of life. Serotonin (5-HT) in the central nervous system (CNS) has been recognized as an important neurotransmitter and neuromodulator which regulates various physiological functions, such as pain sensation, cognition, and emotions–especially anxiety and depression. Its widespread and diverse receptors underlie the functional complexity of 5-HT in the CNS. Recent studies found that both chronic pain and anxiety are associated with synaptic plasticity in the anterior cingulate cortex (ACC), the insular cortex (IC), and the spinal cord. 5-HT exerts multiple modulations of synaptic transmission and plasticity in the ACC and the spinal cord, including activation, inhibition, and biphasic actions. In this review, we will discuss the multiple actions of the 5-HT system in both chronic pain and injury-related anxiety, and the synaptic mechanisms behind them. It is likely that the specific 5-HT receptors would be new promising therapeutic targets for the effective treatment of chronic pain and injury-related anxiety in the future.

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          Cognitive and emotional control of pain and its disruption in chronic pain.

          Chronic pain is one of the most prevalent health problems in our modern world, with millions of people debilitated by conditions such as back pain, headache and arthritis. To address this growing problem, many people are turning to mind-body therapies, including meditation, yoga and cognitive behavioural therapy. This article will review the neural mechanisms underlying the modulation of pain by cognitive and emotional states - important components of mind-body therapies. It will also examine the accumulating evidence that chronic pain itself alters brain circuitry, including that involved in endogenous pain control, suggesting that controlling pain becomes increasingly difficult as pain becomes chronic.
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            Neuroinflammation and Central Sensitization in Chronic and Widespread Pain.

            Chronic pain is maintained in part by central sensitization, a phenomenon of synaptic plasticity, and increased neuronal responsiveness in central pain pathways after painful insults. Accumulating evidence suggests that central sensitization is also driven by neuroinflammation in the peripheral and central nervous system. A characteristic feature of neuroinflammation is the activation of glial cells, such as microglia and astrocytes, in the spinal cord and brain, leading to the release of proinflammatory cytokines and chemokines. Recent studies suggest that central cytokines and chemokines are powerful neuromodulators and play a sufficient role in inducing hyperalgesia and allodynia after central nervous system administration. Sustained increase of cytokines and chemokines in the central nervous system also promotes chronic widespread pain that affects multiple body sites. Thus, neuroinflammation drives widespread chronic pain via central sensitization. We also discuss sex-dependent glial/immune signaling in chronic pain and new therapeutic approaches that control neuroinflammation for the resolution of chronic pain.
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              Chronic pain: an update on burden, best practices, and new advances

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                Author and article information

                Contributors
                Journal
                Front Synaptic Neurosci
                Front Synaptic Neurosci
                Front. Synaptic Neurosci.
                Frontiers in Synaptic Neuroscience
                Frontiers Media S.A.
                1663-3563
                18 April 2023
                2023
                : 15
                : 1122381
                Affiliations
                [1] 1Department of Pharmacology, School of Pharmacy, Qingdao University , Qingdao, Shandong, China
                [2] 2Oujiang Laboratory, Zhejiang Lab for Regenerative Medicine, Vision and Brain Health , Wenzhou, Zhejiang, China
                [3] 3International Institute of Brain Research, Forevercheer Medicine Pharmac Inc. , Qingdao, Shandong, China
                [4] 4Center for Neuron and Disease, Frontier Institute of Science and Technology, Xi’an Jiaotong University , Xi’an, Shaanxi, China
                [5] 5The Brain Cognition and Brain Disease Institute, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences , Shenzhen, Guangdong, China
                [6] 6Department of Physiology, Faculty of Medicine, University of Toronto , Toronto, ON, Canada
                Author notes

                Edited by: Natalia Alenina, Helmholtz Association of German Research Centers (HZ), Germany

                Reviewed by: Gary C. Mouradian, Medical College of Wisconsin, United States; Magdalena Zaniewska, The Polish Academy of Sciences, Poland; Hongxing Zhang, Xuzhou Medical University, China

                *Correspondence: Min Zhuo, min.zhuo@ 123456utoronto.ca
                Article
                10.3389/fnsyn.2023.1122381
                10151796
                37143481
                adc960cc-fe97-4764-ab08-f691e03630ec
                Copyright © 2023 Hao, Shi, Liu, Chen and Zhuo.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 12 December 2022
                : 03 April 2023
                Page count
                Figures: 2, Tables: 0, Equations: 0, References: 100, Pages: 12, Words: 10414
                Funding
                This study was funded by the EJLB-CIHR Michael Smith Chair in Neurosciences and Mental Health in Canada, the Canada Research Chair, the Ontario-China Research and Innovation Fund (OC-RIF), and the Canadian Institute for Health Research operating and project Grants (MOP-124807; PJT-148648 and 419286) for funding support to MZ.
                Categories
                Neuroscience
                Review

                Neurosciences
                5-ht,5-ht receptors,chronic pain,anxiety,synaptic modulation,acc,insular cortex,amygdala
                Neurosciences
                5-ht, 5-ht receptors, chronic pain, anxiety, synaptic modulation, acc, insular cortex, amygdala

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