The Distinct Functions of Dopaminergic Receptors on Pain Modulation: A Narrative Review

Chronic pain is considered an economic burden on society as it often results in disability, job loss, and early retirement. Opioids are the most common analgesics prescribed for the management of moderate to severe pain. However, chronic exposure to these drugs can result in opioid tolerance and opi...

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Main Authors: Xia-qing Wang, Tahmineh Mokhtari, Yu-xuan Zeng, Lu-peng Yue, Li Hu
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Neural Plasticity
Online Access:http://dx.doi.org/10.1155/2021/6682275
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author Xia-qing Wang
Tahmineh Mokhtari
Yu-xuan Zeng
Lu-peng Yue
Li Hu
author_facet Xia-qing Wang
Tahmineh Mokhtari
Yu-xuan Zeng
Lu-peng Yue
Li Hu
author_sort Xia-qing Wang
collection DOAJ
description Chronic pain is considered an economic burden on society as it often results in disability, job loss, and early retirement. Opioids are the most common analgesics prescribed for the management of moderate to severe pain. However, chronic exposure to these drugs can result in opioid tolerance and opioid-induced hyperalgesia. On pain modulation strategies, exploiting the multitarget drugs with the ability of the superadditive or synergistic interactions attracts more attention. In the present report, we have reviewed the analgesic effects of different dopamine receptors, particularly D1 and D2 receptors, in different regions of the central nervous system, including the spinal cord, striatum, nucleus accumbens (NAc), and periaqueductal gray (PAG). According to the evidence, these regions are not only involved in pain modulation but also express a high density of DA receptors. The findings can be categorized as follows: (1) D2-like receptors may exert a higher analgesic potency, but D1-like receptors act in different manners across several mechanisms in the mentioned regions; (2) in the spinal cord and striatum, antinociception of DA is mainly mediated by D2-like receptors, while in the NAc and PAG, both D1- and D2-like receptors are involved as analgesic targets; and (3) D2-like receptor agonists can act as adjuvants of μ-opioid receptor agonists to potentiate analgesic effects and provide a better approach to pain relief.
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spelling doaj-art-012666c39bf84d118f0d26f88fb6db202025-02-03T01:24:38ZengWileyNeural Plasticity2090-59041687-54432021-01-01202110.1155/2021/66822756682275The Distinct Functions of Dopaminergic Receptors on Pain Modulation: A Narrative ReviewXia-qing Wang0Tahmineh Mokhtari1Yu-xuan Zeng2Lu-peng Yue3Li Hu4CAS Key Laboratory of Mental Health, Institute of Psychology, Beijing, ChinaCAS Key Laboratory of Mental Health, Institute of Psychology, Beijing, ChinaCAS Key Laboratory of Mental Health, Institute of Psychology, Beijing, ChinaCAS Key Laboratory of Mental Health, Institute of Psychology, Beijing, ChinaCAS Key Laboratory of Mental Health, Institute of Psychology, Beijing, ChinaChronic pain is considered an economic burden on society as it often results in disability, job loss, and early retirement. Opioids are the most common analgesics prescribed for the management of moderate to severe pain. However, chronic exposure to these drugs can result in opioid tolerance and opioid-induced hyperalgesia. On pain modulation strategies, exploiting the multitarget drugs with the ability of the superadditive or synergistic interactions attracts more attention. In the present report, we have reviewed the analgesic effects of different dopamine receptors, particularly D1 and D2 receptors, in different regions of the central nervous system, including the spinal cord, striatum, nucleus accumbens (NAc), and periaqueductal gray (PAG). According to the evidence, these regions are not only involved in pain modulation but also express a high density of DA receptors. The findings can be categorized as follows: (1) D2-like receptors may exert a higher analgesic potency, but D1-like receptors act in different manners across several mechanisms in the mentioned regions; (2) in the spinal cord and striatum, antinociception of DA is mainly mediated by D2-like receptors, while in the NAc and PAG, both D1- and D2-like receptors are involved as analgesic targets; and (3) D2-like receptor agonists can act as adjuvants of μ-opioid receptor agonists to potentiate analgesic effects and provide a better approach to pain relief.http://dx.doi.org/10.1155/2021/6682275
spellingShingle Xia-qing Wang
Tahmineh Mokhtari
Yu-xuan Zeng
Lu-peng Yue
Li Hu
The Distinct Functions of Dopaminergic Receptors on Pain Modulation: A Narrative Review
Neural Plasticity
title The Distinct Functions of Dopaminergic Receptors on Pain Modulation: A Narrative Review
title_full The Distinct Functions of Dopaminergic Receptors on Pain Modulation: A Narrative Review
title_fullStr The Distinct Functions of Dopaminergic Receptors on Pain Modulation: A Narrative Review
title_full_unstemmed The Distinct Functions of Dopaminergic Receptors on Pain Modulation: A Narrative Review
title_short The Distinct Functions of Dopaminergic Receptors on Pain Modulation: A Narrative Review
title_sort distinct functions of dopaminergic receptors on pain modulation a narrative review
url http://dx.doi.org/10.1155/2021/6682275
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