Literature DB >> 32422213

Endogenous opioid peptides in the descending pain modulatory circuit.

Elena E Bagley1, Susan L Ingram2.   

Abstract

The opioid epidemic has led to a serious examination of the use of opioids for the treatment of pain. Opioid drugs are effective due to the expression of opioid receptors throughout the body. These receptors respond to endogenous opioid peptides that are expressed as polypeptide hormones that are processed by proteolytic cleavage. Endogenous opioids are expressed throughout the peripheral and central nervous system and regulate many different neuronal circuits and functions. One of the key functions of endogenous opioid peptides is to modulate our responses to pain. This review will focus on the descending pain modulatory circuit which consists of the ventrolateral periaqueductal gray (PAG) projections to the rostral ventromedial medulla (RVM). RVM projections modulate incoming nociceptive afferents at the level of the spinal cord. Stimulation within either the PAG or RVM results in analgesia and this circuit has been studied in detail in terms of the actions of exogenous opioids, such as morphine and fentanyl. Further emphasis on understanding the complex regulation of endogenous opioids will help to make rational decisions with regard to the use of opioids for pain. We also include a discussion of the actions of endogenous opioids in the amygdala, an upstream brain structure that has reciprocal connections to the PAG that contribute to the brain's response to pain.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Amygdala; Beta-endorphin; Enkephalin; Opioid; Pain; Periaqueductal gray; Rostral ventromedial medulla

Mesh:

Substances:

Year:  2020        PMID: 32422213      PMCID: PMC7313723          DOI: 10.1016/j.neuropharm.2020.108131

Source DB:  PubMed          Journal:  Neuropharmacology        ISSN: 0028-3908            Impact factor:   5.250


  214 in total

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Journal:  J Neurosci       Date:  2015-02-04       Impact factor: 6.167

4.  Opioid presynaptic disinhibition of the midbrain periaqueductal grey descending analgesic pathway.

Authors:  Benjamin K Lau; Bryony L Winters; Christopher W Vaughan
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5.  Suppressive influences from periaqueductal gray and nucleus raphe magnus on respiration and related reflex activities and on solitary tract neurons, and effect of naloxone.

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Journal:  J Neurosci       Date:  2001-04-01       Impact factor: 6.167

7.  Activity of murine raphe magnus cells predicts tachypnea and on-going nociceptive responsiveness.

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Journal:  J Neurophysiol       Date:  2007-10-03       Impact factor: 2.714

8.  Stimulation of guanosine-5'-O-(3-[35S]thio)triphosphate binding by endogenous opioids acting at a cloned mu receptor.

Authors:  A Alt; A Mansour; H Akil; F Medzihradsky; J R Traynor; J H Woods
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Journal:  Neurosci Lett       Date:  1987-10-29       Impact factor: 3.046

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Authors:  You-Qing Cai; Wei Wang; Yuan-Yuan Hou; Zhizhong Z Pan
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Review 3.  Opioid Receptor-Mediated Regulation of Neurotransmission in the Brain.

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Review 5.  The Periaqueductal Gray and Its Extended Participation in Drug Addiction Phenomena.

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6.  Kappa Opioid Signaling at the Crossroads of Chronic Pain and Opioid Addiction.

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Review 7.  Alternative pain management via endocannabinoids in the time of the opioid epidemic: Peripheral neuromodulation and pharmacological interventions.

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8.  Noninvasive vagus nerve stimulation and morphine transiently inhibit trigeminal pain signaling in a chronic headache model.

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9.  Green Light Antinociceptive and Reversal of Thermal and Mechanical Hypersensitivity Effects Rely on Endogenous Opioid System Stimulation.

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10.  β-endorphin at the intersection of pain and cancer progression: Preclinical evidence.

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