Literature DB >> 10742719

Presynaptic and postsynaptic relations of mu-opioid receptors to gamma-aminobutyric acid-immunoreactive and medullary-projecting periaqueductal gray neurons.

K G Commons1, S A Aicher, L M Kow, D W Pfaff.   

Abstract

The ventrolateral portion of the periaqueductal gray (PAG) is one brain region in which ligands of the mu-opioid receptor (MOR) produce analgesia. In the PAG, MOR ligands are thought to act primarily on inhibitory [e.g., gamma-aminobutyric acidergic (GABAergic)] neurons to disinhibit PAG output rather than directly on medullary-projecting PAG neurons. In this study, the ultrastructural localization of MOR immunolabeling was examined with respect to either GABAergic PAG neurons or PAG projection neurons that were labeled retrogradely from the rostral ventromedial medulla. Immunoreactivity for MOR and GABA often coexisted within dendrites. Dual-labeled profiles accounted for subpopulations of dendrites containing immunoreactivity for either MOR (65 of 145 dendrites; 45%) or GABA (65 of 183 dendrites; 35%). In addition, nearly half of PAG neuronal profiles (148 of 344 profiles) that were labeled retrogradely from the ventromedial medulla contained MOR immunoreactivity. MOR was distributed equally among retrogradely labeled neuronal profiles in the lateral and ventrolateral columns of the caudal PAG. With respect to the presynaptic distribution of MOR, approximately half of MOR-immunolabeled axon terminals (35 of 69 terminals) also contained GABA. Some MOR and GABA dual-immunolabeled axon terminals contacted unlabeled dendrites (11 of 35 terminals), whereas others contacted GABA-immunoreactive dendrites (15 of 35 terminals). Furthermore, axon terminals synapsing on medullary-projecting PAG neurons sometimes contained immunoreactivity for MOR. These data support the model that MOR ligands can act by inhibiting GABAergic neurons, but they also provide evidence that MOR ligands may act directly on PAG output neurons. In addition, MOR at presynaptic sites could affect both GABAergic neurons and output neurons. Thus, the disinhibitory model represents only partially the potential mechanisms by which MOR ligands can modulate output of the PAG. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10742719     DOI: 10.1002/(sici)1096-9861(20000417)419:4<532::aid-cne8>3.0.co;2-6

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  27 in total

1.  Sex differences in the anatomical and functional organization of the periaqueductal gray-rostral ventromedial medullary pathway in the rat: a potential circuit mediating the sexually dimorphic actions of morphine.

Authors:  Dayna R Loyd; Anne Z Murphy
Journal:  J Comp Neurol       Date:  2006-06-10       Impact factor: 3.215

2.  Mechanism Underlying the Analgesic Effect Exerted by Endomorphin-1 in the rat Ventrolateral Periaqueductal Gray.

Authors:  Tao Chen; Jing Li; Ban Feng; Rui Hui; Yu-Lin Dong; Fu-Quan Huo; Ting Zhang; Jun-Bin Yin; Jian-Qing Du; Yun-Qing Li
Journal:  Mol Neurobiol       Date:  2015-04-16       Impact factor: 5.590

Review 3.  Inflammatory mediators of opioid tolerance: Implications for dependency and addiction.

Authors:  Lori N Eidson; Anne Z Murphy
Journal:  Peptides       Date:  2019-03-16       Impact factor: 3.750

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

Authors:  Benjamin K Lau; Bryony L Winters; Christopher W Vaughan
Journal:  Br J Pharmacol       Date:  2020-02-15       Impact factor: 8.739

5.  Tolerance to the antinociceptive effect of morphine in the absence of short-term presynaptic desensitization in rat periaqueductal gray neurons.

Authors:  Leon W Fyfe; Daniel R Cleary; Tara A Macey; Michael M Morgan; Susan L Ingram
Journal:  J Pharmacol Exp Ther       Date:  2010-08-25       Impact factor: 4.030

6.  Periaqueductal gray neuroplasticity following chronic morphine varies with age: role of oxidative stress.

Authors:  D Bajic; C B Berde; K G Commons
Journal:  Neuroscience       Date:  2012-09-19       Impact factor: 3.590

7.  Central Amygdala Circuits Mediate Hyperalgesia in Alcohol-Dependent Rats.

Authors:  Elizabeth M Avegno; Thomas D Lobell; Christy A Itoga; Brittni B Baynes; Annie M Whitaker; Marcus M Weera; Scott Edwards; Jason W Middleton; Nicholas W Gilpin
Journal:  J Neurosci       Date:  2018-07-27       Impact factor: 6.167

8.  Mu-opioid receptor trafficking on inhibitory synapses in the rat brainstem.

Authors:  Kirsteen N Browning; Alexander E Kalyuzhny; R Alberto Travagli
Journal:  J Neurosci       Date:  2004-08-18       Impact factor: 6.167

9.  Sexually dimorphic activation of the periaqueductal gray-rostral ventromedial medullary circuit during the development of tolerance to morphine in the rat.

Authors:  Dayna R Loyd; Michael M Morgan; Anne Z Murphy
Journal:  Eur J Neurosci       Date:  2008-03       Impact factor: 3.386

10.  Neonatal injury alters adult pain sensitivity by increasing opioid tone in the periaqueductal gray.

Authors:  Jamie L Laprairie; Anne Z Murphy
Journal:  Front Behav Neurosci       Date:  2009-09-30       Impact factor: 3.558

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