Activation of MORs in the VTA induces changes on cFos expression in different projecting regions: Effect of inflammatory pain.
Analgesics, Opioid
/ administration & dosage
Animals
Enkephalin, Ala(2)-MePhe(4)-Gly(5)-
/ administration & dosage
Freund's Adjuvant
Gene Expression Regulation
Genes, fos
/ genetics
Immunohistochemistry
Inflammation
/ chemically induced
Male
Microinjections
Neural Pathways
/ drug effects
Pain
/ metabolism
Rats
Receptors, Opioid, mu
/ agonists
Ventral Tegmental Area
/ drug effects
Inflammatory pain
Mesocorticolimbic system
Mu opioid receptor
VTA
cFos
Journal
Neurochemistry international
ISSN: 1872-9754
Titre abrégé: Neurochem Int
Pays: England
ID NLM: 8006959
Informations de publication
Date de publication:
12 2019
12 2019
Historique:
received:
07
06
2019
revised:
19
07
2019
accepted:
12
08
2019
pubmed:
17
8
2019
medline:
4
9
2020
entrez:
17
8
2019
Statut:
ppublish
Résumé
Chronic pain is a worldwide major health problem and many pain-suffering patients are under opioid based therapy. Epidemiological data show that pain intensity correlates with the risk of misuse of prescription opioids, and other drugs of abuse including alcohol. This increased vulnerability to suffer Substance Use Disorders could be, in part, caused by functional changes that occur over the mesocorticolimbic system, a brain pathway involved in reward processing and addiction. Previous data in rats revealed that inflammatory pain desensitizes mu opioid receptors (MORs) in the ventral tegmental area (VTA). As a consequence, pain alters dopamine release in the nucleus accumbens (NAc) derived from MOR activation in the VTA and also increases intake of high doses of heroine. Given that the VTA neurons target different brain regions, in the present study we first analyzed changes induced by inflammatory pain in the MOR dependent activation pattern of the main VTA projecting areas. To do that, we administered two doses (7 or 14 ng) of DAMGO (MORs agonist) or artificial cerebrospinal fluid (aCSF) focally into the VTA of rats and measured the activation in projection areas by cFos immunohistochemistry. Our results show that focal injections of DAMGO in the VTA increases cFos expression in the majority of its projecting areas, namely NAc, basolateral amygdala (BLA), cingulate cortex (ACC) and bed nucleus of the stria terminalis (BNST), as compared to aCSF. Second, we analyzed whether inflammatory pain would affect to cFos expression using a group of rats injected with CFA in the hind paw. In this case, we found that cFos expression was not significantly different between DAMGO and aCSF administered rats in BLA, ACC and BNST. Our results confirm that inflammatory pain induces desensitization of VTA MORs in a region dependent manner which can be very relevant for addictive behaviours.
Identifiants
pubmed: 31419453
pii: S0197-0186(19)30315-8
doi: 10.1016/j.neuint.2019.104521
pii:
doi:
Substances chimiques
Analgesics, Opioid
0
Receptors, Opioid, mu
0
Enkephalin, Ala(2)-MePhe(4)-Gly(5)-
100929-53-1
Freund's Adjuvant
9007-81-2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
104521Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.