Projections from lateral habenular to tail of ventral tegmental area contribute to inhibitory effect of stress on morphine-induced conditioned place preference.
Animals
Brain
/ metabolism
Calcium-Calmodulin-Dependent Protein Kinase Type 2
/ metabolism
Conditioning, Classical
/ drug effects
Conditioning, Operant
/ drug effects
Habenula
/ metabolism
Male
Morphine
/ pharmacology
Narcotics
/ pharmacology
Nucleus Accumbens
/ metabolism
Rats
Rats, Sprague-Dawley
Stress, Physiological
/ drug effects
Ventral Tegmental Area
/ metabolism
CaMΚII
Conditioned place preference
Forced swimming stress
Lateral habenular
Morphine
Tail of the ventral tegmental area
Journal
Brain research
ISSN: 1872-6240
Titre abrégé: Brain Res
Pays: Netherlands
ID NLM: 0045503
Informations de publication
Date de publication:
15 08 2019
15 08 2019
Historique:
received:
09
12
2018
revised:
17
03
2019
accepted:
22
03
2019
pubmed:
28
3
2019
medline:
25
9
2020
entrez:
28
3
2019
Statut:
ppublish
Résumé
Physical stress is one of the most important factors affecting morphine-induced conditioned place preference (CPP). Convincing evidences demonstrate that physical stress can activate lateral habenular (LHb) neurons. However, the mechanism by which physical stress regulates morphine-induced CPP through LHb remains unclear. In this study, we examined the impact of forced swimming stress (FSS) on morphine-induced CPP in rats. We found that FSS significantly decreased the CPP scores of rats compared with the normal morphine administration rats. Meanwhile, we detected the expression of DARPP-32 phosphorylation (p-DARPP-32) in the nucleus accumbens (NAc), and CaMKII in LHb. The results show that FSS enhanced the expression of CaMΚII in LHb, while it reduced the level of p-DARPP-32 expression in the NAc. Furthermore, by microinjecting AAV-CaMKII or AAV-RNAi into LHb, we demonstrated that an overexpression of CaMKII could reduce morphine-induced CPP scores of rats, while knock-down CaMΚII could restore morphine-induced CPP scores, which were interfered by FSS. In addition, by microinjecting DiI into the ventral tegmental area (VTA) and tail of VTA (tVTA) unilaterally, and an anterograde tracing virus (AAV-CaMKII-mCherry) into LHb unilaterally, we verified the neural projections from LHb to tVTA. Taken together, our findings suggest that FSS could activate LHb neurons through CaMΚII, and inhibit morphine-induced CPP through the LHb-tVTA pathway.
Identifiants
pubmed: 30914248
pii: S0006-8993(19)30165-9
doi: 10.1016/j.brainres.2019.03.026
pii:
doi:
Substances chimiques
Narcotics
0
Morphine
76I7G6D29C
Calcium-Calmodulin-Dependent Protein Kinase Type 2
EC 2.7.11.17
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
35-43Informations de copyright
Copyright © 2019. Published by Elsevier B.V.