This Week in The Journal

Ventral tegmental area (VTA) dopamine neurons regulate reward-related behavior and are hijacked by drugs of abuse, like opiates, to facilitate addiction.However, how opiates interact with distinct VTA dopamine neuron subpopulations is unclear.In this issue, Quiles et al. used mice to explore how the opiate morphine targets VTA dopamine neuron subpopulations.The researchers looked at gene expression changes in VTA dopamine neurons following long-term morphine exposure and discovered increased expression of the neuropeptide neuromedin S (NMS).Using a genetic mouse model enabling the targeting of NMS-expressing neurons, Quiles and colleagues found that artificially stimulating or inhibiting these neurons bidirectionally influenced locomotor activity associated with morphine use.Inhibiting NMS neurons also reduced morphine reward as measured by a conditioned place preference paradigm.The researchers used more experimental controls to highlight the morphine and NMS specificity of their findings.This identification of a new neuron subpopulation that morphine interacts with to affect behavior may inform treatment development for opiate addiction.

Publication Details

Journal
Journal of Neuroscience
Published
2025-03-26
DOI
https://doi.org/10.1523/jneurosci.twij-45-13-2025
Primary Topic
Opioid Use Disorder Treatment
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

This Week in The Journal

Journal of Neuroscience
Opioid Use Disorder Treatment
article

This Week in The Journal

article en

Abstract

Ventral tegmental area (VTA) dopamine neurons regulate reward-related behavior and are hijacked by drugs of abuse, like opiates, to facilitate addiction.However, how opiates interact with distinct VTA dopamine neuron subpopulations is unclear.In this issue, Quiles et al. used mice to explore how the opiate morphine targets VTA dopamine neuron subpopulations.The researchers looked at gene expression changes in VTA dopamine neurons following long-term morphine exposure and discovered increased expression of the neuropeptide neuromedin S (NMS).Using a genetic mouse model enabling the targeting of NMS-expressing neurons, Quiles and colleagues found that artificially stimulating or inhibiting these neurons bidirectionally influenced locomotor activity associated with morphine use.Inhibiting NMS neurons also reduced morphine reward as measured by a conditioned place preference paradigm.The researchers used more experimental controls to highlight the morphine and NMS specificity of their findings.This identification of a new neuron subpopulation that morphine interacts with to affect behavior may inform treatment development for opiate addiction.

Journal of NeuroscienceVol. 45(13)
Openalex Percentile: Top 92%
Opioid Use Disorder Treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.