Evidence map›Paper›PMID 37535645›Full record

ArticleEMBO reports2023

mPFC DUSP1 mediates adolescent cocaine exposure-induced higher sensitivity to drug in adulthood.

Xiaoyan Wei, Jiasong Chang, Zhen Cheng, Wenwen Chen, Hao Guo, Zhaoyu Liu, Yuning Mai, Tao Hu, Yuanyuan Zhang, Qinglong Cai and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Xiaoyan WeiDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.ORCID 0000-0003-3599-0449
Jiasong ChangDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.
Zhen ChengDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.ORCID 0000-0003-1290-0180
Wenwen ChenDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.
Hao GuoDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.
Zhaoyu LiuDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.
Yuning MaiDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.ORCID 0000-0001-8209-0289
Tao HuDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.ORCID 0000-0001-7893-096X
Yuanyuan ZhangDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.
Qinglong CaiDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.
Feifei GeDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.
Yu FanDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.ORCID 0000-0001-6813-6797
Xiaowei GuanDepartment of Human Anatomy and Histoembryology, Nanjing University of Chinese Medicine, Nanjing, China.ORCID 0000-0002-0886-4706
Nanjing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adolescent cocaine abuse increases the risk for developing addiction in later life, but the underlying molecular mechanism remains poorly understood. Here, we establish adolescent cocaine-exposed (ACE) male mouse models. A subthreshold dose of cocaine (sdC) treatment, insufficient to produce conditioned place preference (CPP) in adolescent mice, induces CPP in ACE mice during adulthood, along with more activated CaMKII-positive neurons, higher dual specificity protein kinase phosphatase-1 (Dusp1) mRNA, lower DUSP1 activity, and lower DUSP1 expression in CaMKII-positive neurons in the medial prefrontal cortex (mPFC). Overexpressing DUSP1 in CaMKII-positive neurons suppresses neuron activity and blocks sdC-induced CPP in ACE mice during adulthood. On the contrary, depleting DUSP1 in CaMKII-positive neurons activates more neurons and further enhances sdC-induced behavior in ACE mice during adulthood. Also, ERK1/2 might be a downstream signal of DUSP1 in the process. Our findings reveal a role of mPFC DUSP1 in ACE-induced higher sensitivity to the drug in adult mice. DUSP1 might be a potential pharmacological target to predict or treat the susceptibility to addictive drugs caused by adolescent substance use.

Indexed as

CocaineCocaine-Related DisordersAnimalsCalcium-Calmodulin-Dependent Protein Kinase Type 2MaleMiceNeuronsPrefrontal CortexCalcium-Calmodulin-Dependent Protein Kinase Type 2Cocaineadolescent cocaine exposureDUSP1mPFC activationsensitivity to cocaine

Identifiers

PMID37535645
PMCPMC10481668
OpenAlexW4385525164

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.