Evidence map›Paper›PMID 25740916›Full record

ArticleThe international journal of neuropsychopharmacology2015

Dopamine Receptor D2 and Associated microRNAs Are Involved in Stress Susceptibility and Resistance to Escitalopram Treatment.

Yi Zhang, Yuting Wang, Lei Wang, Mei Bai, Xiuwu Zhang, Xiongzhao Zhu

Open access · goldAbstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 106 citations in OpenAlex.

  1. Pooled it
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  17. Oxycodone, an opioid like the others?Frontiers in psychiatry · 2023
    Review
  18. Article
  19. Therapeutic Implications of microRNAs in Depressive Disorders: A Review.International journal of molecular sciences · 2022
    Review
  20. Article
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

6 authors at 3 institutions in 2 countries.

Yi ZhangMedical Psychological Institute, Second Xiangya Hospital, Central South University,Changsha, PR China (Drs Y. Zhang, Y. Wang, L. Wang, Bai, and Zhu); Department of Radiation Oncology, University of Maryland, Baltimore, MD (Drs Y. Zhang and X. Zhang); National Technology Institute of Psychiatry, Central South University, Changsha, PR China (Drs Y. Wang and L. Wang); Key Laboratory of Psychiatry and Mental Health of Hunan Province, Central South University, Changsha, PR China (Drs Bai and Zhu).
Yuting WangMedical Psychological Institute, Second Xiangya Hospital, Central South University,Changsha, PR China (Drs Y. Zhang, Y. Wang, L. Wang, Bai, and Zhu); Department of Radiation Oncology, University of Maryland, Baltimore, MD (Drs Y. Zhang and X. Zhang); National Technology Institute of Psychiatry, Central South University, Changsha, PR China (Drs Y. Wang and L. Wang); Key Laboratory of Psychiatry and Mental Health of Hunan Province, Central South University, Changsha, PR China (Drs Bai and Zhu).
Lei WangMedical Psychological Institute, Second Xiangya Hospital, Central South University,Changsha, PR China (Drs Y. Zhang, Y. Wang, L. Wang, Bai, and Zhu); Department of Radiation Oncology, University of Maryland, Baltimore, MD (Drs Y. Zhang and X. Zhang); National Technology Institute of Psychiatry, Central South University, Changsha, PR China (Drs Y. Wang and L. Wang); Key Laboratory of Psychiatry and Mental Health of Hunan Province, Central South University, Changsha, PR China (Drs Bai and Zhu).
Mei BaiMedical Psychological Institute, Second Xiangya Hospital, Central South University,Changsha, PR China (Drs Y. Zhang, Y. Wang, L. Wang, Bai, and Zhu); Department of Radiation Oncology, University of Maryland, Baltimore, MD (Drs Y. Zhang and X. Zhang); National Technology Institute of Psychiatry, Central South University, Changsha, PR China (Drs Y. Wang and L. Wang); Key Laboratory of Psychiatry and Mental Health of Hunan Province, Central South University, Changsha, PR China (Drs Bai and Zhu).
Xiuwu ZhangMedical Psychological Institute, Second Xiangya Hospital, Central South University,Changsha, PR China (Drs Y. Zhang, Y. Wang, L. Wang, Bai, and Zhu); Department of Radiation Oncology, University of Maryland, Baltimore, MD (Drs Y. Zhang and X. Zhang); National Technology Institute of Psychiatry, Central South University, Changsha, PR China (Drs Y. Wang and L. Wang); Key Laboratory of Psychiatry and Mental Health of Hunan Province, Central South University, Changsha, PR China (Drs Bai and Zhu).
Xiongzhao ZhuMedical Psychological Institute, Second Xiangya Hospital, Central South University,Changsha, PR China (Drs Y. Zhang, Y. Wang, L. Wang, Bai, and Zhu); Department of Radiation Oncology, University of Maryland, Baltimore, MD (Drs Y. Zhang and X. Zhang); National Technology Institute of Psychiatry, Central South University, Changsha, PR China (Drs Y. Wang and L. Wang); Key Laboratory of Psychiatry and Mental Health of Hunan Province, Central South University, Changsha, PR China (Drs Bai and Zhu). xiongzhaozhu@163.com.
University of Maryland, Baltimore · USCentral South University · CNSecond Xiangya Hospital of Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarly life stress has been demonstrated to increase the risk of developing depression in adulthood. However, the roles and associated molecular mechanisms of stresses in the onset and relapse of depression have yet to be fully elucidated.

methodsDepression-like behaviors were induced in rats by maternal deprivation and chronic unpredictable stress. Depression- and anxiety-like behaviors of rats, dopamine receptor D2 level, and microRNAs expression in rats' brain tissues were measured.

resultsChronic unpredictable stress alone induced depression-like behaviors in rats, but maternal deprivation enhanced the effect of chronic unpredictable stress. Escitalopram significantly decreased depression-like behaviors in chronic unpredictable stress rats but was less effective in maternal deprivation with chronic unpredictable stress rats. Maternal deprivation increased dopamine receptor D2 messenger RNA expression and decreased microRNA-9 expression in the striatum. Chronic unpredictable stress increased dopamine receptor D2 mRNA and protein levels and decreased microRNA-9 expression in the nucleus accumbens. Furthermore, maternal deprivation enhanced the effect of chronic unpredictable stress on dopamine receptor D2 gene and microRNA-9 expression. Chronic unpredictable stress increased the expression of microRNA-326 in the nucleus accumbens but decreased it in the striatum, whereas maternal deprivation elevated microRNA-326 expression in the striatum. Escitalopram normalized microRNA-326 expression but had no effect on the expression of microRNA-9, dopamine receptor D2 mRNA, and dopamine receptor D2 protein in both the nucleus accumbens and striatum. The in vitro study showed that only microRNA-9 directly targeted the 3' untranslated region of dopamine receptor D2 mRNA and inhibited dopamine receptor D2 protein expression.

conclusionEarly life stress enhanced the susceptibility to late life stress and resistance to escitalopram treatment through decreasing microRNA-9 expression and subsequently upregulating dopamine receptor D2 expression in the nucleus accumbens. microRNA-326 may be a novel target of escitalopram.

Indexed as

AnimalsAntidepressive Agents, Second-GenerationChronic DiseaseCitalopramCorpus StriatumDepressive DisorderDepressive Disorder, Treatment-ResistantDisease Models, AnimalDrug ResistanceMaleMaternal DeprivationMicroRNAsNucleus AccumbensRandom AllocationRats, Sprague-DawleyReceptors, Dopamine D2Antidepressive Agents, Second-GenerationCitalopramMicroRNAsMIRN326 microRNA, ratMIRN9 microRNA, ratReceptors, Dopamine D2RNA, Messengerdepressiondopamine receptor D2microRNAsstress

Identifiers

PMID25740916
PMCPMC4571637
OpenAlexW2095128214

What OpenQuestion holds

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Registered trials

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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.