Evidence map›Paper›PMID 33483691›Full record

ArticleMolecular psychiatry2021

Decoding the temporal nature of brain GR activity in the NFκB signal transition leading to depressive-like behavior.

Young-Min Han, Min Sun Kim, Juyeong Jo, Daiha Shin, Seung-Hae Kwon, Jong Bok Seo, Dongmin Kang, Byoung Dae Lee, Hoon Ryu, Eun Mi Hwang and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 20 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

15 authors at 8 institutions in 2 countries.

Young-Min HanSeoul Centre, Korea Basic Science Institute, Seoul, South Korea.
Min Sun KimSeoul Centre, Korea Basic Science Institute, Seoul, South Korea.
Juyeong JoSeoul Centre, Korea Basic Science Institute, Seoul, South Korea.
Daiha ShinSeoul Centre, Korea Basic Science Institute, Seoul, South Korea.
Seung-Hae KwonSeoul Centre, Korea Basic Science Institute, Seoul, South Korea.
Jong Bok SeoSeoul Centre, Korea Basic Science Institute, Seoul, South Korea.
Dongmin KangDepartment of Life Science, Ewha Womans University, Seoul, South Korea.ORCID http://orcid.org/0000-0001-5997-625X
Byoung Dae LeeDepartment of Physiology, School of Medicine, Kyung Hee University, Seoul, South Korea.
Hoon RyuNeuroscience Centre, Korea Institute of Science and Technology, Seoul, South Korea.
Eun Mi HwangCenter for Functional Connectomics, Korea Institute of Science and Technology, Seoul, South Korea.
Jae-Min KimDepartment of Psychiatry, Chonnam National University Medical School, Seoul, South Korea.
Paresh D PatelDepartment of Psychiatry, Molecular and Behavioral Neuroscience Institute, University of Michigan Medical Centre, Ann Arbor, MI, USA.
David M LyonsDepartments of Psychiatry, Stanford University Medical Centre, Stanford, CA, USA.
Alan F SchatzbergDepartments of Psychiatry, Stanford University Medical Centre, Stanford, CA, USA.
Song HerSeoul Centre, Korea Basic Science Institute, Seoul, South Korea. swher@kbsi.re.kr.ORCID http://orcid.org/0000-0001-9678-3203
Korea Basic Science Institute · KRStanford University · USChonnam National University Hospital · KREwha Womans University · KRKorea Institute of Science and Technology · KRKorean Association Of Science and Technology Studies · KRKyung Hee University · KRUniversity of Michigan · US

Funding

National Research Foundation of Korea (NRF) NRF-2016M3C7A1904362
6 · The paper itself

Abstract

The fine-tuning of neuroinflammation is crucial for brain homeostasis as well as its immune response. The transcription factor, nuclear factor-κ-B (NFκB) is a key inflammatory player that is antagonized via anti-inflammatory actions exerted by the glucocorticoid receptor (GR). However, technical limitations have restricted our understanding of how GR is involved in the dynamics of NFκB in vivo. In this study, we used an improved lentiviral-based reporter to elucidate the time course of NFκB and GR activities during behavioral changes from sickness to depression induced by a systemic lipopolysaccharide challenge. The trajectory of NFκB activity established a behavioral basis for the NFκB signal transition involved in three phases, sickness-early-phase, normal-middle-phase, and depressive-like-late-phase. The temporal shift in brain GR activity was differentially involved in the transition of NFκB signals during the normal and depressive-like phases. The middle-phase GR effectively inhibited NFκB in a glucocorticoid-dependent manner, but the late-phase GR had no inhibitory action. Furthermore, we revealed the cryptic role of basal GR activity in the early NFκB signal transition, as evidenced by the fact that blocking GR activity with RU486 led to early depressive-like episodes through the emergence of the brain NFκB activity. These results highlight the inhibitory action of GR on NFκB by the basal and activated hypothalamic-pituitary-adrenal (HPA)-axis during body-to-brain inflammatory spread, providing clues about molecular mechanisms underlying systemic inflammation caused by such as COVID-19 infection, leading to depression.

Indexed as

NF-kappa BReceptors, GlucocorticoidAnimalsBrainDepressionHypothalamo-Hypophyseal SystemMicePituitary-Adrenal SystemNF-kappa BReceptors, Glucocorticoid

Identifiers

PMID33483691
PMCPMC7821461
OpenAlexW3121811057

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.