Evidence map›Paper›PMID 34272506›Full record

ArticleActa pharmacologica Sinica2022

Sulforaphane activates anti-inflammatory microglia, modulating stress resilience associated with BDNF transcription.

Rui Tang, Qian-Qian Cao, Sheng-Wei Hu, Lu-Juan He, Peng-Fei Du, Gang Chen, Rao Fu, Fei Xiao, Yi-Rong Sun, Ji-Chun Zhang and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 48 citations in OpenAlex.

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  18. Microglia at the blood brain barrier in health and disease.Frontiers in cellular neuroscience · 2024
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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

11 authors at 5 institutions in 1 country.

Rui Tang *Department of Physiology, School of Medicine, Jinan University, Guangzhou, 510632, China.
Qian-Qian Cao *Department of Physiology, School of Medicine, Jinan University, Guangzhou, 510632, China.
Sheng-Wei Hu *MOE Key Laboratory of Tumor Molecular Biology, Clinical Translational Center for Targeted Drug, Department of Pharmacology, School of Medicine, Jinan University, Guangzhou, 510632, China.
Lu-Juan HeDepartment of Physiology, School of Medicine, Jinan University, Guangzhou, 510632, China.
Peng-Fei DuSecond Affiliated Hospital of Jiaxing, Jiaxing, 4564496, China.
Gang ChenSchool of traditional Chinese Medicine, Jinan University, Guangzhou, 510632, China.
Rao FuDepartment of Anatomy, School of Medicine (Shenzhen), Sun Yat-sen University, Guangzhou, 510080, China.
Fei XiaoDepartment of Pharmacology, School of Pharmacy, Jinan University, Guangzhou, 510632, China.
Yi-Rong SunGuangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, 510530, China. sun_yirong@gibh.ac.cn.
Ji-Chun ZhangDepartment of Physiology, School of Medicine, Jinan University, Guangzhou, 510632, China. jczhang@jnu.edu.cn.
Qi QiMOE Key Laboratory of Tumor Molecular Biology, Clinical Translational Center for Targeted Drug, Department of Pharmacology, School of Medicine, Jinan University, Guangzhou, 510632, China. qiqikc@jnu.edu.cn.
Jinan University · CNFirst Hospital of Jiaxing · CNGuangzhou Institutes of Biomedicine and Health · CNSun Yat-sen University · CNXi’an University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sulforaphane (SFN) is an organic isothiocyanate and an NF-E2-related factor-2 (Nrf2) inducer that exerts prophylactic effects on depression-like behavior in mice. However, the underlying mechanisms remain poorly understood. Brain-derived neurotrophic factor (BDNF), a neurotrophin, is widely accepted for its antidepressant effects and role in stress resilience. Here, we show that SFN confers stress resilience via BDNF upregulation and changes in abnormal dendritic spine morphology in stressed mice, which is accompanied by rectifying the irregular levels of inflammatory cytokines. Mechanistic studies demonstrated that SFN activated Nrf2 to promote BDNF transcription by binding to the exon I promoter, which is associated with increased Nrf2, and decreased methyl-CpG binding protein-2 (MeCP2), a transcriptional suppressor of BDNF, in BV2 microglial cells. Furthermore, SFN inhibited the pro-inflammatory phenotype and activated the anti-inflammatory phenotype of microglia, which was associated with increased Nrf2 and decreased MeCP2 expression in microglia of stressed mice. Hence, our findings support that Nrf2 induces BDNF transcription via upregulation of Nrf2 and downregulation of MeCP2 in microglia, which is associated with changes in the morphology of damaged dendritic spines in stressed mice. Meanwhile, the data presented here provide evidence for the application of SFN as a candidate for the prevention and intervention of depression.

Indexed as

Brain-Derived Neurotrophic FactorMicrogliaAnimalsAnti-Inflammatory AgentsIsothiocyanatesMiceNF-E2-Related Factor 2SulfoxidesAnti-Inflammatory AgentsBrain-Derived Neurotrophic FactorIsothiocyanatesNF-E2-Related Factor 2sulforaphaneSulfoxidesBDNFmicrogliaNrf2stress resiliencesulforaphane

Identifiers

PMID34272506
PMCPMC8976037
OpenAlexW3178403178

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.