Evidence map›Paper›PMID 36697976›Full record

ArticleActa pharmacologica Sinica2023

CB2R agonist GW405833 alleviates acute liver failure in mice via inhibiting HIF-1α-mediated reprogramming of glycometabolism and macrophage proliferation.

Sheng-Lan Cai, Xue-Gong Fan, Jie Wu, Yang Wang, Xing-Wang Hu, Si-Ya Pei, Yi-Xiang Zheng, Jun Chen, Yan Huang, Ning Li and 1 more

Open access · greenAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

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  15. Inhibition of Expression of the Circadian Clock GeneInternational journal of molecular sciences · 2023
    Article
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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 3 institutions in 1 country.

Sheng-Lan CaiDepartment of Infectious Diseases, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008, China.
Xue-Gong FanDepartment of Infectious Diseases, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008, China.
Jie WuShantou University Medical College, Shantou, 515041, China.
Yang WangHunan Key Laboratory of Viral Hepatitis, Xiangya Hospital, Central South University, Changsha, 410008, China.
Xing-Wang HuDepartment of Infectious Diseases, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008, China.
Si-Ya PeiDepartment of Infectious Diseases, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008, China.
Yi-Xiang ZhengDepartment of Infectious Diseases, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008, China.
Jun ChenDepartment of Infectious Diseases, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008, China.
Yan HuangDepartment of Infectious Diseases, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008, China.
Ning LiHunan Key Laboratory of Viral Hepatitis, Xiangya Hospital, Central South University, Changsha, 410008, China.
Ze-Bing HuangDepartment of Infectious Diseases, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008, China. 36165934@qq.com.
Xiangya Hospital Central South University · CNCentral South University · CNShantou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The inflammatory responses involving infiltration and activation of liver macrophages play a vital role in acute liver failure (ALF). In the liver of ALF mice, cannabinoid receptor 2 (CB2R) is significantly upregulated on macrophages, while CB2R agonist GW405833 (GW) could protect against cell death in acute liver damage. In this study, we investigated the molecular mechanisms underlying the protective effects of GW against ALF in vivo and in vitro from a perspective of macrophage glycometabolism. Mice were pretreated with GW (10 mg/kg, i.p.), then were injected with D-GalN (750 mg/kg, i.p.) and LPS (10 mg/kg, i.p.) to induce ALF. We verified the protective effects of GW pretreatment in ALF mice. Furthermore, GW pretreatment significantly reduced liver macrophage infiltration and M1 polarization, and inhibited the release of inflammatory factors TNF-α and IL-1β in ALF mice. These protective effects were eliminated by CB2R antagonist SR144528 or in CB2R

Indexed as

LipopolysaccharidesLiver Failure, AcuteAnimalsCell ProliferationCytokinesHypoxia-Inducible Factor 1, alpha SubunitIndolesMacrophagesMiceMorpholines1-(2,3-dichlorobenzoyl)-5-methoxy-2-methyl-(2-(mopholin-4-yl)ethyl)-1H-indoleCytokinesHypoxia-Inducible Factor 1, alpha SubunitIndolesLipopolysaccharidesMorpholinesacute liver failurecannabinoid receptor 2glycolysisGW405833hypoxia-inducible factor 1αmacrophagesRAW264.7 cellsSR144528

Identifiers

PMID36697976
PMCPMC10310807
OpenAlexW4317931203

What Socratic 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 Socratic graph.