Evidence map›Paper›PMID 37436491›Full record

ArticlePsychopharmacology2023

18β-glycyrrhetinic acid ameliorates MPTP-induced neurotoxicity in mice through activation of microglial anti-inflammatory phenotype.

Hanyue Luo, Caishi Zhang, Lujuan He, Zefang Lin, Ji-Chun Zhang, Qi Qi, Jia-Xu Chen, Wei Yao

Abstract read
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In one paragraph

Article in Psychopharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

7 citing papers in PubMed, 11 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

8 authors at 1 institution in 1 country.

Hanyue LuoGuangzhou Key Laboratory of Formula-Pattern Research Center, School of Traditional Chinese Medicine, Jinan University, Guangzhou, 510632, China.
Caishi ZhangSchool of Pharmacy, Jinan University, Guangzhou, 510632, Guangdong, China.
Lujuan HeDepartment of Physiology, School of Medicine, Jinan University, Guangzhou, 510632, China.
Zefang LinDepartment of Physiology, School of Medicine, Jinan University, Guangzhou, 510632, China.
Ji-Chun ZhangDepartment of Physiology, School of Medicine, Jinan University, Guangzhou, 510632, China.
Qi QiMOE Key Laboratory of Tumor Molecular Biology, Department of Pharmacology, School of Pharmacy, Jinan University, Guangzhou, 510632, China. qiqikc@jnu.edu.cn.
Jia-Xu ChenGuangzhou Key Laboratory of Formula-Pattern Research Center, School of Traditional Chinese Medicine, Jinan University, Guangzhou, 510632, China. chenjiaxu@hotmail.com.
Wei YaoGuangzhou Key Laboratory of Formula-Pattern Research Center, School of Traditional Chinese Medicine, Jinan University, Guangzhou, 510632, China. weiyao@jnu.edu.cn.
Jinan University · CN

Funding

National Natural Science Foundation of China 81973341National Natural Science Foundation of China 81973748National Natural Science Foundation of China 82174278National Natural Science Foundation of China 82204786National Natural Science Foundation of China 82271563
6 · The paper itself

Abstract

rationale18β-glycyrrhetinic acid (18β-GA) has been reported to have anti-inflammatory and neuroprotective effects. However, the therapeutic effect of 18β-GA in Parkinson's disease (PD) has not been defined.

objectiveThe current study aimed to evaluate the potential therapeutic effects of 18β-GA in treating PD by mitigating 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neurotoxicity.

resultsThe study showed that 18β-GA has anti-inflammatory effects by upregulating TREM2 expression in BV2 cells, which correlates with the presence of NF-E2-related factor-2 (Nrf2). 18β-GA reduced inflammation in BV2 cells treated with 1-methyl-4- phenylpyridinium (MPP

conclusionsIt is probable that activating microglial anti-inflammatory response through TREM2 expression might serve as a novel therapeutic strategy for PD. Additionally, 18β-GA seems to hold potential as a new therapeutic agent for PD.

Indexed as

Neuroprotective AgentsParkinson DiseaseAnimalsAnti-Inflammatory AgentsBrain-Derived Neurotrophic FactorDisease Models, AnimalGlycyrrhetinic AcidMiceMice, Inbred C57BLMicrogliaPhenotype18alpha-glycyrrhetinic acidAnti-Inflammatory AgentsBrain-Derived Neurotrophic FactorGlycyrrhetinic AcidNeuroprotective Agents18β-glycyrrhetinic acidAnti-inflammationMicrogliaNeuroprotectionParkinson’s disease

Identifiers

PMID37436491
OpenAlexW4383999145

What OpenQuestion holds

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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.