Evidence map›Paper›PMID 31278631›Full record

ArticleNeurochemical research2019

Licorisoflavan A Exerts Antidepressant-Like Effect in Mice: Involvement of BDNF-TrkB Pathway and AMPA Receptors.

Dong Xiao, Li Liu, Yuanjie Li, Jie Ruan, Hanqing Wang

Abstract read
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In one paragraph

Article in Neurochemical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
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  3. 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

5 authors at 3 institutions in 1 country.

Dong XiaoCollege of Pharmacy, Guangdong Medical University, Dongguan, 523808, China.
Li LiuCollege of Pharmacy, Guangdong Medical University, Dongguan, 523808, China. liuli-44@163.com.
Yuanjie LiCollege of Pharmacy, Ningxia Medical University, Ningxia, 750004, China.
Jie RuanCollege of Traditional Chinese Medicine, China Pharmaceutical University, Nanjing, 210009, China.
Hanqing WangCollege of Pharmacy, Ningxia Medical University, Ningxia, 750004, China. hqwangnx@tom.com.
Guangdong Medical College · CNNingxia Medical University · CNChina Pharmaceutical University · CN

Funding

National Natural Science Foundation of China 81460645National Natural Science Foundation of China 81503465National Natural Science Foundation of China 81603227National Natural Science Foundation of China 81873096
6 · The paper itself

Abstract

Depression is a highly debilitating and life-threatening psychiatric disorder. The classical antidepressants are still not adequate due to undesirable side effects. Therefore, the development of new drugs for depression treatment is an urgent strategic to achieving clinical needs. Licorisoflavan A is a bioactive ingredient isolated from Glycyrrhizae Radix and has been recently reported for neuroprotective effects. In this study, the antidepressant-like effect and neural mechanism of licorisoflavan A were explored. In the mice behavioral despair test, we observed that licorisoflavan A exhibited powerful antidepressant-like effect in forced swimming test (FST), tail suspension test (TST), without affecting locomotor activity in open field test (OFT). Additionally, licorisoflavan A administration significantly restored Chronic mild stress (CMS)-induced changes in sucrose preference test (SPT), FST, and TST, without altering the locomotion in OFT. In chronical-stimulated mice, the licorisoflavan A treatment effectively attenuated the expressions of Brain-derived neurotrophic factor (BDNF), tyrosine kinase B (TrkB), the phosphorylations of cAMP response element binding protein (CREB), extracellular signal-regulated kinase (ERK)-1/2, eukaryotic elongation factor 2 (eEF2), mammalian target of rapamycin (mTOR), initiation factor 4E-binding protein 1 (4E-BP-1), and p70 ribosomal protein S6 kinase (p70S6K) in hippocampus of CMS-induced mice. Additionally, licorisoflavan A could reverse the decreases in synaptic proteins post-synaptic density protein 95 (PSD-95) and α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA) receptor subunit glutamate receptor 1 (GluR1) caused by CMS, and its antidepressant-like effect was blocked by the AMPA receptor antagonist NBQX. These findings served as preclinical evidence that licorisoflavan A exerted potent antidepressant-like effects involving BDNF-TrkB pathway and AMPA receptors. Licorisoflavan A might be used as a potential medicine against depression-like disorder.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAntidepressive AgentsBehavior, AnimalBenzopyransBrain-Derived Neurotrophic FactorCell Cycle ProteinsCyclic AMP Response Element-Binding ProteinDepressionHippocampusLocomotionMaleMembrane GlycoproteinsMicePhosphorylationProtein Serine-Threonine KinasesAdaptor Proteins, Signal TransducingAntidepressive AgentsBdnf protein, mouseBenzopyransBrain-Derived Neurotrophic FactorCell Cycle ProteinsCreb1 protein, mouseCyclic AMP Response Element-Binding ProteinEif4ebp1 protein, mouselicorisoflavan AMembrane GlycoproteinsNtrk2 protein, mouseProtein Serine-Threonine KinasesProtein-Tyrosine KinasesReceptors, AMPAReceptor, trkBAMPAAntidepressant-like effectBDNF-TrkB signaling pathwayChronic mild stressLicorisoflavan A

Identifiers

PMID31278631
OpenAlexW2994193757

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.