Evidence map›Paper›PMID 22445602›Full record

ArticleNeuropharmacology2012

The natural products magnolol and honokiol are positive allosteric modulators of both synaptic and extra-synaptic GABA(A) receptors.

Mikhail Alexeev, Denise K Grosenbaugh, David D Mott, Janet L Fisher

Open access · greenAbstract read
In one paragraph

Article in Neuropharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
6.7field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 74 citations in OpenAlex.

  1. Neuroprotective Potency of Neolignans inFrontiers in pharmacology · 2022
    Pooled it
  2. Pooled it
  3. Review
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  9. Antioxidants (Basel, Switzerland) · 2022
    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

4 authors at 1 institution in 1 country.

Mikhail AlexeevHonors College, University of South Carolina, Columbia, SC 29208, USA.
Denise K Grosenbaugh
David D Mott
Janet L Fisher
University of South Carolina · US

Funding

Structural Determinants of GABA-A receptor functionR01NS045950 · NINDS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI FISHER, JANET L · 2004 to 2007
$795k
NINDS NIH HHS R01 NS045950NINDS NIH HHS R01-NS045950
6 · The paper itself

Abstract

The National Center for Complementary and Alternative Medicine (NCCAM) estimates that nearly 40% of adults in the United States use alternative medicines, often in the form of an herbal supplement. Extracts from the tree bark of magnolia species have been used for centuries in traditional Chinese and Japanese medicines to treat a variety of neurological diseases, including anxiety, depression, and seizures. The active ingredients in the extracts have been identified as the bi-phenolic isomers magnolol and honokiol. These compounds were shown to enhance the activity of GABA(A) receptors, consistent with their biological effects. The GABA(A) receptors exhibit substantial subunit heterogeneity, which influences both their functional and pharmacological properties. We examined the activity of magnolol and honokiol at different populations of both neuronal and recombinant GABA(A) receptors to characterize their mechanism of action and to determine whether sensitivity to modulation was dependent upon the receptor's subunit composition. We found that magnolol and honokiol enhanced both phasic and tonic GABAergic neurotransmission in hippocampal dentate granule neurons. In addition, all recombinant receptors examined were sensitive to modulation, regardless of the identity of the α, β, or γ subunit subtype, although the compounds showed particularly high efficacy at δ-containing receptors. This direct positive modulation of both synaptic and extra-synaptic populations of GABA(A) receptors suggests that supplements containing magnolol and/or honokiol would be effective anxiolytics, sedatives, and anti-convulsants. However, significant side-effects and risk of drug interactions would also be expected.

Indexed as

Allyl CompoundsAnimalsBiphenyl CompoundsDrugs, Chinese HerbalGABA AgentsHEK293 CellsHippocampusHumansInhibitory Postsynaptic PotentialsLignansNeuronsPhenolsRatsReceptors, GABA-ASynaptic TransmissionAllyl CompoundsBiphenyl CompoundsDrugs, Chinese HerbalGABA AgentshonokiolLignansmagnololPhenolsReceptors, GABA-A

Identifiers

PMID22445602
PMCPMC3652012
OpenAlexW2064291335

What OpenQuestion holds

Textmetadata
LicenceTDM
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.