Evidence map›Paper›PMID 40063637›Full record

ArticlePloS one2025

Kaempferia parviflora extract and its methoxyflavones as potential anti-Alzheimer assessing in vitro, integrated computational approach, and in vivo impact on behaviour in scopolamine-induced amnesic mice.

Pitchayakarn Takomthong, Pornthip Waiwut, Chavi Yenjai, Jinda Wangboonskul, Kusawadee Plekratoke, Puguh Novi Arsito, Carlo Ballatore, Chantana Boonyarat

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
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.

Pitchayakarn TakomthongFaculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, Thailand.ORCID 0000-0002-8358-0420
Pornthip WaiwutFaculty of Pharmaceutical Sciences, Ubon Ratchathani University, Ubon Ratchathani, Thailand.
Chavi YenjaiFaculty of Sciences, Khon Kaen University, Khon Kaen, Thailand.
Jinda WangboonskulFaculty of Pharmacy, Thammasat University, Bangkok, Thailand.
Kusawadee PlekratokeFaculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, Thailand.
Puguh Novi ArsitoSchool of Pharmacy, Faculty of Medicine and Health Sciences, Universitas Muhammadiyah Yogyakarta, Yogyakarta, Indonesia.
Carlo BallatoreSkaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, San Diego, California, United States of America.
Chantana BoonyaratFaculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, Thailand.ORCID 0000-0003-4065-6090

Funding

Fundamental Fund of Khon Kaen University under the National Science, Research and Innovation Fund, Thailand; Program Management Unit for Human Resources & Institutional Development, Research and Innovation (PMU-B), Thailand B38G670003Khon Kaen University, Thailand 631JH218
6 · The paper itself

Abstract

Alzheimer's disease (AD), a growing global challenge, lacks effective preventive and therapeutic strategies. This study explored the promising potential of the Kaempferia parviflora (KP) and its methoxyflavones (MFs) against the disease. We evaluated KP extract and its five MFs for antioxidant capacity, cholinesterase inhibition (AChE, and BChE), amyloid plaque (Aβ) reduction, neuroprotection, and memory improvement in a mouse model. HPLC quantified the five MFs in KP extract, with 5,7-dimethoxyflavone (F1) being the most abundant. 5,7,4'-Trimethoxyflavone (F3) and 5-hydroxy-3,7-dimethoxyflavone (F4) exhibited the strongest AChE and BChE inhibitory activities, respectively. MFs hindered Aβ1-42 aggregation and destabilized fibrils, with F3 showing the potent anti-aggregation and the strongest fibril destabilization. They also protected SH-SY5Y cells from Aβ1-42-induced damage. Notably, F3 combined anti-cholinesterase and anti-Aβ activities, suggesting its potential as a multi-target agent. KP extract ameliorated scopolamine-induced memory deficits in mice, suggesting its potential for cognitive improvement. These findings revealed that KP can be a promising candidate for herbal medicine development against AD. Its multi-target MFs offered a unique advantage by targeting multiple AD pathways. KP may have a great potential to modify the disease and overcome the challenge of drug development as cognitive enhancing herbal medicine.

Indexed as

Alzheimer DiseaseAmnesiaFlavonesPlant ExtractsZingiberaceaeAcetylcholinesteraseAmyloid beta-PeptidesAnimalsAntioxidantsBehavior, AnimalButyrylcholinesteraseCell Line, TumorCholinesterase InhibitorsDisease Models, AnimalHumansMaleAcetylcholinesteraseAmyloid beta-Peptidesamyloid beta-protein (1-42)AntioxidantsButyrylcholinesteraseCholinesterase InhibitorsFlavonesNeuroprotective AgentsPeptide FragmentsPlant ExtractsScopolamine

Identifiers

PMID40063637
PMCPMC11892870

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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.