Evidence map›Paper›PMID 40491366›Full record

ArticleCurrent Alzheimer research2025

Assessment of the Inhibition of AChE and BChE by

Assia Keniche, Chaimaa Kalache, Mohammed El Amine Dib, Ibtissem El Ouar

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Article in Current Alzheimer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Assia KenicheThe Laboratory of Organic Chemistry, Natural Substances and Analyses (COSNA), Aboubekr Belkaïd University, Tlemcen, Algeria.
Chaimaa KalacheThe Laboratory of Organic Chemistry, Natural Substances and Analyses (COSNA), Aboubekr Belkaïd University, Tlemcen, Algeria.
Mohammed El Amine DibThe Laboratory of Natural and Bioactive Substances (LASNABIO), Faculty of Sciences, Abou Bekr-Belkaid University, Tlemcen, Algeria.ORCID 0000-0003-4612-5303
Ibtissem El OuarLaboratory of Cellular and Molecular Immunology, Faculty of Life and Natural Sciences, University Constantine 1, Constantine, Algeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlzheimer's disease is associated with dysfunction of the cholinergic system, making the inhibition of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) a promising therapeutic approach.

objectiveThis study aimed to evaluate the neuroprotective effects and toxicity of essential oil (EO) and carlina oxide from Carthamus caeruleus in mice, assessing their potential for Alzheimer's disease treatment.

methodsThe chemical composition of the essential oil extracted from the roots of Carthamus caeruleus was analyzed using gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS). The main component, carlina oxide, was isolated via column chromatography. The inhibitory activities of AChE and BChE were evaluated in vitro for both the essential oil and carlina oxide. Additionally, in vivo, toxicity was assessed in laboratory mice.

resultsChemical analysis identified carlina oxide (81.6%) as the major constituent, along with minor compounds such as 13-methoxycarlin oxide and hexadecanoic acid. Both the essential oil and its main component, carlina oxide, exhibited significant inhibitory activity against AChE and BChE, enzymes associated with Alzheimer's disease. The essential oil demonstrated promising IC DISCUSSION: The essential oil and carlina oxide demonstrated potent BChE inhibition, particularly relevant in advanced Alzheimer's disease. While effective at low doses, signs of toxicity were observed at higher concentrations, highlighting the importance of dose optimization. These findings suggest that C. caeruleus may serve as a natural source of cholinesterase inhibitors, pending further

conclusionCarthamus caeruleus essential oil and carlina oxide show promising inhibitory effects on AChE and BChE, suggesting their potential as neuroprotective agents. However, their toxicity at higher doses highlights the need for cautious use and further investigation.

Indexed as

AcetylcholinesteraseAlzheimer DiseaseButyrylcholinesteraseCholinesterase InhibitorsNeuroprotective AgentsOils, VolatileAnimalsDisease Models, AnimalDose-Response Relationship, DrugMaleMicePlant OilsAcetylcholinesteraseButyrylcholinesteraseCholinesterase InhibitorsNeuroprotective AgentsOils, VolatilePlant Oilsacetylcholinesterase (AChE)Alzheimer’s diseasebutyrylcholinesterase (BChE)carlina oxideCarthamus caeruleusessential oilneuroprotectiontoxicity.

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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.