Current Alzheimer Research

Current Alzheimer Research

Editor-in-Chief

ISSN (Print): 1567-2050
ISSN (Online): 1875-5828

Back Subscribe
Translate in Chinese
Research Article

Assessment of the Inhibition of AChE and BChE by Carthamus caeruleus Essential Oil and Carline Oxide: Neuroprotective Effects and In Vivo Toxicity Assessment for the Management of Alzheimer’s Disease

Author(s): Assia Keniche, Chaimaa Kalache, Mohammed El Amine Dib*orcid of author and Ibtissem El Ouar

Volume 22, Issue 5, 2025

Published on: 05 June, 2025

Page: [368 - 375] Pages: 8

DOI: 10.2174/0115672050383227250529072253

Price: $65

Become a Editorial Board Member
Become a Reviewer
Become a Editor
Become a Section Editor

Abstract

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

Objective: This 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.

Methods: The 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.

Results: Chemical 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 IC50 values, with stronger anti-BChE activity compared to the reference drug, galantamine. Toxicity tests in mice revealed no adverse effects at lower doses (0.2-0.5 g/kg). However, higher doses (1.0-2.0 g/kg) resulted in mild to significant toxicity, including weight loss and mortality.

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 in vivo studies and clinical validation.

Conclusion: Carthamus 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.

Keywords: Carthamus caeruleus, essential oil, carlina oxide, acetylcholinesterase (AChE), butyrylcholinesterase (BChE), neuroprotection, Alzheimer’s disease, toxicity.

[1]
Ahmad FB, Cisewski JA, Xu J, Anderson RN. Provisional Mortality Data — United States, 2022. MMWR Morb Mortal Wkly Rep 2023; 72(18): 488-92.
[http://dx.doi.org/10.15585/mmwr.mm7218a3] [PMID: 37141156]
[2]
Selkoe DJ, Hardy J. The amyloid hypothesis of Alzheimer’s disease at 25 years. EMBO Mol Med 2016; 8(6): 595-608.
[http://dx.doi.org/10.15252/emmm.201606210] [PMID: 27025652]
[3]
Birks JS, Harvey RJ. Donepezil for dementia due to Alzheimer’s disease. Cochrane Libr 2018; 2018(6): CD001190.
[http://dx.doi.org/10.1002/14651858.CD001190.pub3] [PMID: 29923184]
[4]
Yiannopoulou KG, Papageorgiou SG. Current and future treatments in Alzheimer disease: An update. J Cent Nerv Syst Dis 2020; 12: 1179573520907397.
[http://dx.doi.org/10.1177/1179573520907397] [PMID: 32165850]
[5]
Howes MJ, Houghton PJ. Ethnobotanical treatment strategies against Alzheimer’s disease. Curr Alzheimer Res 2012; 9(1): 67-85.
[http://dx.doi.org/10.2174/156720512799015046] [PMID: 22329652]
[6]
Hancianu M, Cioanca O, Mihasan M, Hritcu L. Neuroprotective effects of inhaled lavender oil on scopolamine-induced dementia via anti-oxidative activities in rats. Phytomedicine 2013; 20(5): 446-52.
[http://dx.doi.org/10.1016/j.phymed.2012.12.005] [PMID: 23351960]
[7]
Lopresti AL. Salvia (Sage): A review of its potential cognitive-enhancing and protective effects. Drugs R D 2017; 17(1): 53-64.
[http://dx.doi.org/10.1007/s40268-016-0157-5] [PMID: 27888449]
[8]
Chaiyana W, Okonogi S. Inhibition of cholinesterase by essential oil from food plant. Phytomedicine 2012; 19(8-9): 836-9.
[http://dx.doi.org/10.1016/j.phymed.2012.03.010]
[9]
Panel I. A.; Owokotomo, O.; Ekundayo, T.G.; Abayomi, A.V.: Chukwuka. In vitro anti-cholinesterase activity of essential oil from four tropical medicinal plants. Toxicol Rep 2015; 2: 850-7.
[http://dx.doi.org/10.1016/j.toxrep.2015.05.003] [PMID: 28962420]
[10]
Rahman MA, Sultana A, Khan MF, Boonhok R, Afroz S. Tea tree oil, a vibrant source of neuroprotection via neuroinflammation inhibition: a critical insight into repurposing Melaleuca alternifolia by unfolding its characteristics. J Zhejiang Univ Sci B 2023; 24(7): 554-73.
[http://dx.doi.org/10.1631/jzus.B2300168] [PMID: 37455134]
[11]
Lai SMS, Liew SY, Chear NJY, Goh BH, Tan WN, Khaw KY. Plant terpenoids as the promising source of cholinesterase inhibitors for anti-AD therapy. Biology 2022; 11(2): 307.
[http://dx.doi.org/10.3390/biology11020307] [PMID: 35205173]
[12]
Benmansour N, Said RM, El Hanbali F, Cherif H, Akssira M. Study of the anti-inflammatory and healing properties of the rhizomes of Carthamus Caeruleus L. (asteraceae) harvested in the region of tipaza. Med Technol J 2020; 4(1): 525-6.
[http://dx.doi.org/10.26415/2572-004X-vol4iss1p525-526]
[13]
Mami IR, Belabbes R, Dib MA, Tabti B. Costa, J.; Muselli, A. Biological activities of carlina oxide isolated from the roots of Carthamus caeruleus. Nat Prod J 2020; 10(2): 145-52.
[http://dx.doi.org/10.2174/2210315509666190117152740]
[14]
Đorđević S, Petrović S, Dobrić S, et al. Antimicrobial, anti-inflammatory, anti-ulcer and antioxidant activities of Carlina acanthifolia root essential oil. J Ethnopharmacol 2007; 109(3): 458-63.
[http://dx.doi.org/10.1016/j.jep.2006.08.021] [PMID: 17011148]
[15]
Hammoudi A, Tabet Zatla A, Mami IR, et al. α-amylase inhibition activity of carlina oxide and aplotaxene isolated from the roots of and Rhaponticum acaule. Curr Chem Biol 2024; 18(2): 94-103.
[http://dx.doi.org/10.2174/0122127968317328240918041222]
[16]
Adams R. Identification of essential oils by Capillary Gas Chromatography/Mass Spectroscopy, Allured Publ Corp. IL: Carol Stream 2001.
[17]
Kçnig W, Joulain D, Hochmuth D. Terpenoids and Related Constituents of Essential Oils, Library of Mass Finder 21. Hamburg: Institute of Organic Chemistry, University of Hamburg 2001.
[18]
McLafferty FW, Stauffer DB. Registry of Mass Spectral Data, 6th electronic ed Wiley. New York 1994.
[19]
McLafferty FW, Stauffer DB. PC Version 17 of The NIST/EPA/NIH Mass Spectral Library. PerkinElmer Corporation 1999.
[20]
Bensaad MS, Dassamiour S, Hambaba L, Bensouici C, Haba H. In vitro assessment of antioxidant, anti-inflammatory, neuroprotective and antimicrobial activities of Centaurea tougourensis Boiss. & Reut. J Pharm Pharmacogn Res 2021; 9(6): 790-802.
[http://dx.doi.org/10.56499/jppres21.1103_9.6.790]
[21]
Benhamidat L, Amine Dib ME, Bensaid O, et al. Chemical composition and antioxidant, anti-inflammatory and anticholinesterase properties of the aerial and root parts of Centaurea acaulis essential oils: Study of the combinatorial activities of aplotaxene with reference standards. J Essent Oil-Bear Plants 2022; 25(1): 126-46.
[http://dx.doi.org/10.1080/0972060X.2022.2046177]
[22]
Semaoui M, Dib MEA, Djabou N, Costa J, Muselli A. Chemical composition, biological activities and toxicity study of carduncellus pinnatus essential oil from West Algeria. Curr Bioact Compd 2022; 18(3): e020821195186.
[http://dx.doi.org/10.2174/1573407217666210802113423]
[23]
Mejdoub K, Mami IR, Belabbes R, et al. Chemical variability of Atractylis gummifera essential oils at three developmental stages and investigation of their antioxidant, antifungal and insecticidal activities. Curr Bioact Compd 2020; 16(4): 489-97.
[http://dx.doi.org/10.2174/1573407215666190126152112]
[24]
Schmidt B, Audörsch S. Stereoselective total syntheses of polyacetylene plant metabolites via ester-tethered ring closing metathesis. J Org Chem 2017; 82(3): 1743-60.
[http://dx.doi.org/10.1021/acs.joc.6b02987] [PMID: 28085285]
[25]
Semmler FW. Zusammensetzung des ätherischen Oels der Eberwurzel (Carlina acaulis L.). Ber Dtsch Chem Ges 1906; 39(1): 726-31.
[http://dx.doi.org/10.1002/cber.190603901108]
[26]
Dosoky NS, Setzer WN. Biological activities of Cistus spp. essential oils. Int J Mol Sci 2018; 19(7): 1966.
[http://dx.doi.org/10.3390/ijms19071966] [PMID: 29976894]
[27]
Loizzo MR, Menichini F, Tundis R, et al. In vitro biological activity of Salvia leriifolia benth essential oil relevant to the treatment of Alzheimer’s disease. J Oleo Sci 2009; 58(8): 443-6.
[http://dx.doi.org/10.5650/jos.58.443] [PMID: 19584571]
[28]
Garcion E, Wion-Barbot N, Montero-Menei CN, Berger F, Wion D. New clues about vitamin D functions in the nervous system. Trends Endocrinol Metab 2002; 13(3): 100-5.
[http://dx.doi.org/10.1016/S1043-2760(01)00547-1] [PMID: 11893522]
[29]
Grimm M, Mett J, Hartmann T. The impact of vitamin E and other fat-soluble vitamins on Alzheimer´s disease. Int J Mol Sci 2016; 17(11): 1785.
[http://dx.doi.org/10.3390/ijms17111785] [PMID: 27792188]
[30]
Ciro A, Park J, Burkhard G, Yan N, Geula C. Biochemical differentiation of cholinesterases from normal and Alzheimer’s disease cortex. Curr Alzheimer Res 2012; 9(1): 138-43.
[http://dx.doi.org/10.2174/156720512799015127] [PMID: 21244353]
[31]
Darreh-Shori T, Brimijoin S, Kadir A, Almkvist O, Nordberg A. Differential CSF butyrylcholinesterase levels in Alzheimer’s disease patients with the ApoE ε4 allele, in relation to cognitive function and cerebral glucose metabolism. Neurobiol Dis 2006; 24(2): 326-33.
[http://dx.doi.org/10.1016/j.nbd.2006.07.013] [PMID: 16973370]
[32]
Herrmann F, Hamoud R, Sporer F, Tahrani A, Wink M. Carlina oxide--a natural polyacetylene from Carlina acaulis (Asteraceae) with potent antitrypanosomal and antimicrobial properties. Planta Med 2011; 77(17): 1905-11.
[http://dx.doi.org/10.1055/s-0031-1279984] [PMID: 21678234]
[33]
Stojanović-Radić Z, Čomić L, Radulović N, Blagojević P, Mihajilov-Krstev T, Rajković J. Commercial Carlinae radix herbal drug: Botanical identity, chemical composition and antimicrobial properties. Pharm Biol 2012; 50(8): 933-40.
[http://dx.doi.org/10.3109/13880209.2011.649214] [PMID: 22480199]
[34]
Djordjevic S, Petrovic S, Ristic M, Djokovic D. Composition of Carlina acanthifolia root essential oil. Chem Nat Compd 2005; 41(4): 410-2.
[http://dx.doi.org/10.1007/s10600-005-0163-2]
[35]
Mami IR, Amina TZ, Pérard J, Arrar Z, Dib MEA. Hemisyntheses and in-silico study of new analogues of carlina oxide from Carthamus Caeruleus roots. Comb Chem High Throughput Screen 2021; 24(9): 1503-13.
[http://dx.doi.org/10.2174/1386207323999201103214141] [PMID: 33155891]
[36]
Benelli G, Pavoni L, Zeni V, et al. Developing a highly stable Carlina acaulis essential oil nanoemulsion for managing Lobesia botrana. Nanomaterials 2020; 10(9): 1867.
[http://dx.doi.org/10.3390/nano10091867] [PMID: 32961890]
[37]
Belabbes R, Mami IR, Dib MEA, et al. I.R.; Dib, M.A.; Mejdoub, K.; Tabti, B.; Costa, J.; Muselli, M. Chemical composition and biological activities of essential oils of Echinops spinosus and Carlina vulgaris rich in polyacetylene compounds. Curr Nutr Food Sci 2020; 16(4): 563-70.
[http://dx.doi.org/10.2174/1573401315666190206142929]
[38]
Mejdoub K, Mami IR, Belabbes R, et al. DJabou, N.; Tabti, B.; Benyelles, N.; Costa, J.; Muselli, A. Chemical variability of Atractylis gummifera essential oils at three developmental stages and investigation of their antioxidant, antifungal and insecticidal activities. Curr Bioact Compd 2020; 16(4): 489-97.
[http://dx.doi.org/10.2174/1573407215666190126152112]
[39]
Benelli G, Pavela R, Petrelli R, et al. Carlina oxide from Carlina acaulis root essential oil acts as a potent mosquito larvicide. Ind Crops Prod 2019; 137: 356-66.
[http://dx.doi.org/10.1016/j.indcrop.2019.05.037]
[40]
Ayaz M, Junaid M, Ahmed J, et al. Phenolic contents, antioxidant and anticholinesterase potentials of crude extract, subsequent fractions and crude saponins from Polygonum hydropiper L. BMC Complement Altern Med 2014; 14(1): 145.
[http://dx.doi.org/10.1186/1472-6882-14-145] [PMID: 24884823]
[41]
Ahmad S, Ullah F, Sadiq A, et al. Chemical composition, antioxidant and anticholinesterase potentials of essential oil of Rumex hastatus D. Don collected from the North West of Pakistan. BMC Complement Altern Med 2016; 16(1): 29.
[http://dx.doi.org/10.1186/s12906-016-0998-z] [PMID: 26810212]
[42]
Souza A, Silva MC, Cardoso-Lopes EM, et al. Differential acetyl cholinesterase inhibition by volatile oils from two specimens of Marlierea racemosa (Myrtaceae) collected from different areas of the Atlantic Rain Forest. Nat Prod Commun 2009; 4(8): 1934578X0900400826.
[http://dx.doi.org/10.1177/1934578X0900400826] [PMID: 19769001]
[43]
Okello E, Dimaki C, Howes M, Houghton P, Perry E. In vitro inhibition of human acetyl-and butyryl-cholinesterase by Narcissus poeticus L. (Amaryllidaceae) flower absolute. Int J Essent Oil Ther 2008; 2: 105-10.
[44]
Hung NH, Quan PM, Satyal P, et al. Acetylcholinesterase inhibitory activities of essential oils from Vietnamese traditional medicinal plants. Molecules 2022; 27(20): 7092.
[http://dx.doi.org/10.3390/molecules27207092] [PMID: 36296686]
[45]
Staton Laws J III, Smid SD. Sesquiterpene-evoked phytochemical toxicity in PC12 neuronal cells reveals a variable degree of oxidative stress and alpha-tocopherol and glutathione-dependent protection. Curr Res Toxicol 2024; 6: 100144.
[http://dx.doi.org/10.1016/j.crtox.2023.100144] [PMID: 38193034]
[46]
Salvi M, Fiore C, Battaglia V, Palermo M, Armanini D, Toninello A. Carbenoxolone induces oxidative stress in liver mitochondria, which is responsible for transition pore opening. Endocrinology 2005; 146(5): 2306-12.
[http://dx.doi.org/10.1210/en.2004-1128] [PMID: 15677764]
[47]
Preeti D, Sambhakar S, Malik R, et al. Nanoemulsion: An emerging novel technology for improving the bioavailability of drugs. Scientifica (Cairo) 2023; 2023: 1-25.
[http://dx.doi.org/10.1155/2023/6640103] [PMID: 37928749]
[48]
Ávila-Gálvez MÁ, Marques D, Figueira I, et al. Costunolide and parthenolide: Novel blood-brain barrier permeable sesquiterpene lactones to improve barrier tightness. Biomed Pharmacother 2023; 167: 115413.
[http://dx.doi.org/10.1016/j.biopha.2023.115413] [PMID: 37683593]

Rights & Permissions Print Cite