Chemical profiles and biological properties of methanol extracts of Allium pallens L. from different localities in Turkey
Keywords:
Allium, phenolics, antioxidant, anticholinesterase, antityrosinaseAbstract
Paper description:
- Due to their wide range of biological effects, phenolic compounds are one of the most significant secondary metabolite groups of plants.
- The determination of phenolics, total bioactive compounds, and antioxidant and enzyme inhibitory activities of Allium pallens L. was carried out by chromatographic and spectrophotometric methods.
- Stem parts of A. pallens collected from different locations were rich in phenolics and possessed notable biological activities.
- A. pallens may be a natural source of bioactive compounds and help to advance in vivo research on diseases related to cholinesterase and tyrosinase inhibition.
Abstract: Many species of the Allium genus, principally the cultivated forms, are widely used as vegetables, spices and natural therapeutics due to their beneficial health properties. This study aimed to identify the phenolic composition and biological activities of the bulb, stem and flower parts of Allium pallens L., collected from two different localities. A total of 28 phenolic compounds were investigated by LC-ESI-MS/MS, and gallic acid, 4-hydroxybenzoic acid, and benzoic acid were found to be the major phenolic compounds in the plants from both locations. Total phenolic- and flavonoid-content analyses of samples were carried out using spectrophotometry, and the stem extracts were found to be rich in phenolics. DPPH, ABTS, FRAP and CUPRAC assays were used to determine the antioxidant capacities of the extracts. A linear relation was observed between the phenolic contents of the extracts and their antioxidant activities, and the stem extracts of plants from both locations were found to have potent antioxidant capacity. The inhibitory activities of the extracts against acetylcholinesterase, butyrylcholinesterase and tyrosinase were determined using a 96-well microplate reader. The anti-butyrylcholinesterase activity of the extracts was found to be the highest. The outcomes of these investigations were further explored, and the underlying structure of multivariate data was revealed using principal component analysis. This study presents the distribution of chemical constituents and biological activities of the different parts of A. pallens, and also contributes to further investigations of Allium species.
https://doi.org/10.2298/ABS200226013E
Received: February 26, 2020; Revised: April 20, 2020; Accepted: April 20, 2020; Published online: April 20, 2020
How to cite this article: Emir A, Emir C. Chemical profiles and biological properties of methanol extracts of Allium pallens L. from different localities in Turkey. Arch Biol Sci. 2020;72(2):193-201.
Downloads
References
Lattanzio V. Phenolic Compounds: Introduction. In: Ramawat KG, Merillon JM, editors. Handbook of natural products. Berlin, Heidelberg: Springer-Verlag; 2013. p. 1544-73.
Reis Giada ML. Food phenolic compounds: main classes, sources and their antioxidant power In: Morales-Gonzalez A, editor. Oxidative stress and chronic degenerative diseases. London: IntechOpen; 2013. p. 27-112.
Zhang H, Tsao R. Dietary polyphenols, oxidative stress and antioxidant and anti-inflammatory effects. Curr Opin Food Sci. 2016;8:33-42.
Castellano G, Tena J, Torrens F. Classification of phenolic compounds by chemical structural indicators and its relation to antioxidant properties of Posidonia Oceanica (L.) Delile. Match. 2012;67(1):231-50.
Gonçalves S, Romano A. Inhibitory properties of phenolic compounds against enzymes linked with human diseases. In: Soto-Hernández M, editor. Phenolic compounds - biological activity. London: IntechOpen; 2017. p. 99-118.
Hopkins AL, Groom CR. The druggable genome. Nat Rev Drug Discov. 2002;1(9):727-30.
Weinstock M. Selectivity of cholinesterase inhibition: clinical implications for the treatment of Alzheimer’s Disease. CNS Drugs. 1999;12(4):307-23.
Govaerts R, Kington S, Friesen N, Fritsch R, Snijman DA, Marcucci R, Silverstone-Sopkin PA, Brullo S. 2005-2019, World checklist of Amaryllidaceae [Internet]. Facilitated by the Royal Botanic Gardens, Kew. [cited 2019 Apr 25]. Available from: http://apps.kew.org/wcsp/.
Fritsch RM, Abbasi M. New taxa and other contributions to the taxonomy of Allium L. (Alliaceae) in Iran. Rostaniha. 2008;10(2008):1-76.
Angiosperm Phylogeny Group. An update of the Angiosperm Phylogeny Group classification for the orders and the families of the flowering plants: APG III. Bot J Linn Soc. 2009;161:105-21.
Iciek M, Kwiecien I, Włodek L. Biological properties of garlic and garlic-derived organosulfur compounds. Environ Mol Mutagen. 2009;50:247-65.
Corzo-Martínez M, Corzo N, Villamiel M. Biological properties of onions and garlic. Trends Food Sci Tech. 2007;18:609-25.
Hadacova V, Vackova K, Klozova E, Kutacek M, Pitterova K. Cholinesterase activity in some species of the Allium Genus. Biologia plantarum. 1983;25(3).
Mollica A, Zengin G, Locatelli M, Picot-Allain CMN. Mahomoodally MF. Multidirectional investigations on different parts of Allium scorodoprasum L. subsp. rotundum (L.) Stearn: Phenolic components, in vitro biological, and in silico propensities. Food Res Int. 2018;108:641-9.
Emir A, Emir C, Yıldırım H. Characterization of phenolic profile by LC-ESI-MS/MS and enzyme inhibitory activities of two wild edible garlic : Allium nigrum L. and Allium subhirsutum L. J Food Biochem. 2020;44(4):e13165.
Brullo S, Guglielmo A, Pavone P, Salmeri C. Cytotaxonomical remarks on Allium pallens and its relationships with A. convallarioides ( Alliaceae ). Bocconea. 2003;16(2):557-71.
Kollmann F. Allium L., In: Davis PH, editor. Flora of Turkey and the East Aegean Islands 8. Edinburgh: Edinburgh University Press; 1984. p. 98-211.
Singleton VL, Orthofer R, Lamuela-Raventos RM. Analysis of total phenols and other oxidation substrates and antioxidants by means of Folin-Ciocalteu reagent. Method Enzymol. 1999;299:152-78.
Chang C, Yang M, Wen H, Chern J. Estimation of total flavonoid content in propolis by two complementary colorimetric methods. J Food Drug Anal. 2002;10:178-82.
Ellman L, Courtney KD, Andres Jr V, Featherstone RM. New and rapid colorimetric determination of acetylcholinesterase activity. Biochem Pharmacol. 1961;7:88-95.
Emir C, Emir A, Bozkurt B, Somer NU. Phytochemical constituents from Galanthus alpinus Sosn. var. alpinus and their anticholinesterase activities. S Afr J Bot. 2019;12:63-7.
Masuda T, Yamashita D, Takeda Y, Yonemori S. Screening for tyrosinase inhibitors among extracts of seashore plants and identification of potent inhibitors from Garcinia subelliptica. Biosci Biotechnol Biochem. 2005;69(1):197-201.
Blois MS. Antioxidant determinations by the use of a stable free radical. Nature. 1958;181:1199-200.
Stämpfli R, Brühwiler P, Mourad S, Verdejo R, Shaffer M. Development and characterisation of carbon nanotube-reinforced polyurethane foams. EMPA Activities. 2007;26(2007):51.
Apak R, Güçlü K, Özyürek M, Çelik SE. Mechanism of antioxidant capacity assays and the CUPRAC (cupric ion reducing antioxidant capacity) assay. Mikrochim Acta. 2008;160(4):413-19.
Benzie I, Strain J. The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Anal Biochem. 1996;239(1):70-6.
Mesulam M, Geula C. Butyrylcholinesterase reactivity differentiates the amyloid plaques of aging from those of dementia. Ann Neurol. 1994;36:722-7.
Zolghadri S, Bahrami A, Hassan Khan MT, Munoz-Munoz J, Garcia-Molina F, Garcia-Canovas F, Saboury AA. A comprehensive review on tyrosinase inhibitors. J Enzyme Inhib Med Chem. 2019;34(1):279-309.
Martinez MV, Whitaker JR. The biochemistry and control of enzymatic browning. Trends Food Sci Tech. 1995;6:195-200.
Asanuma M, Miyazaki I, Ogawa N. Dopamine- or L-DOPA-induced neurotoxicity: The role of dopamine quinone formation and tyrosinase in a model of Parkinson’s disease. Neurotox Res. 2003;5(3):165-76.
Tessari I, Bisaglia M, Valle F, Samorì B, Bergantino E, Mammi S, Bubacco L. The reaction of α-synuclein with tyrosinase: Possible implications for Parkinson disease. J Biol Chem. 2008;283(24):16808-17.
Dziri S, Hassen I, Fatnassi S, Mrabet Y, Casabianca H, Hanchi B, et al. Phenolic constituents, antioxidant and antimicrobial activities of rosy garlic (Allium roseum var. odoratissimum). J Funct Foods. 2012;4(2):423-32.
Lachowicz S, Kolniak-Ostek J, Oszmiański J, Wiśniewski R. Comparison of phenolic content and antioxidant capacity of bear garlic (Allium ursinum L.) in different maturity stages. J Food Process Preserv. 2017;41(1).
Ceylan O, Alic H. Antibiofilm, antioxidant, antimutagenic activities and phenolic compounds of Allium orientale Boiss. Braz Arch Biol Technol. 2015;58(6):935-43.
Park SY, Je JY, Ahn CB. Phenolic composition and hepatoprotective activities of Allium hookeri against hydrogen-peroxide-induced oxidative stress in cultured hepatocytes. J Food Biochem. 2016;40(3):284-93.
Simin N, Orcic D, Cetojevic-Simin D, Mimica-Dukic N, Anackov G, Beara I, Mitic-Culafic D, Bozin B. Phenolic profile, antioxidant, anti-inflammatory and cytotoxic activities of small yellow onion (Allium flavum L. subsp. flavum, Alliaceae). Lebenson Wiss Technol. 2013;54(1):139-46.
Demirci Kayiran S, Eroglu Ozkan E, Mataraci Kara E, Yilmaz MA, Zengin G, Boga M. Comprehensive analysis of an uninvestigated wild edible medicinal garlic species from Turkey: Allium macrochaetum Boiss. & Hausskn. J Food Biochem. 2019;43:e12928.
Katalinić M, Rusak G, Domaćinović Barović J, Šinko G, Jelić D, Antolović R Kovarik Z. Structural aspects of flavonoids as inhibitors of human butyrylcholinesterase. Eur J Med Chem. 2010;45(1):186-92.
Remya C, Dileep KV, Tintu I, Variyar EJ Sadasivan C. Design of potent inhibitors of acetylcholinesterase using morin as the starting compound. Front Life Sci. 2012;6(3-4):107-17.
Balkis A, Tran K, Lee YZ, Ng K. Screening flavonoids for inhibition of acetylcholinesterase identified baicalein as the most potent inhibitör. J Agr Sci. 2015;7:26-35.
Wang HM, Chou YT, Hong ZL, Chen HA, Chang YC, Yang WL, Chang HC, Mai CT, Chen CY. Bioconstituents from stems of Synsepalum dulcificum Daniell (Sapotaceae) inhibit human melanoma proliferation, reduce mushroom tyrosinase activity and have antioxidant properties. J Taiwan Inst Chem Eng. 2011;42:204-11.
Boo YC. p-Coumaric acid as an active ingredient in cosmetics: A review focusing on its antimelanogenic effects. Antioxidants. 2019;8(8):E275.
Parvez S, Kang M, Chung H and Bae H. Naturally occurring tyrosinase inhibitors: mechanism and applications in skin health, cosmetics and agriculture industries. Phytother Res. 2007;21(9):805-16.
Downloads
Published
How to Cite
Issue
Section
License
Authors grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution 4.0 International License that allows others to share the work with an acknowledgment of the work’s authorship and initial publication in this journal.