Comparative Analysis of Phenolic Compounds, Carotenoid, and Antioxidant Activity of Leaf and Stem of Acanthus ebracteatus Vahl (Sea Holly)
Main Article Content
Abstract
Introduction: In Thailand, Acanthus ebracteatus Vahl (Sea Holly), known locally as ‘Nguak Pla Mo,’ has been used for anti-inflammatory, analgesic, and diuretic properties. This study aimed to explore Sea Holly’s antioxidant and phytochemical attributes, open avenues for pharmaceutical applications, and emphasize the importance of conserving Thailand's ethnobotanical wisdom and biodiversity. The primary objectives of this study were to characterize the amount of carotenoid, total phenolic compounds, and antioxidant activity in the leaf and stem of Sea Holly, as well as identify the main chemical constituents in plant extracts.
Methods: The plant extracts were analyzed for their carotenoid and total phenolic content. Their antioxidant activity was evaluated using ABTS, FRAP, and DPPH assays, and the chemical constituents were characterized using GC-MS and IR spectroscopy.
Results: Sea Holly leaf extract contains higher amounts of both carotenoid (0.2261 mg/g sample) and total phenolic compounds (344.67 mg GAE/g DW) than its stem, which has 0.0103 mg/g sample for carotenoid and 92.75 mg GAE/g DW for total phenolic compounds. Consequently, the extraction from leaves exhibits higher antioxidant activity (%DPPH: 18.73; %ABTS: 81.4 and FRAP: 3.46 mmolFe2+/g sample) than stem extract (%DPPH: 14.48; %ABTS: 69.0 and FRAP: 2.40 mmolFe2+/g sample). The GC-MS and IR analysis reveals that the main phytochemicals contained in both stem and leaf extracts are hexadecenoic acid, triolein, campesterol, stigmasterol, and g-sitosterol.
Conclusion: Sea Holly leaf contains higher total phenolic compounds, carotenoid content, and antioxidant activity than Sea Holly stem, a potential application for treatment in oxidative-stress-related diseases and a promising opportunity to develop alternative healthcare and medicinal products.
Article Details
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
JHSAM publishes all articles in full open access, meaning unlimited use and reuse of articles with appropriate credit to the authors.
All our articles are published under a Creative Commons "CC-BY-NC-ND 4.0". License which permits use, distribution and reproduction in any medium,
provided that the original work is properly cited and is used for noncommercial purposes.
References
Prasansuklab A, Tencomnao T. Acanthus ebracteatus leaf extract provides neuronal cell protection against oxidative stress injury induced by glutamate. BMC Complement Altern Med. 2018; 18(1): 278-292.
Olatunji OJ, Olatunde OO, Jayeoye, TJ, Singh S, Nalinbenjapun S, Sripetthong S, et al. New insights on Acanthus ebracteatus Vahl: UPLC-ESI-QTOF-MS Profile, antioxidant, antimicrobial and anticancer activities. Molecules. 2022; 27: 1981-1994.
Kanchanapoom T, Kasai R, Picheansoonthon C, Yamasaki K. Megastigmane, aliphatic alcohol and benzoxazinoid glycosides from Acanthus ebracteatus. Phytochemistry. 2001; 58(5): 811-818.
Hokputsa S, Harding SE, Inngjerdingen K, Jumel K, Michaelsen TE, Heinze T, et al. Bioactive polysaccharides from the stems of the Thai medicinal plant Acanthus ebracteatus: their chemical and physical feature. Carbohydr Res. 2004; 339(4): 753-62.
Williams GM and Jeffrey AM. Oxidative DNA damage: Endogenous and chemically induced. Regul Toxicol Pharm. 2000; 32: 283-292.
Halliwell B. Establishing the significance and optimal intake of dietary antioxidants: the biomarker concept. Nutr Rev. 1999; 57: 104-113.
Williams WB, Cuvelier AE and Berset, C. Use of a free radical method to evaluate antioxidant activity. LWT-Food Sci Technol. 1995; 28: 25-30.
Rakkhitawatthana V, Sillapachaiyaporn C, Nilkhet S, Brimson JM, and Tencomnao T. Effect of Thai medicinal plants Acanthus ebracteatus Vahl., Carthamus tinctorius L. and Streblus asper Lour. on neurite outgrowth activity in Neuro-2A cells. J Assoc Med Sci. 2023;56(1) :71-84.
Kanlayavattanakul M, Chaikul P, Kongkow M, Iempridee T, Lourith N. Anti-aging of phenolic-rich Acanthus ebracteatus Vahl. extracts. Chem Biol Technol Agric. 2023;10(1):1-14.
Wisuitiprot V. The development of hair growth promoting product containing Acanthus ebracteatus Vahl. extract [dissertation]. Phitsanulok: Naresuan University; 2022.
Sommer TR, D'Souza FML, Morrissy NM. Pigmentation of adult rainbow trout, Oncorhynchus mykiss, using the green alga Haematococcus pluvialis. Aquaculture. 1992; 106(1): 63 - 74.
Arnao MB, Cano A, Acosta M. The hydrophilic and lipophilic contribution to total antioxidant activity. Food Chem. 2001; 73: 239 - 244.
Benzie IFF, Strain, JJ. The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power” the FRAP assay. Anal Biochem. 1996; 239: 70 - 76.
Alothman M, Bhat R, Karim AA. Antioxidant capacity and phenolic content of selected tropical fruits from Malaysia, extracted with different solvent. Food Chem. 2009; 115: 785 - 788.
Panpimanmas S, Sithipongsri S, Sukdanon C, Manmee C. Experimental comparative study of the efficacy and side effects of Cissus quadrangularis L. (Vitaceae) to Daflon (Servier) and placebo in the treatment of acute hemorrhoids. J Med Assoc Thai. 2010; 93: 1360 - 1367.
Lisiewska Z, Kmiecik W, Korus A. Content of vitamin C, carotenoids, chlorophylls, and polyphenols in green parts of dill (Anethum graveolens L.) depending on plant height. J Food Comp Anal. 2006; 19: 134 -140.
Khwairakpam AD, Bodoloi D, Thakur KK, Monisha J, Arfuso F, Sethi G, et al. Possible use of Punica granutum (Pomengranate) in cancer therapy. Pharmacol Res. 2018; 133: 53-64.
de Carvalho LMJ, Gomes PB, de Oliveira Godoy RL, Pacheco S, do Monte PHF, de Carvalho JLV, et al. Total carotenoid content, α-carotene and β-carotene, of landrace pumpkins (Cucurbita moschata Duch): A preliminary study. Food Res Int. 2012; 47(2): 337-40.
Ferraces-Casais P, Lage-Yusty MA, Rodríguez-Delgado MA, Valcárcel J, Fernández-Martínez JM, García-Ríos A. Carotenoids: Their role in human health, food applications and determination methods. Curr Pharm Des. 2020; 26(18): 2224-2239.
Arscott SA, Tanumihardjo SA. Carrots of many colors provide basic nutrition and bioavailable phytochemicals acting as a functional food. Compr Rev Food Sci Food Saf. 2010; 9(2): 223-239.
Prapasanobol V, Sudta P, Chaocharoen W. Phytochemical screening, total phenolic, flavonoid and alkaloid contents, cytotoxicity, and antioxidant activities of Capparis monantha, Jacobs extracts. Asia Pac J Sci Technol. 2022; 27(6): 1-7.
Rakkhitawatthana V, Sillapachaiyaporn C, Nilkhet S, Brimson J, Tencomnao T. Effect of Thai medicinal plants Acanthus ebracteatus Vahl. Carthamus tinctorius L. and Streblus asper Lour on neurite outgrowth activity in Neuro-2A cells. J Assoc Med Sci. 2023; 56(1): 71 - 84.
Burri SCM, Ekholm A, Håkansson Å, Tornberg E, Rumpunen K. Antioxidant capacity and major phenol compounds of horticultural plant materials not usually used. J Funct Foods. 2017; 38(Pt A): 119 - 127.
Gründemann, C., Gruber, C. W., Hertrampf, A., Zöll, M., Burstein, C., & Huber, R. An aqueous melissa extract induces gastric relaxation via activation of endogenous prostaglandin pathways. Planta Medica. 2011; 77(05): 494-499.
Kubola J, Siriamornpun S. Phenolic contents and antioxidant activities of bitter gourd (Momordica charantia L.) leaf, stem and fruit fraction extracts in vitro. Food Chem. 2008; 110(4): 881-90.
Gülçin İ. Antioxidant activity of food constituents: an overview. Arch
Toxicol. 2012; 86(3):345-91.
Litz RE, Ratnayake C, Bach-Pham K. Genetic resources of mango. In: Genetic Resources of Tropical Underutilized Fruits. Academic Press; 2022. p. 133-165.
Juntachote T, Berghofer E. Antioxidative properties and stability of ethanolic extracts of Holy basil and Galangal. Food Chem. 2005; 92(2): 193-202.
Sulaiman SF, Sajak AAB, Ooi KL, Supriatno, Seow EM. Antioxidant activities, flavonoids, ascorbic acid and phenolic contents of Malaysian vegetables. J. Med. Plant Res. 2010; 4(7): 592-599.
Tyagi T, Agarwal M. Phytochemical screening and GC-MS analysis of bioactive constituents in the ethanolic extract of Pistia stratiotes L. and Eichhornia crassipes (Mart.) solms. J Pharmacogn Phytochem. 2017; 6(1): 195-206.
Sahu N, Saxena J. Phytochemical Analysis of Bougainvillea Glabra Choisy by FTIR and UV-VIS Spectroscopic Analysis. Int J Pharm Sci Rev Res. 2013;21(1):196-198.
Bohn T. Dietary factors affecting polyphenol bioavailability. Nutr Rev. 2014 Jul;72(7):429-52.
Duperon R, Thiersault M, Duperon P. High level of glycosylated sterols in species of solanum and sterol changes during the development of the tomato. Phytochemistry. 1984; 23(4): 743 - 746.
Yoshida Y, Niki E. Antioxidant effects of phytosterol and its components. J Nutr Sci Vitaminol. 2003; 49(4): 277 - 280.
Mitra S, Choudhury A, Ghosh A, Dutta J. The role of hydrophobic substances in leaves in adaptation of plants to periodic submersion by tidal water in a mangrove ecosystem. J Ecol. 1984; 72: 621-625.
Mitra S, Choudhury A, Dutta J, Ghosh A. Hydrocarbon and wax ester compositions of the leaves of some flooded and emergent plants of Sunderban mangrove forest. In: Krishnamurthy V, Untawale AG, editors. All-India Symposium on Marine Plants, their Biology, Chemistry and Utilization; 1985. p. 273-276.
Yelmate AA, Thonte SS. Phytochemical screening by FTIR spectroscopic analysis of some Indian medicinal plants. Eur. J. Mol. Clin. Med. 2020; 7(11): 4362 - 4371.
Ashokkumar R and Ramaswamy M. Phytochemical screening by FTIR spectroscopic analysis of leaf extracts of selected Indian medicinal plants. Int J Curr Microbiol App Sci. 2014; 3(1): 395-406.
Brangule A, Šukele R, Bandere D. Herbal medicine characterization perspectives using advanced FTIR sample techniques – diffuse reflectance (DRIFT) and photoacoustic spectroscopy (PAS). Front Plant Sci. 2020: (11): 1-11.