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Keywords: n Costus afern , Polyphenolic content, Antioxidant activity, Glycemic index, Enzyme inhibitory activity, Medicinal plant
This study evaluated the polyphenolic content, estimated glycemic index, antioxidant potential, and enzyme inhibitory activities of aqueous extract from different parts of Costus afer (Ker Gawl). The leaf extract exhibited the highest total phenolic content (45.87 ± 0.03 mg GAE/g) and flavonoid contents (32.39 ± 0.03 mg QE/g), while the stem showed the lowest value. The estimated glycemic index was lowest in the leaf (20.14 ± 0.035%), indicating its potential to better regulate blood glucose levels compared to the stem and rhizome. Antioxidant activities assessed using DPPH, ABTS, NO, and FRAP assays, revealed variable results. The stem and leaf demonstrated statistically similar DPPH radical scavenging abilities, while the rhizome showed the strongest FRAP activity. ABTS and NO assays highlighted the rhizome superior free radical scavenging capacities. Additionally, the rhizome exhibited the highest inhibition of FeSO₄-induced lipid peroxidation (469.10 ± 2.67 µg/ml). The α-amylase and α-glucosidase inhibitory activities were significantly higher in all Costus afer extracts compared to acarbose. The rhizome had the strongest α-amylase inhibition (27.52 ± 0.59 mg/ml), while the stem exhibited the highest α-glucosidase inhibition (18.71 ± 0.94 mg/ml). HPLC analysis identified quercetin, caffeic acid, kaempferol, and other bioactive phenolics, with the leaf showing the highest quercetin content. These findings suggest that Costus afer extracts, particularly the leaf and rhizome, exhibit promising antioxidant, antidiabetic, and bioactive properties, supporting their potential use in managing oxidative stress and diabetes.
Ajayi OB, Oyetayo FL, Akomolafe SF (2020) Starch composition, glycemic indices, antioxidant properties and carbohydrate hydrolyzing enzymes activities of African star apple fruit parts. BMC Compl Med Ther 20:260
Bathaie S, Mokarizade N, Shirali S (2012) An overview of the mechanisms of plant ingredients in the treatment of diabetes mellitus. J Med Plant 4(44):1–24
Benzie I, Strain J (1998) The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power: the FRAP assay.” Anal Biochem 239:70–76
Borquaye LS, Layea MK, Gasu EN, Boateng MA, Baffor PK, Kyeremateng A, Doh G (2020) Anti-inflammatory an antioxidant activities of extracts of Reisantia indica, Cissus cornifolia and Grosseria vignei. Congent Biol 6(1):1785755. https://doi.org/10.1080/233025.2020.1785755
Brand-Miller JC, Stockmann K, Atkinson F, Petocz P, Denyer G (2008) Glycemic index, postprandial glycemia, and the shape of the curve in healthy subjects: analysis of a database of more than 1000 foods. Ame J Clin Nut 89(1):97–105
Cheplick S, Kwon Y, Bhowmik P, Shetty K (2007) Clonal variation in raspberry fruit phenolics and relevance for diabetes and hypertension management. J Food Biochem 31:656–679
Chu Y, Sun J, Wu X, Liu RH (2002) Antioxidant and antiproliferative activity of common vegetables. J Agric Food Chem 50:6910–6916
Costa ASG, Alves RC, Vinha AF, Barriera SUP, Nunes MA, Cunha LM, Oliverira MBP (2014) Optimization of antioxidants extraction from coffee, silverskin a roasting by-product, living in view a sustainable process. Ind Crop Prod 3:350–357
Dastmalchi K, Dorman HJD, Kosar M, Hiltunen R (2007) Chemical composition and in vitro antioxidant evaluation of a water soluble Moldavian balm (Dracocephalum oldavica L.) extract. Leb Wiss Technol 40:239–248. https://doi.org/10.1016/j.lwt.2005.09.019
Edeoga HO, Okoli BE (2000) Chromosome numbers of Costus lucanusianus (Costaceae) in Nigeria. Folia Geobot 35:315–318
Eleazu CO (2016) The concept of low glycemic index and glycemic load foods as panacea for type 2 diabetes mellitus; prospects, challenges and solutions. Afr Health Sci 16(2):468–479
Ezeigwe OC, Onwusulu DN, Adindu CS, Okani CO, Onuegbu ME (2022) Effect of ethyl acetate fraction of Costus afer on glycaemic control and essential haematological and biochemical indices of streptozotocin-induced diabetic rats. J Herbmed Pharmacol 11(4):575–584
Gella FJ, Gubern G, Vidal R, Canalias F (1997) Determination of total and pancreatic α- amylase in human serum with 2-chloro-4-nitrophenyl-α-d-maltotrioside as substrate. Clin Chim Acta 259(1-2):147–160
Goñi I, Garcia-Alonso A, Saura-Calixto F (1997) A starch hydrolysis procedure to estimate glycemic index. Nutr Res 17:427–437
Gu C, Zhang H, Putri CY, Ng K (2015) Evaluation of α-amylase and α-glucosidase inhibitory activity of flavonoids. Int J Food Nutr Sci 2(6):1–6
Atlas ID (2019) International Diabetes Federation (IDF) Diabetes Atlas Brussels, Belgium, 9th edn
Iqbal T, Hussain AI, Chatha SAS, Naqvi SAR, Bokhari TH (2013) Antioxidant activity and volatile and phenolic profile of essentials oil and different extract of wild mint (Mentha longifolia) from Parkistani flora. Anal Mtd Chem 55:64–90
Kim Y, Keogh JB, Clifton PM (2016) Polyphenols and glycemic control. Nutrients 8(1):17
Liu RH (2003) Health benefit of fruit and vegetable from additive and synergistic combination of phytochemicals. Am J Clin Nutr 78(3):5175–5205
Lushchak V (2011) Adaptive response to oxidative stress; bacteria, fungi, plants and animals comparative. Biochem Physiol C Toxicol Pharma CPB 153(2):175–190
Momoh S, Yusuf OW, Adamu MM, Agwu C, Atanu FO (2011) Evaluation of the phytochemical composition and hypoglycaemic activity of methanolic leaves extract of Costus afer in albino rats. Br J Pharm Res 1(1):1–8
Neha P, Dushyant B (2011) Antioxidant activity of ethanolic extract of Annona squamosa Linn bark. Int J Res Pharm Biomed Sci 2:1692–1697
Nehete J, Bhatia M, Narkhedeb M (2020) In-vitro evaluation of antioxidant activity and phenolic content of costus speciosus (Keon). Iran J Pharm Res 9(3):27
Oboh G, Puntel RL, Rocha JBT (2007) Hot pepper (Capsicum annuum, tepin and Capsicum chinese, Habanero) prevents Fe2+-induced lipid peroxidation in brain in vitro. Food Chem 102:178–185
Ohkawa H, Ohishi N, Yagi K (1979) Assay of lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 95:351–358
Ojo OA, Ajiboye BO, Olayide I, Fadaka A, Olasehinde OR (2016) Ethyl acetate fraction of bark of Bridelia ferruginea Benth. inhibits carbohydrate hydrolyzing enzymes associated with type 2 diabetes (α-glucosidase and α-amylase). Adv Biores 7(3):126–133
Ojo OA, Oyetayo FL, Oladipo A, Oluwatosin V (2023) In vitro antioxidant and inhibitory activities of Acacia nilotica (L.) Delile seeds and pods on enzymes relevant to type-2 diabetes. Vegetos. https://doi.org/10.1007/s42535-019-00022-7
Okoko T (2009) Stem extracts from the monocot Costus afer ameliorates paracetamol induced issue injury in rats. Int J Pure Appl Sci 3:21–25
Ou B, Prior RL, Huang D (2005) The chemistry behind dietary antioxidant capacity assays. J Agric Food Chem 53:1841–1856
Oyetayo FL, Akomolafe SF, Odeniyi IA (2019) Effects of dietary supplementation of Chrysophyllum albidum fruit pulp powder on some biochemical parameters in a type 2 diabetes rat model. Vegetos. https://doi.org/10.1007/s42535-019-00022-7
Phuyal N, Jha PK, Raturi PP, Rajibhandry S (2020) Total phenolic, flavonoid contents and antioxidant activities of fruit, seed and bark extracts of Zanthoxylum armatum DC. Sci World e8780704:1–7
Pietta PG (2000) Flavonoids as antioxidants. J Nat Products 63:1035–1042
Re R, Pellegrini N, Proteggente A, Yang M, Rice-Evans C (1999) Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radic Biol Med 26:1231–1237
Rubiya K, Sachin KS, Sheetu W, Monica G, Ankit A (2020) Enhancing the potential preclinical and clinical benefits of quercetin through novel drug delivery systems. Drug Deliv Today 25(1):209–222
Singleton VL, Orthofer R, Lamuela-Raventos RM (1999) Analysis of total phenols and other oxidation substrates and antioxidants by means of Folin–Ciocalteu reagent. Mtd Enzy 29:152–178. https://doi.org/10.1016/S0076-6879(99)99017-1
Tafrihil M, Imran M, Tufail T, Gondal T, Caruso G, Sharma S (2021) The wonderful activities of the genus menthe: not only antioxidant properties. Molecules 26:1118
Tanaka T, Kohno H, Mori H (1998) Chemoprevention of colon carcinogenesis by dietary nonnutritive compounds. Asian Pac J Can Prev 2:1–13
Tchamgoue AD, Tchokouaha LR, Tarkang PA, Kuiate JR, Agbor GA (2015) Costus afer possesses carbohydrate hydrolyzing enzymes inhibitory activity and antioxidant capacity in vitro. Evid Based Complementary Altern Medicine 2015(1):987984
Tchamgoue AD, Tchokouaha LR, Tsabang N, Tarkang PA, Kuiate JR, Agbor GA (2018) Costus afer protects cardio-, hepato-, and reno-antioxidant status in streptozotocin-intoxicated Wistar rats. Biomed Res Int 2018(1):4907648
Telagari M, Hullatti K (2015) In-vitro α-amylase and α-glucosidase inhibitory activity of Adiantum caudatum Linn. and Celosia argentea Linn. extracts and fractions. Ind J Pharm 47(4):425–429
Zago MP, Verstraeten SV, Oteiza PI (2000) Zinc in the prevention of Fe2+ initiated lipid and protein oxidation. Biol Res 33:143–150
Department of Biochemistry, Ekiti State University, Ado Ekiti, Nigeria