A Comparative Study on Polyphenol, Flavonoid Content, Antioxidant and AntiInflammatory Capacity of Different Solvent Extract from Portulaca oleracea in Carrageenan-Induced Paw Edema in Mice

http://www.doi.org/10.26538/tjnpr/v7i10.6

Authors

  • Truong T.P Thao Department of Biology, College of Natural Sciences, Can Tho University, Can Tho City, Vietnam 900000
  • Phan T.C Tu Faculty of aquatic biology and environmental science, College of Aquaculture and Fisheries, Can Tho University, Can Tho City, Vietnam 900000
  • Tran T Men Department of Biology, College of Natural Sciences, Can Tho University, Can Tho City, Vietnam 900000

Keywords:

polyphenol absorption, oxidative index, Portulaca oleracea, carrageenan-induced inflammation in mice, anti-inflammatory, antioxidant

Abstract

Portulaca oleracea L., belonging to the Portulacaceae family, is a succulent annual plant, that has been used as vegetables and folk medicine in many Asian countries. There is no systematic and comprehensive research on the comparison of phytochemical quantification and biological activities from various extracts of this plant. This study examined the total polyphenol and
flavonoid content of various Portulaca oleracea extracts and assessed their antioxidant and antiinflammatory properties. Comparing four extracts (methanol, aqueous, ethyl acetate, n-hexane) from P. oleracea, methanolic extract (ME) showed the greatest total polyphenol (60.52±1.88, mg GAE/g DW) and flavonoid content (44.78±1.17 mg QE/g DW). Thus, across all activities
examined, ME had the strongest in vitro antioxidant (IC50=43.52 g/mL for DPPH, IC50=9.71 g/mL for FRAP), and anti-inflammatory effects (80% protein denaturation and 74.81% protection of HRBC membrane). Remarkably, after treatment of ME for 5 h, ME has significantly reduced paw volume (0.098 mL) and thickness (0.62 mm) on carrageenan-induced inflammation (hind paw edema model), compared to the inflamed model (0.19 mL and 1.52 mm). Moreover, ME helps protect the inflamed site in mice based on its ability to reduce malondialdehyde (MDA) and increase glutathione (GSH). The applications of ME in the treatment of inflammatory illnesses and oxidative damage are pharmacologically supported by our results. Also, 60 minutes after ingestion of ME, it dramatically raised the plasma levels of polyphenols and flavonoids as well as the antiradical capacity in healthy mice. Our results showed that ME consumption can support in vivo diet-related health advantages. 

References

White M. Mediators of inflammation and the inflammatory process. J Allergy Clin Immunol. 1999; 103(3): 378-381.

Nagy G, Clark JM, Buzás EI, Gorman CL, Cope AP. Nitric oxide, chronic inflammation and autoimmunity. Vol. 111, Immunology Letters. 2007; 111(1): 1-5.

O’Byrne KJ, Dalgleish AG. Chronic immune activation and inflammation as the cause of malignancy. Vol. 85, British Journal of Cancer. 2001; 85(4): 473-483.

Okada Y. Pathoetiology of chronic rheumatoid arthritis-- from inflammation to bone destruction. 3) From the viewpoint of pathology. Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine. 2000; 89(10): 2072-2080.

Tokmachev RE, Budnevsky A V., Kravchenko AY. The role of inflammation in the pathogenesis of chronic heart failure. Vol. 88, Terapevticheskii Arkhiv. 2016; 88(9): 106-111.

Pawelec G, Goldeck D, Derhovanessian E. Inflammation, ageing and chronic disease. Current Opinion in Immunology.2014; 29: 23-8.

Thanan R, Oikawa S, Hiraku Y, Ohnishi S, Ma N, Pinlaor S, et al. Oxidative stress and its significant roles in neurodegenerative diseases and cancer. International Journal of Molecular Sciences. 2014; 16(1): 193-217.

Lei Y, Wang K, Deng L, Chen Y, Nice EC, Huang C. Redox regulation of inflammation: Old elements, a new story. Med Res Rev. 2015; 35(2): 306-340.

Burns J, Gardner PT, Matthews D, Duthie GG, Lean MEJ, Crozier A. Extraction of phenolics and changes in antioxidant activity of red wines during vinification. J Agric Food Chem. 2001; 49(12): 5797-5808.

Anand David AV, Arulmoli R, Parasuraman S. Overviews of biological importance of quercetin: A bioactive flavonoid. Pharmacognosy Reviews. 2016; 10(20): 84.

Karimi G, Khoei A, Omidi A, Kalantari M, Babaei J, Taghiabadi E, Razavi BM. Protective effect of aqueous and ethanolic extracts of Portulaca oleracea against cisplatin induced nephrotoxicity. Iran J Basic Med Sci. 2010; 13(2 SPRING): 31-35.

Lim YY, Quah EPL. Antioxidant properties of different cultivars of Portulaca oleracea. Food Chem. 2007; 103(3): 734-740.

Zhou YX, Xin HL, Rahman K, Wang SJ, Peng C, Zhang H. Portulaca oleracea L.: A review of phytochemistry and pharmacological effects. BioMed Research International. 2015; 2015.

Sultana A, Rahman K. Portulaca oleracea Linn: A global panacea with ethnomedicinal and pharmacological potential. International Journal of Pharmacy and Pharmaceutical Sciences. 2013; 5(2): 33-39.

Mousavi SM, Bagheri G, Saeidi S. Antibacterial Activities of the Hydroalcoholic Extract of Portulaca oleracea Leaves and Seeds in Sistan Region, Southeastern Iran. Int J Infect. 2015; 2(2): e23214.

Voynikov Y, Gevrenova R, Balabanova V, Doytchinova I, Nedialkov P, Zheleva-Dimitrova D. LC-MS analysis of phenolic compounds and oleraceins in aerial parts of Portulaca oleracea L. J Appl Bot Food Qual. 2019; 92.

Farag MA, Shakour ZTA. Metabolomics driven analysis of 11 Portulaca leaf taxa as analysed via UPLC-ESI-MS/MS and chemometrics. Phytochemistry. 2019; 161: 177-129.

Guo G, Yue L. Antioxidant and Antiproliferative Activities of Purslane Seed Oil. J Hypertens Open Access. 2016; 05(02): 1-19.

Tan GCS, Wong KM, Pearle-Wong GQ, Yeo SL, Yeap SK, Yiap BC, huEh ZAN. In vitro cytotoxic and antiproliferative effects of Portulaca oleracea methanol extract on breast, cervical, colon and nasopharyngeal cancerous cell lines. Sains Malaysiana. 2013; 42(7): 927-935.

Allahmoradi E, Taghiloo S, Omrani-Nava V, Shobeiri SS, Tehrani M, Ebrahimzadeh MA, Asgarian-Omran H. Antiinflammatory effects of the Portulaca oleracea hydroalcholic extract on human peripheral blood mononuclear cells. Med JIslam Repub Iran. 2018; 32(1): 80.

Odion EE, Falodun A, Adelusi SA. Total flavonoid, Total Phenolic and antioxidant potential of root bark extract and fractions of from Cola rostrata (Sterculiaceae) K. Schum.University of Benin. J Sci Tech. 2013; 1(2): 38-42.

Okolie NP aulinu., Falodun A, Davids O. Evaluation of theantioxidant activity of root extract of pepper fruit (Dennetia tripetala), and it’s potential for the inhibition of lipid peroxidation. Afr J Tradit Complement Altern Med. 2014; 11(3): 221-227.

Egharevba E, Chukwuemeke-Nwani P, Eboh U, Okoye E, Bolanle IO, Oseghale IO, Imieje VO, Erharuyi O, Falodun A. Evaluation of the antioxidant and hypoglycaemic potentials of the leaf extracts of Stachytarphyta jamaicensis (Verbenaceae). Trop J Nat Prod Res. 2019; 3(5): 170-174.

Gambhire M, Juvekar AR, Wankhede S. Evaluation of antiinflammatory activity of methanol extract Barleria cristata leaves by in vivo and in vitro methods. Internet J Pharmacol. 2009; 7(1): 1-4.

Gunathilake KDPP, Ranaweera KKDS, Rupasinghe HPV. Influence of boiling, steaming and frying of selected leafy vegetables on the in vitro anti-inflammation associated biological activities. Plants. 2018; 7(1): 22.

Gandhidasan R, Thamaraichelvan A, Baburaj S. Antiinflammatory action of Lannea coromandelica by HRBC membrane stabilization. Fitoterapia. 1991; 62(1): 81-83.

Winter CA, Risley EA, Nuss GW. Carrageenin-Induced Edema in Hind Paw of the Rat as an Assay for Antiinflammatory Drugs. Proc Soc Exp Biol Med. 1962; 111(3):544-547.

Sinha P, Clements VK, Fulton AM, Ostrand-Rosenberg S. Prostaglandin E2 promotes tumor progression by inducing myeloid-derived suppressor cells. Cancer Res. 2007; 67(9): 4507-4513.

Draper HH, Hadley M. Malondialdehyde determination as index of lipid Peroxidation. Methods Enzymol. 1990;186(C): 421-431.

Jollow D, Mitchell JR, Zampaglione N, Gillette JR. Bromobenzene-induced liver necrosis. Protective role of glutathione and evidence for 3,4-bromobenzene oxide as the hepatotoxic metabolite. Pharmacology. 1974;11(3): 151- 169.

Soobrattee MA, Neergheen VS, Luximon-Ramma A, Aruoma OI, Bahorun T. Phenolics as potential antioxidant therapeutic agents: Mechanism and actions. Mutat Res - Fundam Mol Mech Mutagen. 2005; 579(1-2): 200-213.

Amarowicz R, Pegg RB, Rahimi-Moghaddam P, Barl B, Weil JA. Free-radical scavenging capacity and antioxidant activity of selected plant species from the Canadian prairies. Food Chem. 2004; 84(4): 551-562.

Shrestha PM, Dhillion SS. Diversity and traditional knowledge concerning wild food species in a locally managed forest in Nepal. Agrofor Syst. 2006; 66(1): 55-63.

Azeem AK, Dilip C, Prasanth SS, Shahima VJH, Sajeev K, Naseera C. Anti-inflammatory activity of the glandular extracts of Thunnus alalunga. Asian Pac J Trop Med. 2010; 3(10): 794-796.

Bouaziz A, Djidel S, Bentaher A, Khennouf S. Polyphenolic content, Antioxidant and Anti-inflammatory activities of Melon (Cucumis melo L. var. inodorus) Seeds. J Drug Deliv Ther. 2020; 10(2-s): 22-6.

Bigagli E, D’ambrosio M, Cinci L, Niccolai A, Biondi N, Rodolfi L, et al. A comparative in vitro evaluation of the antiinflammatory effects of a tisochrysis lutea extract and fucoxanthin. Mar Drugs. 2021; 19(6): 334.

Wang T, Li X, Zhou B, Li H, Zeng J, Gao W. Anti-diabetic activity in type 2 diabetic mice and α-glucosidase inhibitory, antioxidant and anti-inflammatory potential of chemically profiled pear peel and pulp extracts (Pyrus spp.). J Funct Foods. 2015; 13: 276-88

Kim JH, Kim MY. The potential use of citrus juice waste as sources of natural phenolic antioxidants. J Appl Pharm Sci. 2016; 6(12): 202-5.

De Oliveira NG, Teixeira IT, Theodoro H, Branco CS. Dietary total antioxidant capacity as a preventive factor against depression in climacteric women. Dement eNeuropsychol. 2019; 13 (3): 305-311.

Bardaa S, Turki M, Ben Khedir S, Mzid M, Rebai T, Ayadi F, Sahnoun Z. The Effect of Prickly Pear, Pumpkin, and Linseed Oils on Biological Mediators of Acute Inflammation and Oxidative Stress Markers. Biomed Res Int. 2020; 2020.

Shafiq M, Chen Y, Hashim R, He C, Mo X, Zhou X. Reactive Oxygen Species-Based Biomaterials for Regenerative Medicine and Tissue Engineering Applications. Frontiers in Bioengineering and Biotechnology. 2021; 9: 821288.

Sousa-Neto BP, Cunha FVM, Nunes DB, Gomes BS, Amorim LV, Lopes EM, Gutierrez SJ, Almeida FR, Arcanjo DD, Souza MF, Oliveira FA. Anti-Inflammatory and Antioxidant Effects of the Indole-Derived NSalicyloyltryptamine on Peritonitis and Joint Disability Induced by Carrageenan in Rodents. Evidence-based Complement Altern Med. 2022; 2022.

Milutinović M, Dimitrijević-Branković S, Rajilić-Stojanović M. Plant Extracts Rich in Polyphenols as Potent Modulators in the Growth of Probiotic and Pathogenic Intestinal Microorganisms. Front Nutr. 2021; 8: 688843.

Liu K, Luo M, Wei S. The bioprotective effects of polyphenols on metabolic syndrome against oxidative stress: Evidences and perspectives. Oxidative Medicine and Cellular Longevity. 2019; 2019.

Sharifi-Rad M, Anil Kumar NV, Zucca P, Varoni EM, Dini L, Panzarini E, et al. Lifestyle, Oxidative Stress, and Antioxidants: Back and Forth in the Pathophysiology of Chronic Diseases. Frontiers in Physiology. 2020; 11: 694.

Salehi B, Azzini E, Zucca P, Varoni EM, Kumar NVA, Dini L, et al. Plant-derived bioactives and oxidative stress-related disorders: A key trend towards healthy aging and longevity promotion. Applied Sciences (Switzerland). 2020; 10(3): 947.

Published

2023-10-29

How to Cite

Thao, T. T., Tu, P. T., & Men, T. T. (2023). A Comparative Study on Polyphenol, Flavonoid Content, Antioxidant and AntiInflammatory Capacity of Different Solvent Extract from Portulaca oleracea in Carrageenan-Induced Paw Edema in Mice: http://www.doi.org/10.26538/tjnpr/v7i10.6. Tropical Journal of Natural Product Research (TJNPR), 7(10), 4152–4159. Retrieved from https://tjnpr.org/index.php/home/article/view/2794