EVALUATION OF ETHANOLIC ROOT EXTRACT OF PARTHENIUM HYSTEROPHORUS LINN FOR ANTIOXIDANT AND ANTI-INFLAMMATORY ACTIVITY

##article.authors##

  • Pankaj Lohumi Department of Pharmaceutical Sciences, Kumaun University, Bhimtal Campus, Nainital, Uttarakhand, India 263136
  • Tirath Kumar Department of Pharmaceutical Sciences, Kumaun University, Bhimtal Campus, Nainital, Uttarakhand, India 263136
  • Lipi Nogai Department of Pharmaceutical Sciences, Kumaun University, Bhimtal Campus, Nainital, Uttarakhand, India 263136

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Parthenium##common.commaListSeparator## Ethanolic extract##common.commaListSeparator## Antioxidant##common.commaListSeparator## Anti-inflammatory activity

##article.abstract##

Objective: The work is aimed to draw out the health beneficial properties of a weed (Parthenium hysterophorus Linn). The present work is organized to evaluate the antioxidant and anti-inflammatory activity of the ethanolic root extract of Parthenium hysterophorus Linn.

Methods: In the present work the ethanolic extract was determined by using soxhlet apparatus. The antioxidant scavenging activity of this extract was determined by applying three different assay methods: (1) DPPH (1, 1-diphenyl-2-picryl hydrazyl) free radical method. (2) Nitric oxide scavenging assay and (3) Reducing power method. The anti-inflammatory activity was determined by in vivo method i.e. Carrageenan induced rat paw edema.

Results: DPPH radical scavenging activities of the standard antioxidant and extracts were found to be increased in dose dependent manner. The percentage inhibition increases from 4.19% to 97.09% within the concentration range of 10µg/ml to 160µg/ml. Parthenium hysterophorus Linn effectively reduced the generation of nitric oxide radicals from sodium nitroprusside solution in a concentration dependent manner and percentage inhibition increases from 3.53% to 55.21% within the concentration range 10µg/ml to 160µg/ml. All the concentrations of extract significantly showed higher absorbance than the absorbance of control reaction (0.9705) in reducing power assay. A Higher absorbance indicates high reducing power due to the formation of reduced intermediates. Parthenium hysterophorus Linn showed highly significant anti-inflammatory activity at a dose of 200 mg/kg and the lesser effect was observed at 100 mg/kg with the percentage change in paw volume at 0 min, 30 min, 60 min, 90 min and 120 min.

Conclusion: Thus, from above experimental observations, it can be stated that Parthenium is a natural antioxidant and bearing anti-inflammatory activity.

 

##submission.citations##

Parr A, Bolwell GP. Phenols in the plant and in man: the potential for possible nutritional enhancement of the diet by modifying the phenols content or profile. J Sci Food Agric 2000;80:985-1012.

Hussain SR, Cillard P. Hydroxyl radical scavenging activity of flavonoids. Phytochemistry 1987;26:2489-97.

Gupta M, Mazumdar UK, Gomathi P. In vitro antioxidant and free radical scavenging activities of Galena purpurea root. Pharmacogn Mag 2007;3:219-25.

Kaur IP, Geetha T. Screening methods for antioxidants-a review, mini reviews. Med Chem 2006;6:305-12.

Kehrer JP. Free radicals as mediators of tissue injury and diseases. Crit Rev Toxicol 1993;23:21-48.

Yener Z, Celik I, Ilhan F, Bal R. Effect of Urtica diocia L. seed on lipid peroxidation, antioxidant and liver pathology in aflatoxin-induced tissue injury in rats. Food Chem Toxicol 2009;47:418-24.

Abbas AB, Litcthman AH. In saunderes basic immunology functions and disorders of the immune system. ch 2. 3rd ed. innate immunity; 2009. p. 19-21.

Filomena C. In vivo anti-inflammatory and in vitro antioxidant activities of mediterranean dietry plants. J Ethnopharmacol 2008;116:144-51.

Pro Sono. Principles of the inflammatory response. Professional ultrasound services; 2011. p. 22-4.

Khan F, Khan M. Design and evaluation of levofloxacin hemihydrate floating tablets. Int J Appl Biol Pharm Technol 2010;1:25-7.

Hatano T, Edmatsu R, Mori A, Yasuhara T, Yoshida T, Okuda T. Effects of the interactions of tannins with co-existing substances on 1,1-diphenylpicrylhydrazyl radical. Chem Pharm Bull 1989;37:2016-21.

Oyaizu M. Studies on product of browning reaction prepared from glucose amine. Jpn J Nutr 1986;44:307-15.

Sreejayan N, Rao MNA. Free radical scavenging by curcuminoids. Drug Res 1996;46:169-71.

Kulkarni SK. Handbook of experimental pharmacology. Vallabh Prakashan. 3rd edition reprint; 2010. p. 128-31.

##submissions.published##

21-09-2017

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Original Article(s)