EVALUATION OF ANTICHOLINERGIC, ANTIDIABETIC AND ANTIOXIDANT ACTIVITY OF LEAF EXTRACTS OF OCHNA OBTUSATA DC USING IN VITRO ASSAYS

Authors

  • Tirupati Reddy Gourigari Department of Biology, Rajiv Gandhi University of Knowledge of Technologies, Vempalli, Kadapa (Dt), 516330, Andhra Pradesh, India
  • Bhakshu Md Lepakshi Department of Botany, Government College for Men, Kadapa, 516004, Andhra Pradesh, India
  • Ratnam V Kamsala Department of Botany, Rayalaseema University, Kurnool, 518 007, Andhra Pradesh, India
  • Venkata Raju R R Department of Botany, Sri Krishnadevaraya University, Ananthapuramu, 515 003, Andhra Pradesh, India.

Keywords:

Ochna obtusata, Anticholenergic, Antidiabetic, Antioxidant

Abstract

Objective: To study the antidiabetic, anticholinergic and antioxidant activity of leaf extracts of Ochna obtusata DC. using in vitro methods.

Methods: Alcoholic extract and a decoction of Ochna obtusata DC. leaf was screened for antidiabetic, anticholinergic and antioxidant activity by using in vitro methods. Total phenolic and total antioxidant capacity of Ochna obtusata DC. leaf extracts were quantified as gallic acid equivalents, using the spectrophotometric method.

Results: The ethanol extract and water decoction showed strong inhibition to 1,1-diphenyl-2-picrylhydrazyl radical (IC50 0.3±0.01 µg/ml, 90±5.1 µg/ml), Nitric Oxide (IC50 of 43±1 µg/ml, 82±1 µg/ml) hydrogen peroxide(IC50 of 45±2.1 µg/ml, 92±1.3 µg/ml), hydroxyl radical (IC50 of 22±2.3 µg/ml, above 200), lipid peroxidation (IC50 of 4.37±0.5 µg/ml, 1.68±0.3 µg/ml)equivalents of gallic acid (EGA), whereas the Acetylcholinesterase (IC50 of 0.5±0.2, 40±2.12) and α-Glucosidase IC50 of 3.5±.04 µg/ml, 45±3.03 µg/ml against the standard drug (acarbose equivalents) respectively. The present investigation revealed that the alcoholic extract of Ochna obtusata DC (except lipid peroxide) is effective than water decoction.

Conclusion: The present observations suggest that Ochna. obtusata DC leaves may be considered as a new source for anticholinergic, antidiabetic and antioxidant constituents for therapeutic use.

Keywords: Ochna obtusata DC, Acetylcholinesterase, α-Glucosidase, Antioxidant

Downloads

Download data is not yet available.

References

Rendle AB. The classification of flowering plants. Vol. II. Cambridge University Press: London; 1952.

Mathew KM. The flora of Tamilnadu and carnatic. Vol. I-III. Dioceran Press: Madras; 1983.

Rao KV, Sreeramulu K, Venkata Rao, Gunasekhar D. Two New Biflavonoids from Ochna obtusata DC. J Nat Prod 1997;60:632-4.

Thammanna H, Narayana Rao K. Medicinal plants of Tirumala. Gayatri art printers, Hyderabad; 1998.

Chopra RN, Nayar SL, Chopra IC. Glossary of Indian medicinal plants. Council of Scientific and Industrial Research, New Delhi; 1956.

Jain SK. Dictionary of Indian Folk Medicine and Ethnobotany. Deep Publication, New Delhi, India; 1991.

Kirtikar KR, Basu BD. Indian medicinal plants. Vol. I-IV. International book distributors, Dehra Dun, India; 1981.

Hemadri KA. Treatise on tribal medicine. Dr Koppula Hemadri’s House of Tribal Medicine, Vijayawada, India; 2006.

Anuradha V, Pullella V Srinivas, Ranga Rao R, Manjulatha K, Muralidhar G Purohit. Isolation and synthesis of analgesic and anti-inflammatory compounds from Ochna squarrosa L. Bioorg Med Chem 2006;14:6820-6.

Jain SK, Tarafder CR. Native plant remedies for snakebite among Adivasis of central India. Indian Med J 1963;57:307-9.

Devasagayam TPA, Tilak JC, Boloor KK, Ketaki S Sane, Saroj S Ghaskadbi. Free radicals and antioxidants in human health: current status and future prospects. J Assoc Physicians India 2004;52:794-804.

Halliwell Band, Gutteridge JMC. Free radicals in biology and medicine. Oxford University Press: Oxford; 1997.

Lipinsky B. Pathophysiology of oxidative stress in diabetes mellitus. J Diabetes Complications 2001;15:203-10.

Subhasree B, Baskar R, Laxmi Keerthana R, Lijina Susan R, Rajasekaran P. Evalution of antioxidant potential in selected green leafy vegetables. Food Chem 2009;115:1213-20.

Maryam Zahin, Farrukh Aqil, Iqbal Ahmad. The in vitro antioxidant activity and total phenolic content of four Indian medicinal plants. Int J Pharm Pharm Sci 2009;1:88-95.

Fawole OA, Amoo SO, Ndhlala AR, Light ME, Finnie. Anti-inflammatory, anticholinesterase, antioxidant and phytochemical properties of medicinal plants used for pain-related ailments in South Africa. J Ethnopharmacol 2010;127:235-41.

Lee WL, Downey GP. Leukocyte elastase: physiological function and role in acute lung injury. Am J Respir Crit Care Med 2001;164:896–904.

Pohanka M. Acetylcholinesterase inhibitors; a patent review (2008-present). Expert Opin Ther Pat 2012;22:871–86.

Colovic MB, Krstic, Danijela Z, Lazarevic-Pasti, Tamara D, Bondzic, et al. Acetylcholinesterase inhibitors: pharmacology and toxicology. Curr Neuropharmacol 2013;11:315–35.

Inglis F. The tolerability and safety of cholinesterase inhibitors in the treatment of dementia. Int J Clin Prac 2002;127:45–63.

Yuschak Thomas. Advanced lucid dreaming: the power of supplements. Lulu Enterprises; 2006.

Singh J, Kour K, Jayaram MB. Acetylcholinesterase inhibitors for schizophrenia. Cochrane Database Syst Rev 2012;1:CD007967. Doi:10.1002/14651858.CD007967. [Article in Press]

Choi KH, Wykes T, Kurtz MM. Adjunctive pharmacotherapy for cognitive deficits in schizophrenia: meta-analytical investigation of efficacy. The British J Psychiatry 2013;3:172–8.

Ribeiz SR, Bassitt DP, Arrais JA, Avila R, Steffens DC, Bottino CM. Cholinesterase inhibitors as adjunctive therapy in patients with schizophrenia and schizoaffective disorder a review and meta-analysis of the literature. CNS Drugs 2010;24:303–17.

Matsuura H, Asakawa C, Kurimoto M. Mizutani J. α-Glucosidase inhibitor from the seeds of balsam pear (Momordica charantia) and the fruit bodies of Grifola frondosa. Biosci Biotech Biochem 2002;66:1576–8.

Gamble JS. Flora of the presidency of madras. Vol. I-III. Bishen Singh Mahendra Pal Singh, Dehra Dun, India; 1995.

Pullaiah T. Flora of Andhra Pradesh (India). Vol. I-IV. Scientific Publishers, Jodhpur, India; 1997.

Rama Rao, Henry AN. The ethnobotany of eastern ghats in Andhra Pradesh, India. Botanical Survey of India, Calcutta; 1996.

Venakata Raju RR, Pullaiah T. Flora of Kurnool. Bishen Singh Mahendra Pal Singh, Dehra Dun, India; 1995.

Hagerman A, Harvey MI, Makkar HPS. Quantification of tannins in tree foliage. A Laboratory Manual 2000;537:4-7.

Preito P, Pineda M, Aguilar M. Spectrophotometric quantification of antioxidant capacity through the formation of a phospho- molybdenum complex: specific application to the determination of Vitamin E. Anal Biochem 1999;269:337-41.

Yaushisakono A. DPPH free radical scavenging activity of medicinal plant extract. Biochem Biophy 1978;136:189-95.

Long LH, Lan ANB, Hsuan FTY, Halliwell B. Generation of hydrogen peroxide by antioxidant beverages and the effect of milk addition. Is cocoa the best beverage? Free Radical Res 1999;37:67–71.

Halliwel B. Reactive oxygen species in living systems: source, biochemistry and role in human disease. Am J Med 1991;91(3C):14–22.

Green LC, Wagner DA, Glogowski J. Analysis of nitrate, nitrite and nitrate in biological fluids. Anal Biochem 1982;126:131–8.

Bandi AKR, Nimmanapalli PR, Gunasekhar D, Alain B, Bernard B. Biflavonoids from Ochna lanceolata. Phytochem Lett 2008;1:27-30.

Mukherjee PK, Venkatesan Kr, Mainak M, Houghton PJ. Acetylcholinesterase inhibitors from plants. Phytomedicine 2007;14:289-300.

Rickwood CJ, Galloway TS. Acetylcholinesterase inhibition as a biomarker of adverse effect, A study of Mytilus edulis exposed to the priority pollutant chlorfenvinphos. Aquatic Toxicol 2004;67:45-56.

Inglis F. The tolerability and safety of cholinesterase inhibitors in the treatment of dementia. Int J Clin Pract 2002;127:45-63.

Wang H, Yu M Ochani. Nicotinic acetylcholine receptor a-7 subunit is an essential regulator of inflammation. Nature 2003;421:384-8.

Shytle RD, Mori T, Townsend K. Cholinergic modulation of microglial activation by a7 nicotinic receptors. J Neurochem 2004;89:337–43.

Kim KS, Seo EK, Lee YC, Lee TK, Cho YW, Ezaki O Kim. Effect of dietary Platycodon grandiflorum on the improvement of insulin resistance in obese Zucker rats. J Nutr Biochem 2000;11:420-4.

Pontes DBC, Polizello AC, Spadaro AC. Clinical and biochemical evaluation of the saliva of patients with xerostomia induced by radiotherapy. Brazilian Oral Res 2004;18:69-74.

Bernfeld P. Amylases α-and β. Methods Enzymol 1955;1:149-58.

Casirola DM, Ferraris RP. Alpha-Glucosidase inhibitors prevent diet-induced increases in intestinal sugar transport in diabetic mice. Metabolism 2006;55:832-41.

Published

01-06-2016

How to Cite

Gourigari, T. R., B. M. Lepakshi, R. V. Kamsala, and V. R. R R. “EVALUATION OF ANTICHOLINERGIC, ANTIDIABETIC AND ANTIOXIDANT ACTIVITY OF LEAF EXTRACTS OF OCHNA OBTUSATA DC USING IN VITRO ASSAYS”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 8, no. 6, June 2016, pp. 82-87, https://journals.innovareacademics.in/index.php/ijpps/article/view/10620.

Issue

Section

Original Article(s)