SEED EXTRACT OF ABELMOSCHUS MOSCHATUS MEDIK REVERSES NAF-INDUCED BEHAVIORAL CHANGES THROUGH NEURODEGENERATION AND OXIDATIVE STRESS IN BRAIN OF RAT

Authors

  • Kurmeti Sudhakar Department of Zoology, Osmania University, Hyderabad, India.
  • Mesram Nageshwar Department of Zoology, Osmania University, Hyderabad, India.
  • Pratap Reddy K Department of Zoology, Osmania University, Hyderabad, India.

DOI:

https://doi.org/10.22159/ajpcr.2017.v10i10.20215

Keywords:

Abelmoschus moschatus, Fluoride, Oxidative stress, Neurodegeneration, Nociception

Abstract

 

 Objective: This study reports protective effect of Abelmoschus moschatus seed extract against sodium fluoride-induced neurodegeneration through oxidative stress, neurohistological, and behavioral observations in Wistar rats.

Methods: A total of 20 Wistar rats (around 250 g) were randomly classified into four groups, namely, control, fluoride (NaF), fluoride + A. moschatus seed aqueous extract (AMAE), and fluoride + A. moschatus seed ethanol extract (AMEE). The control group animals received normal tap water, fluoride group received fluoridated water at the rate of 40 mg/kg b. wt., 3rd group rats treated with fluoride (40 mg/kg b. wt.) + AMAE (300 mg/kg b. wt.), and 4th group rats treated with fluoride (40 mg/kg b. wt.) + AMEE (300 mg/kg b. wt.). Neurobehavioral responses of rotarod, hot plate, and maze learning tests and oxidantive stress markers including lipid peroxidation (LPO), GSH levels, superoxide dismutase, CAT, and GSH peroxidase (GPx) activities, and also histology with H and E as well as congo red staining were studied in control, fluoride, and A. moschatus seed extract treated against fluoride groups.

Results: Decreased neurobehavioral responses with rotarod, hot plate, and maze and enhanced LPO (p<0.05) levels were found in fluoride received animals. Whereas, the superoxide dismutase (SOD), CAT, GSH, and GPx were decreased (p<0.05) in NaF treatment. The rats received seed extract along with NaF showed significant reversal of behavioral and oxidative stress markers and the effect of ethanol extract was more pronounced than aqueous extract. The fluoride-treated group showed disturbed cell structure and reduced number of cells in H and E as well as congo red staining which was reversed in cell morphology and restored cell number in seed extract against NaF-treated group. As a result of increased LPO, decreased antioxidant system, and decreased number of cells, neurodegeneration was observed resulting in the disturbance in functions associated with reported behavior.

Conclusion: Okra with high antioxidants activity, seed extract showed reversal of LPO levels and antioxidant status in the brain tissue. And also plant extract administered rats displayed normal cell structure and number of cells than only fluoride received group. Therefore, the aqueous and ethanolic extract of A. moschatus plant seeds has neuroprotective effects against fluoride-induced motor, nociceptive, learning behavior, and on histological structure of brain through antioxidant mechanism. The ethanol extract has shown more efficacy than aqueous extract.

Downloads

Download data is not yet available.

Author Biographies

Kurmeti Sudhakar, Department of Zoology, Osmania University, Hyderabad, India.

Dept. of Zoology

Professor

Mesram Nageshwar, Department of Zoology, Osmania University, Hyderabad, India.

Dept. of Zoology

PhD scholar

Pratap Reddy K, Department of Zoology, Osmania University, Hyderabad, India.

Dept. of Zoology

PhD scholar

References

Lu Y, Sun ZR, Wu LN, Wang X, Lu W, Liu SS. Effect of high-fluoride water on intelligence in children. Fluoride 2000;33(2):74-8.

Sharma A, Chinoy N. Role of free radicals in fluoride-induced toxicity in liver and kidney of mice and its reversal. Fluoride 1998;31:26-30.

Mesram N, Nagapuri K, Banala RR, Nalagoni CR, Karnati PR. Quercetin treatment against NaF induced oxidative stress related neuronal and learning changes in developing rats. J King Saud Univ Sci 2017;29:221-9.

Niedzielska E, Smaga I, Gawlik M, Moniczewski A, Stankowicz P, Pera J, et al. Oxidative stress in neurodegenerative diseases. Mol Neurobiol 2016;53(6):4094-125.

Kamel MM, El-Lethey H, Shaheed I, Kamel G. Black tea forestalls sodium fluoride induced neurobehavioral toxicity in laboratory rats. J Am Sci 2010;6(12):1655-73.

Ailton M, Larissa M, Rute MF, Lima Di ego M, de Oliveira, Martins D, et al. Oxidative stress in neurodegenerative diseases: Mechanisms and therapeutic perspectives. Oxid Med Cell Longevity 2011;2011:Article ID: 467180, 14.

Banala RR, Karnati PR. Vitamin A deficiency: An oxidative stress marker in sodium fluoride (NaF) induced oxidative damage in developing rat brain. Int J Devl Neurosci 2015;47:298-303.

Reddy KP, Sailaja G, Krishnaiah C. Protective effects of selenium on fluoride induced alterations in certain enzymes in brain of mice. J Environ Biol 2009;30 5 Suppl:859-64.

Gul MZ, Bhakshu LM, Ahmad F, Kondapi AK, Qureshi IA, Ghazi IA. Evaluation of Abelmoschus moschatus extracts for antioxidant, free radical scavenging, antimicrobial and antiproliferative activities using in vitro assays. BMC Complement Altern Med 2011;11:64.

Khandare AL, Kumar PU, Lakshmaiah N. Beneficial effect of tamarind ingestion on fluoride toxicity in dogs. Fluoride 2000;33(1):33-8.

Reddy MM, Reddy KP. Protective effects of aqueous extract of fruit pulp of Tamarindus indica on motor activity and metabolism of the gastrocnemius muscle of rats treated with fluoride. Int J Toxicol Pharmcol Res 2015;7(5):241-8.

Vasant RA, Narasimhacharya AV. Alleviatory effects of Emblica officinalis G. as a food supplement in fluoride induced hyperlipemia and oxidative stress. Int J Pharm Pharm Sci 2012;4(1):404-8.

Nabavi SF, Moghaddam AH, Eslami S, Nabavi SM. Protective effects of curcumin against sodium fluoride-induced toxicity in rat kidneys. Biol Trace Elem Res 2012;145(3):369-74.

Nabavi SF, Nabavi SM, Mirzaei M, Moghaddam AH. Protective effect of quercetin against sodium fluoride induced oxidative stress in rat’s heart. Food Funct 2012;3(4):437-41.

Al-Hayani A, Elshal EB, Aal IH, Al-Shammer E. Does vitamin E protect against sodium fluoride toxicity on the cerebellar cortex of albino rats? Middle East J Sci Res 2013;16(7):1019-26.

Pal S, Sarkar C. Protective effect of resveratrol on fluoride induced alteration in protein and nucleic acid metabolism, DNA damage and biogenic amines in rat brain. Environ Toxicol Pharmacol 2014;38(2):684-99.

Reddy CH, Reddy PK. Protective effects of resveratrol against neuronal damage through oxidative stress in cerebral hemisphere of aluminum and fluoride treated rats. Interdiscip Toxicol 2016;9(2):101-5.

Sheik HS, Vedhaiyan N, Singaravel S. Evaluation of Abelmoschus moschatus seed extract in psychiatric and neurological disorders. Int J Basic Clin Pharmacol 2014;3(5):845-53.

Christina AJ, Muthumani P. Phytochemical investigation and diuretic activity of Abelmoschus moschatus Medik us. Int J Pharm Chem Sci 2012;1(4):1311-4.

Arapitsas P. Identification and quantification of polyphenolic compounds from okra seeds and skins. Food Chem 2008;110(4):1041-5.

Adelakun OE, Oyelade OJ, Ade-Omowaye BI, Adeyemi IA, Van de Venter M. Chemical composition and the antioxidative properties of Nigerian okra Seed (Abelmoschus esculentus Moench) Flour. Food Chem Toxicol 2009;47(6):1123-6.

Kumar DM, Prasad DS. Antimicrobial activity of a trypsin inhibitor from the seeds of Abelmoschus moschatus L. Int J Curr Microbiol Appl Sci 2014;3(5):184-99.

Du Z, Clery RA, Hammond CJ. Volatile organic nitrogen-containing constituents in ambrette seed Abelmoschus moschatus Medik (Malvaceae). J Agric Food Chem 2008;56(16):7388-92.

Nandhini S, Vadivu R, Jayshree N. Memory strengthening activity on seeds of Abelmoschus moschatus. Int J Res Pharm Chem 2014;4(2):346-50.

Wen JY, Chen ZW. Protective effect of pharmacological preconditioning of total flavones of abelmoschl manihot on cerebral ischemic reperfusion injury in rats. Am J Chin Med 2007;35(4):653-61.

Tongjaroenbuangam W, Ruksee N, Chantiratikul P, Pakdeenarong N, Kongbuntad W, Govitrapong P. Neuroprotective effects of quercetin, rutin and okra (Abelmoschus esculentus Linn.) in dexamethasone-treated mice. Neurochem Int 2011;59(5):677-85.

Hutter-Saunders JA, Gendelman HE, Mosley RL. Murine motor and behavior functional evaluations for acute 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) intoxication. J Neuroimmune Pharmacol 2012;7(1):279-88.

Gunn A, Bobeck EN, Weber C, Morgan MM. The influence of non-nociceptive factors on hot-plate latency in rats. J Pain 2011;12(2):222-7.

Randall LO, Selitto JJ. A method for measurement of analgesic activity on inflamed tissue. Arch Int Pharmacodyn Ther 1957;111(4):409-19.

Bromley-Brits K, Deng Y, Song W. Morris water maze test for learning and memory deficits in Alzheimer’s disease model mice. J Vis Exp 2011;53:pii: 2920.

Marklund S, Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem 1974;47(3):469-74.

Bhuyan KC, Bhuyan DK, Johansen N. Estimation of malondialdehyde. IRCS Med Sci 1981;9:126-7.

Brannan TS, Maker HS, Raes IP. Regional distribution of catalase in the adult rat brain. J Neurochem 1981;36(1):307-9.

Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys 1959;82:70-7.

Rotruck JT, Pope AL, Ganther HE, Swanson AB, Hafeman DG, Hoekstra WG. Selenium: Biochemical role as a component of glutathione peroxidase. Science 1973;179(4073):588-90.

Lillie RD, Fullmer HM. Histopathologic Technic and Practical Histochemistry. New York: McGraw-Hill; 1976.

Elghetany MT, Saleem A, Barr K. The congo red stain revisited. Ann Clin Lab Sci 1989;19(3):190-5.

Bera I, Sabatini R, Auteri P, Flace P, Sisto G, Montagnani M, et al. Neurofunctional effects of developmental sodium fluoride exposure in rats. Eur Rev Med Pharmacol Sci 2007;11(4):211-24.

Spittle B. Psychopharmacology of fluoride: A review. Int Clin Psychopharmacol 1994;9(2):79-82.

Tsunoda H, Seki T, Hayakawa H, Yamashita F, Yoshida R. Chronic fluoride poisoning. Pediatr Toxicol 1981;6:255-64.

Knoll J, Kelemen K, Knoll B. Experimental studies on the higher nervous activity of animals. I. A method for the elaboration of a non-extinguishable conditioned reflex in the rat. Acta Physiol Hung 1955;8:327-44.

Paul V, Ekambaram P, Jayakumar AR. Effects of sodium fluoride on locomotor behavior and a few biochemical parameters in rats. Environ Toxicol Pharmacol 1998;6(3):187-91.

Nagilla B, Reddy PK. Neuroprotective and antinociceptive effect of curcumin in diabetic neuropathy in rats. Int J Pharm Pharm Sci 2014;6(5):131-8.

Al-Enazi MM. Protective effects of combined therapy of rutin with silymarin on experimentally induced diabetic neuropathy in rats. Pharmacol Pharm 2014;5:876-89.

Banji D, Banji OJ, Pratusha NG, Annamalai AR. Investigation on the role of Spirulina platensis in ameliorating behavioural changes, thyroid dysfunction and oxidative stress in offspring of pregnant rats exposed to fluoride. Food Chem 2013;140(1-2):321-31.

Rzeuski R, Chlubek D, Machoy Z. Interactions between fluoride and biological free radical reactions. Fluoride 1998;31(l):43-5.

Yan MH, Wang X, Zhu X. Mitochondrial defects and oxidative stress in Alzheimer disease and Parkinson disease. Free Radic Biol Med 2013;62:90-101.

Inkielewicz-Stepniak I, Czarnowski W. Oxidative stress parameters in rats exposed to fluoride and caffeine. Food Chem Toxicol 2010;48(6):1607-11.

Zhang M, Wang A, He W, He P, Xu B, Xia T, et al. Effects of fluoride on the expression of NCAM, oxidative stress, and apoptosis in primary cultured hippocampal neurons. Toxicology 2007;236(3):208-16.

Barbier O, Arreola-Mendoza L, Del Razo LM. Molecular mechanisms of fluoride toxicity. Chem Biol Interact 2010;188(2):319-33.

Trivedi MH, Verma RJ, Sangai NP, Chinoy NJ. Mitigation by black tea extract of sodium fluoride induced histopathological changes in brain of mice. Fluoride 2012;45(1):13-26.

Shui G, Peng LL. An improved method for the analysis of major antioxidants of Hibiscus esculentus Linn. Chromatogr A J 2004;1048(1):17-24.

Atawodi SE, Atawodi JC, Idakwo GA, Pfundstein B, Haubner R, Wurtele G, et al. Evaluation of the polyphenol composition and antioxidant activity of African variety of Dacryodes edulis (G. Don) H.J Lam fruit. J Med Food 2009;12(6):1321-5.

Ansari NM, Houlihan L, Hussain B, Pieroni A. Antioxidant activity of five vegetables traditionally consumed by South-Asian migrants in Bradford, Yorkshire, UK. Phytother Res 2005;19(10):907-11.

Gemede HF, Ratta N, Haki GD, Woldegiorgis AZ, Beyene F. Nutritional quality and health benefits of okra (Abelmoschus esculentus): A review. Pak J Food Sci 2015;25(1):16-25.

Zhavoronkov AA. Non-skeletal forms of fluorosis. Arkh Patol 1977;39:83-91.

Shivarajashankara YM, Shivashankara AR. Neurotoxic effects of fluoride in endemic skeletal fluorosis and in experimental chronic fluoride toxicity. J Clin Diagn Res 2012;6:740-4.

Shivarajashankara YM, Shivashankara AR, Bhat PG, Rao SH. Effect of fluoride intoxication on the lipid peroxidation and the antioxidant system in rats. Fluoride 2002;34:108-13.

Guan ZZ, Wang YN, Xiao KQ, Dai DY, Chen YH, Liu JL, et al. Influence of chronic fluorosis on membrane lipids in rat brain. Neurotoxicol Teratol 1998;20(5):537-42.

Kamel OA. Effect of sodium fluoride on the cerebellar cortex of adult albino rats and the possible protective role of vitamin B6: A light and electron microscopic study. Egypt J Histol 2009;32(2):358-67.

Bhatnagar M, Rao P, Sushma J, Bhatnagar R. Neurotoxicity of fluoride: Neurodegeneration in hippocampus of female mice. Indian J Exp Biol 2002;40(5):546-54.

Zhu JT, Choi RC, Xie HQ, Zheng KY, Guo AJ, Bi CW, et al. Hibifolin, a flavonol glycoside, prevents beta-amyloid-induced neurotoxicity in cultured cortical neurons. Neurosci Lett 2009;461(2):172-6.

Published

01-10-2017

How to Cite

Sudhakar, K., M. Nageshwar, and P. Reddy K. “SEED EXTRACT OF ABELMOSCHUS MOSCHATUS MEDIK REVERSES NAF-INDUCED BEHAVIORAL CHANGES THROUGH NEURODEGENERATION AND OXIDATIVE STRESS IN BRAIN OF RAT”. Asian Journal of Pharmaceutical and Clinical Research, vol. 10, no. 10, Oct. 2017, pp. 165-71, doi:10.22159/ajpcr.2017.v10i10.20215.

Issue

Section

Original Article(s)