NEUROPROTECTIVE ACTIVITY OF FRACTIONAL FLOWER EXTRACTS OF MIRABILIS JALAPA AGAINST ALUMINIUM HYDROCHLORIDE INDUCED NEUROTOXICITY IN MALE WISTER RATS

Authors

  • Sitty Manohar Babu Southern Institute of Medical Sciences, College of Pharmacy, SIMS Group of Institutions, Mangaladas Nagar, Vijayawada Road, Guntur 522001, Andhra Pradesh, India
  • Suryakanta Swain Southern Institute of Medical Sciences, College of Pharmacy, SIMS Group of Institutions, Mangaladas Nagar, Vijayawada Road, Guntur 522001, Andhra Pradesh, India
  • Karanam Renuka Southern Institute of Medical Sciences, College of Pharmacy, SIMS Group of Institutions, Mangaladas Nagar, Vijayawada Road, Guntur 522001, Andhra Pradesh, India

DOI:

https://doi.org/10.22159/ijpps.2017v9i5.17584

Keywords:

Mirabilis jalapa, Memantine, Oxidative stress, Thiobarbituric acid reactive substances, Neuroprotective activity

Abstract

Objective: The major objective of this present study was to evaluate the neuroprotective effect of fractional flower extracts (acetone, petroleum ether, methanol and aqueous) of Mirabilis jalapa (MJ) against aluminium hydrochloride-induced neurotoxicity in male wister rats.

Methods: From the different fractional flower extracts of Mirabilis jalapa (MJ), two doses (250 and 500 mg/kg body weight) of each extract was initially selected and administered per orally 30 min prior to aluminium hydrochloride administration to the different animal groups once a day for a period of 45 d. Rat serum was collected from different animal groups on 1st, 15th, 30th and 45th days for estimation of marker enzymes, where a reduction in marker was observed. Animal was sacrificed by decapitation and the whole brain of rats was analyzed to estimate the levels of nitrite, thiobarbituric acid reactive substances (TBARS), superoxide dismutase (DOS), catalase, reduced glutathione and acetylcholinesterase (AchE).

Results: On the 9th day the Wister rats were sacrificed and cerebral cortex was removed. One-half of the cerebral cortex samples from different groups of Aluminium hydrochloride treated rats were stored in FAM mixture (40% formaldehyde, acetic acid and methanol in the ratio of 1:1:8) for histological analysis. From the study confirmed that dose of 250 and 500 mg/kg bwt of methanolic extract of MJ significantly (p˂0.001) increases the reduced glutathione, superoxide dismutase and catalase level, whereas petroleum ether, acetone and aqueous fractional flower extracts of MJ significantly (p˂0.01) decreases nitrite, TBARS and AchE levels of aluminium hydrochloride treated groups.

Conclusion: This result is indicating evidence for Mirabilis jalapa had a significant neuroprotective effect on aluminium hydrochloride-induced neurotoxicity and also supports by histopathological studies.

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References

Subin MZ, Aleykutty NA, Vidya V, Sonu J, Visakh P. In vitro antioxidant potential of methanolic extracts of mirabilis jalapa linn. Free Radicals Antioxid 2011;1:82-6.

Kumar A, Prakash A, Dogra S. Neuroprotective effect of carvedilol against aluminium induced toxicity: possible behavioural and biochemical alterations in rats. Pharmacol Rep 2011;63:915-23.

Manno C, Lipari A, Bono V, Taiello AC, Bella VLa. Sporadic parkinson disease and amyotrophic lateral sclerosis complex (Brait-Fahn-Schwartz disease). J Neurol Sci 2013;326:104-6.

Maheswari SL, Murali RV, Balaji R. Aluminium induced cholinotoxicity in zebra fish brain-a sequel of oxidative stress. Int Adv Res 2014;2:322-35.

Singh T, Goel RK. Neuroprotective effect of Allium cepa L. in aluminium chloride induced neurotoxicity. Neurotoxicology 2015;49:1-7.

Baptiste AF, Marie-Elise MB, Carole H, Jean-Jacques, Yves A, Etienne CH. Neuromelanin associated redox-active iron is increased in the substantia nigra of patients with Parkinson's disease. J Neurochem 2003;86:1142–8.

Sumithra M, Arunachalam G, Arunachalam G, Chitra V, Arunachalam G. Neuroprotective effect of Sargassum ilicifolium Turner c. agardh on acetylcholinesterase activity and attenuation of scopolamine-induced amnesia in rodents. Asian J Pharm Clin Res 2016;9:93-6.

OECD guidelines. Proc Indian Natl Sci Acad 1999;65 Suppl B:179-204.

Piper DW, Stiel DD. Pathogenesis of chronic peptic ulcer. DW Clin Implications Med 1986;2:7-10.

Dimitrios T. Analysis of nitrite and nitrate in biological fluids by assays based on the griess reaction: an appraisal of the Griess reaction in the L-arginine/nitric oxide area of research. J Chromatogr B: Anal Technol Biomed Life Sci 2007;851:51-70.

Hermann E, HC Kevin. Determination of aldehydic lipid peroxidation products, malonaldehyde and 4-hydroxynonenal. Methods Enzymol 1990;186:407-21.

Himani B, Saumya S, Promila S, Syed MW. Investigation of phytochemical composition, evaluation of antioxidant, antibacterial activities and toxicity study of Emblica officinalis and Terminalia bellirica fruits. Asian J Pharm Clin Res 2016;9:96-102.

Misra HP, Fridovich I. The role of superoxide anion in the auto oxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem 1972;247:3170-5.

Aebi H. Catalase in vitro methods. Methods Enzymol 1984;105:121-6.

Zacharoula IL, Malvina GO, Alexandros GK, Fotini NL, Marigoula M. Investigation of the neuroprotective action of saffron (Crocus sativus L.) in aluminum-exposed adult mice through behavioural and neurobiochemical assessment. Food Chem Toxicol 2013;52:163-70.

Kumar A, Dogra S, Prakash A. Protective effect of curcumin, against aluminium hydrochloride toxicity. Possible behavioral and biochemical alterations in rats. Behavioural Brain Res 2009;205:384-90.

Deloncle R, Guillard O. Mechanism of Alzeimer’s disease: arguments for a neurotransmitter aluminium hydrochloride complex implication. Neurochem Res 1990;15:1239-45.

Yokel RA. The toxicology of aluminium in the brain: a review. Neurotoxicology 2000;21:813-28.

Canales JJ, Corbalan, Montoliu C, Llansola M, Monfor P, Erceg S, et al. Aluminium impairs the glutamate-nitric oxide-c-GMP pathway in cultured neurons and in rat brain in vivo: molecular mechanisms and implications for neuropathology. J Inorg Biochem 2001;87:63-9.

Ghribi O, DeWitt DA, Forbes MS, Arad A, Herman MM, J Savory. Cyclosporin a inhibits al-induced cytochrome c release from mitochondria in aged rabbits. J Alzheimer's Disease 2012;3:387-91.

Marvanova M, Lakso M, Pirhonen J, Nawa H, Wong G, Castren E. The neuroprotective agent memantine induces brain-derived neurotrophic factor and trkB receptor expression in rat brain. Mol Cell Neurosci 2001;18:247-58.

Drever BD, Anderson WG, Johnson H, O'Callaghan M, Seo S, Choi DY, et al. Memantine acts as a cholinergic stimulant in the mouse hippocampus. J Alzheimer's Disease 2007;12:319-33.

Lo D, Grossberg GT. Use of memantine for the treatment of dementia. Expert Rev Neurother 2011;11:1359-70.

Sondheimer JH, Mahajan SK, Rye DL, Abu-Hamdan DK, Migdal SD, Prasad AS, et al. Elevated plasma copper in chronic renal failure. Am J Clin Nutr 1988;47:896-9.

Benzi G, Marzatico F, Pastoris O Villa. The relationship between aging, drug treatment and the cerebral enzymatic antioxidant system. Exp Gerontol 1989;24:137-48.

Swegert CV, Dave KR, Katyare SS. Effect of aluminium-induced Alzheimer-like condition on oxidative energy metabolism in rat liver, brain and heart mitochondria. Mechanisms Ageing Dev 1999;112:27-42.

Yu SP. Na+/K+-ATPase: the new face of an old player in pathogenisism and apoptotic or hybrid cell death. Biochem Pharmacol 2003;66:1601-9.

Jyoti A, Sethi P, Sharma D. Bacopa monniera prevents from aluminium hydrochloride neurotoxicity in the cerebral cortex of rat brain. J Ethnopharmacol 2007;111:56-62.

Published

01-05-2017

How to Cite

Babu, S. M., S. Swain, and K. Renuka. “NEUROPROTECTIVE ACTIVITY OF FRACTIONAL FLOWER EXTRACTS OF MIRABILIS JALAPA AGAINST ALUMINIUM HYDROCHLORIDE INDUCED NEUROTOXICITY IN MALE WISTER RATS”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 9, no. 5, May 2017, pp. 216-21, doi:10.22159/ijpps.2017v9i5.17584.

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