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World Journal of Agricultural Research. 2018, 6(3), 87-93
DOI: 10.12691/WJAR-6-3-3
Original Research

Mitigation by Aqueous Extract of Celastrus Paniculatus Seeds against Monosodium Glutamate Induced Impairments in Human Neuronal cells IMR-32

Naumita Shah1, Ankit Nariya1, Ambar Pathan1, Alpesh Patel2, Shiva Shankaran Chettiar2 and Devendrasinh Jhala1,

1Department of Zoology, University School of Sciences, Gujarat University, Ahmedabad-380009, Gujarat, India

2GeneXplore Diagnostics and Research Centre Pvt. Ltd., Ellis Bridge, Ahmedabad-380006, Gujarat, India

Pub. Date: October 16, 2018

Cite this paper

Naumita Shah, Ankit Nariya, Ambar Pathan, Alpesh Patel, Shiva Shankaran Chettiar and Devendrasinh Jhala. Mitigation by Aqueous Extract of Celastrus Paniculatus Seeds against Monosodium Glutamate Induced Impairments in Human Neuronal cells IMR-32. World Journal of Agricultural Research. 2018; 6(3):87-93. doi: 10.12691/WJAR-6-3-3

Abstract

The free radicals are considered as primary culprit for many multifactorial diseases. These free radicals scavenging remains a foremost challenge in most neurological disorders, which can be subjected with least collateral damage by herbal extracts. In this study, Celastrus paniculatus (CP) seeds aqueous extract (AE) (0.25, 0.5 and 1.0 µg/ml) was used to evaluate the neuroprotective efficacy against adverse effects of monosodium glutamate (MSG) (7 mM) in neuroblastoma cell line IMR-32. Preliminary pharmacological investigations and free radical scavenging capacity were evaluated for AE. Cytotoxicity and oxidative stress were studied using MTT assay and some biochemical parameters (total protein and glutathione level as well as activity of superoxide dismutase and catalase). Moreover, genotoxicity due to free radicals was also assessed using comet assay in IMR-32 cells. Results showed presence of various phytochemicals in AE and its significant inhibition of DPPH and NO radicals. AE was not only enhancing the activity of antioxidant enzymes but also reduced the free radical mediated cytotoxicity of MSG in IMR-32 cells. The DNA damage found in neuronal cells due to free radical toxicity of MSG was reduced in presence of free radical inhibitory phytochemical present in AE. From these results it can be concluded that AE of CP seeds is an effective antioxidant agent and potent neuroprotective herb to mitigate MSG induced neuronal impairments in IMR-32 cells.

Keywords

celastrus paniculatus, genotoxicity, monosodium glutamate, neurodegeneration, oxidative stress

Copyright

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

References

[1]  Giacoppo, S., Mandolino, G., Galuppo, M., Bramanti, P. and Mazzon, E., “Cannabinoids: new promising agents in the treatment of neurological diseases”, Molecules, 19. 18781-18816. 2014.
 
[2]  Kandale, V. V., Mujawar, S. N., Welasly, P. J. and Nimbalkar, J. M., “Development of integrated database of neurodegenerative diseases (IDND)”, Review of Research, 2. 1-5. 2013.
 
[3]  Lee, O. H., Lee, B. Y., Lee, J., Lee, H. B., Son, J. Y., Park, C. S. and Kim, Y. C., “Assessment of phenolics-enriched extract and fractions of olive leaves and their antioxidant activities”, Bioresource Technology, 100. 6107-6113. 2009.
 
[4]  Farooqui, T. and Farooqui, A. A., “Aging: an important factor for the pathogenesis of neurodegenerative diseases”, Mechanisms of Ageing and Development, 130. 203-215. 2009.
 
[5]  Blaylock, R. L., “A possible central mechanism in autism spectrum disorders, part 3: the role of excitotoxin food additives and the synergistic effects of other environmental toxins”, Alternative Therapies in Health and Medicine, 15. 56-60. 2009.
 
[6]  Lipton, S. A. and Rosenberg, P. A., “Excitatory amino acids as a final common pathway for neurologic disorders”, New England Journal of Medicine, 330. 613-622. 1994.
 
[7]  Rothman, S. M. and Olney, J. W., “Excitotoxicity and the NMDA receptor-still lethal after eight years”, Trends in Neurosciences, 18. 57-58. 1995.
 
[8]  Ikonomidou, C., Bosch, F., Miksa, M., Bittigau, P., Vöckler, J., Dikranian, K., Tenkova, T. I., Stefovska, V., Turski, L. and Olney, J. W., “Blockade of NMDA receptors and apoptotic neurodegeneration in the developing brain”, Science, 283, 70-74. 1999.
 
[9]  Husarova, V. and Ostatnikova, D., “Monosodium glutamate toxic effects and their implications for human intake: a review”, JMED Research, 2013. 1-12. 2013.
 
[10]  Veni, N. K., Karthika, D., Devi, M. S., Rubini, M. F., Vishalini, M. and Pradeepa, Y. J., “Analysis of monosodium l-glutamate in food products by high-performance thin layer chromatography”, Journal of Young Pharmacists, 2. 297-300. 2010.
 
[11]  Federico, A., Cardaioli, E., Da Pozzo, P., Formichi, P., Gallus, G. N. and Radi, E., “Mitochondria, oxidative stress and neurodegeneration”, Journal of the Neurological Sciences, 322. 254-262. 2012.
 
[12]  Uttara, B., Singh, A. V., Zamboni, P. and Mahajan, R. T., “Oxidative stress and neurodegenerative diseases: a review of upstream and downstream antioxidant therapeutic options”, Current Neuropharmacology, 7. 65-74. 2009.
 
[13]  Deodhar, K. A. and Shinde, N. W., “Celastrus paniculatus: Traditional uses and Ethnobotanical study”, Indian Journal of Advances in Plant Research, 2. 18-21. 2015.
 
[14]  Karuppusamy, S. and Rajasekaran, K. M., “High throughput antibacterial screening of plant extracts by resazurin redox with special reference to medicinal plants of Western Ghats”, Global Journal of Pharmacology, 3. 63-68. 2009.
 
[15]  Godkar, P. B., Gordon, R. K., Ravindran, A. and Doctor, B. P., “Celastrus paniculatus seed oil and organic extracts attenuate hydrogen peroxide-and glutamate-induced injury in embryonic rat forebrain neuronal cells”, Phytomedicine, 13. 29-36. 2006.
 
[16]  Harborne, J. B., Methods of plant analysis. Springer, Dordrecht. 1984.
 
[17]  Macdonald‐Wicks, L. K., Wood, L. G. and Garg, M. L., “Methodology for the determination of biological antioxidant capacity in vitro: a review”, Journal of the Science of Food and Agriculture, 86. 2046-2056. 2006.
 
[18]  Parul, R., Saha, P. and Kundu, S. K., “In vitro nitric oxide scavenging activity of methanol extracts of three Bangladeshi medicinal plants”, The Pharma Innovation, 1. 83-88. 2013.
 
[19]  Mosmann, T., “Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays”, Journal of Immunological Methods, 65. 55-63. 1983.
 
[20]  Shah, N., Nariya, A., Pathan, A., Patel, A., Chettiar, S. S. and Jhala, D., “Neuroprotection Effects of Celastrus paniculatus seed oil against monosodium glutamate in human IMR-32 cells”, Annual Research & Review in Biology, 24. 1-9. 2018.
 
[21]  Shen, H. M., Yang, C. F., Ding, W. X., Liu, J. and Ong, C. N., “Superoxide radical–initiated apoptotic signalling pathway in selenite-treated HepG2 cells: mitochondria serve as the main target”, Free Radical Biology and Medicine, 30. 9-21. 2001.
 
[22]  Lowry, O. H., Rosebrough, N. J., Farr, A. L. and Randall, R. J., “Protein measurement with the Folin phenol reagent”, Journal of Biological Chemistry, 193. 265-275. 1951.
 
[23]  Ellman, G. L., “Tissue sulfhydryl groups”, Archives of Biochemistry and Biophysics, 82. 70-77. 1959.
 
[24]  Kakkar, P., Das, B. and Viswanathan, P. N., “A modified spectrophotometric assay of superoxide dismutase”, Indian Journal of Biochemistry and Biophysics, 21. 130-132. 1984.
 
[25]  Sinha, A. K., “Colorimetric assay of catalase”, Analytical Biochemistry, 47. 389-394. 1972.
 
[26]  Singh, N. P., Mccoy, M. T., Tice, R. R. and Schneider, E. L., “A simple technique for quantitation of low levels of DNA damage in individual cells”, Experimental Cell Research, 175. 184-191. 1988.
 
[27]  Kumar, G. P. and Khanum, F., “Neuroprotective potential of phytochemicals”, Pharmacognosy Reviews, 6. 81-90. 2012.
 
[28]  Sofowora, A., Ogunbodede, E. and Onayade, A., “The role and place of medicinal plants in the strategies for disease prevention”, African Journal of Traditional, Complementary and Alternative Medicines, 10. 210-229. 2013.
 
[29]  Kumar, M. H. V. and Gupta, Y. K., “Antioxidant property of Celastrus paniculatus willd.: A possible mechanism in enhancing cognition”, Phytomedicine, 9. 302-311. 2002.
 
[30]  Kulkarni, Y. A., Agarwal, S. and Garud, M. S., “Effect of Jyotishmati (Celastrus paniculatus) seeds in animal models of pain and inflammation”, Journal of Ayurveda and Integrative Medicine, 6. 82-88. 2015.
 
[31]  Gamlath, C. B., Gunatilaka, A. L., Tezuka, Y., Kikuchi, T. and Balasubramaniam, S., “Quinone-methide, phenolic and related triterpenoids of plants of Celastraceae: further evidence for the structure of Celastranhydride”, Phytochemistry, 29. 3189-3192. 1990.
 
[32]  Venkataramaiah, C. and Rajendra, W., “Phytochemical screening of bioactive compounds present in the seed of Celastrus paniculatus: Role in traditional medicine”, Indo American Journal of Pharmacology Research, 3. 9104-9112. 2013.
 
[33]  Wink, D. A., Hines, H. B., Cheng, R., Switzer, C. H., Flores‐Santana, W., Vitek, M. P., Ridnour, L. A. and Colton, C. A., “Nitric oxide and redox mechanisms in the immune response”, Journal of Leukocyte Biology, 89. 873-891. 2011.
 
[34]  Hetrick, E. M. and Schoenfisch, M. H., “Analytical chemistry of nitric oxide” Annual Review of Analytical Chemistry, 2. 409-433. 2009.
 
[35]  Zohera, F. T., Habib, M. R., Imam, M. Z., Mazumder, M. E. H. and Rana, M. S., “Comparative antioxidant potential of different extracts of Celastrus paniculatus wild Seed”, Stamford Journal of Pharmaceutical Sciences, 3. 68-74. 2010.
 
[36]  Lakhanpal, P. and Rai, D. K., “Quercetin: a versatile flavonoid”, Internet Journal of Medical Update, 2. 22-37. 2007.
 
[37]  Godkar, P. B., Gordon, R. K., Ravindran, A. and Doctor, B. P., “Celastrus paniculatus seed water soluble extracts protect against glutamate toxicity in neuronal cultures from rat forebrain”, Journal of Ethnopharmacology, 93. 213-219. 2004.
 
[38]  Imlay, J. A., “Cellular defenses against superoxide and hydrogen peroxide”, Annual Review of Biochemistry, 77. 755-776. 2008.
 
[39]  Kim, G. H., Kim, J. E., Rhie, S. J. and Yoon, S. “The role of oxidative stress in neurodegenerative diseases”, Experimental Neurobiology, 24. 325-340. 2015.
 
[40]  Dugan, L. L. and Choi, D. W., “Excitotoxicity, free radicals, and cell membrane changes”, Annals of Neurology, 35. S17-S21. 1994.
 
[41]  Ataseven, N., Yuzbaşioglu, D., Keskin, A. C. and Unal, F., “Genotoxicity of monosodium glutamate”, Food and Chemical Toxicology, 91. 8-18. 2016.
 
[42]  Kannan, K. and Jain, S. K., “Oxidative stress and apoptosis”, Pathophysiology, 7. 153-163. 2000.
 
[43]  Circu, M. L. and Aw, T. Y., “Reactive oxygen species, cellular redox systems and apoptosis”, Free Radical Biology & Medicine, 48. 749-762. 2010.
 
[44]  Liao, W., Mcnutt, M. A. and Zhu, W. G., “The comet assay: a sensitive method for detecting DNA damage in individual cells”, Methods, 48. 46-53. 2009.
 
[45]  Hartmann, A., Schumacher, M., Plappert‐Helbig, U., Lowe, P., Suter, W. and Mueller, L., “Use of the alkaline in vivo Comet assay for mechanistic genotoxicity investigations”, Mutagenesis, 19. 51-59. 2004.
 
[46]  Russo, A., Izzo, A. A., Cardile, V., Borrelli, F., and Vanella, A., “Indian medicinal plants as antiradicals and DNA cleavage protectors”, Phytomedicine, 8. 125-132. 2001.