Characterization and Anti-stroke Activity of Stem Extract of Colebrookea oppositifolia Smith

Reference

• Guzik, A., Bushnell, C. (2017). Stroke Epidemiology and Risk Factor Management. Continuum. 23: 15-39.
   PubMedGoogle Scholar
• Kaur, J., Zhao, Z., Klein, G.M., Lo, E.H., Buchan, A.M. (2004). The neurotoxicity of tissue plasminogen activator? J. Cereb. Blood Flow Metab. 24(9): 945-963.
   PubMed Web of Science ®Google Scholar
• Mahendran, G., Thamotharan, G., Sengottuvelu, S., Bai, V.N. (2014). Evaluation of anticonvulsant, sedative, anxiolytic, and phytochemical profile of the methanol extract from the aerial parts of Swertia corymbosa (Griseb.) wight ex CB Clarke. BioMed Research International. Article ID 542385.
   Google Scholar
• Anaeigoudari, A., Hosseini, M., Karami, R., Vafaee, F., Mohammadpour, T., Ghorbani, A., Sadeghnia, H.R. (2016). The effects of different fractions of Coriandrum sativum on pentylenetetrazole-induced seizures and brain tissues oxidative damage in rats. Avicenna J. Phytomed. 6(2): 223-235.
   PubMed Web of Science ®Google Scholar
• Karami, R., Hosseini, M., Mohammadpour, T., Ghorbani, A., Sadeghnia, H.R., Rakhshandeh, H., Esmaeilizadeh, M. (2015). Effects of hydroalcoholic extract of Coriandrum sativum on oxidative damage in pentylenetetrazole-induced seizures in rats. Iran J. Neurol. 14(2): 59-66.
   PubMed Web of Science ®Google Scholar
• Mora-Perez, A., Hernández-Medel, M.D.R. (2016). Anticonvulsant activity of methanolic extract from Kalanchoe pinnata (Lam.) stems and roots in mice: A comparison to diazepam. Neurología. 31(3): 161-168.
   PubMed Web of Science ®Google Scholar
• Parkash, O., Kumar, D., Kumar, S. (2015). Screening of methanol extract and ethyl acetate fraction of Abies webbiana Lindl. for neuropharmacological activities. Ind. J. Pharm. Sci. 77(5): 536-541.
   PubMed Web of Science ®Google Scholar
• Malami, S., Kyari, H., Danjuma, N.M., Ya’u, J., Hussaini, I.M. (2016). Anticonvulsant properties of methanol leaf extract of Laggera aurita Linn. F. (Asteraceae) in laboratory animals. J. Ethnopharmacol. 191: 301-306.
   PubMed Web of Science ®Google Scholar
• da Costa Júnior, J.S., de Almeida, A.A.C., da Rocha Tomé, A., Citó, A.M.D.G.L., Saffi, J., de Freitas, R.M. (2011). Evaluation of possible antioxidant and anticonvulsant effects of the ethyl acetate fraction from Platonia insignis Mart (Bacuri) on epilepsy models. Epilepsy Behav. 22(4): 678-684.
   PubMed Web of Science ®Google Scholar
• Viswanatha, G.L., Venkataranganna, M.V., Prasad, N.B.L., Hanumanthappa, S. (2018). Chemical characterization and cerebroprotective effect of methanolic root extract of Colebrookea oppositifolia in rats. J. Ethnopharmacol. 223: 63-75.
   PubMed Web of Science ®Google Scholar
• Ali, I., Sharma, P., Suri, K.A., Satti, N.K., Dutt, P., Afrin, F., Khan, I.A. (2011). In vitro antifungal activities of amphotericin B in combination with acteoside, a phenylethanoid glycoside from Colebrookea oppositifolia. J. Med. Microbiol. 60(9): 1326-1336.
   PubMed Web of Science ®Google Scholar
• Panda, S.K., Padhi, L., Leyssen, P., Liu, M., Neyts, J., Luyten, W. (2017). Antimicrobial, anthelmintic, and antiviral activity of plants traditionally used for treating infectious disease in the similipal biosphere reserve, Odisha, India. Front. Pharmacol. 8: 658.
   PubMed Web of Science ®Google Scholar
• Gupta, R.S., Yadav, R.K., Dixit, V.P., Dobhal, M.P. (2001). Antifertility studies of Colebrookia oppositifolia leaf extract in male rats with special reference to testicular cell population dynamics. Fitoterapia. 72(3): 236-245.
   PubMed Web of Science ®Google Scholar
• Riaz, T., Abbasi, M., Shahzadi, T., Rehman, A., Siddiqui, S., Ajaib, M. (2001). Colebrookia oppositifolia: A valuable source for natural antioxidants. J. Med. Plants Res. 5: 4180-4187.
   Google Scholar
• Pallab, K., Kush, B., Kumar, P., Girraj, T., Kishor, T., Singh, N., Kumar, S., Shivani, G. (2011). In vitro-in vivo evaluation of cardioprotective effect of the leaf extract of Colebrookea oppositifolia Sm. J. Global Trend Pharm. Sci. 2: 310-324.
   Google Scholar
• Ghaisas, M.M., Sharma, S., Ganu, G.P., Limaye, R.P. (2010). Antiulcer Activity of Colebrookea oppositifolia Sm. Res. J. Pharmacol. Pharmacodyn. 2(1): 66-70.
   Google Scholar
• Viswanatha, G.L., Venkataranganna, M.V., Prasad, N.B.L. (2017). Ameliorative potential of Colebrookea oppositifolia methanolic root extract against experimental models of epilepsy: Possible role of GABA mediated mechanism. Biomed. Pharmacother. 90: 455-465.
   PubMed Web of Science ®Google Scholar
• Viswanatha, G.L., Sowmya, G.P., Shylaja, H., Yogananda, M. (2020). Methanolic Stem Extract of Colebrookea oppositifolia Attenuates Epilepsy in Experimental Animal Models: Possible Role of GABA Pathways. Journal of Biologically Active Substance from Nature 2(3) :44-58.
   Google Scholar
• Sharma, J., Gairola, S., Gaur, R.D., Painuli, R.M., Siddiqi, T.O. (2013). Ethnomedicinal plants used for treating epilepsy by indigenous communities of sub-Himalayan region of Uttarakhand, India. J. Ethnopharmacol. 150: 353-70.
   PubMed Web of Science ®Google Scholar
• Viswanatha, G.L., Venkataranganna, M.V., Prasad, N.B.L. (2019). Methanolic leaf extract of Punica granatum attenuates ischemia-reperfusion brain injury in Wistar rats: Potential antioxidant and anti-inflammatory mechanisms. Iran J. Basic Med. Sci. 22(2): 187-196.
   PubMed Web of Science ®Google Scholar
• Shah, Z.A., Gilani, R.A., Sharma, P., Vohora, S.B. (2005). Cerebroprotective effect of Korean ginseng tea against global and focal models of ischemia in rats. J. Ethnopharmacol. 101(1-3): 299-307.
   PubMed Web of Science ®Google Scholar
• Viswanatha, G.L., Kumar, L.M.S., Rafiq, M., Kavya, K.J., Thippeswamy, A.H., Yuvaraj, H.C., Ramakrishnan, S. (2015). LC-MS/MS profiling and neuroprotective effects of Mentat® against transient global ischemia and reperfusion-induced brain injury in rats. Nutrition. 31(7-8): 1008-1017.
   PubMed Web of Science ®Google Scholar
• Saraf, M.K., Prabhakar, S., Anand, A. (2010). Neuroprotective effect of Bacopa monniera on ischemia induced brain injury. Pharmacol. Biochem. Behav. 97(2): 192-197.
   PubMed Web of Science ®Google Scholar
• Mansoorali, K.P., Prakash, T., Kotresha, D., Prabhu, K., Rao, N.R. (2012). Cerebroprotective effect of Eclipta alba against global model of cerebral ischemia induced oxidative stress in rats. Phytomedicine. 19(12): 1108-16.
   PubMed Web of Science ®Google Scholar
• Itoh, J., Nabeshima, T., Kameyama, T. (1990). Utility of an elevated plus-maze for the evaluation of memory in mice: effects of nootropics, scopolamine and electroconvulsive shock Psychopharmacology. (Berl).
   Google Scholar
• Bederson, J.B., Pitts, L. H., Germano, S.M., Nishimura, M.C., Davis, R.L., Bartkowski, H.M. (1986). Evaluation of 2, 3, 5-triphenyltetrazolium chloride as a stain for detection and quantification of experimental cerebral infarction in rats. Stroke. 17(6): 1304-1308.
   PubMed Web of Science ®Google Scholar
• Buch, P., Patel, V., Ranpariya, V., Sheth, N., Parmar, S. (2012). Neuroprotective activity of Cymbopogon martinii against cerebral ischemia/reperfusion-induced oxidative stress in rats. J. Ethnopharmacol. 142(1): 35-40.
   PubMed Web of Science ®Google Scholar
• Claiborne, A. (1985). Handbook of methods for oxygen radical research. Florida: CRC Press, Boca Raton.
   Google Scholar
• Pi, J., Bai, Y., Zhang, Q., Wong, V., Floering, L.M., Daniel, K., Collins, S. (2007). Reactive oxygen species as a signal in glucose-stimulated insulin secretion. Diabetes. 56(7): 1783-91.
   PubMed Web of Science ®Google Scholar
• Wills, E. (1966). Mechanisms of lipid peroxide formation in animal tissues. Biochem. J. 99(3): 667-76.
   PubMed Web of Science ®Google Scholar
• Prabhakar, K.R., Veerapur, V.P., Parihar, K.V., Priyadarsini, K.I., Rao, B.S.S., Unnikrishnan, M.K. (2006). Evaluation and optimization of radioprotective activity of Coronopus didymus Linn. in gamma-irradiated mice. Int. J. Radiat. Biol. 82(8): 525-36.
   PubMed Web of Science ®Google Scholar
• Devendra, S.K., Mohd, T.S., Hemant, K., Singh., Ali, A., Verma, V.K. (2012). In vivo Hepatoprotective Potential of Nigella sativa Extract Against Rifampicin Induced Sub-chronic Hepatotoxicity and Altered Redox Status. Journal of Biologically Active Substance from Nature. 2(3): 167-177.
   Google Scholar
• Samapika, N., Anindita, M., Anuradha, M., Abhijit, D. (2017). Efficacious Naturally Occurring Anti-cerebral Ischaemia Extracts, Compounds and Formulations Data from Animal Models. Journal of Biologically Active Substance from Nature. 7(3): 178-199.
   Google Scholar
• Ainsworth, E.A., Gillespie, K.M. (2007). Estimation of total phenolic content and other oxidation substrates in plant tissues using Folin-Ciocalteu reagent. Nat. Protoc. 2(4): 875-7.
   PubMed Web of Science ®Google Scholar
• Tsuchiya, M., Sako, K., Yura, S., Yonemasu, Y. (1993). Local cerebral glucose utilisation following acute and chronic bilateral carotid artery ligation in Wistar rats: relation to changes in local cerebral blood flow. Exp. Brain Res. 95(1): 1-7.
   PubMed Web of Science ®Google Scholar
• Benedek, A., Móricz, K., Jurányi, Z., Gigler, G., Lévay, G., Hársing Jr, L.G., Albert, M. (2006). Use of TTC staining for the evaluation of tissue injury in the early phases of reperfusion after focal cerebral ischemia in rats. Brain Res. 1116(1): 159-65.
   PubMedGoogle Scholar
• Reglodi, D., Tamas, A., Lengvari, I. (2003). Examination of sensorimotor performance following middle cerebral artery occlusion in rats. Brain Res. Bull. 59(6): 459-66.
   PubMed Web of Science ®Google Scholar
• Rodrigues, F.T.S., de Sousa, C.N.S., Ximenes, N.C., Almeida, A.B., Cabral, L.M., Patrocínio, C.F.V., Vasconcelos, S.M.M. (2017). Effects of standard ethanolic extract from Erythrina velutina in acute cerebral ischemia in mice. Biomed. Pharmacother. 96: 1230-9.
   PubMed Web of Science ®Google Scholar
• Peng, X.M., Gao, L., Huo, S.X., Liu, X.M., Yan, M. (2015). The mechanism of memory enhancement of acteoside (verbascoside) in the senescent mouse model induced by a combination of d gal and AlCl3. Phytother. Res. 29(8): 1137-44.
   PubMed Web of Science ®Google Scholar
• Yuan, J., Ren, J., Wang, Y., He, X., Zhao, Y. (2016). Acteoside binds to caspase-3 and exerts neuroprotection in the rotenone rat model of Parkinson’s disease. PLoS One. 11(9): e0162696.
   PubMed Web of Science ®Google Scholar
• Viswanatha, G.L., Yogish Kumar, H., Venkataranganna, M.V., Prasad, N.B.L., Shylaja, H. (2019). Anticonvulsant Activity Guided Isolation of Acteoside from Methanolic Root Extracts of Colebrookea oppositifolia Smith. Journal of Biologically Active Substance from Nature. 9(5): 328-334.
   Google Scholar
• Viswanatha, G.L., Mohan, C.G., Shylaja, H., Yuvaraj, H.C., Sunil, V. (2013). Anticonvulsant activity of 1, 2, 3, 4, 6-penta-O-galloyl-β-D-glucopyranose isolated from leaves of Mangifera indica. Naunyn Schmiedebergs Arch Pharmacol. 386(7): 599-604.
   PubMed Web of Science ®Google Scholar
• Rivera, F., Costa, G., Abin, A., Urbanavicius, J., Arruti, C., Casanova, G., Dajas, F. (2008). Reduction of ischemic brain damage and increase of glutathione by a liposomal preparation of quercetin in permanent focal ischemia in rats. Neurotox Res. 13(2): 105-14.
   PubMed Web of Science ®Google Scholar
• Viswanatha, G.L., Venkataranganna, M.V., Prasad, N.B.L., Shylaja, H. (2019). Achyranthes aspera Linn. alleviates cerebral ischemia-reperfusion-induced neurocognitive, biochemical, morphological and histological alterations in Wistar rats. J. Ethnopharmacol. 228: 58-69.
   PubMed Web of Science ®Google Scholar