Potential evaluation of central nervous system anti-depressant activity of Cleome rutidosperma in mice
Keywords:
CNS, anxiolytic, hole cross test, thiopental, motor neuron activityAbstract
Introduction: This investigation was carried out to analyze the central nervous system (CNS) depressant effect of the plant Cleome rutidosperma extract, after it was found to have been used by the local people in the Philippine for that purpose.
Methods: In this study presented below, the CNS depressant effects of the extract was evaluated in in vivo mice models; using the standard procedures of Open field, Hole cross and Thiopental sodium induced sleeping time tests.
Results: Using two test extracts at a concentration of 100 and 200 mg/kg, it was seen that the extracts showed significant (p< 0.01) dose dependent suppression of motor activity in both open field and hole cross test, 4.67 ± 0.68** and 3.00 ± 0.45**, respectively at 200 mg/kg. It also showed significant (p< 0.01) decrease in the time for the onset of sleep (5.00 ± 0.45 at 200 mg/kg); and an increase in sleeping duration (70.20 ± 0.66 at 200 mg/kg), when compared with the positive control Thiopental sodium.
Conclusion: Overall, the study demonstrates that the extracts used, showed promising CNS depressant effect. Further study needs to be carried out on the extract to isolate the active constituent, so that it can be assessed for therapeutic use.
References
Yadav, A.V., Kawale, L.A., and Nade, V.S. (2008). Effect of Morus alba L. (mulberry) leaves on anxiety in mice. Indian Journal of Pharmacology 40, 32-36.
Titov. N., Andrews. G., Kemp. A., and Robinson. E. (2010). Characteristics of adults with anxiety or depression treated at an internet clinic: comparison with a national survey and an outpatient clinic. PLOS ONE 5(5), e10885.
Katzung. B.G., Masters. S.B., and Trevor. A.J. (2009). Basic and Clinical Pharmacology, McGraw-Hill, New York, NY, USA, 11th edition.
Dhawan. K., Dhawan. S., and Chhabra. S. (2003). Attenuation of benzodiazepine dependence in mice by atri-substituted benzoflavone moiety of Passiflora incarnata Linneaus: a non-habit forming anxiolytic. Journal of Pharmacy & Pharmaceutical Sciences 6(2), 215–222.
Bose A., Saravanan V.S., Karunanidhi N., and Gupta J.K. (2004). Analgesic and locomotor activity of extracts of Cleome rutidosperma DC. Indian Journal of Pharmaceutical Sciences 66(6), 795-797.
Walker, C.I.B., Trevisan, G., Rossato, M.F., Franciscato, C., Pereira, M.E., Ferreira, J., and Manfron, M.P. (2008). Antinociceptive activity of Mirabilis jalapa in mice. Journal of Ethnopharmacology 120, 169-175.
Imam, M.Z., and Sumi, C.D. (2014). Evaluation of antinociceptive activity of Hydromethanol extract of Cyperus rotundus in mice. BMC Compl Alt Med 14, 83.
Gupta, B.D., Dandiya, P.C., and Gupta. M.L. (1971). A psychopharmacological analysis of behaviour in rats. The Japanese Journal of Pharmacology 21(3), 293–298.
Takagi. K., Watanabe. M., and Saito. H. (1971). Studies of the spontaneous movement of animals by the hole cross test; effect of 2-dimethyl-aminoethanol and its acyl esters on the central nervous system. The Japanese Journal of Pharmacology 21(6), 797–810.
Ferrini. R., Miragoli. G., Taccardi. B. (1974). Neuro-pharmacological studies on SB 5833, a new psychotherapeutic agent of the benzodiazepine class. Arzneim-Forsch (Drug Res) 24, 2029-2032.
Nyeem. M.A.B., Alam. M.A., Awal. M.A., Mostofa. M., Uddin. S.J., Islam. N., and Rouf. R. (2006). CNS depressant effect of the crude ethanolic extract of the flowering tops of Rosa damascena. Iranian Journal of Pharmacology and Therapy 5, 171-174.
Hasan. R.S.M., Hossain. M.M., Akter. R., Jamila. M., Mazumder. E.H.M., and Rahman. S. (2009). Sedative and anxiolytic effects of different fractions of the Commelina benghalensis Linn. Drug Discovery and Therapeutics 3, 221-227.
Squires. R.F., and Braestrup. C. (1977). Benzodiazepine receptors in rat brain. Nature 266, 732-734.
Trofimiuk. E., Walesiuk. A., and Braszko. J.J. (2005). St John's wort (Hyperium perforatum) diminishes cognitive impairment caused by the chronic restraint stress in rats. Pharmacol Res 51, 239-246.
Mansur. R.M., Martz. W., Carlini. E.A. (1980). Effect of acute and chronic administration of Cannabis satis and (-) 9-trans tetrahydro cannabinaol on the behaviour of rats in open field arena. Psychopharmacology 2, 5-7.
Rakotonirina. V.S., Bum. E.N., Rakotonirena. A., and Bopelet. M. (2001). Sedative properties of the decoction of the rhizome of Cyperus anticulatives. Fitoterapia 72, 22-29.
Ozturk. Y., Aydini. S., Beis. R., Baser. K.H.C., and Berberoglu. H. (1996). Effect of Hypericum pericum L. and Hypericum calycinum L. extracts on the central nervous system in mice. Phytomedicine 3, 139 - 146.
Briskin. D.P. (2000). Medicinal plants and phytomedicines - linking plant biochemistry and physiology to human health. Plant Physiol 124, 507 - 514.
Kaufman. P.B., Cseke. L.J., Warber. S., Duke. J.A., Brielmann. H.L. (1999). Natural Products from Plants. CRC Press, Boca Raton, FL, USA.
Marder. M., and Paladini. A.C. (2002). GABAA receptor ligands of flavonoid structure. Curr Top Med Chem 2, 853 - 867.
Johnston. G.A. (2005). GABAA receptor channel pharmacology. Curr Pharm Des 11, 1867 -1885.
Goutman. J.D., Waxemberg. M.D., Doñate-Oliver. F., Pomata. P.E., and Calvo. D.J. (2003). Flavonoid modulation of ionic currents mediated by GABA(A) and GABA(C) receptors. Eur J Pharmacol 461, 79 - 87.
Campbell. E.L., Chebib. M., and Johnston. G.A. (2004). The dietary flavonoids apigenin and (-)-epigallocatechin gallate enhance the positive modulation by diazepam of the activation by GABA of recombinant GABAA receptors. Biochem Pharmacol 68, 1631 - 1638.
Kavvadias. D., Sand. P., Youdim. K.A., Qaiser. M.Z., Evans. R.C., Baur. R.., Sigel. E., Rausch. W.D., Riederer. P., and Schreier. P. (2004). The flavone hispidulin, a benzodiazepine receptor ligand with positive allosteric properties, traverses the blood-brain barrier and exhibits anticonvulsive effects. Br J Pharmacol 142, 811 - 820.
Downloads
Published
Issue
Section
License
Copyright The Author(s) 2017. This article is published with open access by BioMedPress. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.