EVALUATION OF LIPOSOMAL GOSSYPIN IN ANIMAL MODELS OF EPILEPSY

Authors

  • Dheeraj Nagpal
  • Nidhi Agarwal
  • Deepshikha Katare Professor and Assistant Director, Amity Institute of Biotechnology, Amity University, Noida, Uttar Pradesh, India

Abstract

Objective: Epilepsy is a chronic neurological disorder affecting 1 % of the population worldwide. A number of studies have reported neuroprotective, anticonvulsant and anti-oxidant activity of gossipin a bioflavonoid isolated from Hibiscus vitifolius. The present study was carried out to evaluate the acute effects of liposome entrapped gossypin on Increasing Current electroshock seizures (ICES) test; Pentylenetetrazole (PTZ) induced seizures and status epilepticus in mice.

Methods: Gossypin liposomes were prepared by film hydration technique, and the effect of liposomal Gossypin formulations was studied in two doses i.e. 2.5 mg/kg and 5 mg/kg given per oral on ICES test and PTZ induced seizures in mice. Same doses of the formulation were administered by intravenous route during PTZ induces status epilepticus in mice.

Results: The results indicated that liposome entrapped Gossypin in doses 2.5 mg/Kg and 5 mg/Kg demonstrated significant increase in seizure threshold and latency to generalized seizures in ICES test and PTZ induced seizures respectively. Oxidative stress parameters like malondialdehyde (MDA) and glutathione were estimated in brain tissues in mice. Increased levels of MDA and glutathione were reduced and liposomal Gossypin suppressed the progression of kindling in mice. These results suggest that liposomal Gossypin appears to possess protective activity against kindling in mice.

Conclusion: To conclude, the study supports that liposomal Gossypin offers protection against PTZ kindling in mice. Liposomal Gossypin administration significantly reduced the progression of kindling in mice therefore it could be a promising candidate to control both development of seizures and oxidative stress during epilepsy.

Keywords: Epilepsy, Gossypin, Liposomes, ICES and PTZ induced seizures, Status epilepticus

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References

Namara M. Drugs are effective in the therapy of the epilepsies. In: Goodman and Gillman’s The Pharmacological basis of therapeutics. New York: McGraw-Hill; 2001.

Maertns P, Dyken P, Graf W, Pippenger C, Chronister R, Shah A. Free radicals, anticonvulsants and the neuronal ceroid-lipofuscinoses. Am J Med Genet 1995;57:225-8.

Jesberger J, Richard J. Oxygen free radicals and brain dysfunction. Int J Neurosci 1991;57:1-17.

Bhakuni DS, Dhar ML, Dhar MM, Dhawan BN, Mehrotra BN. Screening of Indian plants for biological activity. Indian J Exp Biol 1969;6:232.

Babu BH, Jayram HN, Nair MG, Ajai KB, Padikkala J. Free radical scavenging, anti-tumor and anti-carcinogenic activity of gossypin. Exp Clin Cancer Res 2003;22:581-9.

Vidyasagar J, Srinivas M, Nagulu M, Venkatasam A, Udyakiran B, Krishna DR. Protein binding study of gossypin by equilibrium dialysis. Curr Trends Biotechnol Pharm 2008;2:396–401.

Ganapaty S, Chandrashekhar VM, Narsu ML. Evaluation of the anti-allergic activity of gossypin and suramin in mast cell mediated allergy model. Indian J Biochem Biophys 2010;2:90-5.

Venktesan T, Sorimuthu Pillai S. Anti-diabetic activity of gossypin a Penta hydroxyl flavone glucoside, in streptozotocin-induced experimental diabetes in rats. J Diabetes 2012;1:41-6.

Mad SR, Metukuri MR, Burugula L, Reddanna P, Krisna DR. Anti-inflammatory and anti-nociceptive activities of gossypin and procumbentin-cyclooxygenase-2 (COX-2) inhibition studies. Phytother Res 2009;6:874-8.

Chandrashekhar VM, Ganapaty S, Ramkishan A, Narsu ML. Neuroprotective activity of gossypin from Hibiscus vitifolius against cerebral ischemia in rats. Indian J Pharmacol 2013;45:575-80.

Rasilingam D, Duraisamy S, Subramania. Anticonvulsant activity of bioflavonoid gossypin. Bangladesh J Pharmacol 2009;4:51-4.

Xu X, Khan MA, Burgers DJ. A two stage reverse dialysis in-vitro dissolution testing method for passive targeted liposomes. Int J Pharm 2012;426:211-8.

Roozi B. AFM, ESFM, TEM and CLSM in liposomal characterization: a Comparative study. Int J Nanomed 2011;6:557-63.

Kitano Y, Usui C, Takasuna K, Hirohashi M, Nomura M. Increasing current electroshock seizure test: a new method for assessment of anti-and pro-convulsant activities of drugs in mice. J Pharmacol Toxicol Methods 1996;35:25-9.

Marwah R, Pal SN, Pillai KK. Effect of Fluoxetine on increasing current electro-shock (ICES) in mice. Indian J Pharmacol 1999;31:350-3.

Bharal N, Pillai KK, Vohra D. Effects of Sparfloxacin on CNS functions urinary hydroxyproline in mice. Pharmacol Res 2006;54:111-7.

Raines A, Henderson TR, Swinyard EA, Kenneth LD. Comparison of midazolam and diazepam by the intramuscular route for the control of seizures in a mouse model of status epilepticus. Epilepsia 1996;31:313-7.

Okhawa H, Ohishi N, Yagi K. Assay of lipid peroxides in animal tissue by thiobarbituric acid reaction. Anal Biochem 1979;95:351-8.

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

Ali A, Pillai KK, Jalees FA, Dua Y, Iqbal Z, Vohora D. Comparative efficacy of liposome entrapped amiloride and free Amiloride in an animal model of seizures and serum potassium in mice. Eur Neuropsychopharmacol 2007;17:227-9.

Loeb C, Bessio G, Mainardi P. Liposome-entrapped GABA inhibits Isoniazid induced epileptogenic activity in rats. Epilepsia 1986;27:98-102.

Mori N, Fukatsu T. Anticonvulsant effect of DN-1417, a derivative of thyrotropin-releasing hormone, and liposome entrapped DN-147, on amygdaloid kindled rats. Epilepsia 1992;33:994-1001.

Published

01-04-2016

How to Cite

Nagpal, D., N. Agarwal, and D. Katare. “EVALUATION OF LIPOSOMAL GOSSYPIN IN ANIMAL MODELS OF EPILEPSY”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 8, no. 4, Apr. 2016, pp. 247-51, https://mail.innovareacademics.in/journals/index.php/ijpps/article/view/8897.

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