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Hypothalamic digoxin-mediated model for epileptogenesis

Published online by Cambridge University Press:  24 June 2014

Ravi Kumar Kurup
Affiliation:
Department of Medicine, Medical College Hospital, Trivandrum
Parameswara Achutha Kurup*
Affiliation:
Metabolic Disorders Research Center, Trivandrum, Kerala, India
*
Gouri Sadan, T.C.4/1525, North of Cliff House, Kattu Road, Kowdiar P.O.,Trivandrum, Kerala, India, Tel: 0471-541607; Fax: 91-0471-550782; E-mail: [email protected]

Abstract

Background/aims:

This study assessed the changes in the isoprenoid pathway and its metabolites in seizure disorder (ILAE classification – I generalized – idiopathic generalized epilepsy with age-related onset – epilepsy with generalized tonic clonic seizures on awakening) and the metabolic cascade produced by isoprenoid pathway dysregulation.

Methods:

The following parameters were assessed in seizure disorder: isoprenoid pathway metabolites, tyrosine and tryptophan catabolites, glycoconjugates metabolism and red blood cell (RBC) membrane composition.

Results:

There was elevation in plasma HMG-CoA reductase activity, serum digoxin and dolichol and a reduction in RBC membrane Na-K+ ATPase activity, serum magnesium and ubiquinone levels. Serum tryptophan, serotonin, strychnine, nicotine and quinolinic acid were elevated while tyrosine, dopamine, morphine and norepinephrine were decreased. The total serum glycosaminoglycans and glycosaminoglycan fractions (except dermatan sulfate), the activity of glycosaminoglycans (GAG) degrading enzymes and glycohydrolases, carbohydrate residues of glycoproteins and serum glycolipids were elevated. Total serum cholesterol, LDL cholesterol and free fatty acids were increased while HDL cholesterol and triglycerides were unaltered. The concentration of membrane hexose, fucose, cholesterol and phospholipids in the RBC membrane decreased significantly but the total RBC membrane GAG was unaltered.

Conclusions:

Epileptogenesis could be due to a dysfunctional isoprenoidal pathway and paroxysmal hypothalamic digoxin hypersecretion.

Type
Research Article
Copyright
Copyright © 2003 Blackwell Munksgaard

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References

Haupert, GT. Sodium pump regulation by endogenous inhibition. Curr Rop Member Transport 1989;34: 345349. CrossRefGoogle Scholar
Mikhailov, IB, Biull EskspR. Effect of strophanthin and digoxin on the activity of an experimental epileptogenic focus in the frog hippocampus. Biol Med 1987;104 :586588. Google ScholarPubMed
Rapport, RC, Harris, AB, Fried, PN. Human epileptic brain Na+-K+ ATPase content. Arch Neurol 1965;32: 549554. CrossRefGoogle Scholar
Hisaka, A, Kasamatu, S, Takenaga, N. Absorption of a novel prodrug of DOPA. Drug–Metabolism Disposal 1990;19: 621625. Google Scholar
Freese, A, Swartz, KJ, During, MJ, Martin, JB. Kynurenine pathway. Neurology 1990;40: 691695.CrossRefGoogle Scholar
Sheng, JG, Boop, FA, Mark, RE, Griffin, WS T. Increase neuronal beta amyloid precursor protein expression in human temporal lobe epilepsy association with interleukin-1 –alpha immunoreactivity. J Neurochem 1994; 63: 18721879.CrossRefGoogle ScholarPubMed
Hosford, DA, Caddick, SJ, Lin, FH. Generalised epilepsies: emerging insights into cellular and genetic mechanisms. Curr Opin Neurol 1997;10: 115120.CrossRefGoogle ScholarPubMed
Rao, AV, Ramakrishnan, S. Estimation of HMG CoA reductase activity. Clin Chem 1975;21: 15231528.CrossRefGoogle Scholar
Wallach, DFH, Kamath, VB. Assay for membrane Na+K+ ATPase activity. In: Colowick, SP, Kaplan, O, eds. Methods in Enzymology. New York: Academic Press, 1966: 164165. Google Scholar
Arun, P, Ravi Kumar, A, Leelamma, S, Kurup, PA. Identification and estimation of endogenous digoxin in biological fluids and tissues by TLC and HPLC. Indian J Biochem Biophys 1998;35: 308312.Google ScholarPubMed
Palmer, DN, Maureen, AA, Robert, DJ. Separation of some neutral lipids by normal phase high performance liquid chromatography on a cyanopropyl column: ubiquinone, dolichol and cholesterol levels in sheep liver. Anal Biochem 1984;140: 315319.CrossRefGoogle ScholarPubMed
The applications of atomic absorption analysis. In: Price, WJ, ed. Spectrochemical Analysis by Atomic Absorption. New York: John Wiley, 1985: 259263. Google Scholar
Ravikumar, A, Arun, P, Deepa Devi, KV, Kurup, PA. Tryptophan and tyrosine catabolic patterns in neuropsychiatric disorders. Neurol India 2000;3: 231238. Google Scholar
Arun, P, Ravi Kumar, A, Leelamma, S, Kurup, PA. Endogenous alkaloids in the brain of rats loaded with tyrosine/tryptophan and in the serum of patients of neurodegnerative and psychiatric disorders. Ind J Med Res 1998;107: 231238. Google Scholar
Manoj, AJ, Kurup, PA. Changes in the glycosaminoglycans and glycoproteins in the rat brain during protein calorie malnutrition. J Clin Biochem Nutr 1998;25: 149157. Google Scholar
Falholt, K, Lund, B, Falholt, W. Estimation of free fatty acids. Clin Chem Acta 1973;46: 105107. CrossRefGoogle Scholar
Zilversmiths, DB, Davis, AK. Estimation of phospholipids. J Laboratory Clin Med 1950;35: 100110. Google Scholar
Ravi Kumar, A, Augustine, J, Kurup, PA. Studies on digoxin –14C-acetate incorporation in to digoxin and degenerative changes in the brain in rats administered digoxin. Ind J Exp Biol 2001;22: 121132. Google Scholar
Haga, H. Effects of dietary magnesium supplementation on diurnal variation of B and plasma Na+-K+ ATPase activity in essential hypertension. Jpn Heart J 1992;33: 785798.CrossRefGoogle Scholar
Stefano, GB, Scharrer, B. Endogenous morphine and related opiates, a new class of chemical messengers. Adv Neuroimmunol 1994;4: 5769.CrossRefGoogle ScholarPubMed
Babb, TL, Pretorius, JK. Pathological substrates of epilepsy . In: Wyllie, E, ed. The Treatment of Epilepsy: Principles and Practice, 2nd edn. Baltimore: Williams & Wilkins, 1997: 106121. Google Scholar
Greenamyre, JT, Poter, RhP. Anatomy and physiology of glutamate in CNS. Neurology 1994;44: 713. Google ScholarPubMed
Ishimaru, M, Kurumaji, A, Toru, M. Increases in strychnine-insensitive glycine binding sites in cerebral cortex of chronic schizophrenics: evidence for glutamate hypothesis. Biol Psychiatry 1994; 35: 84.CrossRefGoogle ScholarPubMed
Jaya, P, Kurup, PA. Effect of magnesium deficiency on the metabolism of glycosaminoglycans in rats. J Bioscience 1986;10: 487497. CrossRefGoogle Scholar
Green, DR, Reed, JC. Mitochondria and apoptosis. Science 1998;281: 13091316.CrossRefGoogle ScholarPubMed
Finkel, Th. T-cell development and transmembrane signalling. Changing biological responses through a unchanging receptor. Immunol Today 1991;12: 7986.CrossRefGoogle ScholarPubMed
Feinmann, R, Sawyer, J, Hardin, J, Tricot, G. Cytogenetics and molecular genetics in multiple myeloma. Hematology – Oncol Clin N Am 1997;11: 121. CrossRefGoogle Scholar