Skip to main content
Log in

γ-Vinyl GABA: comparison of neurochemical and anticonvulsant effects in mice

  • Original Papers
  • Published:
Journal of Neural Transmission Aims and scope Submit manuscript

Summary

Biochemical and pharmacological effects ofγ-vinyl GABA (Vigabatrin®, GVG), an irreversible enzyme-activated inhibitor of 4-aminobutyrate: 2-oxoglutarate aminotransferase (EC 2.6.1.19; GABA-T), were measured in mice. This anticonvulsant produced a time- and dose-dependent elevation of the GABA, phenylalanine and lysine contents of cortical tissue and simultaneously decreased glutamate, aspartate and alanine levels. In addition, GVG caused a biphasic change in glutamine concentrations (a decline 1–4 hours after administration, followed 20 hours later by an increase). Moreover, we found a new, as yet unidentified amino acid in the brain eluting with the same retention time as α-aminoadipic acid from an HPLC cation-exchange column. The level of this novel chemical entity was greatly increased by GVG 20 hours after injection of the drug. At all tested intervals between 1 and 60 hours after injection, GVG was ineffective against maximal electroshock. The GABA-T inhibitor dose-dependently protected mice against isoniazid-induced seizures, simultaneously causing an increase in brain GABA concentrations. However, this apparent correlation applied only until 4 hours after treatment. To better define the anticonvulsant profile of GVG, groups of mice were treated, 1, 2, 4, and 24 hours prior to challenge with convulsant doses of strychnine, pentetrazole (PTZ), and picrotoxin, and brain amino acid levels, including brain concentrations of GVG, were measured. In all instances, the time dependency of the anticonvulsant effects of GVG and of increases in brain GABA levels differed. Amino acid concentrations in animals treated only with GVG were similar to those in animals given GVG and a chemical convulsant. GVG showed no selectivity for seizures produced by impairment of GABA-ergic neurotransmission. Although GVG is an effective GABA-T inhibitor, it apparently affects several other pyridoxal-phosphate-dependent cerebral enzymes and/or interacts with other neurotransmitter systems as well.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Benson JR, Hare PE (1975) o-Phthaldehyde: fluorogenic detection of primary amines in the picomole range. Comparison with fluorescamine and ninhydrin. Proc Natl Acad Sci USA 72: 619–622

    Google Scholar 

  • Bernasconi R, Maitre L, Martin P, Raschdorf F (1982) The use of inhibitors of GABA-transaminase for the determination of GABA turnover in mouse brain regions: an evaluation of aminooxyacetic acid and gabaculine. J Neurochem 38: 56–66

    Google Scholar 

  • Bernasconi R, Klein M, Martin P, Portet C, Maitre L, Jones RSG, Baltzer V, Schmutz M (1985) The specific protective effect of diazepam and valproate against isoniazid-induced seizures is not correlated with increased GABA levels. J Neural Transm 63: 169–189

    Google Scholar 

  • Bernasconi R, Jones RSG, Bittiger H, Olpe HR, Heid J, Martin P, Klein M, Loo P, Braunwalder A, Schmutz M (1986) Does pipecolic acid interact with the central GABA-ergic system? J Neural Transm 67: 175–189

    Google Scholar 

  • Chapman AG, Riley K, Evans MC, Meldrum BS (1982) Acute effects of sodium valproate andγ-vinyl GABA on regional amino acid metabolism in the rat brain: incorporation of 2-[14C]glucose into amino acids. Neurochem Res 7: 1089–1105

    Google Scholar 

  • Costa E, Guidotti A, Mao CC, Suria A (1975) New concepts on the mechanism of action of benzodiazepines. Life Sci 17: 167–187

    Google Scholar 

  • Enna SJ, Kendall DA, Browner M (1981) Differential effects ofγ-Vinyl GABA on chemically induced seizures. In: Morselli PL, Lloyd KG, Loescher W, Meldrum B, Reynolds EH (eds) Neurotransmitters, seizures and epilepsy, vol 1. Raven Press, New York, pp 107–115

    Google Scholar 

  • Fariello RG (1985) Biochemical approaches to seizure mechanisms: the GABA and glutamate systems. In: Porter RJ, Morselli P (eds) The epilepsies. Butterworth, London, pp 1–19

    Google Scholar 

  • Fonnum F, Fosse VM, Paulsen R (1986) The compartmentation and turnover of glutamate and GABA: a better understanding by the use of drugs. In: Boulton AA, Baker GB, Wood JD (eds) Neuromethods, vol. 3, amino acids. Humana Press, Clufton, New Jersey, pp 67–83

    Google Scholar 

  • Gale K (1986) Role of the substantia nigra in GABA-mediated anticonvulsant action. In: Delgado-Escueta AV, Ward AA, Woodbury DM, Porter RJ (eds) Basic mechanisms of the epilepsies. Molecular and cellular approaches. Raven Press, New York (Advances in Neurology, vol 44, pp 343–364)

    Google Scholar 

  • Gale K, Iadarola MJ (1980) Seizure protection and increased nerve terminal GABA: delayed effects of GABA transaminase inhibition. Science 208: 288–291

    Google Scholar 

  • Iadarola MJ, Gale K (1981) Cellular compartments of GABA in brain and their relationship to anticonvulsant activity. Mol Cell Biochem 39: 305–330

    Google Scholar 

  • Jung MJ, Lippert B, Metcalf BW, Bohlen P, Schechter PJ (1977)γ-Vinyl GABA (4-aminohex-5-enoic acid), a new selective irreversible inhibitor of GABA-T: effect on brain GABA metabolism in mice. J Neurochem 29: 797–802

    Google Scholar 

  • Jung MJ (1982) GABA-transaminase inhibitors and neuronal function. In: Bradford HF (ed) Neurotransmitter interaction and compartmentation. Plenum Press, New York, pp 329–344

    Google Scholar 

  • Kendall DA, Fox DA, Enna SJ (1981) Effects ofγ-Vinyl GABA on bicuculline-induced seizures. Neuropharmacology 20: 351–355

    Google Scholar 

  • Klein M (1985) Thesis, Strasbourg

  • Krall RL, Penry JK, Kuperberg HJ, Swinyard EA (1978) Antiepileptic drug development. II. Anticonvulsant drug screening. Epilepsia 19: 409–428

    Google Scholar 

  • Loiseau P, Hardenberg JP, Pestre M, Guyot M, Schechter PJ, Tell GP (1986) Doubleblind, placebo-controlled study of vigabatrin (γ-vinyl GABA) in drug-resistant epilepsy. Epilepsia 27: 115–120

    Google Scholar 

  • Meldrum BS, Balzano E, Gadea M, Naquet R (1970) Photic and drug-induced epilepsy in the baboon (Papio papio): the effects of isoniazid, thiosemicarbazide, pyridoxine and amino-oxyacetic acid. Electroencephalogr Clin Neurophysiol 29: 333–347

    Google Scholar 

  • Meldrum BS (1975) Epilepsy andγ-aminobutyric-acid-mediated inhibition. Int Rev Neurobiol 17: 1–35

    Google Scholar 

  • Meldrum B, Horton R (1978) Blockade of epileptic responses in the photosensitive baboon, Papio papio, by two irreversible inhibitors of GABA-transaminase,γ-Acetylenic GABA (4-amino-hex-5-ynoic acid) andγ-Vinyl GABA (4-amino-5-enoic acid). Psychopharmacology 59: 47–50

    Google Scholar 

  • Miller RG (1966) Simultaneous statistical inference. McGraw-Hill, New York, pp 143–153

    Google Scholar 

  • Palfreyman MG, Schechter PJ, Buckett WR, Tell GP, Koch-Weser J (1981) The pharmacology of GABA-transaminase inhibitors. Biochem Pharmacol 30: 817–824

    Google Scholar 

  • Perry TL, Kish SJ, Hansen S (1979)γ-Vinyl GABA: effects of chronic administration on the metabolism of GABA and other amino compounds in rat brain. J Neurochem 32: 1641–1645

    Google Scholar 

  • Schechter PJ, Tranier Y, Jung MJ, Boehlen P (1977) Audiogenic seizure protection by elevated brain GABA concentration in mice: effects ofγ-Acetylenic GABA andγ- Vinyl GABA, two irreversible GABA-T inhibitors. Eur J Pharmacol 45: 319–328

    Google Scholar 

  • Schechter PJ (1986) Vigabatrin. In: Meldrum BS, Porter RJ (eds) New anticonvulsant drugs. John Libbey, London, pp 265–275

    Google Scholar 

  • Schmid R, Karobath M (1977) Specific and sensitive method for the determination ofγ- aminobutyric acid using gas chromatography with electron-capture or mass fragmentographic detection. J Chromatogr 139: 101–109

    Google Scholar 

  • Straughan DV (1974) Convulsant drugs: amino acid antagonism and central inhibition. Neuropharmacology 13: 495–508

    Google Scholar 

  • Ticku MK, Rastogi SK (1986) Convulsant/anticonvulsant drugs and GABAergic transmission. In: Nistico G, Morselli PL, Lloyd KG, Fariello RG, Engel J (eds) Neurotransmitters, seizures and epilepsy, vol 3. Raven Press, New York, pp 163–177

    Google Scholar 

  • Winer BJ (1971) Statistical principles in experiment design. McGraw-Hill, New York, pp 201–204

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bernasconi, R., Klein, M., Martin, P. et al. γ-Vinyl GABA: comparison of neurochemical and anticonvulsant effects in mice. J. Neural Transmission 72, 213–233 (1988). https://doi.org/10.1007/BF01243421

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01243421

Keywords

Navigation