Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1979 Feb;65(2):339–345. doi: 10.1111/j.1476-5381.1979.tb07835.x

Depolarization of neurones in the isolated olfactory cortex of the guinea-pig by γ-aminobutyric acid

DA Brown, CN Scholfield
PMCID: PMC1668608  PMID: 216454

Abstract

1 Effects of γ-aminobutyric acid (GABA) on single neurones in slices of guinea-pig olfactory cortex maintained in vitro were recorded with single intracellular microelectrodes. The average resting potential of 52 cells was -75 mV and apparent input resistance ranged from 20 to 200 MΩ.

2 Superfusions of GABA over the slice invariably depolarized the neurones and reduced their input resistance. The minimum effective concentration was 50 to 200 μM.

3 The reversal potential for the depolarization produced by 0.1 mM GABA (Eg) was -66 ± 2 mV. At concentrations >0.1 mM the reversal potential became progressively more positive (-55 to -50 mV).

4 Reduction of external chloride, with isethionate as the substitute anion, increased the amplitude of the depolarization.

5 GABA reduced the amplitude of the excitatory postsynaptic potential produced by lateral olfactory tract stimulation, and occluded or reversed the subsequent depolarizing recurrent inhibitory postsynaptic potential.

6 Action potentials elicited by injection of depolarizing current or by focal antidromic stimulation were slowed and reduced in amplitude by GABA.

7 The effects of GABA on membrane conductance (potency = 1) were duplicated by 3-aminopropanesulphonic acid (potency = 20), β-alanine (0.5), β-amino-n-butyric acid (0.5), glycine (0.3) and L-2,4-diaminobutyric acid (0.2). For a given conductance change, 3-aminopropanesulphonic acid, glycine and β-alanine produced less depolarization than did GABA.

8 It is concluded that the action of GABA on the neurones is compatible with a role in mediating recurrent postsynaptic inhibition.

Full text

PDF
339

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Adams P. R., Brown D. A. Actions of gamma-aminobutyric acid on sympathetic ganglion cells. J Physiol. 1975 Aug;250(1):85–120. doi: 10.1113/jphysiol.1975.sp011044. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brown D. A., Galvan M. Influence of neuroglial transport on the action of gamma-aminobutyric acid on mammalian ganglion cells. Br J Pharmacol. 1977 Feb;59(2):373–378. doi: 10.1111/j.1476-5381.1977.tb07502.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Curtis D. R., Hösli L., Johnston G. A., Johnston I. H. The hyperpolarization of spinal motoneurones by glycine and related amino acids. Exp Brain Res. 1968;5(3):235–258. doi: 10.1007/BF00238666. [DOI] [PubMed] [Google Scholar]
  4. Deschenes M., Feltz P. GABA-induced rise of extracellular potassium in rat dorsal root ganglia: an electrophysiological study in vivo. Brain Res. 1976 Dec 24;118(3):494–499. doi: 10.1016/0006-8993(76)90319-x. [DOI] [PubMed] [Google Scholar]
  5. Deschenes M., Feltz P., Lamour Y. A model for an estimate in vivo of the ionic basis of presynaptic inhibition: an intracellular analysis of the GABA-induced depolarization in rat dorsal root ganglia. Brain Res. 1976 Dec 24;118(3):486–493. doi: 10.1016/0006-8993(76)90318-8. [DOI] [PubMed] [Google Scholar]
  6. Dreifuss J. J., Kelly J. S., Krnjević K. Cortical inhibition and gamma-aminobutyric acid. Exp Brain Res. 1969;9(2):137–154. doi: 10.1007/BF00238327. [DOI] [PubMed] [Google Scholar]
  7. Gallagher J. P., Higashi H., Nishi S. Characterization and ionic basis of GABA-induced depolarizations recorded in vitro from cat primary afferent neurones. J Physiol. 1978 Feb;275:263–282. doi: 10.1113/jphysiol.1978.sp012189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Ginsborg B. L., House C. R., Silinsky E. M. Conductance changes associated with the secretory potential in the cockroach salivary gland. J Physiol. 1974 Feb;236(3):723–731. doi: 10.1113/jphysiol.1974.sp010462. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Ginsborg B. L. Ion movements in junctional transmission. Pharmacol Rev. 1967 Sep;19(3):289–316. [PubMed] [Google Scholar]
  10. Harvey J. A., Scholfield C. N., Brown D. A. Evoked surface-positive potentials in isolated mammalian olfactory cortex. Brain Res. 1974 Aug 16;76(2):235–245. doi: 10.1016/0006-8993(74)90457-0. [DOI] [PubMed] [Google Scholar]
  11. Krnjević K., Puil E., Werman R. GABA and glycine actions on spinal motoneurons. Can J Physiol Pharmacol. 1977 Jun;55(3):658–669. doi: 10.1139/y77-090. [DOI] [PubMed] [Google Scholar]
  12. Legge K. F., Randic M., Straughan D. W. The pharmacology of neurones in the pyriform cortex. Br J Pharmacol Chemother. 1966 Jan;26(1):87–107. doi: 10.1111/j.1476-5381.1966.tb01814.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Obata K. Transmitter sensitivities of some nerve and muscle cells in culture. Brain Res. 1974 Jun 14;73(1):71–88. doi: 10.1016/0006-8993(74)91008-7. [DOI] [PubMed] [Google Scholar]
  14. Ransom B. R., Bullock P. N., Nelson P. G. Mouse spinal cord in cell culture. III. Neuronal chemosensitivity and its relationship to synaptic activity. J Neurophysiol. 1977 Sep;40(5):1163–1177. doi: 10.1152/jn.1977.40.5.1163. [DOI] [PubMed] [Google Scholar]
  15. Richards C. D., Sercombe R. Electrical activity observed in guinea-pig olfactory cortex maintained in vitro. J Physiol. 1968 Aug;197(3):667–683. doi: 10.1113/jphysiol.1968.sp008581. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Scholfield C. N. A barbiturate induced intensification of the inhibitory potential in slices of guinea-pig olfactory cortex. J Physiol. 1978 Feb;275:559–566. doi: 10.1113/jphysiol.1978.sp012208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Scholfield C. N. A depolarizing inhibitory potential in neurones of the olfactory cortex in vitro. J Physiol. 1978 Feb;275:547–557. doi: 10.1113/jphysiol.1978.sp012207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Scholfield C. N. Electrical properties of neurones in the olfactory cortex slice in vitro. J Physiol. 1978 Feb;275:535–546. doi: 10.1113/jphysiol.1978.sp012206. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Yamamoto C., Kawai N. Generation of the seizure discharge in thin sections from the guinea pig brain in chloride-free medium in vitro. Jpn J Physiol. 1968 Oct 15;18(5):620–631. doi: 10.2170/jjphysiol.18.620. [DOI] [PubMed] [Google Scholar]
  20. Yamamoto C., McIlwain H. Electrical activities in thin sections from the mammalian brain maintained in chemically-defined media in vitro. J Neurochem. 1966 Dec;13(12):1333–1343. doi: 10.1111/j.1471-4159.1966.tb04296.x. [DOI] [PubMed] [Google Scholar]

Articles from British Journal of Pharmacology are provided here courtesy of The British Pharmacological Society

RESOURCES