Literature DB >> 2311696

Effects of ketamine on GABA-evoked excitability of peripheral nerve.

S Liske1, A Li, M E Morris.   

Abstract

The effects of the dissociative anaesthetic, ketamine on GABA-evoked changes in the excitability of myelinated fibers of dorsal and ventral roots of isolated bullfrog sciatic nerves were examined. Ketamine alone (0.01-1000 microM) evoked small increases (less than 5%) in dorsal root fiber excitability, as reflected in the half-maximal A-fiber compound action potential when concentrations were greater than 10 microM; with greater than or equal to 0.1 microM even larger increases (greater than or equal to 10%) were elicited in the ventral root fibers. As well, the increases evoked by greater than or equal to 10 microM ketamine were followed by graded decreases. 0.1 and 10 microM ketamine, concentrations which by themselves had small or no effect, produced a dose-dependent depression of the large increases in excitability which are induced by activation of GABA receptors. In the presence of ketamine GABA concentration-response curves of the dorsal root fibers showed depression of the maximal response, while those of the ventral root fibers were shifted to the right. This apparent antagonism of GABA responses by ketamine may arise from blockade of receptor-mediated effects (e.g. K+/Cl- currents and/or secondary depolarization from K+ accumulation), but could also be caused by a selective potentiation of hyperpolarizing receptors.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2311696     DOI: 10.1007/bf00228888

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  27 in total

1.  Effects of GABA, THIP, and potassium on excitability of myelinated axons of isolated amphibian spinal roots.

Authors:  S Liske; M E Morris
Journal:  Can J Physiol Pharmacol       Date:  1989-06       Impact factor: 2.273

2.  Pharmacological estimation of drug-receptor dissociation constants. Statistical evaluation. I. Agonists.

Authors:  R B Parker; D R Waud
Journal:  J Pharmacol Exp Ther       Date:  1971-04       Impact factor: 4.030

3.  General anesthetics hyperpolarize neurons in the vertebrate central nervous system.

Authors:  R A Nicoll; D V Madison
Journal:  Science       Date:  1982-09-10       Impact factor: 47.728

4.  Ketamine-induced changes in the GABA system of mouse brain.

Authors:  J D Wood; L Hertz
Journal:  Neuropharmacology       Date:  1980-08       Impact factor: 5.250

5.  Biphasic actions of pentobarbital on synaptic transmission.

Authors:  S H Roth; B H Bland; B M MacIver
Journal:  Prog Neuropsychopharmacol Biol Psychiatry       Date:  1983       Impact factor: 5.067

6.  Development of hyperpolarizing inhibitory postsynaptic potentials and hyperpolarizing response to gamma-aminobutyric acid in rabbit hippocampus studied in vitro.

Authors:  A L Mueller; J S Taube; P A Schwartzkroin
Journal:  J Neurosci       Date:  1984-03       Impact factor: 6.167

7.  Depolarizing action of GABA (gamma-aminobutyric acid) on myelinated fibers of peripheral nerves.

Authors:  M E Morris; G A Di Costanzo; S Fox; R Werman
Journal:  Brain Res       Date:  1983-11-14       Impact factor: 3.252

8.  Phencyclidine in low doses selectively blocks a presynaptic voltage-regulated potassium channel in rat brain.

Authors:  D K Bartschat; M P Blaustein
Journal:  Proc Natl Acad Sci U S A       Date:  1986-01       Impact factor: 11.205

9.  Comparison of the action of baclofen with gamma-aminobutyric acid on rat hippocampal pyramidal cells in vitro.

Authors:  N R Newberry; R A Nicoll
Journal:  J Physiol       Date:  1985-03       Impact factor: 5.182

10.  Discriminant effects of behaviorally active and inactive analogs of phencyclidine on membrane electrical excitability.

Authors:  L G Aguayo; H Weinstein; S Maayani; S D Glick; J E Warnick; E X Albuquerque
Journal:  J Pharmacol Exp Ther       Date:  1984-01       Impact factor: 4.030

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.