The effect of two lipophilic gamma-aminobutyric acid uptake blockers in CA1 of the rat hippocampal slice

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The effect of two lipophilic gamma-aminobutyric acid uptake blockers in CA1 of the rat hippocampal slice. / Rekling, J C; Jahnsen, H; Mosfeldt Laursen, A.

In: British Journal of Pharmacology, Vol. 99, No. 1, 1990, p. 103-6.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Rekling, JC, Jahnsen, H & Mosfeldt Laursen, A 1990, 'The effect of two lipophilic gamma-aminobutyric acid uptake blockers in CA1 of the rat hippocampal slice', British Journal of Pharmacology, vol. 99, no. 1, pp. 103-6.

APA

Rekling, J. C., Jahnsen, H., & Mosfeldt Laursen, A. (1990). The effect of two lipophilic gamma-aminobutyric acid uptake blockers in CA1 of the rat hippocampal slice. British Journal of Pharmacology, 99(1), 103-6.

Vancouver

Rekling JC, Jahnsen H, Mosfeldt Laursen A. The effect of two lipophilic gamma-aminobutyric acid uptake blockers in CA1 of the rat hippocampal slice. British Journal of Pharmacology. 1990;99(1):103-6.

Author

Rekling, J C ; Jahnsen, H ; Mosfeldt Laursen, A. / The effect of two lipophilic gamma-aminobutyric acid uptake blockers in CA1 of the rat hippocampal slice. In: British Journal of Pharmacology. 1990 ; Vol. 99, No. 1. pp. 103-6.

Bibtex

@article{041a80b0cdea11dd9473000ea68e967b,
title = "The effect of two lipophilic gamma-aminobutyric acid uptake blockers in CA1 of the rat hippocampal slice",
abstract = "1. Drugs that increase inhibitory synaptic transmission in the central nervous system may be valuable tools in the treatment of seizures. Theoretically, substances that block the uptake of inhibitory transmitters such as gamma-aminobutyric acid (GABA) into intracellular compartments should also increase inhibition and therefore have potential value as antiepileptic drugs. However, most of these substances penetrate the blood-brain barrier poorly and have therefore until now had limited value. NO-05-0328 and NO-05-0329 are two new lipophilic GABA uptake inhibitors that readily enter the CNS from the blood. 2. We have investigated the effect of these two uptake inhibitors on the responses to exogenous GABA and on GABA-mediated inhibitory synaptic potentials in pyramidal neurones of the CA1 region in the rat hippocampal slice. 3. We found that both drugs increased the amplitude and duration of responses to exogenous GABA. Furthermore, the inhibitory synaptic potentials increased in amplitude. This increase was seen in both early and late phases of the synaptic potentials. We conclude that NO-05-0328 and NO-05-0329, at least in vitro, are more effective than older GABA uptake inhibitors such as nipecotic acid and they therefore deserve consideration for clinical use.",
author = "Rekling, {J C} and H Jahnsen and {Mosfeldt Laursen}, A",
note = "Keywords: Animals; Dendrites; Electric Stimulation; Electrodes; Female; GABA Antagonists; Hippocampus; Iontophoresis; Male; Membrane Potentials; Nipecotic Acids; Rats",
year = "1990",
language = "English",
volume = "99",
pages = "103--6",
journal = "British Journal of Pharmacology",
issn = "0007-1188",
publisher = "Wiley",
number = "1",

}

RIS

TY - JOUR

T1 - The effect of two lipophilic gamma-aminobutyric acid uptake blockers in CA1 of the rat hippocampal slice

AU - Rekling, J C

AU - Jahnsen, H

AU - Mosfeldt Laursen, A

N1 - Keywords: Animals; Dendrites; Electric Stimulation; Electrodes; Female; GABA Antagonists; Hippocampus; Iontophoresis; Male; Membrane Potentials; Nipecotic Acids; Rats

PY - 1990

Y1 - 1990

N2 - 1. Drugs that increase inhibitory synaptic transmission in the central nervous system may be valuable tools in the treatment of seizures. Theoretically, substances that block the uptake of inhibitory transmitters such as gamma-aminobutyric acid (GABA) into intracellular compartments should also increase inhibition and therefore have potential value as antiepileptic drugs. However, most of these substances penetrate the blood-brain barrier poorly and have therefore until now had limited value. NO-05-0328 and NO-05-0329 are two new lipophilic GABA uptake inhibitors that readily enter the CNS from the blood. 2. We have investigated the effect of these two uptake inhibitors on the responses to exogenous GABA and on GABA-mediated inhibitory synaptic potentials in pyramidal neurones of the CA1 region in the rat hippocampal slice. 3. We found that both drugs increased the amplitude and duration of responses to exogenous GABA. Furthermore, the inhibitory synaptic potentials increased in amplitude. This increase was seen in both early and late phases of the synaptic potentials. We conclude that NO-05-0328 and NO-05-0329, at least in vitro, are more effective than older GABA uptake inhibitors such as nipecotic acid and they therefore deserve consideration for clinical use.

AB - 1. Drugs that increase inhibitory synaptic transmission in the central nervous system may be valuable tools in the treatment of seizures. Theoretically, substances that block the uptake of inhibitory transmitters such as gamma-aminobutyric acid (GABA) into intracellular compartments should also increase inhibition and therefore have potential value as antiepileptic drugs. However, most of these substances penetrate the blood-brain barrier poorly and have therefore until now had limited value. NO-05-0328 and NO-05-0329 are two new lipophilic GABA uptake inhibitors that readily enter the CNS from the blood. 2. We have investigated the effect of these two uptake inhibitors on the responses to exogenous GABA and on GABA-mediated inhibitory synaptic potentials in pyramidal neurones of the CA1 region in the rat hippocampal slice. 3. We found that both drugs increased the amplitude and duration of responses to exogenous GABA. Furthermore, the inhibitory synaptic potentials increased in amplitude. This increase was seen in both early and late phases of the synaptic potentials. We conclude that NO-05-0328 and NO-05-0329, at least in vitro, are more effective than older GABA uptake inhibitors such as nipecotic acid and they therefore deserve consideration for clinical use.

M3 - Journal article

C2 - 2331564

VL - 99

SP - 103

EP - 106

JO - British Journal of Pharmacology

JF - British Journal of Pharmacology

SN - 0007-1188

IS - 1

ER -

ID: 9256155