The anaesthetic action and modulation of GABA(A) receptor activity by the novel water-soluble aminosteroid Org 20599

C. Hill-Venning, J. A. Peters, H. Callachan, J. J. Lambert (Lead / Corresponding author), D. K. Gemmell, A. Anderson, A. Byford, N. Hamilton, D. R. Hill, R. J. Marshall, A. C. Campbell

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

The anaesthetic profile of a novel water-soluble aminosteroid, Org 20599 [(2β,3α,5α)-21-chloro-3-hydroxy-2-(4-morpholinyl)pregnan-20-one methanesulphonate], and the ability of the compound to allosterically regulate the activity of the GABA(A) receptor, have been studied in comparison to the properties of established intravenous general-anaesthetic agents. Intravenously administered Org 20599 produced a rapid onset, short duration loss of the righting reflex in mice. The anaesthetic potency of Org 20599 was comparable to that of the steroids 5α-pregnan-3α-ol-20-one or alphaxalone, and exceeded that of propofol, thiopentone or pentobarbitone. Org 20599 and the reference anaesthetic agents allosterically displaced the binding of [35S]-t-butylbicyclophosphorothionate (TBPS) from GABA(A) receptors of rat-brain membranes with the order of potency: 5α-pregnan-3α-ol-20-one > Org 20599 > alphaxalone > propofol > thiopentone > pentobarbitone. At human recombinant α1, β2, γ(2L) subunit-containing GABA(A) receptors expressed in Xenopus laevis oocytes, the anaesthetic agents produced a concentration-dependent and reversible potentiation of the peak amplitude of GABA-evoked currents. A similar positive allosteric action of Org 20599 was observed for the GABA(A) receptors expressed by bovine adrenal chromaffin cells maintained in culture. The rank order of potency in the aforementioned assays was identical to that determined from the displacement of TBPS binding. At concentrations greater than those required for potentiation of GABA, the anaesthetics exhibited GABA-mimetic effects with a rank order of potency that paralleled their modulatory activity. Such direct agonism varied greatly in maximal effect between compounds. The modulatory and direct agonist actions of Org 20599 were additionally confirmed utilizing rat hippocampal neurones in culture. The results indicate Org 20599 to be a potent and short-acting intravenous anaesthetic agent in mice and suggest positive allosteric regulation of GABA(A) receptor function to be a plausible molecular mechanism of action for the drug.

Original languageEnglish
Pages (from-to)1209-1222
Number of pages14
JournalNeuropharmacology
Volume35
Issue number9-10
DOIs
Publication statusPublished - 1996

Fingerprint

GABA-A Receptors
Anesthetics
Water
Intravenous Anesthetics
Thiopental
Propofol
Pentobarbital
gamma-Aminobutyric Acid
GABA Agents
Allosteric Regulation
Righting Reflex
21-chloro-3-hydroxy-2-(4-morpholinyl)pregnan-20-one
General Anesthetics
Chromaffin Cells
Aptitude
Xenopus laevis
Oocytes
Steroids
Neurons
Membranes

Keywords

  • Chromaffin cells
  • GABA(A) receptor
  • Hippocampal neurones
  • Human GABA(A) receptor subunits
  • Intravenous anaesthetic agents
  • Org 20599

Cite this

Hill-Venning, C. ; Peters, J. A. ; Callachan, H. ; Lambert, J. J. ; Gemmell, D. K. ; Anderson, A. ; Byford, A. ; Hamilton, N. ; Hill, D. R. ; Marshall, R. J. ; Campbell, A. C. / The anaesthetic action and modulation of GABA(A) receptor activity by the novel water-soluble aminosteroid Org 20599. In: Neuropharmacology. 1996 ; Vol. 35, No. 9-10. pp. 1209-1222.
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Hill-Venning, C, Peters, JA, Callachan, H, Lambert, JJ, Gemmell, DK, Anderson, A, Byford, A, Hamilton, N, Hill, DR, Marshall, RJ & Campbell, AC 1996, 'The anaesthetic action and modulation of GABA(A) receptor activity by the novel water-soluble aminosteroid Org 20599', Neuropharmacology, vol. 35, no. 9-10, pp. 1209-1222. https://doi.org/10.1016/S0028-3908(96)00069-X

The anaesthetic action and modulation of GABA(A) receptor activity by the novel water-soluble aminosteroid Org 20599. / Hill-Venning, C.; Peters, J. A.; Callachan, H.; Lambert, J. J. (Lead / Corresponding author); Gemmell, D. K.; Anderson, A.; Byford, A.; Hamilton, N.; Hill, D. R.; Marshall, R. J.; Campbell, A. C.

In: Neuropharmacology, Vol. 35, No. 9-10, 1996, p. 1209-1222.

Research output: Contribution to journalArticle

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T1 - The anaesthetic action and modulation of GABA(A) receptor activity by the novel water-soluble aminosteroid Org 20599

AU - Hill-Venning, C.

AU - Peters, J. A.

AU - Callachan, H.

AU - Lambert, J. J.

AU - Gemmell, D. K.

AU - Anderson, A.

AU - Byford, A.

AU - Hamilton, N.

AU - Hill, D. R.

AU - Marshall, R. J.

AU - Campbell, A. C.

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N2 - The anaesthetic profile of a novel water-soluble aminosteroid, Org 20599 [(2β,3α,5α)-21-chloro-3-hydroxy-2-(4-morpholinyl)pregnan-20-one methanesulphonate], and the ability of the compound to allosterically regulate the activity of the GABA(A) receptor, have been studied in comparison to the properties of established intravenous general-anaesthetic agents. Intravenously administered Org 20599 produced a rapid onset, short duration loss of the righting reflex in mice. The anaesthetic potency of Org 20599 was comparable to that of the steroids 5α-pregnan-3α-ol-20-one or alphaxalone, and exceeded that of propofol, thiopentone or pentobarbitone. Org 20599 and the reference anaesthetic agents allosterically displaced the binding of [35S]-t-butylbicyclophosphorothionate (TBPS) from GABA(A) receptors of rat-brain membranes with the order of potency: 5α-pregnan-3α-ol-20-one > Org 20599 > alphaxalone > propofol > thiopentone > pentobarbitone. At human recombinant α1, β2, γ(2L) subunit-containing GABA(A) receptors expressed in Xenopus laevis oocytes, the anaesthetic agents produced a concentration-dependent and reversible potentiation of the peak amplitude of GABA-evoked currents. A similar positive allosteric action of Org 20599 was observed for the GABA(A) receptors expressed by bovine adrenal chromaffin cells maintained in culture. The rank order of potency in the aforementioned assays was identical to that determined from the displacement of TBPS binding. At concentrations greater than those required for potentiation of GABA, the anaesthetics exhibited GABA-mimetic effects with a rank order of potency that paralleled their modulatory activity. Such direct agonism varied greatly in maximal effect between compounds. The modulatory and direct agonist actions of Org 20599 were additionally confirmed utilizing rat hippocampal neurones in culture. The results indicate Org 20599 to be a potent and short-acting intravenous anaesthetic agent in mice and suggest positive allosteric regulation of GABA(A) receptor function to be a plausible molecular mechanism of action for the drug.

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KW - Chromaffin cells

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