Protein Information

ID 291
Name glycine receptors (protein family or complex)
Synonyms Glycine receptor; Glycine receptors

Compound Information

ID 336
Name strychnine
CAS strychnidin-10-one

Reference

PubMed Abstract RScore(About this table)
9622238 Kira T, Harata N, Sakata T, Akaike N: Kinetics of sevoflurane action on GABA- and glycine-induced currents in acutely dissociated rat hippocampal neurons. J Neurophysiol. 2009 Jun;101(6):3063-74. Epub 2009 Mar 25.
Effects of a new kind of volatile anaesthetics, sevoflurane, on GABA- and glycine-gated chloride current (ICl) were examined in single pyramidal neurons acutely dissociated from the rat hippocampal CA1 region, using the voltage-clamp mode of the nystatin-perforated patch-clamp technique. Rapid application of sevoflurane-induced ICl by itself, with the time to peak reduced as the sevoflurane concentration was increased from 10 (-3) to 3 x 10 (-3) M. Although a pretreatment with 10 (-3) M sevoflurane enhanced the peak amplitude of GABA (3 x 10 (-6) M)-induced ICl and suppressed the peak amplitude when the GABA concentration was increased to 10 (-4) M, the pretreatment decreased the time to peak of the ICl induced by any concentration of GABA (from 3 x 10 (-6) to 10 (-4) M). The treatment also accelerated the decay phase of the GABA-induced ICl. On the other hand, sevoflurane suppressed the peak ICl induced by 3 x 10 (-5) M glycine in a concentration-dependent manner. In the presence of 3 x 10 (-4) M sevoflurane, the peak amplitude of the glycine-induced ICl was decreased without changes in EC50 or Hill coefficients. Pretreatment with 10 (-3) M sevoflurane did not affect the time to peak of the ICl induced by any concentration of glycine (from 3 x 10 (-5) to 10 (-3) M). Pretreatment with 3 x 10 (-8) M strychnine markedly prolonged the time to peak of the glycine-induced ICl. These results suggest that sevoflurane modulated the amplitude of the GABA responses, depending on the balance of the accelerated activation and decay phases, and that sevoflurane suppressed the glycine-induced ICl in a non-competitive manner without noticeable effect on the kinetics. The reversible and differential modulation of GABA (A) and glycine receptors might underlie a part of the anaesthetic actions and less adverse clinical effects of sevoflurane.
1(0,0,0,1)