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Inhibition by propofol (2,6 di‐isopropylphenol) of the N‐methyl‐D‐aspartate subtype of glutamate receptor in cultured hippocampal neurones

1995; Wiley; Volume: 116; Issue: 2 Linguagem: Inglês

10.1111/j.1476-5381.1995.tb16660.x

1476-5381

Beverley A. Orser, Maria Bertlik, Lu‐Yang Wang, John F. MacDonald,

Anesthesia and Sedative Agents

The effects of propofol (2,6 di‐isopropylphenol) on responses to the selective glutamate receptor agonists, N‐methyl‐D‐aspartate (NMDA) and kainate, were investigated in cultured hippocampal neurones of the mouse. Whole cell and single channel currents were recorded by patch‐clamp techniques. Drugs were applied with a multi‐barrel perfusion system Propofol produced a reversible, dose‐dependent inhibition of whole cell currents activated by NMDA. The concentration of propofol which induced 50% of the maximal inhibition (IC50) was approximately 160 μ m . The maximal inhibition was incomplete leaving a residual current of about 33% of the control response. This inhibitory action of propofol was neither voltage‐ nor use‐dependent Analysis of the dose‐response relation for whole cell NMDA‐activated currents indicated that propofol caused no significant change in the apparent affinity of the receptor for NMDA Outside‐out patch recordings of single channel currents evoked by NMDA (10 μ m ) revealed that propofol (100 HM) reversibly decreased the probability of channel opening but did not influence the average duration of channel opening or single channel conductance Whole‐cell currents evoked by kainate (50 μ M) were insensitive to propofol (1 μ m ‐1 mM) These results indicate that propofol inhibits the NMDA subtype of glutamate receptor, possibly through an allosteric modulation of channel gating rather than by blocking the open channel. Depression of NMDA‐mediated excitatory neurotransmission may contribute to the anaesthetic, amnesic and anticonvulsant properties of propofol.