EFFECTS OF KETAMINE AND OF HIGH PRESSURE ON THE RESPONSES TO γ‐AMINOBUTYRIC ACID OF THE RAT SUPERIOR CERVICAL GANGLION in vitro

1 The method of Brown & Marsh (1974) for recording of surface potentials from the rat superior cervical ganglion has been adapted for use in a high pressure chamber in order to study the effects of high pressure of helium and the possible interactions with the effects of general anaesthetics. 2 Helium pressure of 130 atm did not alter the amplitude of the responses recorded from the ganglion in response to γ‐aminobutyric acid (GABA) application (9.7 and 19.4 μm) but the amplitude of responses to a nicotinic agonist were depressed. 3 Ketamine, at concentrations between 18 and 180 μm, considerably potentiated the responses of the ganglion to GABA. 4 Helium pressure (130 atm) did not reverse the potentiation of GABA by ketamine. 5 The results are discussed in connection with the ability of ketamine to oppose the behavioural effects of high pressure.

[1]  H. Little,et al.  DRUGS THAT INCREASE γ‐AMINOBUTYRIC ACID TRANSMISSION PROTECT AGAINST THE HIGH PRESSURE NEUROLOGICAL SYNDROME , 1982, British journal of pharmacology.

[2]  D. Koblin,et al.  Brain monoamines and the high pressure neurological syndrome , 1980, Neuropharmacology.

[3]  L. Hertz,et al.  Ketamine-induced changes in the gaba system of mouse brain , 1980, Neuropharmacology.

[4]  J. Barker,et al.  Pentobarbital: stereospecific actions of (+) and (-) isomers revealed on cultured mammalian neurons. , 1980, Science.

[5]  R. W. Beaver,et al.  Stages in development of high-pressure neurological syndrome in the mouse. , 1979, Journal of applied physiology: respiratory, environmental and exercise physiology.

[6]  E. Eger,et al.  Nonlinear Antagonism of Anesthesia in Mice by Pressure , 1979, Anesthesia and analgesia.

[7]  J J Kendig,et al.  Pressure, temperature, and repetitive impulse generation in crustacean axons. , 1978, Journal of applied physiology: respiratory, environmental and exercise physiology.

[8]  C. Green,et al.  Pressure reversal of general anaesthesia--a multi-site expansion hypothesis. , 1978, British journal of anaesthesia.

[9]  K. Miller,et al.  Pressure resolves two sites of action of inert gases. , 1978, Molecular pharmacology.

[10]  K. Miller,et al.  The Pressure Reversal of a Variety of Anesthetic Agents in Mice , 1978, Anesthesiology.

[11]  M. Halsey,et al.  Possible protection against some of the physiological effects of high pressure [proceedings]. , 1977, The Journal of physiology.

[12]  K. Miller,et al.  The opposing physiological effects of high pressures and inert gases. , 1977, Federation proceedings.

[13]  M. Galvan,et al.  INFLUENCE OF NEUROGLIAL TRANSPORT ON THE ACTION OF γ‐AMINOBUTYRIC ACID ON MAMMALIAN GANGLION CELLS , 1977, British journal of pharmacology.

[14]  J. Trudell,et al.  A Unitary Theory of Anesthesia Based on Lateral Phase Separations in Nerve Membranes , 1977, Anesthesiology.

[15]  E. Eger,et al.  Pressure Antagonism of Barbiturate Anesthesia , 1976, Anesthesiology.

[16]  D. Gilbert,et al.  Slowing of ionic currents in the voltage-clamped squid axon by helium pressure , 1975, Nature.

[17]  J. Trudell,et al.  Effects of pressure and anesthetics on conduction and synaptic transmission. , 1975, The Journal of pharmacology and experimental therapeutics.

[18]  M. Halsey,et al.  Pressure reversal of narcosis produced by anaesthetics, narcotics and tranquillisers , 1975, Nature.

[19]  R. Campenot,et al.  The effects of high hydrostatic pressure on transmission at the crustacean neuromuscular junction. , 1975, Comparative biochemistry and physiology. B, Comparative biochemistry.

[20]  D. A. Brown,et al.  Actions of gamma‐aminobutyric acid on sympathetic ganglion cells. , 1975, The Journal of physiology.

[21]  D. A. Brown,et al.  A very simple method for recording ganglion depolarization. , 1975, The Journal of physiology.

[22]  M. Cohen,et al.  On the cerebral accumulation of ketamine and the relationship between metabolism of the drug and its pharmacological effects. , 1974, The Journal of pharmacology and experimental therapeutics.

[23]  D. Brown,et al.  DEPOLARIZING ACTIONS OF γ‐AMINOBUTYRIC ACID AND RELATED COMPOUNDS ON RAT SUPERIOR CERVICAL GANGLIA IN VITRO , 1974, British journal of pharmacology.

[24]  M. Cohen,et al.  Distribution in the Brain and Metabolism of Ketamine in the Rat after Intravenous Administration , 1973, Anesthesiology.

[25]  R. Nicoll The effects of anaesthetics on synaptic excitation and inhibition in the olfactory bulb , 1972, The Journal of physiology.

[26]  W. D. M. PATON,et al.  Pressure Reversal of Anaesthesia , 1971, Nature.

[27]  A. Macdonald,et al.  The effects of pressure on excitable cells , 1980 .

[28]  R. Mccall,et al.  Comparative physiology of the high-pressure neurological syndrome--compression rate effects. , 1979, Journal of applied physiology: respiratory, environmental and exercise physiology.

[29]  D. Gilbert,et al.  Helium pressure alteration of function in squid giant synapse. , 1977, Undersea biomedical research.