Abstract
Intracellular recordings were made from reticulo-spinal cells in the medulla of lamprey ammocoetes; potential changes in response to iontophoretically applied L-glutamate were measured before, during and after the preparation was superfused with anaesthetic solutions. Of the anaesthetics pentobarbitone, ketamine, alphaxalone/alphadolone (Saffan) and metomidate, only pentobarbitone (greater than 10 microM) had a consistent dose-related depressant effect on glutamate responses. Spontaneous excitatory postsynaptic potentials (e.p.s.ps) and inhibitory postsynaptic potentials (i.p.s.ps) were diminished in frequency by high concentrations (1 mM) of all anaesthetics. Anaesthetic concentrations of all drugs also reduced i.p.s.ps; for e.p.s.ps this was true of pentobarbitone (100 microM) immediately, and of ketamine (370 microM) and alphaxalone (10-30 microM) after a transitory increase in activity. Consideration of the results in the light of previous observations on inhibitory responses suggests a basis for some of the excitatory side effects of these compounds, assuming that the equivalent mammalian cells are similarly affected.
Full text
PDF







Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Andersen P., Dingledine R., Gjerstad L., Langmoen I. A., Laursen A. M. Two different responses of hippocampal pyramidal cells to application of gamma-amino butyric acid. J Physiol. 1980 Aug;305:279–296. doi: 10.1113/jphysiol.1980.sp013363. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Anis N. A., Berry S. C., Burton N. R., Lodge D. The dissociative anaesthetics, ketamine and phencyclidine, selectively reduce excitation of central mammalian neurones by N-methyl-aspartate. Br J Pharmacol. 1983 Jun;79(2):565–575. doi: 10.1111/j.1476-5381.1983.tb11031.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ault B., Evans R. H., Francis A. A., Oakes D. J., Watkins J. C. Selective depression of excitatory amino acid induced depolarizations by magnesium ions in isolated spinal cord preparations. J Physiol. 1980 Oct;307:413–428. doi: 10.1113/jphysiol.1980.sp013443. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Barker J. L., Ransom B. R. Pentobarbitone pharmacology of mammalian central neurones grown in tissue culture. J Physiol. 1978 Jul;280:355–372. doi: 10.1113/jphysiol.1978.sp012388. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Buchanan J. T., Cohen A. H. Activities of identified interneurons, motoneurons, and muscle fibers during fictive swimming in the lamprey and effects of reticulospinal and dorsal cell stimulation. J Neurophysiol. 1982 May;47(5):948–960. doi: 10.1152/jn.1982.47.5.948. [DOI] [PubMed] [Google Scholar]
- Buchanan J. T. Identification of interneurons with contralateral, caudal axons in the lamprey spinal cord: synaptic interactions and morphology. J Neurophysiol. 1982 May;47(5):961–975. doi: 10.1152/jn.1982.47.5.961. [DOI] [PubMed] [Google Scholar]
- Crawford J. M., Curtis D. R. Pharmacological studies on feline Betz cells. J Physiol. 1966 Sep;186(1):121–138. doi: 10.1113/jphysiol.1966.sp008024. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cullen K. D., Martin R. J. Dissimilar influences of some injectable anaesthetics on the responses of reticulo-spinal neurones to inhibitory transmitters in the lamprey. Br J Pharmacol. 1982 Nov;77(3):493–504. doi: 10.1111/j.1476-5381.1982.tb09323.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Evans R. H., Watkins J. C. Specific antagonism of excitant amino acids in the isolated spinal cord of the neonatal rat. Eur J Pharmacol. 1978 Jul 15;50(2):123–129. doi: 10.1016/0014-2999(78)90007-9. [DOI] [PubMed] [Google Scholar]
- Gold M. R., Martin A. R. Characteristics of inhibitory post-synaptic currents in brain-stem neurones of the lamprey. J Physiol. 1983 Sep;342:85–98. doi: 10.1113/jphysiol.1983.sp014841. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson E. S., Roberts M. H., Straughan D. W. The responses of cortical neurones to monoamines under differing anaesthetic conditions. J Physiol. 1969 Aug;203(2):261–280. doi: 10.1113/jphysiol.1969.sp008863. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KRNJEVIC K., PHILLIS J. W. Iontophoretic studies of neurones in the mammalian cerebral cortex. J Physiol. 1963 Feb;165:274–304. doi: 10.1113/jphysiol.1963.sp007057. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Matthews G., Wickelgren W. O. Glutamate and synaptic excitation of reticulospinal neurones of lamprey. J Physiol. 1979 Aug;293:417–433. doi: 10.1113/jphysiol.1979.sp012897. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nicoll R. A., Wojtowicz J. M. The effects of pentobarbital and related compounds on frog motoneurons. Brain Res. 1980 Jun 2;191(1):225–237. doi: 10.1016/0006-8993(80)90325-x. [DOI] [PubMed] [Google Scholar]
- Richards C. D., Smaje J. C. Anaesthetics depress the sensitivity of cortical neurones to L-glutamate. Br J Pharmacol. 1976 Nov;58(3):347–357. [PMC free article] [PubMed] [Google Scholar]
- Scholfield C. N. Potentiation of inhibition by general anaesthetics in neurones of the olfactory cortex in vitro. Pflugers Arch. 1980 Feb;383(3):249–255. doi: 10.1007/BF00587527. [DOI] [PubMed] [Google Scholar]
- Wickelgren W. O. Physiological and anatomical characteristics of reticulospinalneurones in lamprey. J Physiol. 1977 Aug;270(1):89–114. doi: 10.1113/jphysiol.1977.sp011940. [DOI] [PMC free article] [PubMed] [Google Scholar]
