Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow E-Letters: Submit a response to the article
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (66)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by LODGE, D.
Right arrow Articles by ANIS, N. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by LODGE, D.
Right arrow Articles by ANIS, N. A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

British Journal of Anaesthesia, 1984, Vol. 56, No. 10 1143-1152
© 1984 The Board of Management and Trustees of the British Journal of Anaesthesia


research-article

EFFECTS OF KETAMINE AND THREE OTHER ANAESTHETICS ON SPINAL REFLEXES AND INHIBITIONS IN THE CAT

D. LODGE, B.V.SC, M.R.C.V.S., D.V.A., PH.D.1 and N. A. ANIS, B.V.SC, M.V.S.S.E., PH.D.

Department of Physiology, Royal Veterinary College Royal College Street, London NW1 0TU.

1Correspondence to D. L.

The effects of ketamine, alphaxalone/alphadolone, methohexitone and di-isopropylphenol have been compared on synaptic excitations and inhibitions in the spinal cord of decerebrate or pentobarbitone-anaesthetized cats. Ketamine selectively and reversibly decreased polysynaptic reflexes over a wide dose range. With the other three anaesthetic drugs decreases in reflex activity were accompanied by increases in the prolonged inhibition of reflexes, and in the amplitude and time course of dorsal root potentials. It was concluded that ketamine decreases synaptic transmission at terminals of excitatory interneurones, whereas the other three anaesthetics enhance synaptic inhibitions mediated by {gamma}-aminobutyric acid. Such specific effects of anaesthetics on particular synaptic processes do not support a unitary hypotheses of anaesthesia.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
C. T. Moritz, T. H. Lucas, S. I. Perlmutter, and E. E. Fetz
Forelimb Movements and Muscle Responses Evoked by Microstimulation of Cervical Spinal Cord in Sedated Monkeys
J Neurophysiol, January 1, 2007; 97(1): 110 - 120.
[Abstract] [Full Text] [PDF]


Home page
Br J AnaesthHome page
C. D. Richards
Anaesthetic modulation of synaptic transmission in the mammalian CNS
Br. J. Anaesth., July 1, 2002; 89(1): 79 - 90.
[Abstract] [Full Text] [PDF]


Home page
Br J AnaesthHome page
J. J. Kendig
In vitro networks: subcortical mechanisms of anaesthetic action
Br. J. Anaesth., July 1, 2002; 89(1): 91 - 101.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
R. Kalb
Regulation of motor neuron dendrite growth by NMDA receptor activation
Development, January 11, 1994; 120(11): 3063 - 3071.
[Abstract] [PDF]


Home page
ScienceHome page
R. Kalb and S Hockfield
Induction of a neuronal proteoglycan by the NMDA receptor in the developing spinal cord
Science, October 12, 1990; 250(4978): 294 - 296.
[Abstract] [PDF]


Home page
ScienceHome page
T Honore, S. Davies, J Drejer, E. Fletcher, P Jacobsen, D Lodge, and F. Nielsen
Quinoxalinediones: potent competitive non-NMDA glutamate receptor antagonists
Science, August 5, 1988; 241(4866): 701 - 703.
[Abstract] [PDF]


Home page
ScienceHome page
M. Majewska, N. Harrison, R. Schwartz, J. Barker, and S. Paul
Steroid hormone metabolites are barbiturate-like modulators of the GABA receptor
Science, May 23, 1986; 232(4753): 1004 - 1007.
[Abstract] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.