JN AJP: Lung Cellular and Molecular Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


J Neurophysiol (July 5, 2007). doi:10.1152/jn.00057.2007
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
98/3/1697    most recent
00057.2007v1
Right arrow Alert me when this article is cited
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 Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bengtsson, F.
Right arrow Articles by Jorntell, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bengtsson, F.
Right arrow Articles by Jorntell, H.
Submitted on January 17, 2007
Accepted on June 26, 2007

Ketamine and xylazine depress sensory-evoked parallel fiber and climbing fiber responses

Fredrik Bengtsson1 and Henrik Jorntell1*

1 Section for Neuroscience, Dept. Exp. Med. Sciences, Lund, Sweden

* To whom correspondence should be addressed. E-mail: henrik.jorntell{at}med.lu.se.

The last few years have seen an increase in the variety of in vivo experiments used for studying cerebellar physiological mechanisms. A combination of ketamine and xylazine has become a particularly popular form of anesthesia. However, because non-anesthetized control conditions is lacking in these experiments, so far there has been no evaluation of the effects of these drugs on the physiological activity in the cerebellar neuronal network. In the present study, we used the mossy fiber, parallel fiber and climbing fiber field potentials evoked in the non-anesthetized, decerebrated rat to serve as a control condition against which the effects of intravenous drug injections could be compared. All anesthetics were applied at doses required for normal maintenance of anesthesia. We found that ketamine substantially depressed the evoked N3 field potential, which is an indicator of the activity in the parallel fiber synapses, (-40%), and nearly completely abolished evoked climbing fiber field potentials (-90%). Xylazine severely depressed the N3 field (-75%) and completely abolished the climbing fiber field (-100%). In a combination which is commonly used for general anesthesia (20:1), ketamine+xylazine injections also severely depressed the N3 field (-75%) and nearly completely abolished the climbing fiber field (-90%). We also observed that lowered body and surface temperatures (below 34 degrees C) resulted in a substantial depression of the N3 field (-50%). These results urge for some caution in the interpretations of studies on cerebellar network physiology performed in animals anesthetized with these drugs.




This article has been cited by other articles:


Home page
J. Neurosci.Home page
L. Roggeri, B. Rivieccio, P. Rossi, and E. D'Angelo
Tactile Stimulation Evokes Long-Term Synaptic Plasticity in the Granular Layer of Cerebellum
J. Neurosci., June 18, 2008; 28(25): 6354 - 6359.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
W. Hevers, S. H. Hadley, H. Luddens, and J. Amin
Ketamine, But Not Phencyclidine, Selectively Modulates Cerebellar GABAA Receptors Containing {alpha}6 and {delta} Subunits
J. Neurosci., May 14, 2008; 28(20): 5383 - 5393.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 2007 by the The American Physiological Society.