Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
This Article
Right arrow Full Text (PDF)
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
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Oren, R. E.
Right arrow Articles by Rubinstein, E. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Oren, R. E.
Right arrow Articles by Rubinstein, E. H.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Hazardous Substances DB
*KETAMINE HYDROCHLORIDE

Stroke, Vol 18, 441-444, Copyright © 1987 by American Heart Association


ARTICLES

Effect of ketamine on cerebral cortical blood flow and metabolism in rabbits

RE Oren, NA Rasool and EH Rubinstein

The effects of intravenous ketamine (1 mg/kg) on cerebral cortical blood flow and O2 uptake were evaluated in 13 anesthetized, ventilated rabbits. Blood flow was measured either directly (Group 1) or by the H2 clearance method (Group 2). In those animals of Groups 1 and 2 with normal control arterial pH (pHa), ketamine produced a significant increase in cerebral cortical blood flow of 18 and 34%, respectively, but had no effect on cerebral cortical O2 uptake. However, in rabbits with low control pHa, ketamine caused an increase in blood flow (30%) accompanied by a significant increase in O2 uptake (22%). Ketamine produced nonsignificant changes in mean arterial blood pressure and arterial blood gases, except for a significant reduction in pressure in animals with low pHa. It is concluded that ketamine is a cerebral vasodilator without cerebral metabolic effect when mean arterial blood pressure and arterial PCO2, PO2, and pH are held constant at physiologic levels. The vasodilator effect of ketamine is probably due to direct dilating action or activation of a cholinergic cerebral vasodilator system.


This article has been cited by other articles:


Home page
Canadian J. AnesthesiaHome page
G. J. Crystal, A. A. Metwally, and M. R. Salem
Isoflurane preserves central nervous system blood flow during intraoperative cardiac tamponade in dogs: [L'isoflurane maintient le debit sanguin du systeme nerveux central pendant une tamponnade pericardique peroperatoire chez des chiens]
Can J Anesth, December 1, 2004; 51(10): 1011 - 1017.
[Abstract] [Full Text] [PDF]


Home page
Anesth. Analg.Home page
H. Hou, O. Y. Grinberg, S. Taie, S. Leichtweis, M. Miyake, S. Grinberg, H. Xie, M. Csete, and H. M. Swartz
Electron Paramagnetic Resonance Assessment of Brain Tissue Oxygen Tension in Anesthetized Rats
Anesth. Analg., May 1, 2003; 96(5): 1467 - 1472.
[Abstract] [Full Text] [PDF]


Home page
Canadian J. AnesthesiaHome page
K. Engelhard, C. Werner, O. Mollenberg, and E. Kochs
S(+)-ketamine/propofol maintain dynamic cerebrovascular autoregulation in humans : [Une combinaison de S(+)ketamine et de propofol maintient l'autoregulation vasculaire cerebrale dynamique chez l'humain]
Can J Anesth, November 1, 2001; 48(10): 1034 - 1039.
[Abstract] [Full Text] [PDF]


Home page
ChestHome page
H. A. Werner
Status Asthmaticus in Children : A Review
Chest, June 1, 2001; 119(6): 1913 - 1929.
[Abstract] [Full Text] [PDF]