Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
Stroke. 1988;19:1383-1387

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
Right arrow Citation Map
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 Chopp, M.
Right arrow Articles by Helpern, J. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chopp, M.
Right arrow Articles by Helpern, J. A.

Stroke, Vol 19, 1383-1387, Copyright © 1988 by American Heart Association


ARTICLES

Global cerebral ischemia and intracellular pH during hyperglycemia and hypoglycemia in cats

M Chopp, KM Welch, CD Tidwell and JA Helpern
Department of Neurology, Henry Ford Hospital, Detroit, MI 48202.

In 27 cats treated to vary arterial serum glucose concentrations, we measured cerebral high-energy phosphate metabolite concentration and intracellular pH using in vivo phosphorus-31 nuclear magnetic resonance spectroscopy during transient global cerebral ischemia and reperfusion. Hypoglycemia was induced with 4 units/kg i.v. insulin in six cats before ischemia; hyperglycemia was induced with 1.5 g/kg i.v. glucose in six cats before and in six cats during ischemia. Nine untreated cats subjected to ischemia without manipulation of blood glucose concentration served as controls. During ischemia, intracellular pH fell to similar levels in the control and both hyperglycemic groups. During reperfusion, the hyperglycemic before ischemia group initially exhibited a severe further decline in intracellular pH (p less than 0.003); this further decline was not observed in the control or the hyperglycemic during ischemia groups. Intracellular acidosis was attenuated both during ischemia and early after reperfusion in the hypoglycemic before ischemia group. In all groups, cerebral high-energy phosphate metabolite concentrations were depleted during ischemia and then recovered to the same degree during reperfusion. Our data suggest that brain glucose stores before ischemia determine the severity and time course of intracellular acidosis during ischemia and reperfusion.


This article has been cited by other articles:


Home page
StrokeHome page
A. Martin, S. Rojas, A. Chamorro, C. Falcon, N. Bargallo, and A. M. Planas
Why Does Acute Hyperglycemia Worsen the Outcome of Transient Focal Cerebral Ischemia?: Role of Corticosteroids, Inflammation, and Protein O-Glycosylation
Stroke, May 1, 2006; 37(5): 1288 - 1295.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
B. A. Coert, R. E. Anderson, and F. B. Meyer
Is neuroprotective efficacy of nNOS inhibitor 7-NI dependent on ischemic intracellular pH?
Am J Physiol Heart Circ Physiol, January 1, 2003; 284(1): H151 - H159.
[Abstract] [Full Text] [PDF]


Home page
Ann. Thorac. Surg.Home page
B. P. Conroy, M. R. Grafe, L. W. Jenkins, A. H. Vela, C. Y. Lin, D. S. DeWitt, and W. E. Johnston
Histopathologic consequences of hyperglycemic cerebral ischemia during hypothermic cardiopulmonary bypass in pigs
Ann. Thorac. Surg., April 1, 2001; 71(4): 1325 - 1334.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
G. A. Ewy and J. P. Ornato
Emergency cardiac care: introduction
J. Am. Coll. Cardiol., March 15, 2000; 35(4): 825 - 880.
[Full Text] [PDF]


Home page
Physiol. Rev.Home page
P. Lipton
Ischemic Cell Death in Brain Neurons
Physiol Rev, October 1, 1999; 79(4): 1431 - 1568.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
N. Kawai, R. F. Keep, A. L. Betz, and W. D. Dietrich
Hyperglycemia and the Vascular Effects of Cerebral Ischemia
Stroke, January 1, 1997; 28(1): 149 - 154.
[Abstract] [Full Text]