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PMID: 6496667 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Diabetes-induced alterations of glucose metabolism in rat cerebral microvessels.

The American journal of physiology ·Vol. 247 ·No. 4 Pt 1 ·1984-10-00 ·Pages E462-7

McCall AL, Gould JB, Ruderman NB

Abstract

The effect of diabetes on the metabolism of glucose and lactate was examined in isolated rat cerebral microvessels. In rats with diabetes induced with streptozotocin, glucose oxidation to CO2 by the microvessels was decreased by 54-83% and its conversion to lactate by 21-61%. Insulin therapy for several days or starvation for 48 h both lowered blood glucose levels in the diabetic rats and restored microvessel glucose metabolism to normal. Cerebral microvessels consist principally of the capillaries that constitute the blood-brain barrier. Direct assessment of the blood-brain barrier in vivo using the brain uptake index (BUI) technique revealed a close parallel to the findings in the microvessels. Thus, hexose transport was diminished in diabetic rats and restored to normal by both insulin therapy and starvation. The oxidation of [1-14C]lactate to CO2 like that of glucose was depressed in microvessels of diabetic rats. In contrast to glucose, however, the transport of lactate across the blood-brain barrier in vivo was not altered. These findings suggest that diabetes suppresses glucose metabolism in rat cerebral microvessels and downregulates glucose transport across the blood-brain barrier. They also suggest that both of these processes are regulated by chronic alterations in blood glucose concentration rather than by insulin per se.

MeSH Terms
Animals Biological Transport Blood Glucose/analysis Blood-Brain Barrier Capillaries/metabolism Cerebral Cortex/blood supply Diabetes Mellitus/blood Lactates/blood Male Rats Rats, Inbred Strains
Chemicals
Blood Glucose Lactates
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
McCall A L
Gould J B
Ruderman N B
Article Info
Journal
The American journal of physiology
Abbr.
Am J Physiol
ISSN
0002-9513
Published
1984-10-00
Pages
E462-7
Language
English
Region
United States
NLM ID
0370511
Subset
IM
Grants
NIADDK NIH HHS · AM-01006 · United States
NHLBI NIH HHS · HL-26895 · United States
NCRR NIH HHS · RR-05487 · United States
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