Increased sarcolemmal glucose transporter, abundance in myocardial ischemia

Frank C. Brosius, Ngoc Nguyen, Silvia Egert, Zhiwu Lin, G. Michael Deeb, F. Haas, Markus Schwaiger, Daqing Sun

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

Abstract

Many clinical and laboratory studies suggest that an increase in glucose uptake and metabolism by ischemic myocardium helps protect myocardial cells from irreversible injury. We have examined whether increased sarcolemmal abundance of cardiomyocyte glucose transporters plays a role in this adaptive response. We have shown that acute myocardial ischemia in perfused rat hearts results in increased sarcolemmal abundance of the major glucose transporter, GLUT4, by causing translocation of GLUT4 molecules from an intracellular compartment to the sarcolemma. In nonischemic control hearts only 18 ± 2.8% of GLUT4 molecules were on the sarcolemma whereas in ischemic hearts this increased to 41 ± 9.3%. Insulin also caused translocation of GLUT4 molecules to the sarcolemma, and resulted in 61 ± 2.6% of GLUT4 molecules on the sarcolemma. The combination of ischemia and insulin did not result in additive increases in sarcolemmal GLUT4 abundance. In more persistent or chronic ischemia, the other major myocardial glucose transporter, GLUT1, appears to play an important role. The mRNA for this transporter, which is constitutively expressed on cardiomyocyte sarcolemma, was increased 2.0-fold in regions of hibernating myocardium in humans with coronary heart disease as well as in persistently hypoxic rat neonatal cardiomyocytes in primary culture. In neither of these conditions was GLUT4 mRNA expression increased. Thus, acute myocardial ischemia increases sarcolemmal glucose transporter abundance mainly by translocating previously synthesized GLUT4 molecules from an intracellular compartment, whereas more chronic ischemia also increases GLUT1 abundance via enhanced mRNA expression. Increased GLUT1 and GLUT4 abundance may participate in the augmented glucose uptake of ischemic myocardium and therefore may help protect ischemic myocardium from irreversible injury.

Original languageEnglish (US)
Pages (from-to)77A-84A
JournalAmerican Journal of Cardiology
Volume80
Issue number3 A
DOIs
StatePublished - Aug 4 1997
Externally publishedYes

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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