Distributed Control of Muscle Glucose Uptake: A Tribute to the Late Dr. David H. Wasserman by Revisiting a 2004 <i>Diabetes</i> Classic by Fueger et al.

The control of muscle glucose uptake (MGU) is distributed across delivery, transport, and phosphorylation of glucose. These steps have been defined as control points of MGU in vivo due to the application of isotopic tracer techniques to transgenic mouse models. Using these techniques in a classic study published in Diabetes, Fueger et al. demonstrated that overexpression in skeletal muscle of hexokinase II (HKII), the enzyme responsible for intracellular glucose phosphorylation, enhanced MGU in insulin-sensitive but not in insulin-resistant mice. Conversely, HKII overexpression enhanced MGU in insulin-resistant mice in response to exercise. Since exercise reduces barriers of glucose delivery and transport, this suggested that these two processes contribute to the dysregulation of MGU in insulin-resistant states. These fundamental findings have spurred subsequent studies highlighting the contribution of glucose delivery and transport to the regulation of MGU in health and disease.

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Publication Details

Journal
Diabetes
Published
2025-10-20
DOI
https://doi.org/10.2337/dbi25-0022
Primary Topic
Adipose Tissue and Metabolism
Type
article
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article

Distributed Control of Muscle Glucose Uptake: A Tribute to the Late Dr. David H. Wasserman by Revisiting a 2004 Diabetes Classic by Fueger et al.

Julio E. Ayala
Diabetes
Adipose Tissue and Metabolism
article

Distributed Control of Muscle Glucose Uptake: A Tribute to the Late Dr. David H. Wasserman by Revisiting a 2004 Diabetes Classic by Fueger et al.

Julio E. Ayala
article en

Abstract

The control of muscle glucose uptake (MGU) is distributed across delivery, transport, and phosphorylation of glucose. These steps have been defined as control points of MGU in vivo due to the application of isotopic tracer techniques to transgenic mouse models. Using these techniques in a classic study published in Diabetes, Fueger et al. demonstrated that overexpression in skeletal muscle of hexokinase II (HKII), the enzyme responsible for intracellular glucose phosphorylation, enhanced MGU in insulin-sensitive but not in insulin-resistant mice. Conversely, HKII overexpression enhanced MGU in insulin-resistant mice in response to exercise. Since exercise reduces barriers of glucose delivery and transport, this suggested that these two processes contribute to the dysregulation of MGU in insulin-resistant states. These fundamental findings have spurred subsequent studies highlighting the contribution of glucose delivery and transport to the regulation of MGU in health and disease.

DiabetesVol. 74(11)
Vanderbilt University (US), Vanderbilt Health (US)
Openalex Percentile: Top 63%
Adipose Tissue and Metabolism
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