» Articles » PMID: 17093944

Impaired in Vivo Mitochondrial Function but Similar Intramyocellular Lipid Content in Patients with Type 2 Diabetes Mellitus and BMI-matched Control Subjects

Overview
Journal Diabetologia
Specialty Endocrinology
Date 2006 Nov 10
PMID 17093944
Citations 130
Authors
Affiliations
Soon will be listed here.
Abstract

Aims/hypothesis: Mitochondrial dysfunction and increased intramyocellular lipid (IMCL) content have both been implicated in the development of insulin resistance and type 2 diabetes mellitus, but the relative contributions of these two factors in the aetiology of diabetes are unknown. As obesity is an independent determinant of IMCL content, we examined mitochondrial function and IMCL content in overweight type 2 diabetes patients and BMI-matched normoglycaemic controls.

Methods: In 12 overweight type 2 diabetes patients and nine controls with similar BMI (29.4 +/- 1 and 29.3 +/- 0.9 kg/m(2) respectively) in vivo mitochondrial function was determined by measuring phosphocreatine recovery half-time (PCr half-time) immediately after exercise, using phosphorus-31 magnetic resonance spectroscopy. IMCL content was determined by proton magnetic resonance spectroscopic imaging and insulin sensitivity was measured with a hyperinsulinaemic-euglycaemic clamp.

Results: The PCr half-time was 45% longer in diabetic patients compared with controls (27.3 +/- 3.5 vs 18.7 +/- 0.9 s, p < 0.05), whereas IMCL content was similar (1.37 +/- 0.30 vs 1.25 +/- 0.22% of the water resonance), and insulin sensitivity was reduced in type 2 diabetes patients (26.0 +/- 2.2 vs 18.9 +/- 2.3 mumol min(-1) kg(-1), p < 0.05 [all mean +/- SEM]). PCr half-time correlated positively with fasting plasma glucose (r (2) = 0.42, p < 0.01) and HbA(1c) (r (2) = 0.48, p < 0.05) in diabetic patients.

Conclusions/interpretation: The finding that in vivo mitochondrial function is decreased in type 2 diabetes patients compared with controls whereas IMCL content is similar suggests that low mitochondrial function is more strongly associated with insulin resistance and type 2 diabetes than a high IMCL content per se. Whether low mitochondrial function is a cause or consequence of the disease remains to be investigated.

Citing Articles

Enhanced fatty acid oxidation in osteoprogenitor cells provides protection from high-fat diet induced bone dysfunction.

Nandy A, Helderman R, Thapa S, Peck S, Richards A, Jayapalan S J Bone Miner Res. 2024; 40(2):283-298.

PMID: 39657629 PMC: 11789392. DOI: 10.1093/jbmr/zjae195.


Effect of a Concurrent Training Program with and Without Metformin Treatment on Metabolic Markers and Cardiorespiratory Fitness in Individuals with Insulin Resistance: A Retrospective Analysis.

Azocar-Gallardo J, Ojeda-Aravena A, Baez-San Martin E, Herrera-Valenzuela T, Tuesta M, Gonzalez-Rojas L Biomolecules. 2024; 14(11).

PMID: 39595646 PMC: 11592327. DOI: 10.3390/biom14111470.


Development of a P magnetic resonance spectroscopy technique to quantify NADH and NAD at 3 T.

Mevenkamp J, Bruls Y, Mancilla R, Grevendonk L, Wildberger J, Brouwers K Nat Commun. 2024; 15(1):9159.

PMID: 39443469 PMC: 11499639. DOI: 10.1038/s41467-024-53292-4.


Role of Cardiorespiratory Fitness and Mitochondrial Oxidative Capacity in Reduced Walk Speed of Older Adults With Diabetes.

Ramos S, Distefano G, Lui L, Cawthon P, Kramer P, Sipula I Diabetes. 2024; 73(7):1048-1057.

PMID: 38551899 PMC: 11189829. DOI: 10.2337/db23-0827.


Parental cardiorespiratory fitness influences early life energetics and metabolic health.

Sadler D, Treas L, Ross T, Sikes J, Britton S, Koch L Physiol Genomics. 2023; 56(2):145-157.

PMID: 38009224 PMC: 11281807. DOI: 10.1152/physiolgenomics.00045.2023.


References
1.
Mattei J, Bendahan D, Cozzone P . P-31 magnetic resonance spectroscopy. A tool for diagnostic purposes and pathophysiological insights in muscle diseases. Reumatismo. 2004; 56(1):9-14. DOI: 10.4081/reumatismo.2004.9. View

2.
Sahlin K, Harris R, Hultman E . Resynthesis of creatine phosphate in human muscle after exercise in relation to intramuscular pH and availability of oxygen. Scand J Clin Lab Invest. 1979; 39(6):551-8. DOI: 10.3109/00365517909108833. View

3.
Taylor D, Crowe M, Bore P, Styles P, Arnold D, Radda G . Examination of the energetics of aging skeletal muscle using nuclear magnetic resonance. Gerontology. 1984; 30(1):2-7. DOI: 10.1159/000212599. View

4.
Stump C, Short K, Bigelow M, Schimke J, Nair K . Effect of insulin on human skeletal muscle mitochondrial ATP production, protein synthesis, and mRNA transcripts. Proc Natl Acad Sci U S A. 2003; 100(13):7996-8001. PMC: 164701. DOI: 10.1073/pnas.1332551100. View

5.
Larson-Meyer D, Newcomer B, Hunter G, Joanisse D, Weinsier R, Bamman M . Relation between in vivo and in vitro measurements of skeletal muscle oxidative metabolism. Muscle Nerve. 2001; 24(12):1665-76. DOI: 10.1002/mus.1202. View