Exp Clin Endocrinol Diabetes 2013; 121(09): 535-538
DOI: 10.1055/s-0033-1349144
Short Communication
© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Low Fructose and Low Salt Diets Increase Mitochondrial DNA in White Blood Cells of Overweight Subjects

R. Hernández-Ríos
1   National Heart Institute, Mexico City
,
S. Hernández-Estrada
1   National Heart Institute, Mexico City
,
D. Cruz-Robles
1   National Heart Institute, Mexico City
,
S. Hernández-Lobato
1   National Heart Institute, Mexico City
,
M. Villalobos-Martín
1   National Heart Institute, Mexico City
,
R. J. Johnson
2   Renal diseases and Hypertension, University of Colorado, Aurora CO USA
,
F. Rodríguez-Castellanos
1   National Heart Institute, Mexico City
,
J. Salazar
1   National Heart Institute, Mexico City
,
F. García-Arroyo
1   National Heart Institute, Mexico City
,
L. G. Sánchez-Lozada
1   National Heart Institute, Mexico City
,
M. Madero
1   National Heart Institute, Mexico City
› Author Affiliations
Further Information

Publication History

received 08 March 2013
first decision 05 June 2013

accepted 19 June 2013

Publication Date:
09 August 2013 (online)

Abstract

Objective:

To evaluate the effect of sodium and fructose restriction on mitochondrial DNA (mtDNA) content and systemic oxidative stress in a sample of overweight and pre hypertensive subjects.

Material/Methods:

Data and blood samples were collected from 36 overweight and pre hypertensive patients randomly assigned to either an isocaloric (with respect to baseline) low sodium-fructose diet or an isocaloric low sodium diet. Patients were followed for 8 weeks. We measured mitochondrial DNA (mtDNA) content from peripheral blood white cells by Real-time PCR and plasma malondialdehyde (MDA) and 2,4-dinitrophenylhydrazine (DNPH) as markers of reactive oxigen species (ROS).

Results:

Compared to baseline, at week 8 there was a continued and significant increase in mtDNA in both the low sodium diet group [2.4 vs. 13.1 (relative copy number), p<0.05] and the low sodium diet-fructose group (1.9 vs. 147.2, p<0.05). By week 8 there was a continued decrease in plasma DNPH levels in the low sodium diet group (4.6 vs. 2.6, p<0.05) and in the low sodium diet-fructose group (5.8 vs. 2.2, p<0.05). No significant differences were found with MDA.

Conclusion:

Our studies suggest that simple dietary measures such as reducing salt with or without restricting fructose can increase mtDNA and improve markers of oxidative stress.

 
  • References

  • 1 Nisoli E, Clementi E, Carruba MO et al. Defective mitocondrial biogenesis: a hallmark of the high cardiovascular risk in the metabolic syndrome?. Circ Res 2007; 100: 795-806
  • 2 Kelley DE, He J, Menshikova EV et al. Dysfunction of mitochondria in human skeletal muscle in type 2 diabetes. Diabetes 2002; 51: 2944-2950
  • 3 Roberts CK, Sindhu KK. Oxidative stress and metabolic syndrome. Life Sci 2009; 84: 705-712
  • 4 Martínez JA. Mitochondrial oxidative stress and inflammation: an slalom to obesity and insulin resistance. Physiol Biochem 2006; 62: 303-306
  • 5 Puddu P, Puddu GM, Cravero E et al. The putative role of mitochondrial dysfunction in hypertension. Clin Exp Hypertens 2007; 29: 427-434
  • 6 Rachek LI, Grishko VI, Ledoux SP et al. Role of nitric oxide induced mtDNA damage in mitochondrial dysfunction and apoptosis. Free Radic Biol Med 2006; 40: 754-762
  • 7 Morino K, Petersen KF, Shulman GI. Molecular mechanisms of insulin resistance in humans and their potential links with mitochondrial dysfunction. Diabetes 2006; 55: S9-S15
  • 8 Park KS, Lee KU, Song JH et al. Decreased mitochondrial DNA content in peripheral blood precedes the development of non-insulin-dependent diabetes mellitus. Diabetes Res Clin Pract 1998; 42: 161-167
  • 9 Ritz P, Berrut G. Mitochondrial function, energy expenditure, aging and insulin resistance. Diabetes Metab 2005; 31: 5S67-5S73
  • 10 Marván L NutriKcal® VO Software
  • 11 Johnson RJ, Gower T, Gollub E. The Sugar Fix: The High-Fructose Fallout That Is Making You Fat and Sick. 2008;
  • 12 Lahiri DK, Nurnberger J. A rapid non-enzymatic method for the preparation of HMWDNA from blood for RFLP studies. Nucleic Acid Res 1991; 19: 5444
  • 13 Bai RK, Perng CL, Hsu CH et al. Quantitative PCR analysis of mitochondrial DNA content in patients with mitochondrial disease. Ann NY Acad Sci 2004; 1011: 304-309
  • 14 Gianotti TF, Sookoian S, Dieuzeide G et al. A decreased mitochondrial DNA content is related to insulin resistance in adolescents. Obesity 2008; 16: 1591-1595
  • 15 Morino K, Petersen KF, Dufour S et al. Reduced mitochondrial density and increased IRS-1 serine phosphorylation in muscle of insulin-resistant offspring of type 2 diabetic parents. J Clin Invest 2005; 115: 3587-3593
  • 16 Ritov VB, Menshikova EV, He J et al. Deficiency of subsarcolemmal mitochondria in obesity and type 2 diabetes. Diabetes 2005; 54: 8-14