Lactate disposal via gluconeogenesis is increased during exercise in patients with mitochondrial myopathy due to complex I deficiency

被引:11
|
作者
Roef, MJ
Kalhan, SC
Reijngoud, DJ
De Meer, K
Berger, R
机构
[1] Vrije Univ Amsterdam, Med Ctr, Dept Clin Chem, Recept K, NL-1007 MB Amsterdam, Netherlands
[2] Univ Utrecht, Childrens Hosp, Dept Pediat Gastroenterol, Utrecht, Netherlands
[3] Univ Utrecht, Childrens Hosp, Lab Metab Dis, Utrecht, Netherlands
[4] Case Western Reserve Univ, Sch Med, Robert Schwartz MD Ctr Metab & Nutr, Metrohlth Med Ctr, Cleveland, OH 44109 USA
[5] Univ Groningen Hosp, Lab Metab Dis, Dept Pediat, Groningen, Netherlands
关键词
D O I
10.1203/00006450-200205000-00008
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
This study evaluated lactate disposal via gluconeogenesis as well as effects of FFA availability on gluconeogenesis via pyruvate (GNG(PYR)) in patients with mitochondrial myopathy due to complex I deficiency (CID). The rates of GNG(PYR) were measured in three CID patients and six healthy controls at rest and during 90 min cycle exercise, using the deuterium-labeled water method. All subjects served as their own control: on one occasion they were studied in the fasting state, and on the second occasion they received an infusion of triacylglycerol plus heparin, At rest. the fractional rate of gluconeogenesis from pyruvate was higher in patients than in controls in the fasting state. Triacylglycerol infusion was associated with increased rates of GNG(PYR) at rest in controls (p < 0.05) but not in patients. Circulating lactate and pyruvate levels were increased 3-fold during exercise in the CID patients. During exercise, GNG(PYR) increased in the CID patients (p < 0.01) and remained unchanged in controls, resulting in 85% and 72% higher absolute rates of GNG(PYR) in the patients than in the controls during fasting and triacylglycerol infusion. respeclively. During exercise. rates of GNG(PYR) were not different between fasting and triacylglycerol infusion within both groups. Our data shock that 1) GNG(PYR) is increased during exercise in CID patients 2) increased pyruvate availability contributes to the higher rates of GNG(PYR) in the CID patients: and 3) exogenous infusion of fatty acids is not associated with increased rates of GNG(PYR) in CID patients at rest or during exercise. GNG(PYR) is a significant mechanism of lactate disposal in exercising CID patients. but triglyceride infusion does not enhance their lactate disposal through this mechanism.
引用
收藏
页码:592 / 597
页数:6
相关论文
共 50 条
  • [1] Lactate Disposal via Gluconeogenesis Is Increased During Exercise in Patients with Mitochondrial Myopathy Due to Complex I Deficiency
    Mark J Roef
    Satish C Kalhan
    Dirk-Jan Reijngoud
    Kees De Meer
    Ruud Berger
    Pediatric Research, 2002, 51 : 592 - 597
  • [2] Triacylglycerol infusion improves exercise endurance in patients with mitochondrial myopathy due to complex I deficiency
    Roef, MJ
    de Meer, K
    Reijngoud, DJ
    Straver, HWHC
    de Barse, M
    Kalhan, SC
    Berger, R
    AMERICAN JOURNAL OF CLINICAL NUTRITION, 2002, 75 (02): : 237 - 244
  • [3] Lactate metabolism during exercise in patients with mitochondrial myopathy
    Jeppesen, Tina D.
    Orngreen, Mette C.
    Van Hall, Gerrit
    Vissing, John
    NEUROMUSCULAR DISORDERS, 2013, 23 (08) : 629 - 636
  • [4] MITOCHONDRIAL MYOPATHY DUE TO COMPLEX-I DEFICIENCY - SECONDARY CHANGES
    BUSCH, HFM
    SCHOLTE, HR
    LUYTHOUWEN, IEM
    ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1986, 488 : 523 - 524
  • [5] Triacylglycerol infusion does not improve hyperlactemia in resting patients with mitochondrial myopathy due to complex I deficiency
    Roef, MJ
    de Meer, K
    Reijngoud, DJ
    Straver, HWHC
    de Barse, M
    Kalhan, SC
    Berger, R
    AMERICAN JOURNAL OF CLINICAL NUTRITION, 2002, 75 (02): : 228 - 236
  • [6] Resting oxygen consumption and in vivo ADP are increased in myopathy due to complex I deficiency
    Roef, MJ
    Reijngoud, DJ
    Jeneson, JAL
    Berger, R
    de Meer, K
    NEUROLOGY, 2002, 58 (07) : 1088 - 1093
  • [7] Increasing fat in the diet does not improve muscle performance in patients with mitochondrial myopathy due to complex I deficiency
    de Meer, K
    Roef, MJ
    de Klerk, JBC
    Bakker, HD
    Smit, GPA
    Poll-The, BT
    JOURNAL OF INHERITED METABOLIC DISEASE, 2005, 28 (01) : 95 - 98
  • [8] Exercise-induced Lactate Production Is Paralleled by Enhanced Lactate Oxidation in Patients with Mitochondrial Myopathy
    Jeppesen, Tina Dysgaard
    Orngreen, Mette Cathrine
    van Hall, Gerrit
    Vissing, John
    NEUROLOGY, 2009, 72 (11) : A17 - A17
  • [9] A CASE OF MITOCHONDRIAL MYOPATHY, LACTIC-ACIDOSIS AND COMPLEX-I DEFICIENCY
    BET, L
    BRESOLIN, N
    MOGGIO, M
    MEOLA, G
    PRELLE, A
    SCHAPIRA, AH
    BINZONI, T
    CHOMYN, A
    FORTUNATO, F
    CERRETELLI, P
    SCARLATO, G
    JOURNAL OF NEUROLOGY, 1990, 237 (07) : 399 - 404
  • [10] CLINICAL AND MOLECULAR HETEROGENEITY IN PATIENTS WITH MITOCHONDRIAL ENCEPHALOMYOPATHIES DUE TO COMPLEX-I DEFICIENCY
    ICHIKI, T
    KOBAYASHI, M
    WADA, Y
    TANAKA, M
    OZAWA, T
    JOURNAL OF INHERITED METABOLIC DISEASE, 1988, 11 (03) : 333 - 336