Is Metabolic Flexibility Altered in Multiple Sclerosis Patients?

被引:43
作者
Maehler, Anja [1 ,2 ,3 ]
Steiniger, Jochen [1 ,2 ]
Bock, Markus [1 ,2 ,3 ]
Brandt, Alexander U. [3 ]
Haas, Verena [1 ,2 ]
Boschmann, Michael [1 ,2 ]
Paul, Friedemann [1 ,2 ,3 ]
机构
[1] Expt & Clin Res Ctr, Berlin, Germany
[2] Max Delbrueck Ctr Mol Med, Berlin, Germany
[3] Charite, NeuroCure Clin Res Ctr, D-13353 Berlin, Germany
关键词
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; MICRODIALYSIS ETHANOL TECHNIQUE; SKELETAL-MUSCLE; HUNTINGTONS-DISEASE; ADIPOSE-TISSUE; BLOOD-FLOW; MITOCHONDRIAL DYSFUNCTION; AUTONOMIC DYSFUNCTION; INSULIN-RESISTANCE; PROGRESSION;
D O I
10.1371/journal.pone.0043675
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Objectives: Metabolic flexibility is defined as ability to adjust fuel oxidation to fuel availability. Multiple sclerosis (MS) results in reduced muscle strength and exercise intolerance. We tested the hypothesis that altered metabolic flexibility contributes to exercise intolerance in MS patients. Methods: We studied 16 patients (all on glatiramer) and 16 matched healthy controls. Energy expenditure (EE), and carbohydrate (COX) and lipid oxidation (LOX) rates were determined by calorimetry, before and after an oral glucose load. We made measurements either at rest (canopy device) or during 40 min low-grade (0.5 W/kg) exercise (metabolic chamber). We also obtained plasma, and adipose tissue and skeletal muscle dialysate samples by microdialysis to study tissue-level metabolism under resting conditions. Results: At rest, fasting and postprandial plasma glucose, insulin, and free fatty acid levels did not differ between patients and controls. Fasting and postprandial COX was higher and LOX lower in patients. In adipose, fasting and postprandial dialysate glucose, lactate, and glycerol levels were higher in patients vs. controls. In muscle, fasting and postprandial dialysate metabolite levels did not differ significantly between the groups. During exercise, EE did not differ between the groups. However, COX increased sharply over 20 min in patients, without reaching a steady state, followed by an immediate decrease within the next 20 min and fell even below basal levels after exercise in patients, compared to controls. Conclusions: Glucose tolerance is not impaired in MS patients. At rest, there is no indication for metabolic inflexibility or mitochondrial dysfunction in skeletal muscle. The increased adipose tissue lipolytic activity might result from glatiramer treatment. Autonomic dysfunction might cause dysregulation of postprandial thermogenesis at rest and lipid mobilization during exercise.
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页数:9
相关论文
共 43 条
[1]
[Anonymous], 2001, HUMAN ENERGY REQUIRE
[2]
Complex I defect in muscle from patients with Huntington's disease [J].
Arenas, J ;
Campos, Y ;
Ribacoba, R ;
Martín, MA ;
Rubio, JC ;
Ablanedo, P ;
Cabello, A .
ANNALS OF NEUROLOGY, 1998, 43 (03) :397-400
[3]
Functional evaluation techniques in mitochondrial disorders [J].
Argov, Z .
EUROPEAN NEUROLOGY, 1998, 39 (02) :65-71
[4]
Systemic energy homeostasis in Huntington's disease patients [J].
Aziz, N. Ahmad ;
Pijl, Hanno ;
Frolich, Marijke ;
Snel, Marieke ;
Streefland, Trea C. M. ;
Roelfsema, Ferdinand ;
Roos, Raymund A. C. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2010, 81 (11) :1233-1237
[5]
Adipose tissue metabolism and CD11b expression on monocytes in obese hypertensives [J].
Boschmann, M ;
Engeli, S ;
Adams, F ;
Gorzelniak, K ;
Franke, G ;
Klaua, S ;
Kreuzberg, U ;
Luedtke, S ;
Kettritz, R ;
Sharma, AM ;
Luft, FC ;
Jordan, J .
HYPERTENSION, 2005, 46 (01) :130-136
[6]
LMNA Mutations, Skeletal Muscle Lipid Metabolism, and Insulin Resistance [J].
Boschmann, Michael ;
Engeli, Stefan ;
Moro, Cedric ;
Luedtke, Angelika ;
Adams, Frauke ;
Gorzelniak, Kerstin ;
Rahn, Gabriele ;
Maehler, Anja ;
Dobberstein, Kerstin ;
Krueger, Antje ;
Schmidt, Saskia ;
Spuler, Simone ;
Luft, Friedrich C. ;
Smith, Steven R. ;
Schmidt, Hartmut H. -J. ;
Jordan, Jens .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2010, 95 (04) :1634-1643
[7]
Brunner E., 2002, Nonparametric analysis of longitudinal data in factorial experiments
[8]
Mitochondrial DNA Deletions and Neurodegeneration in Multiple Sclerosis [J].
Campbell, Graham R. ;
Ziabreva, Iryna ;
Reeve, Amy K. ;
Krishnan, Kim J. ;
Reynolds, Richard ;
Howell, Owen ;
Lassmann, Hans ;
Turnbull, Doug M. ;
Mahad, Don J. .
ANNALS OF NEUROLOGY, 2011, 69 (03) :481-492
[9]
Skeletal muscle characteristics of people with multiple sclerosis [J].
Carroll, CC ;
Gallagher, PM ;
Seidle, ME ;
Trappe, SW .
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 2005, 86 (02) :224-229
[10]
Multiple sclerosis [J].
Compston, Alastair ;
Coles, Alasdair .
LANCET, 2008, 372 (9648) :1502-1517