Validation of a new calibration method for human muscle microdialysis at rest and during exercise

被引:11
作者
Desvigne, N
Barthélémy, JC
Bertholon, F
Gay-Montchamp, JP
Freyssenet, D
Costes, F [1 ]
机构
[1] CHU St Etienne, Hop Nord, Lab Physiol GIP E2S, F-42055 St Etienne 2, France
[2] CHU St Etienne, Hop Bellevue, Lab Cent Pharmacol & Toxicol, F-42055 St Etienne 2, France
关键词
ethanol; interstitial fluid; lactate;
D O I
10.1007/s00421-004-1099-0
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Microdialysis presents the unique possibility to measure metabolite concentrations in human interstitial fluid. During exercise, the recovery of these metabolites should be precisely monitored since it is known to increase greatly with muscle blood flow. The loss of ethanol, perfused at low concentration, can be accurately measured and reflects the changes in dialysis conditions. We evaluated whether using the relationship determined in resting metabolic conditions between the loss of ethanol, as reference substance, and the recovery for lactate or glucose would allow us to calculate precisely the concentration of these substances and their variations during exercise. Using the new catheter calibration method (slope method), the error of estimation of lactate and glucose in vitro was limited to -0.6 (5.8)% and -0.7 (6.2)%, respectively. In resting human muscle, the slope method proved to be as accurate as an established calibration technique ("no net flux method") to evaluate interstitial lactate concentration [1.82 (0.58) vs 1.83 (0.47) mM, respectively]. During dynamic knee-extension exercise or light neuromuscular electrical stimulation, the estimated interstitial lactate and glucose concentrations varied differently, but their time course changes remained consistent with their respective plasma values. We conclude that, after an initial calibration step, the slope method allows accurate measurement of interstitial muscle metabolites and it could be used to monitor rapid metabolic changes during exercise.
引用
收藏
页码:312 / 320
页数:9
相关论文
共 22 条
[1]   DYNAMIC KNEE EXTENSION AS MODEL FOR STUDY OF ISOLATED EXERCISING MUSCLE IN HUMANS [J].
ANDERSEN, P ;
ADAMS, RP ;
SJOGAARD, G ;
THORBOE, A ;
SALTIN, B .
JOURNAL OF APPLIED PHYSIOLOGY, 1985, 59 (05) :1647-1653
[2]   Microdialysis: use in human exercise studies [J].
Arner, P .
PROCEEDINGS OF THE NUTRITION SOCIETY, 1999, 58 (04) :913-917
[3]   MICRODIALYSIS MEASUREMENT OF THE ABSOLUTE GLUCOSE-CONCENTRATION IN SUBCUTANEOUS ADIPOSE-TISSUE ALLOWING GLUCOSE MONITORING IN DIABETIC-PATIENTS [J].
BOLINDER, J ;
UNGERSTEDT, U ;
ARNER, P .
DIABETOLOGIA, 1992, 35 (12) :1177-1180
[4]   Metabolic and hemodynamic responses to exercise in subcutaneous adipose tissue and skeletal muscle [J].
Boschmann, M ;
Rosenbaum, M ;
Leibel, RL ;
Segal, KR .
INTERNATIONAL JOURNAL OF SPORTS MEDICINE, 2002, 23 (08) :537-543
[5]   Microdialysis in peripheral tissues [J].
de la Peña, A ;
Liu, P ;
Derendorf, H .
ADVANCED DRUG DELIVERY REVIEWS, 2000, 45 (2-3) :189-216
[6]   Absolute concentrations of glycerol and lactate in human skeletal muscle, adipose tissue, and blood [J].
HagstromToft, E ;
Enoksson, S ;
Moberg, E ;
Bolinder, J ;
Arner, P .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 273 (03) :E584-E592
[7]   Microdialysis of skeletal muscle at rest [J].
Henriksson, J .
PROCEEDINGS OF THE NUTRITION SOCIETY, 1999, 58 (04) :919-923
[8]   THE ETHANOL TECHNIQUE OF MONITORING LOCAL BLOOD-FLOW CHANGES IN RAT SKELETAL-MUSCLE - IMPLICATIONS FOR MICRODIALYSIS [J].
HICKNER, RC ;
ROSDAHL, H ;
BORG, I ;
UNGERSTEDT, U ;
JORFELDT, L ;
HENRIKSSON, J .
ACTA PHYSIOLOGICA SCANDINAVICA, 1992, 146 (01) :87-97
[9]   Role of nitric oxide in skeletal muscle blood flow at rest and during dynamic exercise in humans [J].
Hickner, RC ;
Fisher, JS ;
Ehsani, AA ;
Kohrt, WM .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 273 (01) :H405-H410
[10]   MUSCLE BLOOD-FLOW DURING INTERMITTENT EXERCISE - COMPARISON OF THE MICRODIALYSIS ETHANOL TECHNIQUE AND XE-133 CLEARANCE [J].
HICKNER, RC ;
BONE, D ;
UNGERSTEDT, U ;
JORFELDT, L ;
HENRIKSSON, J .
CLINICAL SCIENCE, 1994, 86 (01) :15-25