Respiratory gas exchange and metabolic responses during exercise in McArdle's disease

1993 ◽  
Vol 75 (2) ◽  
pp. 745-754 ◽  
Author(s):  
M. Riley ◽  
D. P. Nicholls ◽  
A. M. Nugent ◽  
I. C. Steele ◽  
N. Bell ◽  
...  

During normal progressive exercise, the gas exchange anaerobic threshold occurs when CO2 production (VCO2) and ventilation (VE) increase so as to depart from a linear relationship to O2 consumption (VO2). This is thought to represent a gas exchange response to metabolic acidosis due to lactate accumulation. Patients with McArdle's disease have previously been reported to exhibit a steepened ventilatory response relative to VCO2, despite an inability to produce lactate. However, the VCO2 response has not been studied. We therefore investigated the VCO2-VO2 and VE-VO2 relationships in seven McArdle's disease patients and seven control subjects during symptom-limited maximal treadmill exercise. Analysis of gas exchange showed that whereas all control subjects had an easily identifiable anaerobic threshold, four of the patients had none and the other three displayed an attenuated threshold. The occurrence of the threshold in one patient was associated with a small rise in lactate and in another patient with an abrupt rise in leg discomfort, suggesting a pain response. Ammonia and the purine metabolite hypoxanthine were elevated during exercise in all patients, suggesting that ammonia may be a product of adenosine monophosphate degradation. Free fatty acid levels were also elevated, and a shift toward utilization of lipid may contribute to abnormal gas exchange responses. It is concluded that lactic acidosis contributes to the gas exchange anaerobic threshold but that other factors, such as discomfort, may be involved in the excess Ve seen during heavy exercise.

1986 ◽  
Vol 70 (4) ◽  
pp. 399-401 ◽  
Author(s):  
S. P. T. Sinkeler ◽  
E. M. G. Joosten ◽  
R. A. Wevers ◽  
R. A. Binkhorst ◽  
F. T. Oerlemans ◽  
...  

1. Plasma adenosine, inosine and hypoxanthine concentrations were assayed in seven control subjects, five myoadenylate deaminase deficient (MADD) patients and six McArdle patients before and after ischaemic forearm exercise. 2. The plasma adenosine increase was very low in all test groups and there were no significant differences. 3. The MADD patients showed a significantly lower increase of plasma inosine and hypoxanthine after exercise as compared with the controls. 4. In the McArdle patients the increase in plasma inosine and hypoxanthine after exercise did not differ significantly from the values measured in the controls. 5. The ischaemic exercise test with measurement of plasma inosine and hypoxanthine might be of diagnostic value in MADD, but not in McArdle's disease.


1990 ◽  
Vol 68 (4) ◽  
pp. 1393-1398 ◽  
Author(s):  
J. M. Hagberg ◽  
D. S. King ◽  
M. A. Rogers ◽  
S. J. Montain ◽  
S. M. Jilka ◽  
...  

This study was designed to determine whether patients with McArdle's disease, who do not increase their blood lactate levels during and after maximal exercise, have a slow “lactacid” component to their recovery O2 consumption (VO2) response after high-intensity exercise. VO2 was measured breath by breath during 6 min of rest before exercise, a progressive maximal cycle ergometer test, and 15 min of recovery in five McArdle's patients, six age-matched control subjects, and six maximal O2 consumption- (VO2 max) matched control subjects. The McArdle's patients' ventilatory threshold occurred at the same relative exercise intensity [71 +/- 7% (SD) VO2max] as in the control groups (60 +/- 13 and 70 +/- 10% VO2max) despite no increase and a 20% decrease in the McArdle's patients' arterialized blood lactate and H+ levels, respectively. The recovery VO2 responses of all three groups were better fit by a two-, than a one-, component exponential model, and the parameters of the slow component of the recovery VO2 response were the same in the three groups. The presence of the same slow component of the recovery VO2 response in the McArdle's patients and the control subjects, despite the lack of an increase in blood lactate or H+ levels during maximal exercise and recovery in the patients, provides evidence that this portion of the recovery VO2 response is not the result of a lactacid mechanism. In addition, it appears that the hyperventilation that accompanies high-intensity exercise may be the result of some mechanism other than acidosis or lung CO2 flux.


2004 ◽  
Vol 68 (1) ◽  
pp. 17-22 ◽  
Author(s):  
M. A. Martin ◽  
J. C. Rubio ◽  
R. A. Wevers ◽  
B. G. M. Van Engelen ◽  
G. C. H. Steenbergen ◽  
...  

1990 ◽  
Vol 237 (4) ◽  
pp. 267-270 ◽  
Author(s):  
A. Papadimitriou ◽  
P. Manta ◽  
R. Divari ◽  
A. Karabetsos ◽  
E. Papadimitriou ◽  
...  

1981 ◽  
Vol 59 (23) ◽  
pp. 1319-1320 ◽  
Author(s):  
K. W. Rumpf ◽  
H. Wagner ◽  
H. Kaiser ◽  
H. -M. Meinck ◽  
H. H. Goebel ◽  
...  

Pain ◽  
2006 ◽  
Vol 124 (3) ◽  
pp. 295-304 ◽  
Author(s):  
Oliver Rommel ◽  
Rudolf A. Kley ◽  
Gabriele Dekomien ◽  
Jörg T. Epplen ◽  
Matthias Vorgerd ◽  
...  

2004 ◽  
Vol 11 (2) ◽  
pp. 163-167 ◽  
Author(s):  
Nha Voduc ◽  
Katherine A Webb ◽  
Christine D'Arsigny ◽  
Ian McBride ◽  
Denis E O'Donnell

McArdle's disease is a rare, inherited deficiency of myophosphorylase, an enzyme required for the utilization of glycogen. Patients with myophosphorylase deficiency classically present with exercise intolerance, leg pain and muscle fatigue. The case of a young woman with exertional dyspnea and leg cramps is described. Exercise testing confirmed the presence of exercise intolerance and demonstrated an accelerated heart rate response, despite the absence of an anaerobic threshold and a respiratory exchange ratio of less than 1.0. Subsequent ischemic forearm testing and muscle biopsy confirmed the diagnosis of myophosphorylase deficiency. Evaluation of lung mechanics with esophageal pressure measurements demonstrated the presence of respiratory muscle weakness and early fatiguability, suggesting that the patient's dyspnea might have been attributable to an increased respiratory effort. Dyspnea is not a classic symptom associated with myophosphorylase deficiency, although subclinical respiratory muscle impairment may be present. No previous studies have evaluated respiratory muscle function during exercise in patients with myophosphorylase deficiency.


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