American Journal of Respiratory and Critical Care Medicine

We studied six patients with chronic obstructive pulmonary disease (COPD) (FEV1 = 1.1 ± 0.2 L, 32% of predicted) and six age- and activity level–matched control subjects while performing both maximal bicycle exercise and single leg knee-extensor exercise. Arterial and femoral venous blood sampling, thermodilution blood flow measurements, and needle biopsies allowed the assessment of muscle oxygen supply, utilization, and structure. Maximal work rates and single leg V̇O2max (control subjects = 0.63 ± 0.1; patients with COPD = 0.37 ± 0.1 L/minute) were significantly greater in the control group during bicycle exercise. During knee-extensor exercise this difference in V̇O2max disappeared, whereas maximal work capacity was reduced (flywheel resistance: control subjects = 923 ± 198; patients with COPD = 612 ± 81 g) revealing a significantly reduced mechanical efficiency (work per unit oxygen consumed) with COPD. The patients had an elevated number of less efficient type II muscle fibers, whereas muscle fiber cross-sectional areas, capillarity, and mitochondrial volume density were not different between the groups. Therefore, although metabolic capacity per se is unchanged, fiber type differences associated with COPD may account for the reduced muscular mechanical efficiency that becomes clearly apparent during knee-extensor exercise, when muscle function is no longer overshadowed by the decrement in lung function.

Although researchers have recently focused their attention on the potential involvement of skeletal muscle in the pathophysiology of chronic obstructive pulmonary disease (COPD) (15), there is currently no accord on this matter (6). An issue that has clouded conclusions is the difference between skeletal muscle dysfunction and disuse (7). Certainly, patients with COPD experience locomotor muscle disuse, promoted by the dyspnea that accompanies exercise in this condition. However, should simply deconditioned skeletal muscle be considered dysfunctional? The tendency to answer yes to this question has been promoted by studies that magnify the differences in COPD skeletal muscle by comparisons with relatively physically active control subjects (1, 79). Thus, the selection of appropriately inactive control subjects becomes an essential component of the experimental design of research focused on the assessment of skeletal muscle function and COPD.

Additional support for the concept of dysfunctional muscle in COPD has been provided by the regular use of whole body exercise, such as cycling, to evaluate muscle function (1, 3, 10). The use of a large muscle mass exercise paradigm, in patients with COPD, may shroud peripheral muscle limitations by the attainment of a patient's reduced ventilation ceiling, before truly taxing the locomotor muscles. Ideally, to study muscle function itself in COPD, the amount of muscle recruited should be small enough that the patient can achieve maximal muscular work before the influence of central ventilatory limitations.

The single leg knee-extensor exercise model (11), allows the measurement of oxygen (O2) supply and V̇o2 to a known mass of active muscle (12) under conditions of limited ventilatory demand and thus is an ideal exercise paradigm with which to study the skeletal muscle of patients with COPD (13). The ability to monitor muscle O2 supply in this paradigm is essential because without this metabolic differences may be the consequence of either intrinsic muscle dysfunction or the normal response of healthy (even if detrained) muscle to reduced O2 supply.

Consequently, this study was designed to assess skeletal muscle function in patients with COPD during both cycle and single leg knee-extensor exercise in comparison with that of healthy control subjects that were well matched, both in terms of physical activity and physical characteristics. The purpose of this study was to test the following hypotheses: (1) during cycle exercise the skeletal muscle of patients with COPD will appear dysfunctional in comparison with that of control subjects in terms of maximal work rate, muscle blood flow, and V̇o2, whereas (2) during single leg knee-extensor exercise the skeletal muscle of patients with COPD will have a more similar physiologic response to that of the control subjects. This work has been previously published in abstract form (14).

Subjects

Six patients with COPD (FEV1 = 1.1 ± 0.2, 32 ± 5% predicted) (15) and six healthy age-, weight-, and activity-matched control subjects volunteered according to the University of California San Diego, Human Research Protection Program requirements. Control subjects were determined to be sedentary, and the majority of the patients with COPD had completed the University of California San Diego Pulmonary Rehabilitation Program (within 8–24 months) but did not differ from the control subjects in terms of current physical activity (1618). Subject characteristics are presented in Table 1

TABLE 1. Subject characteristics




Control Subjects

Patients with COPD
Number of subjects66
Age, yr65.4 ± 4.364.0 ± 3.6
Height, cm171.2 ± 3.4179.4 ± 4.8
Weight, kg81.7 ± 6.382.5 ± 11.2
Body mass index, kg/m228.2 ± 1.125.6 ± 1.7
Quadriceps mass, kg2.0 ± 0.11.8 ± 0.2
Leg muscle mass, kg7 ± 0.26.3 ± 0.3
FEV1, L, % predicted3.1 ± 0.3
 (106 ± 4.0)1.1 ± 0.2
 (32.4 ± 4.6)*
FVC, L, % predicted4.0 ± 0.4
 (102.6 ± 0.4)3.1 ± 0.4
 (70.9 ± 4.3)*
FEV1/FVC, %77.8 ± 1.333.6 ± 3.2*
Resting arterial HbO2, %97.0 ± 0.395.2 ± 0.6*
Resting arterial PO2, mm Hg97.7 ± 287.4 ± 3*
Arterial [Hb], g/dl14.0 ± 114.5 ± 0.4
Number of prior steroid
   users
0
2

* Significantly different from control subjects.

Definition of abbreviations: COPD = chronic obstructive pulmonary disease; [Hb] = hemoglobin concentration; HbO2 = oxyhemoglobin.

Percent predicted values derived from Crapo and coworkers (15).

Leg muscle mass estimate based on 3.5 times the measured quadriceps muscle mass (63).

.

Exercise Models

Two exercise modalities were employed in this study, the first being conventional bicycle ergometry performed on an electrically braked bike (Excalibur; Quinton Instruments Co., Gröningen, Holland). Cadence was self-selected, but for most subjects fell between 60 and 80 rpm. The second exercise paradigm was knee-extensor exercise, which limits muscular work to the quadriceps of one leg (11, 12, 19). This was performed with subjects reclined on a padded chair with the knee-extensor exercise ergometer placed in front of them (illustrated in Reference 20) (see online supplement).

Experimental Protocol

Within 1 week of preliminary familiarization studies, subjects returned to the laboratory where two catheters (radial artery and left femoral vein) and a thermocouple (left femoral vein) were emplaced using the sterile technique as previously reported (19, 21) (see online supplement). Blood samples were taken from the arterial and femoral venous catheters to quantify arterial–venous O2 concentration differences.

After the catheterization procedures, two bouts of graded exercise were performed: (1) conventional cycle exercise and (2) single leg knee-extensor exercise. The order of these exercise bouts across subjects was balanced to avoid potential ordering effects. For each exercise bout, the work rate was increased from an unweighted warm-up to the previously determined maximum work rate with a minimum of three work levels. Data were obtained at each level after the attainment of steady-state exercise (2–4 minutes depending on the exercise intensity). Each exercise bout was completed in 8 to 12 minutes. V̇e, pulmonary V̇o2, and V̇co2, were calculated by a commercially available software package (Consentius Technologies, Salt Lake, UT) integrated with a Perkin-Elmer MGA 1,100 mass spectrometer, a gas mixing chamber, and a Fleisch pneumotachograph #3 (Hans-Rudolph, Kansas City, Missouri) (19).

Blood Analyses

Po2, Pco2, pH, O2 saturation, and hemoglobin concentration ([Hb]) were measured on an IL 1306 blood gas analyzer and IL 482 CO-oximeter (Instrumentation Laboratories, Lexington, MA.). O2 concentration was calculated as 1.39 ml O2 × [Hb] g/100 ml × measured O2 saturation (fraction) + 0.003 ml O2/100 ml of blood × measured Po2 (mm Hg). Arterial–venous [O2] difference was calculated from the difference in radial artery and femoral venous O2 concentration. This difference was then divided by arterial concentration to give O2 extraction.

Muscle Biopsy

A percutaneous needle biopsy of vastus lateralis muscle was obtained at approximately 3.5 cm of depth, 15 cm proximal to the knee, and slightly distal to the ventral midline of the muscle in four patients with COPD and four control subjects. The muscle samples from each biopsy were either immediately frozen in liquid nitrogen and stored at −80°C for subsequent histochemical, citrate synthase activity and myoglobin concentration analyses or immersion-fixed in glutaraldehyde fixative (6.25% glutaraldehyde solution in 0.1 M sodium cacodylate buffer; total osmolarity, 1,100 mOsm; pH 7.4) for processing for electron microscopy and morphometry. Details of these specific methodologies are available in the online supplement.

Thigh Volume Measurement

Using thigh length, circumference, and skinfold measurements, thigh volume was calculated to allow an estimate of quadriceps femoris muscle mass (22, 23).

Statistical Analyses

Analysis of variance and a Tukey post hoc analysis were used to determine differences across a series of work intensities. At maximal exercise, variables were tested for a significant difference between the groups by repeated measures t test. All statistics were performed using a commercially available software package (Graph Pad, San Diego, CA). All data are presented as means ± SE. The p value was set at 0.05 or less.

Muscle Biopsy Data

The anthropometric measurement of quadriceps muscle mass revealed no difference between patients with COPD and control subjects (Table 1). The muscle characteristics determined using needle biopsy samples are presented in Table 2

TABLE 2. Vastus lateralis muscle characteristics




Control Subjects

Patients with COPD
% Area of type I fibers50 ± 721 ± 6*
% Area of type II fibers50 ± 779 ± 6*
% Area of type IIA fibers36 ± 1242 ± 4*
% Area of type IIX fibers16 ± 639 ± 2*
Capillary density, capillaries/mm2343 ± 8335 ± 14
Capillary-to-fiber ratio1.01 ± 0.041.07 ± 0.11
Number of capillaries around a fiber2.7 ± 0.22.6 ± 0.2
Mitochondrial volume density, %3.7 ± 0.23.6 ± 0.2
Fiber cross-sectional area, μm22958 ± 903201 ± 290
Citrate synthase activity,
   μmol/min/g tissue12.1 ± 1.112.4 ± 1.4
Myoglobin, mg/g wet weight
7.4 ± 0.9
7.3 ± 1.0

* Significantly different from control subjects.

Number of subjects per group = 4, with the exception of % area of type IIA and IIX fibers (3 per group) and citrate synthase activity (n = 5 per group).

. There were significant differences in the proportions of muscle fiber type, with patients with COPD exhibiting reduced proportion of type I fibers (Figure 1) . The elevated proportion of type II fibers in patients with COPD was evident in both type IIA and type IIX, but the greatest difference was apparent in the type IIX fibers that were approximately 2.5 times as numerous (expressed as a percentage of fibers) compared with control subjects. Patients with COPD did not reveal altered capillarity when expressed as capillary density, capillary fiber ratio, or number capillaries around a fiber. Mitochondrial volume density and cross-sectional area were relatively low in both groups (24) but were not different between patients with COPD and control subjects. It should be noted that these mitochondrial measurements are not fiber type–specific and therefore represent an average for all fibers. Muscle fiber cross-sectional area was not different between the two groups. There was no difference in [myoglobin] between patients with COPD and control subjects, with both groups falling within the previously reported range for this and other techniques used on human tissue (25).

Bicycle Exercise

The major physiologic variables recorded during cycle exercise are reported in Table E1 (see online supplement). In terms of maximum work rate the control subjects achieved a 128% greater work rate than the patients with COPD. As expected, leg V̇o2max and maximal leg blood flow were significantly attenuated in the patients with COPD because of the large reduction in maximal work rate. Indices of arterial O2 availability such as arterial Hb saturation, arterial Po2, and arterial O2 concentration (CaO2) were reduced throughout exercise in the patients with COPD when compared with control subjects. However, leg blood flow at a given work rate was higher in the patients with COPD. This resulted in a tendency for greater O2 delivery at a given work rate to the muscle of patients compared with that of the control subjects. This submaximal leg blood flow was also accompanied by a significantly elevated vascular conductance (at a given work rate) in the patients with COPD. Throughout the progressive exercise test, O2 extraction was slightly, but significantly attenuated in the patients in comparison with that of the control subjects, whereas both leg V̇o2 and pulmonary V̇o2 tended to be elevated but without statistically significant differences. Measures of metabolic stress such as arterial and venous pH and venous lactate outflow revealed similar responses to the submaximal work rates in both patients and control subjects without significant differences. Heart rate was the same at a given work rate in both groups, and thus the patient's maximal heart rate was attenuated when compared with that of the control subjects. Perceived breathlessness was accelerated in the patients with COPD, whereas the assessment of muscle fatigue indicated similar muscular distress at the limited work rates achieved.

Single Leg Knee-Extensor Exercise

The major physiologic variables recorded during knee-extensor exercise are reported in Table E2 (see online supplement). Using this exercise modality, the control subjects achieved a 50% greater maximum work rate than the patients with COPD. However, unlike bicycle exercise, leg V̇o2max and maximal leg blood flow were not attenuated in the patients with COPD despite the difference in maximal work rate. CaO2 was not lower throughout exercise in the patients with COPD when compared with control subjects. Leg blood flow for a given work rate was again elevated in the patients with COPD and again resulted in a greater O2 delivery to the muscle of patients at a given work rate in comparison with that of control subjects. In this exercise modality, the elevated submaximal leg blood flow was not clearly accompanied by a significantly elevated vascular conductance in the patients. Throughout exercise, O2 extraction was again significantly attenuated in the patients in comparison with the control subjects whereas leg V̇o2 was elevated. As during cycle exercise, measures of metabolic stress such as arterial and venous pH and venous lactate outflow revealed very similar responses to the submaximal work rates in both patients and control subjects. Heart rate was the same at a given work rate in both groups, and thus the patient's maximal heart rate was attenuated when compared with that of the control subjects. Subjective assessment of muscle fatigue indicated greater muscular distress at a given work rate in the patients, but maximum levels were equal in both groups. Although perceived breathlessness was accelerated in the patients at a given work rate, the maximal level was not different between groups.

Summary Comparison between Cycle and Single Leg Knee-Extensor Exercise

The disparity in maximal work rate between patients with COPD and control subjects was greatly reduced during single leg knee-extensor exercise when compared with cycle exercise. Unlike cycle exercise, during maximal knee-extensor exercise patients were able to attain the same leg V̇o2max as the control subjects. However, an apparent difference in mechanical efficiency, evident to a lesser degree during cycling, but clearly demonstrated during knee-extension exercise, resulted in an attenuated maximum knee-extension work rate for the patients with COPD compared with the control subjects. Leg blood flow for a given work rate was elevated in the patients with COPD compared with the control subjects during both exercise paradigms. As CaO2 was not severely compromised in the patients, this resulted in an elevated O2 delivery to the exercising muscle at each work rate in each exercise paradigm. Subjectively, the patients indicated that they were less breathless during maximal knee-extensor exercise compared with cycling, and both groups indicated that maximal muscle fatigue was attained at the end of the knee-extensor exercise study, whereas only the control subjects achieved severe muscle fatigue during cycle exercise.

This study reveals significant differences in both skeletal muscle structure and function between activity and anthropometrically matched control subjects and patients with severe COPD. Functionally, the current data indicate that patients with COPD have a tendency for inefficient work economy in skeletal muscle, demonstrated even during cycle exercise, but more clearly during knee-extensor exercise (when the muscles are truly taxed in isolation from the limited pulmonary function). Structurally, the patients with COPD revealed a much greater proportion of type II muscle fibers, most apparent in the form of type IIX. This unique approach of tilting the balance from central to peripheral limitation (bike to knee-extensor exercise comparison) and the clear differences found in muscle structure suggest that the mechanical inefficiency in patients with COPD may be a direct result of an increased percentage of inefficient type II muscle fibers. As a consequence of the small sample size and the relatively constrained features of these patients (minimal muscle wasting, nonhypoxemic, etc.), it is important not to generalize these findings to the whole diverse population of patients with COPD.

Fiber Type, and Fiber Type Energetics

Patients with moderate to severe COPD consistently demonstrate an increase in the proportion of type II fibers, assessed either histochemically (26, 27) (Figure 1) or by the expression of myosin heavy chain isoforms (28, 29). This is the opposite of changes in fiber type associated with healthy aging (30). The cause of this unexpected fiber type composition may be the result of extended or intermittent exposure to conditions of reduced O2 availability (31) or a consequence of disuse (32, 33). In the current study considerable effort was made to find control subjects who exhibited a similar level of activity as the patients with COPD (who for this population were relatively active). Consequently, although possible (34), it is unlikely based on subject selection criteria that disuse alone can account for the greater number of type II fibers in the patient group. In addition, if disuse were a major factor, concomitant changes such as reductions in fiber size, capillary-to-fiber ratio and mitochondrial density that were not observed (Table 2), would be expected. The patients in the current study experienced only mild hypoxia at rest (PaO2 = 87 mm Hg) (Table 1) that increased only slightly (PaO2 = 78 mm Hg) at maximal cycle exercise (Table E1 in the online supplement), despite exhibiting quite severe symptoms of COPD (Table 1). Hence, although the concomitant elevation in the proportion of type IIA fibers with the more typical increase in type IIB fibers is not identical to the previously reported effects of hypoxia (35), these data support the concept that hypoxia itself (albeit mild in this case) may induce the observed shift in fiber type exhibited by these patients (31).

The economy of constant muscular work is, beyond a threshold, inversely related to exercise intensity (36). Therefore, there is an apparent excess O2 cost for a given amount of work during high-intensity muscular contraction, the mechanism for which is not clearly understood (37). As exercise intensity and or rate of force development increases there is a growing reliance on type II muscle fibers that has been proposed to lead to less efficient muscular work (38). There are convincing data at both the in vitro (39, 40) and in vivo (36, 38) levels that the energetic cost of force production is fiber type–specific. The mechanisms associated with a greater cost of developing tension with fast-twitch fibers (type II) may include: lower chemical-to-mechanical coupling efficiency and the adenosine triphosphatase (ATPase)–driven calcium pump whose activity is 5 to 10 times faster in the type II compared with type I fibers (39, 40). However, proportionality between maximum shortening velocities, ATPase activities (41), and between the energy cost of tension development in the extensor digitorum longus (type II) and soleus (type I) suggest that the faster actomyosin turnover is the most likely mechanism (42). Regardless of mechanism, it is apparent that fiber type differences in these patients with COPD may explain the difference in mechanical efficiency observed here during exercise. It should be recognized that, although such a mechanical inefficiency has been documented previously in a COPD study with a similar catheter-based approach to interrogate the muscle itself (10) and not simply assessing the whole body response to exercise, there are certainly many other investigations that have failed to reveal such a finding (6).

O2 Transport and V̇O2

Several studies have reported that exercise tolerance is improved by O2 supplementation in patients with COPD (13, 43, 44). Recognizing the impact of reducing hypoxemia in COPD and evidence of an elevated O2 cost of breathing (45), which may steal blood from the limb muscles (13, 46), it had been suggested that O2 delivery to the exercising muscle of patients with COPD may be compromised (1). However, the current data and the few other studies that have directly assessed blood flow, O2 delivery, and O2 uptake across the exercising muscle of patients with COPD, indicate that at an absolute submaximal work rate these parameters appear to be well preserved or even increased (Tables E1 and E2 in online supplement, Figures 2 and 3)

(1, 10). Healthy subjects have also been documented to increase muscle blood flow to compensate for reductions in CaO2 (47). However, the increase in muscle blood flow and even O2 delivery in the current patients goes beyond a compensation for reduced CaO2, which was somewhat mild during cycle exercise (Table E1 in the online supplement) and not significant during knee-extensor exercise (Table E2 in the online supplement), but appears to more likely linked to the increased metabolic demand of their type II rich muscle.

It has previously been demonstrated, noninvasively, that moving from cycle exercise to isolated single leg knee-extensor exercise resulted in a large increase in the amount of maximal work (per unit of muscle mass) of the quadriceps in patients with COPD (13). This was interpreted as evidence of a metabolic reserve capacity in these patients, as has been previously recognized in normal healthy subjects (48). The current data afford the opportunity to go beyond the work rate per unit of muscle achieved in the whole body exercise and the isolated muscle and to examine the relationship between O2 delivery and V̇o2 during the two exercise modalities in both patients with COPD and matched control subjects (Figure 4)

. Figure 4 illustrates the finding that a large increase in O2 delivery can be used to support a proportional increase in V̇O2 in both groups. This finding supports the concept that patients with COPD have a significant metabolic reserve capacity that is only evident when their muscles are somewhat freed from the constraints of the cardiopulmonary system. It is important to note that this interpretation of the data does not take into account the apparent mechanical inefficiency exhibited by these patients, as already recognized and attributed to fiber type changes. Thus, although these patients with COPD appear to have a large metabolic reserve capacity, this does not appear to directly translate a proportional increase in muscular work capacity. It is also interesting to note that the slope of this relationship between O2 delivery and V̇o2 is similar to that previously reported for the transition between cycle and knee-extensor exercise in well-trained healthy subjects (48). This suggests that similarly across well-trained young, healthy old, and patients with COPD, skeletal muscle has the ability to consume more O2 as O2 demand and delivery are enhanced by switching from an exercise paradigm that is less centrally limited.

Myoglobin has been suggested to be important in O2 transport from blood to muscle cells (49) and has previously been reported to be reduced in patients with COPD (50). The current data (Table 2) are at the high end of the range of myoglobin concentration previously reported in humans of 4 to 8 mg/g of wet muscle (50, 51) but were not different between control subjects and patients. It was previously reported that older subjects, who tend to have a greater predominance of type I fibers than young control subjects, had a small (10%) increase in myoglobin concentration compared with their young counterparts (53). The current data are quite different from the previous findings because neither did the aged control subjects (∼ 65 years) demonstrate a convincing relative increase in type I fibers nor did the patients with COPD reveal a decreased myoglobin concentration despite muscle fiber type changes in the appropriate direction (an increased proportion of type II fibers). Based on studies of diving mammals exposed to long periods of hypoxia (52, 53), in which the intramuscular myoglobin concentration is elevated, it could be hypothesized that patients with COPD may adaptively increase their myoglobin concentration in response to their resting and exercise-induced hypoxemia (Table 2, and Tables E1 and E2 in the online supplement). However, the power of exercise training (54) and inactivity (55) in other animal species suggest that any changes in myoglobin concentration due to hypoxemia may be offset by inactivity in the COPD population.

Skeletal Muscle Capillarity

Typically, the assessment of capillarity in patients with COPD has revealed rarefaction (26, 56). In the current study, we failed to find a difference in capillarity between patients with COPD and control subjects (Table 2). Not only was the capillarity remarkably similar, but comparing the four patients with COPD with eight normal healthy control subjects (four of the current control subjects and four additional control subjects, not matched for age, activity, etc.) showed the same relationship between peak muscle V̇o2 (during knee-extensor exercise) and capillary-to-fiber ratio (Figure 5)

. This finding supports the concept that despite age and health status differences, the structural capacity to transport O2 may be of primary importance in determining maximal O2 flux (57, 58) and that this relationship is intact in patients with COPD. The capillary network is relatively plastic and is consequently altered by exercise and inactivity (59). Although this is not the only research that failed to identify a difference in capillarity between patients with COPD and control subjects (56), a possible explanation for this finding is that a significant effort went into matching the physical activity levels of relatively active patients with COPD (most had recently partaken in the University of California San Diego Pulmonary Rehabilitation Program) with inactive control subjects.

Metabolic Capacity

The current findings that citrate synthase activity and mitochondrial volume are not different between control subjects and patients with COPD (Table 2) are both internally consistent and indicative of a similar metabolic capacity in the two groups. This is supported by the almost identical skeletal muscle V̇o2max achieved during knee-extensor exercise in the control subjects and patients with COPD, albeit with different work efficiencies as discussed (Figure 3). Prior investigations have reported diminished oxidative enzymes (27, 60), such as citrate synthase activity, in patients with COPD. The relatively low and similar values in both groups for both citrate synthase activity and mitochondrial volume suggest that the matching of patients and control subjects in the current research was, based on these exercise sensitive criteria (61, 62), very good. However, it is somewhat surprising that these data are so similar in view of the relative paucity of type I muscle fibers in the patients with COPD (Table 2), expected to be rich in mitochondria. This fall in type I muscle fibers and the potential reduction in mitochondrial volume was somewhat tempered by the rise in type IIA fibers that still have a large oxidative capacity relative to the type IIB fibers. It is also possible that an adaptive process associated with the fiber type changes has altered the mitochondrial volume typically associated with each fiber type in the patients with COPD. Along the same theme, it is interesting to note that despite the significant differences in muscle fiber type, there was no apparent difference in arterial or venous blood pH at the same absolute work rates or at maximal exercise. Venous lactate outflow levels were similar at submaximal workloads but were higher at maximal exercise in the control subjects, accompanying the greater work rate achieved by this group. Again, these data indicate that a given work rate was similar in terms of relative metabolic stress between these two groups.

Disuse, Dysfunction, and Myopathy

Here it is important to clearly define the terms often used to debate issues of muscle function in patients with COPD: disuse being a reduction in muscle use, dysfunction being abnormal or impaired function, and myopathy being a disease of muscle. Continuing to recognize the importance of appropriate control data and within the confines of these definitions, the current data offer some support for the concept that patients with COPD experience a form of myopathy and dysfunction. The elevation in type II fibers and the resultant reduction in mechanical efficiency during muscular work could certainly be considered a destructive process (myopathy) or abnormal or impaired function (dysfunction). However, the current data also reveal similarities in mitochondrial enzyme activities, metabolic scope, metabolic response in terms of lactate production and blood pH, fiber size, and structure–function relationships in the patients with COPD when compared with activity-matched control subjects. Had the patient data been compared with more active individuals, many of these variables may have appeared abnormal and could have easily been classified as the result of muscle disuse. Therefore, it may be concluded that patients with COPD demonstrate limited myopathic or dysfunctional changes in skeletal muscle when compared with appropriate control subjects.

In summary, this research documents a mechanical inefficiency in small subset of patients with COPD that becomes clearly evident when skeletal muscle is studied in isolation from central limitations. Accompanying and perhaps responsible for this altered mechanical efficiency in these patients is a substantial increase in the number of type II muscle fibers. Despite these differences the skeletal muscle of patients with COPD revealed a similar maximal metabolic capacity, mitochondrial density, citrate synthase activity, capillarity, a normal relationship between capillarity and maximal metabolic capacity, and, like the control subjects, the capacity to use more O2 with a change in exercise paradigm that allows greater O2 delivery per unit of muscle. Thus, it must be concluded that although there are apparent differences in the skeletal muscle of patients with COPD, which may to some extent be described as dysfunction or even a myopathy, these differences do not impact all aspects of muscle function and structure.

The authors thank the subjects for their time in volunteering for this involved study.

1. Maltais F, Jobin J, Sullivan MJ, Bernard S, Whittom F, Killian KJ, Desmeules M, Belanger M, LeBlanc P. Metabolic and hemodynamic responses of lower limb during exercise in patients with COPD. J Appl Physiol 1998;84:1573–1580.
2. Kutsuzawa T, Shioya S, Kurita D, Haida M, Ohta Y, Yamabayashi H. Muscle energy metabolism and nutritional status in patients with chronic obstructive disease: a 31P magnetic resonance study. Am J Respir Crit Care Med 1995;152:647–652.
3. Maltais F, Simmard A, Simard C, Jobin J, Desagnes P, LeBlanc P. Oxidative capacity of the skeletal muscle and lactic acid kinetics during exercise in normal subjects and in patients with COPD. Am J Respir Crit Care Med 1996;153:288–293.
4. Mattson J, Poole D. Pulmonary emphysema decreases skeletal muscle oxidative enzyme capacity. J Appl Physiol 1998;85:210–214.
5. Bernard S, LeBlanc P, Whittom F, Carrier G, Jobin J, Belleau R, Maltais F. Peripheral muscle weakness in patients with chronic obstructive pulmonary disease. Am J Respir Crit Care Med 1998;158:629–634.
6. Skeletal muscle dysfunction in chronic obstructive pulmonary disease: a statement of the American Thoracic Society and European Respiratory Society. Am J Respir Crit Care Med 1999;159:S1–S40.
7. Richardson RS. Skeletal muscle dysfunction vs. muscle disuse in patients with COPD. J Appl Physiol 1999;86:1751–1753.
8. Serres I, Gautier V, Varry A, Prefaut C. Impaired skeletal muscle endurance related to physical inactivity and altered lung function in COPD patients. Chest 1998;113:900–905.
9. Maltais F, LeBlanc P, Simard C, Jobin J, Berbue C, Bruneau J, Carrier L, Belleau R. Skeletal muscle adaptation to endurance training in patients with chronic obstructive pulmonary disease. Am J Respir Crit Care Med 1996;154:442–447.
10. Sala E, Roca J, Marrades R, Alonso J, Gonzalez de Suso J, Moreno A, Barbera J, Nadal J, de Jover L, Rodriguez-Roisin R, et al. Effects of endurance training on skeletal muscle bioenergetics in chronic obstructive pulmonary disease. Am J Respir Crit Care Med 1999;159:1726–1734.
11. Andersen P, Adams RP, Sjogaard G, Thorbe A, Saltin B. Dynamic knee extension as a model for study of isolated exercising muscle in humans. J Appl Physiol 1985;59:1647–1653.
12. Richardson RS, Frank RL, Haseler LJ. Dynamic knee-extensor and cycle exercise: functional MRI of muscular activity. Int J Sports Med 1998;19:182–187.
13. Richardson RS, Sheldon J, Poole DC, Hopkins SR, Ries AL, Wagner PD. Evidence of skeletal muscle metabolic reserve during whole body exercise in patients with chronic obstructive pulmonary disease. Am J Respir Crit Care Med 1999;159:881–885.
14. Richardson R, Leak B, Haseler L, Gavin T, Sheldon J, Eltin P, Olfert I, Ries A, Wagner P. Normal skeletal muscle function in patients with COPD when exercise is not centrally limited [abstract]. Med Sci Sports Exerc 1999;31:S277.
15. Crapo RO, Morris AH, Gardner RM. Reference spirometric values using techniques and equipment that meet ATS recommendations. Am Rev Respir Dis 1981;123:659–664.
16. Folsom AR, Jacobs DR Jr, Caspersen CJ, Gomez-Marin O, Knudsen J. Test-retest reliability of the Minnesota Leisure Time Physical Activity Questionnaire. J Chronic Dis 1986;39:505–511.
17. Taylor HL, Jacobs DR Jr, Schucker B, Knudsen J, Leon AS, Debacker G. A questionnaire for the assessment of leisure time physical activities. J Chronic Dis 1978;31:741–755.
18. Jacobs D, Luepker R, Mittelmark M, Folsom A, Pirie P, Mascioli S, Hannan P, Pechacek T, Bracht N, Carlaw R, et al. Community-wide prevention stratergies: evaluation design of the Minnesota Heart Health Program. J Chronic Dis 1986;39:775–788.
19. Richardson RS, Poole DC, Knight DR, Kurdak SS, Hogan MC, Grassi B, Johnson EC, Kendrick K, Erickson BK, Wagner PD. High muscle blood flow in man: is maximal O2 extraction compromised? J Appl Physiol 1993;75:1911–1916.
20. Richardson RS, Noyszewski EA, Kendrick KF, Leigh JS, Wagner PD. Myoglobin O2 desaturation during exercise: evidence of limited O2 transport. J Clin Invest 1995;96:1916–1926.
21. Poole DC, Gaesser GA, Hogan MC, Knight DR, Wagner PD. Pulmonary and leg VO2 during submaximal exercise: implications for muscular efficiency. J Appl Physiol 1992;72:805–810.
22. Andersen P, Saltin B. Maximal perfusion of skeletal muscle in man. J Physiol 1985;366:233–249.
23. Jones PRM, Pearson J. Anthropometric determination of leg fat and muscle plus bone volumes in young male and female adults. J Physiol 1969;294:63P–66P.
24. Hoppeler H, Luthi P, Claasen H, Weibel ER, Howald H. The ultrastructure of normal human skeletal muscle: a morphometric analysis on untrained men, women and well-trained orienteers. Pflugers Arch 1973;344:217–232.
25. Reynafarje B. Simplified method for the determination of myoglobin. J Lab Clin Med 1963;61:138–145.
26. Jobin J, Maltais F, Doyon JF, LeBlanc P, Simard PM, Simard AA, Simard C. Chronic obstructive pulmonary disease: capillarity and fiber-type characteristics of skeletal muscle. J Cardiopulm Rehabil 1998;18:432–437.
27. Jakobsson P, Jordfeldt L, Brunden A. Skeletal muscle metabolites and fibre types in patients with advanced chronic obstructive pulmonary disease (COPD), with and without chronic respiratory failure. Eur Respir J 1990;3:192–196.
28. Maltais F, Sullivan MJ, LeBlanc P, Duscha BD, Schachat FH, Simard C, Blank JM, Jobin J. Altered expression of myosin heavy chain in the vastus lateralis muscle in patients with COPD. Eur Respir J 1999;13:850–854.
29. Satta A, Migliori GB, Spanevello A, Neri M, Bottinelli R, Canepari M, Pellegrino MA, Reggiani C. Fibre types in skeletal muscles of chronic obstructive pulmonary disease patients related to respiratory function and exericse tolerance. Eur Respir J 1997;10:2853–2860.
30. Larsson L. Histochemical characteristics of human skeletal muscle during aging. Acta Physiol Scand 1983;117:469–471.
31. Itoh K, Moritani T, Ishida K, Hirofuji C, Taguchi S, Itoh M. Hypoxia-induced fibre type transformation in rat hindlimb muscles: histochemical and electro-mechanical changes. Eur J Appl Physiol Occup Physiol 1990;60:331–336.
32. Thomason DB, Booth FW. Atrophy of the soleus muscle by hindlimb unweighting. J Appl Physiol 1990;68:1–12.
33. Andersen JL, Mohr T, Biering-Sorensen F, Galbo H, Kjaer M. Myosin heavy chain isoform transformation in single fibres from m. vastus lateralis in spinal cord injured individuals: effects of long-term functional electrical stimulation (FES). Pflugers Arch 1996;431:513–518.
34. Baldwin KM, Haddad F. Effects of different activity and inactivity paradigms on myosin heavy chain gene expression in striated muscle. J Appl Physiol 2001;90:345–357.
35. Bigard AX, Sanchez H, Birot O, Serrurier B. Myosin heavy chain composition of skeletal muscles in young rats growing under hypobaric hypoxia conditions. J Appl Physiol 2000;88:479–486.
36. Hunter GR, Newcomer BR, Larson-Meyer DE, Bamman MM, Weinsier RL. Muscle metabolic economy is inversely related to exercise intensity and type II myofiber distribution. Muscle Nerve 2001;24:654–661.
37. Poole DC, Barstow TJ, Gaesser GA, Willis WT, Whipp BJ. VO2 slow component: physiological and functional significance. Med Sci Sports Exerc 1994;26:1354–1358.
38. Coyle EF, Sidossis LS, Horowitz JF, Beltz JD. Cycling efficiency is related to the percentage of type I muscle fibers. Med Sci Sports Exerc 1992;24:782–788.
39. Gibbs CL, Gibson WR. Energy production of rat soleus muscle. Am J Physiol 1972;223:864–871.
40. Wendt IR, Gibbs CL. Energy production of rat extensor digitorum longus muscle. Am J Physiol 1973;224:1081–1086.
41. Barany M. ATPase activity of myosin correlated with speed of muscle shortening. J Gen Physiol 1967;50:197–218.
42. Crow MT, Kushmerick MJ. Chemical energetics of slow- and fast-twitch muscles of the mouse. J Gen Physiol 1982;79:147–166.
43. Maltais F, Simon M, Jobin J, Desmeules M, Sullivan MJ, Belanger M, Leblanc P. Effects of oxygen on lower limb blood flow and O2 uptake during exercise in COPD. Med Sci Sports Exerc 2001;33:916–922.
44. O'Donnell DE, Bertley JC, Chau LK, Webb KA. Qualitative aspects of exertional breathlessness in chronic airflow limitation: pathophysiologic mechanisms. Am J Respir Crit Care Med 1997;155:109–115.
45. Levison H, Cherniack RM. Ventilatory cost of exercise in chronic obstructive pulmonary disease. J Appl Physiol 1968;25:21–27.
46. Harms CA, Babcock MA, McClaran SR, Pegelow DF, Nickele GA, Nelson WB, Dempsey JA. Respiratory muscle work compromises leg blood flow during maximal exercise. J Appl Physiol 1997;82:1573–1583.
47. Gonzalez-Alonso J, Richardson RS, Saltin B. Exercising skeletal muscle blood flow in humans responds to reduction in arterial oxyhaemoglobin, but not to altered free oxygen. J Physiol 2001;530:331–341.
48. Richardson RS, Grassi B, Gavin TP, Haseler LJ, Tagore K, Roca J, Wagner PD. Evidence of O2 supply-dependent VO2 max in the exercise-trained human quadriceps. J Appl Physiol 1999;86:1048–1053.
49. Richardson RS, Newcomer SC, Noyszewski EA. Skeletal muscle intracellular PO(2) assessed by myoglobin desaturation: response to graded exercise. J Appl Physiol 2001;91:2679–2685.
50. Moller P, Hellstrom K, Hermansson IL. Myoglobin content in leg skeletal muscle in patients with chronic obstructive lung disease. Respiration (Herrlisheim) 1984;45:35–38.
51. Moller P, Sylven C. Myoglobin in human skeletal muscle. Scand J Clin Lab Invest 1981;41:479–482.
52. Kendrew J, Parrish R, Marrack J, Orlans E. The species specfictiy of myoglobin. Nature 1977;174:946.
53. Conley KE, Ordway GA, Richardson RS. Deciphering the mysteries of myoglobin in striated muscle. Acta Physiol Scand 2000;168:623–634.
54. Pattengale PK, Holloszy JO. Augmentation of skeletal muscle myoglobin by a program of treadmill running. Am J Physiol 1967;213:783–785.
55. Oshiro T. Experimental studies of myoglobin in skeletal muscle following denervation and reinervation. Acta Med Fukuoka 1966;36:531–567.
56. Whittom F, Jobin J, Simard PM, Leblanc P, Simard C, Bernard S, Belleau R, Maltais F. Histochemical and morphological characteristics of the vastus lateralis muscle in patients with chronic obstructive pulmonary disease. Med Sci Sports Exerc 1998;30:1467–1474.
57. Mathieu-Costello O, Saurez RK, Howchachka PW. Capillary-to-fiber geometry and mitochondrial density in hummingbird flight muscle. Respir Physiol 1992;89:113–132.
58. Mathieu-Costello O. Compartive aspects of muscle capillary supply. Annu Rev Physiol 1993;55:503–525.
59. Richardson RS, Wagner H, Mudaliar SR, Henry R, Noyszewski EA, Wagner PD. Human VEGF gene expression in skeletal muscle: effect of acute normoxic and hypoxic exercise. Am J Physiol 1999;277:H2247–H2252.
60. Maltais F, LeBlanc P, Whittom F, Simard C, Marquis K, Belanger M, Breton MJ, Jobin J. Oxidative enzyme activities of the vastus lateralis muscle and the functional status in patients with COPD. Thorax 2000;55:848–853.
61. Hoppeler H, Howald H, Conley K, Lindstedt SL, Claasen H, Vock P, Weibel ER. Endurance training in humans: aerobic capacity and structure of skeletal muscle. J Appl Physiol 1985;59:320–327.
62. Leek BT, Mudaliar SR, Henry R, Mathieu-Costello O, Richardson RS. Effect of acute exercise on citrate synthase activity in untrained and trained human skeletal muscle. Am J Physiol Regul Integr Comp Physiol 2001;280:R441–R447.
63. Gallagher D, Visser M, De Meersman RE, Sepulveda D, Baumgartner RN, Pierson RN, Harris T, Heymsfield SB. Appendicular skeletal muscle mass: effects of age, gender and ethnicity. J Appl Physiol 1997;83:229–239.
Correspondence and requests for reprints should be addressed to Russell S. Richardson, Ph.D., Department of Medicine, 0623, University of California San Diego, La Jolla, CA 92093-0623. E-mail:

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