LOW-FREQUENCY ELECTRICAL STIMULATION OF SKELETAL MUSCLES IN PATIENTS WITH CHRONIC HEART FAILURE

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SCRIPTA MEDICA (BRNO) 75 (4): 203 208, August 2002 LOW-FREQUENCY ELECTRICAL STIMULATION OF SKELETAL MUSCLES IN PATIENTS WITH CHRONIC HEART FAILURE JANâÍK J 1. SIEGELOVÁ J. 1, HOMOLKA P. 1, SVAâINOVÁ H. 1, PLACHETA P. 1, VÁRNAYOVÁ L., KOÎANTOVÁ L. 1, DOB ÁK P. 1, DU EK J. 1, FI ER B. 1, PINAROVÁ L. 2, TOMAN J. 2, EICHER J.C. 3 1 Department of Functional Diagnostics and Rehabilitation and 2 Department of Internal Medicine Cardioangiology, St. Anne s Teaching Hospital, Faculty of Medicine, Masaryk University, Brno, Czech Republic 3 Department of Cardiology, University of Dijon, France Abstract The aim of this study was to evaluate the effect of low-frequency electrical stimulation of skeletal muscles in patients with chronic heart failure (CHF).Twelve patients with CHF diagnosed by coronarography (NYHA, III-IV; ejection fraction, 19.33 %) were examined before and after five weeks of the low-frequency electrical stimulation of quadriceps and calf muscles (1 h/day, 5 days/week). The patients were on the waiting list for heart transplantation. The medical regimens of all controlled patients were optimised and they were symptomatically stable. The dynamometry testing of quadriceps muscles was performed. The low-frequency stimulation was well tolerated by all subjects. It is concluded that the low-frequency electrical stimulation of quadriceps muscles lasting one week improved the quadriceps muscle strength by 28 %. The results of magnetic resonance imaging analysis of the gastrocnemius muscle showed a significant increase in muscle volume after stimulation. This procedure could be useful in the treatment of patients with severe chronic heart failure. Key words Chronic heart failure, Low-frequency electrical stimulation, Skeletal muscle, Dynamometry INTRODUCTION Chronic heart failure (CHF) is often accompanied by complete hypoperfusion, which affects a great part of the skeletal muscle mass. The intensity of catabolism increases, the reactive oxygen species and a large amount of circulating cytokines stimulate the development of apoptosis. The skeletal muscle oxidative metabolism is depressed, intracellular ph levels decrease, phosphocreatine depletion during exercise increases and phosphocreatine resynthesis decreases (1). The increased sympathetic tone and stimulation of the renin-angiotensinaldosterone system influence the redistribution of regional blood flow and create endothelial dysfunction of all vessels. This leads to an impaired peripheral vascular dilatation in response to vasodilator stimuli and a reduction of blood flow 203

and O 2 supply in skeletal muscles (2). Chronic hypoxia strongly damages the structural and metabolic integrity of muscle fibers. The resulting general atrophy decreases the power and fatigue resistance of muscles. Sometimes, this situation progresses to cardiac cachexia. The beneficial influence of exercise on the aerometabolic capacity and fatigue tolerance in patients with chronic heart failure (CHF) has been repeatedly reported. The commonly used methods of training, however, are based on systemic exercise and are not always tolerated by all CHF patients, especially by those with severe heart failure or with life-threatening arrhythmia. A new approach to cardiac rehabilitation is represented by the method of low-frequency electrical myostimulation (LFMES) of skeletal muscles. In in vitro conditions, a LFMES of 10 Hz changes the phenotype of stimulated mammalian skeletal muscle fibers. LFMES transforms the myosin chains of fast type to slow type ones, which is characterised by a higher resistance to fatigue (3, 4). LFMES also increases capillary density and enhances perfusion in strength muscles of the rat and rabbit (5, 6). The most important is the fact that all these experimental results are also applicable to human conditions. The aim of our study was to evaluate the long-term effects of LFMES on the metabolic performance and structure of skeletal muscles in patients with chronic heart failure. MATERIALS AND METHODS PATIENTS We evaluated a group of 12 patients who had undergone coronarography (class NYHA, II-IV; both sexes; mean age, 56 ± 9 years; ejection fraction, 19.3 ± 3 %). All of them were symptomatically stable and received an optimal pharmacological treatment (ACEI, betablockers, diuretics) that remained unchanged throughout the study. PROTOCOL OF LFMES APPLICATION The muscles to be stimulated were quadriceps and calf muscles. Special rectangular electrodes (80x100 mm) were positioned on the thighs and calves. Electrical stimulation was performed for an hour per day, 5 days a week for 5 weeks, using the dual-channel stimulators Elpha 2000 (Danmeter, Odense, Denmark). The stimulators delivered a biphasic current of 10 Hz frequency. The pulse duration was 200 msec with an on-off mode of stimulus (20 sec of stimulation followed by 20 sec of pause). The maximal stimulation amplitude was 60 ma. DYNAMOMETRY The dynamometry of quadriceps muscles was performed every week, using the dynamometer PC-2 SDT (Czech Republic). MAGNETIC RESONANCE SPECTROSCOPY To evaluate the muscle metabolic patterns, the phosphorus-31 nuclear magnetic resonance spectroscopy ( 31 P MRS) of gastrocnemius muscle was performed. The exercise protocol for 31 P MRS was based on repeated plantar flexions of equal amplitudes at a frequency of 0.5 Hz against a calibrated load. The initial workload was 1W and increased by 0.25 W every 3 minutes. Spectra were collected every minute; the protocol was discontinued when fatigue appeared. The recovery period was monitored for 10 min and the spectrum was evaluated every 30 seconds. The relative 204

concentrations of inorganic phosphates (Pi) and phosphocreatine (PCr) were calculated by integration and corrected for different saturations. Changes in PCr concentration were expressed as the PCr/PCr+Pi ratio. The PCr recovery rate was calculated and expressed, using the time constant (1/k), according to the standard protocol described by Hanada et al. (7). MAGNETIC RESONANCE IMAGING The volumes of soleus and gastrocnemius muscles were determined by the method of magnetic resonance imaging (MRI), using a FLASH 2D (gradient echo) sequence in the axial plane with a pulse repetition time of 600 msec, an echo time of 10 msec, a slice of 10 mm with a 5-mm interslice gap and a total number of slices equal to 26. Finally, a planimetric estimation of the muscle cross-sectional area was performed and the total muscle volume was calculated. All nuclear magnetic resonance measurements ( 31 P MRS and MRI) were obtained using a Siemens 1.5 T Magneton imaging system (Erlangen, Germany). The experimental protocol completed with the Declaration of Helsinki was approved by the local Ethics Committee. A written informed consent was obtained from each subject prior to their participation. STATISTICAL EVALUATION The Wilcoxon paired test was used for statistical analysis. The statistical significance was defined as P < 0.05. RESULTS The low-frequency electrical stimulation resulted in improved quadriceps muscle strength (F max ) by 28% as early as at one week and persisted until the end of stimulation at 5 weeks. The baseline values of systolic (SBP) and diastolic blood pressure (DBP) and heart rate (HR) remained unchanged during the measurement (Table 1). The analysis of muscle metabolic parameters, using 31 P magnetic resonance spectroscopy of gastrocnemius muscles, did not show any essential changes. There was only a slight tendency to a diminution of the time constant (1/k) of PCr post-exercise resynthesis after 5 weeks of LFMES, but this was without statistical significance (Table 2). In contrast to the results obtained by MRS, the analysis of muscle volumes by MRI showed a significant increase in muscle mass in gastrocnemius muscles after 5 weeks of LFMES (Table 3). DISCUSSION The use of chronic low-frequency stimulation in experimental models has helped to study muscle plasticity. It seems that LFMES involves qualitative and quantitative changes in different elements of the strength muscle fibers. Both structural and functional alterations may probably be caused by transformations of fast protein isoforms to their slow counterparts, which is followed by an increased activity of oxidative enzymes, improved oxygen consumption and growth of the terminal microvascular bed. These changes provide a basis for the general improvement of muscle metabolic patterns, including the diminution and 205

Table 1 Results before and after the low-frequency electrical stimulation of skeletal muscles (mean ± SD) LFMES SBP DBP HR F max (mmhg) (mmhg) (bpm) (N) Before 101 ± 6 67 ± 7 69 ± 3 230 ± 57 stimulation After 1 week 105 ± 5 70 ± 3 67 ± 7 *295 ± 64 After 5 weeks 104 ± 5 71 ± 3 68 ± 6 * 292 ± 61 LFMES, low-frequency electrical stimulation; SBP, systolic blood pressure; DBP, diastolic blood pressure; HR, heart rate, Fmax, maximal strength; *, P < 0.05 Table 2 Results of 31 P magnetic resonance spectrum analysis of the gastrocnemius muscle before and after five weeks of low-frequency electrical stimulation Muscle metabolic pattern Values before LFMES Values after LFMES P value (mean ± SD) (mean ± SD) (Wilcoxon paired test) PCr/PCr+Pi at rest 0.88 ± 0.27 0.89 ± 0.35 NS Maximal workload 1.69 ± 0.53 1.92 ± 0.1 NS PCr/PCr+Pi 0.51 ± 0.1 0.52 ± 0.1 NS at maximal workload PCr resynthesis 81.1 ± 79.1 53.2 ± 28.2 NS time constant LFMES, low-frequency electrical stimulation; PCr, phosphocreatine; Pi, inorganic phosphates; NS, not significant Table 3 Results of magnetic resonance imaging analysis of muscle mass volumes of the soleus and gastrocnemius muscles before and after five weeks of low-frequency electrical stimulation Stimulated muscle Muscle mass volume (cm 3 ) Before LFMES After LFMES Soleus muscle 315.2 ± 65 331.5 ± 44 Gastrocnemius muscle 254.3 ± 47 * 278.6 ± 38 LFMES, low-frequency electrical stimulation; *, P < 0.05 206

prevention of atrophy and increased resistance to fatigue. Such events could play a very important role in the situation of chronic heart failure that is typically characterised by impaired oxidative capacity. The data presented above indicate that the long-term low-frequency electrical stimulation of skeletal muscles can improve some metabolic and circulatory parameters in CHF patients. The previously published results showed a significant improvement of exercise capacity parameters (VO 2peak, VO 2AT ) in patients with CHF after 5 weeks of LFMES (9). In our study, LFMES was well tolerated. Both after 1 and 5 weeks of stimulation, quadriceps muscle strength was improved by 28%. Very similar results were also obtained by MRI. The significantly increased muscle volume mass seems to contribute to the structural and functional (and very probably also metabolic) improvement of both calf and quadriceps muscles. We can conclude that LFMES is a safe and well-tolerated method without any dangerous side-effects. In a relatively short time, it can induce a significant improvement of skeletal muscle conditions, including an increase in muscle strength and mass, in CHF patients. In some cardiac patients, LFMES may be used as an alternative to the conventional exercise training and thus provide an opportunity to improve the quality of their lives. Janãík J., Siegelová J., Homolka P., Svaãinová H., Placheta P., Varnayová L., KoÏantová L., Dob ák P., Du ek J., Fi er B., pinarová L., Toman J., Eicher J.C. NÍZKOFREKVENâNÍ ELEKTRICKÁ STIMULACE KOSTERNÍCH SVALÒ U PACIENTÒ S CHRONICK M SRDEâNÍM SELHÁNÍM Souhrn Cílem této studie bylo posouzení vlivu nízkofrekvenãní elektrické stimulace kosterních svalû u pacientû s chronick m srdeãním selháním (CHF). Dvanáct pacientû s CHF (koronarografie, NYHA III-IV, EF=19,33) bylo vy etfieno pfied pûtit denní nízkofrekvenãní elektrickou stimulací ãtyfihlav ch a l tkov ch svalû a po ní (jedna hodina dennû, 5 dnû t dnû). Pacienti byli na seznamu pro transplantaci srdce. Lékafiské reïimy v ech kontrolovan ch pacientû byly optimalizovány a pacienti byli symptomaticky stabilní. Byla provedena dynamometrie ãtyfihlav ch svalû. Nízkofrekvenãní stimulace byla dobfie sná ena. Dospûli jsme k závûru, Ïe nízkofrekvenãní elektrická stimulace ãtyfihlav ch svalû trvající jeden a pût t dnû zlep ila sílu ãtyfihlavého svalu o 28 %. V sledky anal zy MRI m.gastrocnemius ukázaly signifikantní zv ení svalového objemu po stimulaci. Tento postup by mohl b t uïiteãn pfii léãení pacientû se závaïn m chronick m srdeãním selháním. Acknowledgements This work was supported by grants from the Internal Agency of the Ministry of Health (5878 3) and from the Ministry of Education, Youth and Sports (J037/98:141100004) of the Czech Republic. 207

REFERENCES 1. Wielenga RP, Coats JS, Mosterd W, Huisveld I. The role of exercise training in chronic heart failure. Heart 1997; 78: 431 36. 2. Hornig B, Maier V, Drexler H. Physical training improves endothelial function in patients with chronic heart failure. Circulation, 1996; 93:210 14. 3. Reichmann H, Hoppeler H, Matthieu-Costello O et al. Biochemical and ultrastructural changes of skeletal muscle mitochondria after chronic electrical stimulation in rabbits. Pflugers Arch 1985; 404: 1 9. 4. Termin A, Pette D. Changes in myosin heavy-chain isoform synthesis of chronically stimulated rat fast-twitch muscle. Eur J Biochem 1992; 204: 569 73. 5. Matthieu-Costello O, Agery PJ, Wu L et al. Capillary-to-fiber ratio in rat fast-twitch nindlimb muscle after chronic electrical stimulation. J Appl Physiol 1996; 80: 904 09. 6. Skorjanc D, Jaschinski F, Heine G, Pette D. Sequential increases in capillarization and mitochondria enzymes in low-frequency stimulated rabbit muscle. Am J Physiol 1998; 274: 810 18. 7. Hanada A, Okita K, Yonezawa K et al. Dissociation between muscle metabolism and oxygen kinetics during recovery from exercise in patients with chronic heart failure. Heart 2000; 83: 161 66. 8. Savin E, Siegelová J, Fi er B, Martineaud JP. Détermination non-invasive de la compliance aortique chez l homme. Arch Physiol Biochem 1996 104(3): 257 64. 9. Maillefert JF, Eicher JC, Walker P et al. Effects of low-frequency electrical stimulation of quadriceps and calf muscles in patients with chronic heart failure. J Cardiopulm Rehabil 1998;18:277 82. 208