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Arquivos Brasileiros de Cardiologia

Print version ISSN 0066-782XOn-line version ISSN 1678-4170

Arq. Bras. Cardiol. vol.78 no.3 São Paulo Mar. 2002

http://dx.doi.org/10.1590/S0066-782X2002000300005 

a05v78n3

Original Article


 

Effect of Propafenone on the Contractile Activity of Latissimus Dorsi Muscle Isolated in an Organ Chamber. Experimental Study in Rats

 

Ricardo Simões, Eduardo Luis Guimarães Machado, Odilon Gariglio de Alvarenga Freitas, Maria da Consolação Vieira Moreira, Otoni Moreira Gomes

Belo Horizonte, MG - Brazil

 

 

OBJECTIVE: To study the effect of propafenone on the contractile function of latissimus dorsi muscle isolated from rats in an organ chamber.
METHODS: We studied 20
latissimus dorsi muscles of Wistar rats and divided them into 2 groups: group I (n=10), or control group - we studied the feasibility of muscle contractility; group II (n=10), in which the contralateral muscles were grouped - we analyzed the effect of propafenone on muscle contractility. After building a muscle ring, 8 periods of sequential 2-minute baths were performed, with intervals of preprogrammed electrical stimulation using a pacemaker of 50 stimuli/min. In group II, propafenone, at the concentration of 9.8 µg/mL, was added to the bath in period 2 and withdrawn in period 4.
RESULTS: In group I, no significant depression in muscle contraction occurred up to period 5 (p>0.05). In group II, a significant depression occurred in all periods, except between the last 2 periods (p<0.05). Comparing groups I and II only in period 1, which was a standard period for both groups, we found no significant difference (p>0.05).
CONCLUSION: Propafenone had a depressing effect on the contractile function of
latissimus dorsi muscle isolated from rats and studied in an organ chamber.
Key words: skeletal muscle/drug effect, propafenone/toxicity, cardiomyoplasty

 

 

One aspect of myocardial failure syndrome is the progressive loss of systolic function, and, therefore, dilation of the cardiac cavities; the results obtained with the pharmacological treatment are not totally satisfactory 1-10. In an attempt to increase systolic contraction, pedicled flaps of skeletal muscle involving the heart were projected.

In 1985, Carpentier and Chachques 11 reported the first cardiomyoplasty with successful clinical evolution. Latissimus dorsi (LD) muscle was chosen because it is wide enough, is conveniently located, and is easily mobilized towards the inside of the chest. Another advantage is its long vascular-nervous pedicle, which facilitates electrical conditioning with a pacemaker, and the presence of the thoracodorsal nerve specifically developed for cardiomyoplasty 12,13. This procedure is mainly indicated for patients with New York Heart Association functional class III congestive heart failure, because it provides a myocardial compression effect and also prevents progressive cardiac dilation 11,14,15. Even though a low degree of atrophy and a drop in tension was found in LD muscle, resistance to fatigue was significantly increased when it was electrically conditioned. Adaptation of the skeletal muscle is confirmed by a complete histological transformation, in which the rapid-contraction fibers acquire all the physiological, biochemical, and morphological attributes of the slow-contraction fibers 13,16-18.

Considering that patients with congestive heart failure have an increased incidence of arrhythmias and a higher risk of sudden death, some of them may require antiarrhythmic drugs. Some large studies about the action of antiarrhythmic drugs showed proarrhythmic effects and a myocardial depressing effect of some of these drugs, leading to an increase in mortality 19-23. These effects occurred mainly with drugs of the Ic group 24, such as propafenone, which is frequently used in clinical practice 25-29. Would the skeletal muscle involving the heart be influenced by the depressing action of antiarrhythmic drugs? The objective of our study was to analyze the effects of propafenone [2'-2 hydroxy – 3 –(propylamine) – propoxy – 3 phenylpropylfenone chloride].

 

Methods

We used 10 male Rattus norvegicus of the Wistar variety, with ages ranging from 18 to 24 weeks, and weight from 320 to 360 g (mean = 340±14.53 g). They were divided into 2 groups as follows: group I - 10 LD muscles were isolated with a mean weight of 1.25±0.09 g and were used as controls; group II – 10 LD muscles were isolated with a mean weight of 1.27±0.103 g and were studied after addition of propafenone to the perfusion solution. We used, alternately, one of the muscles as group I and that of the opposite side as group II. The rats were anesthetized with diethyl ether in a fume cupboard, and their mean time of anesthetic induction was 14±5 minutes.

We used Krebs-Henseleit solution bubbled in a carbonic mixture to maintain muscle feasibility (95% O2 and 5% CO2) 30.

For measurements and recordings, we used the GRASS® transducer (USA) FT 03 model, and a BESE-Bio III biomonitor (MG, Brazil).

Electrical stimulation was performed with a BRASCOR 12 pacemaker with the following programming: frequency of 50 stimuli/minute, pulse amplitude of 20 mA, and pulse width of 0.5 milliseconds.

We used the Cleveland Clinic Foundation model (USA) organ chamber with a volume capacity of 25 mL for the nourishing solution and a thermoregulated bath, HC-FM-USP model (SP, Brazil).

We isolated the LD muscles bilaterally and implanted pacemaker electrodes in 2 distinct anatomical planes. In the superior surface of the muscle, 1 electrode was fixed along the extension of that plane with 3 suture stitches (nylon 5-0) and connected to the positive pole of the electrical stimulator. In the inferior surface of the muscle, the 2nd electrode was fixed along the entire circular extension of the ring and connected to the negative pole.

The muscular ring was modeled using the interposition of an acrylic tube, which was surrounded by the LD muscle. After the electrodes were positioned, the mold was removed, and the insertion of the muscle in the scapula was sectioned. Then, the muscle ring was fixed in the organ chamber by traction straps in the inferior rod and in the tensiometer, in its superior part (fig. 1) 30. The mean time elapsed from muscle dissection and isolation until its positioning in the organ chamber was 5.0 ± 2.0 minutes.

 

 

As we could not find any previous report about the technique in the consulted literature, we performed the baths with 8 periods of 2 minutes each for obtaining adequate readings for analysis.

The periods consisted of immersion of the muscular ring in previously warmed Krebs-Henseleit solution bubbled in a carbonic mixture 31, where the muscular ring was maintained at rest for 2 minutes. Then, the muscular structure was removed from the solution to avoid multifocal depolarization and electrical stimulation. After stabilizing the tracing, the contractile muscle force was recorded. We used calibration with equivalence of 1.0cm to 2.0g of tension (22-X amplification) and recorded 3 deflections for measurement; this way, we obtained the mean of the addition of the readings and tabulation of data for analysis. Period 1 was common for the 2 groups. For group II, propafenone (245 µg) was added to the perfusion solution in the bath of period 2, and this was done according to the recommended dosage of propafenone for arrhythmia conversion in bolus of 1 to 2mg/kg. Period 3 consisted of maintaining the same solution of period 2, without or with propafenone for groups I or II, respectively. From period 4 on, the bathing solutions were successively changed until period 8, aiming to promote washing of the drug, when it was present. This procedure was the same for both groups.

At the end of each experiment, the rats and muscles were weighed separately. At the end of periods 1 and 3, the solution present inside the chamber was collected for gas analysis and pH determination for both groups.

In the statistical analysis, we used the following methods: analysis of variance, Duncan multiple range test (for multiple comparisons), and the least significant difference (LSD) test (for comparing mean values).

 

Results

The comparative analysis of the tensions developed by the muscles in group I in the different periods showed no significant difference until period 4 (p>0.05) (tab. I). These data also showed the nonexistence of the so-called "solution effect." That is, the solution maintained between periods 2 and 3 did not influence the contractile muscle force (p>0.05). From period 5 to period 8, the drop was significant with p<0.05 (tab. I).

 

 

Group II exhibited a significant drop in contractile muscle force from period 2 on (p<0.05), except for the last 2 periods (p>0.05) (tab. I).

Figure 2 depicts the means with their respective standard errors, and the difference between the 2 groups can be seen with a more marked drop in the contractile muscle force in group II (p<0.05).

 

 

When comparisons of the percentage drop in contractile muscle force were performed between 2 subsequent periods for group I in regard to group II (fig. 3), we observed that this drop occurred until the last period of the experiment. The mean percentage of total drop was 45.3% for group I and 65.4% for group II.

 

 

Discussion

Left ventricular ejection fraction is one of the major predictors of survival in the analysis of heart disorders, and its drop results from cardiac dilation 19,32,33. Some studies showed the efficacy in generating systolic force by surrounding the heart with muscular flaps 11,14. Several experiments showed the capacity to replace cardiac muscle force, as a pump, synchronous with the QRS complex 11,14,34-41.

Data in the literature have shown that drugs with a primary cardiac effect also act upon skeletal muscle modifying its function 42-44. Dubelaar et al 42 studied the effect of L-carnitine on LD muscle of dogs and showed an increase in its contractile force. Other drugs, such as the steroids methenolon and clenbuterol, may increase skeletal muscle mass and contractile force when associated with the cardiomyoplasty technique 43,44. Howell et al 45 showed the effects of some drugs, such as isoproterenol, acting on skeletal muscle and producing positive inotropism in the rapid-contraction fibers and negative inotropism in the slow-contraction fibers. They also showed that aminophylline and theophylline have an effect on skeletal muscle, which was evidenced through muscle tremor, mainly postural.

Propafenone belongs to the Ic class of antiarrhythmic drugs 24. Its clinical use began in the 1980s due to its characteristics as a local anesthetic and stabilizer of myocardial cell membrane. Propafenone has been shown to reduce the amplitude of the action potential (phase 0), the conduction in the atrioventricular node, and the ascending velocity of the curve of spontaneous diastolic depolarization (phase 4). Depending on the metabolic pathway of hydroxylation of propafenone, different levels of its metabolites (5 - hydroxypropafenone and N-dipropylpropafenone) may result, promoting a mild beta-blocking action 45-47. Propafenone has a predominantly inhibitory effect on sodium (Na+) channels, and a less effective impact on calcium (Ca++) and potassium (K+) channels 24,25. In reality, its effect on calcium (Ca++) channels was considered nonsignificant. However, the hypothesis that this might be the probable cause of myocardial depression was raised, leading to an increase in final diastolic pressure (DP2) and a reduction in systolic indices 26-28.

Some studies have shown the effect of propafenone on vascular smooth muscle relaxation after endothelial skeletonizing, confirming its depressing action on the muscle 29. In 1987, Fierro et al 48 reported 1 case of myasthenia-like syndrome induced by propafenone, but they did not define the drug's action on neuromuscular receptors and myofibrils.

Some animal species have pharmacokinetic characteristics related to the tendency towards a concentration rate (plasma/tissue) below 1 at the skeletal muscle, showing that the muscle serves as a drug reservoir 49.

A great variety of acute and chronic pathophysiological and pharmacological factors may cause changes in skeletal muscle contraction and fatigue and in its adaptive responses 42-45. These facts indirectly support the results obtained in the present study.

Rats were the animals chosen for our study because of the size of and also the constitution of the latissimus dorsi muscle to be analyzed in our study. In small animals, this muscle has a larger number of type I fibers, because it requires a greater resistance to fatigue, as the animals perform repetitive movements more frequently.

Side alternation, left and right, for muscles in groups I or II aimed to alter the disposition of muscle fibers for the confection of the muscle ring, so that muscle feasibility would be the same, independent of the side.

A constant temperature of 37ºC, with a variation of 0.5ºC, was maintained, and it was measured in real time with a catheter inserted into the bath solution, reflecting the baseline levels of the species studied 39. The pH of the medium was maintained even after addition of propafenone, because metabolic acidosis reduced the drug's action; however, variations within physiological limits were respected 50,51.

In the study of the action of propafenone, when the analysis of variance indicated a depressing effect, the least significant difference test for comparing mean values was used to evaluate this effect between the different periods. The interaction, when significant, indicated the existence of differences in the behavior of the muscle for each period when periods were compared with one another.

In group I, no significant (p>0.05) drop in muscle contraction was observed until period 4 (2.78g, 2.75g, 2.68g, 2.58g, respectively); from period 5 on, the reduction in contractile force became significant (p<0.05) (2.39g, 2.17g, 1.79g, 1.52g, respectively). This may be justified by the progressive loss of muscle feasibility during the experiment. In group II, after addition of propafenone in period 2, a drop in muscle contraction could be observed until period 7 (p<0.05) (2.75g, 2.21g, 1.86g, 1.59g, 1.43g, 1.27g, 1.09g, respectively); no difference between the last 2 periods was observed (p>0.05) (1.09g; 0.95g, respectively). One of the hypotheses would be the possible washing away of propafenone impregnated in LD muscle through the consecutive baths performed. Another hypothesis is the progressive loss of muscle feasibility with a drop in contractile force, even when immersed in a solution adequate for study.

In regard to the Krebs-Henseleit solution, which is considered adequate for maintaining muscle feasibility, we analyzed the possibility that it could cause alterations in the results, the so-called "solution effect." To check the effect of the solution on the experiment, the analysis of variance of the results of the means obtained in periods 2, 3, and 4 was performed. In the protocol established, the change of solution between periods 2 and 3 in both groups was not performed, and the action of propafenone was maintained for approximately 5 minutes. Therefore, we admit that no influence of the solution occurred on the results, because group I maintained the stability when the means were compared until period 4 (p>0.05).

In the multiple comparison of the means of the different periods between the groups, we could not reject the hypothesis of equality in the first period only, because it was common to both groups. From period 2 on, the difference was maintained significantly until the end of the experiment (p<0.05).

In regard to LD muscle contractile force, the evaluation of the percentage of its total drop was 45.3% in group I and 65.4% in group II, evidencing a greater percentage of drop with the use of propafenone.

Considering the limitations of the present study, we may conclude that propafenone determines depression of the LD muscle contractile force in rats, with depression of muscle contraction with no recovery, even after sequential baths with a solution with no drug; the use of propafenone, in an acute administration regimen, may affect muscle performance in the cardiomyoplasty technique. Therefore, the control of ventricular function in patients undergoing cardiomyoplasty and requiring the use of propafenone should be carefully observed during the impregnation phase to decide about risks and benefits.

Based on the results of this study, the following facts should be considered because they may constitute obstacles to the immediate clinical application of this technique: LD muscle did not undergo proper preconditioning in the cardiomyoplasty technique; the different types of fibers that constitute LD muscle would be under the influence of the differentiated action of propafenone, as well as that of the dose being used; we still lack adequate definitions of the interference of the species-dependent characteristics for generalizing the conclusions.

 

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