Acessibilidade / Reportar erro

Resistance Training in Spontaneously Hypertensive Rats with Severe Hypertension

Abstract

Background:

Resistance training (RT) has been recommended as a non-pharmacological treatment for moderate hypertension. In spite of the important role of exercise intensity on training prescription, there is still no data regarding the effects of RT intensity on severe hypertension (SH).

Objective:

This study examined the effects of two RT protocols (vertical ladder climbing), performed at different overloads of maximal weight carried (MWC), on blood pressure (BP) and muscle strength of spontaneously hypertensive rats (SHR) with SH.

Methods:

Fifteen male SHR ENT#091;206 ± 10 mmHg of systolic BP (SBP)ENT#093; and five Wistar Kyoto rats (WKY; 119 ± 10 mmHg of SBP) were divided into 4 groups: sedentary (SED-WKY) and SHR (SED-SHR); RT1-SHR training relative to body weight (~40% of MWC); and RT2-SHR training relative to MWC test (~70% of MWC). Systolic BP and heart rate (HR) were measured weekly using the tail-cuff method. The progression of muscle strength was determined once every fifteen days. The RT consisted of 3 weekly sessions on non-consecutive days for 12-weeks.

Results:

Both RT protocols prevented the increase in SBP (delta - 5 and -7 mmHg, respectively; p > 0.05), whereas SBP of the SED-SHR group increased by 19 mmHg (p < 0.05). There was a decrease in HR only for the RT1 group (p < 0.05). There was a higher increase in strength in the RT2 (140%; p < 0.05) group as compared with RT1 (11%; p > 0.05).

Conclusions:

Our data indicated that both RT protocols were effective in preventing chronic elevation of SBP in SH. Additionally, a higher RT overload induced a greater increase in muscle strength.

Keywords:
Hypertension; Strength Muscular; Resistance Exercise; Animal model

Resumo

Fundamentos:

O treinamento de força (TF) tem sido recomendado como tratamento não farmacológico para hipertensão arterial moderada. Apesar do papel importante que a intensidade do exercício desempenha sobre a prescrição do treinamento, ainda não há nenhum dado avaliando os efeitos da intensidade do TF sobre a hipertensão arterial grave (HAG).

Objetivo:

Este estudo analisou os efeitos de dois protocolos do TF(subida em escada vertical), realizados com diferentes sobrecargas do peso máximo carregado (PMC), sobre a pressão arterial (PA) e a força muscular de ratos espontaneamente hipertensos (SHR) com HAG.

Métodos:

Quinze SHR machos (206 ± 10 mmHg de PA sistólica (PAS)) e cinco ratos Wistar Kyoto (WKY; 119 ± 10 mmHg de PAS) foram divididos em 4grupos:sedentários: (SED-WKY) e SHR (SED-SHR); treinados: TF1-SHR conforme o peso corporal (~40% do PMC); e TF2-SHR conforme o teste de PMC (~70% do PMC). Foram coletadas medidas de PAS e a frequência cardíaca (FC) semanalmente usando o método de pressão arterial caudal. A progressão da força muscular foi determinada a cada 15 dias. O TF consistiu de 3 sessões semanais em dias não consecutivos durante 12 semanas.

Resultados:

Os dois protocolos de TF preveniram o aumento da PAS(respectivamente, delta - 5 e -7 mmHg; p > 0, 05), enquanto que a PAS do grupo SED-SHR aumentou em 19 mmHg (p < 0, 05). Houve queda na FC apenas para o grupo TF1 (p < 0, 05). Foi observado um aumento mas significativo de força no grupo do protocolo TF2 (140%; p < 0, 05) em comparação com o TF1 (11%; p>0, 05).

Conclusões:

Nossos dados indicam que ambos os protocolos de TF foram efetivos na prevenção da elevação crônica da PAS na HAG. Além disso, sobrecargas maiores de TF induziram a um maior aumento de força muscular.

Palavras-chave:
Pressão Arterial; Força Muscular; Treinamento Resistido; Modelo Animal

Introduction

Hypertension is well known as one of the main chronic diseases affecting modern society.11 Basu S, Millett C. Social epidemiology of hypertension in middle-income countries: determinants of prevalence, diagnosis, treatment, and control in the WHO SAGE study. Hypertension. 2013;62(1):18-26. It is highly prevalent worldwide and is considered a major risk factor for increased mortality.22 Mancia G, Fagard R, Narkiewicz K, Redon J, Zanchetti A, Bohm M, et al; Task Force for the Management of Arterial Hypertension of the European Society of Hypertension, the European Society of Cardiology. 2013 ESH/ESC Practice Guidelines for the Management of Arterial Hypertension. Blood Press. 2014;23(1):3-16. The progressive increase in BP may result in severe hypertension (SH), with systolic BP (SBP) reaching values over 180 mmHg, leading to subsequent end-organ damage, elevated arterial stiffness and left ventricular hypertrophy.11 Basu S, Millett C. Social epidemiology of hypertension in middle-income countries: determinants of prevalence, diagnosis, treatment, and control in the WHO SAGE study. Hypertension. 2013;62(1):18-26.,33 Dornas WC, Silva ME. Animal models for the study of arterial hypertension. J Biosci. 2011;36(4):731-7. Among the treatment methods, physical exercise is considered an interesting non-pharmacological adjunct to conventional therapy because of its efficacy and low cost, with minimal side effects if prescribed properly.44 Cornelissen VA, Smart NA. Exercise training for blood pressure: a systematic review and meta-analysis. J Am Heart Assoc. 2013;2(1):e004473.

The antihypertensive effects of resistance training (RT) in individuals with hypertension are less studied, with most of these studies being conducted in medicated hypertensive individuals.55 Cornelissen VA, Fagard RH, Coeckelberghs E, Vanhees L. Impact of resistance training on blood pressure and other cardiovascular risk factors: a meta-analysis of randomized, controlled trials. Hypertension. 2011;58(5):950-8. Yet, our studies showed the beneficial effects of RT on muscle strength, body composition and blood pressure (BP) in non-medicated hypertensive stage-1 patients.66 Moraes MR, Bacurau RF, Casarini DE, Jara ZP, Ronchi FA, Almeida SS, et al. Chronic conventional resistance exercise reduces blood pressure in stage 1 hypertensive men. J Strength Cond Res. 2012;26(4):1122-9.,77 Moraes MR, Bacurau RF, Simoes HG, Campbell CS, Pudo MA, Wasinski F, et al. Effect of 12 weeks of resistance exercise on post-exercise hypotension in stage 1 hypertensive individuals. J Hum Hypertens. 2012;26(9):533-9. Other studies with RT evidenced reductions in cardiovascular risk factors,88 Prestes J, Leite RD, Pereira GB, Shiguemoto GE, Bernardes CF, Asano RY, et al. Resistance training and glycogen content in ovariectomized rats. Int J Sports Med. 2012;33(7):550-4. including a lower cardiovascular overload during physical activities.99 Vescovi J, Fernhall B. Cardiac rehabilitation and resistance training: are they compatible? J Strength Condit Res. 2000;14(3):350-8. In turn, muscle strength is also directly associated with lower mortality in hypertensive patients.1010 Artero EG, Lee DC, Ruiz JR, Sui X, Ortega FB, Church TS, et al. A prospective study of muscular strength and all-cause mortality in men with hypertension. J Am Coll Cardiol. 2011;57(18):1831-7.

Of note, a reduced number of studies investigated the effects of the aerobic exercise (AE) intensity on individuals with SH at a high risk of mortality.1111 Kokkinos PF, Narayan P, Fletcher RD, Tsagadopoulos D, Papademetriou V. Effects of aerobic training on exaggerated blood pressure response to exercise in African-Americans with severe systemic hypertension treated with indapamide +/- verapamil +/- enalapril. Am J Cardiol. 1997;79(10):1424-6.,1212 Kokkinos PF, Narayan P, Colleran J, Fletcher RD, Lakshman R, Papademetriou V. Effects of moderate intensity exercise on serum lipids in African-American men with severe systemic hypertension. Am J Cardiol. 1998;81(6):732-5. We have demonstrated that AE intensity influences both nitric oxide release and post-exercise BP reduction in hypertensive women.1313 Santana HA, Moreira SR, Asano RY, Sales MM, Cordova C, Campbell CS, et al. Exercise intensity modulates nitric oxide and blood pressure responses in hypertensive older women. Aging Clin Exp Res. 2013;25(1):43-8. However, the effect of the RT intensity has been less studied.55 Cornelissen VA, Fagard RH, Coeckelberghs E, Vanhees L. Impact of resistance training on blood pressure and other cardiovascular risk factors: a meta-analysis of randomized, controlled trials. Hypertension. 2011;58(5):950-8. Although RT at higher intensity leads to greater neuromuscular adaptations, such as increased strength and muscle hypertrophy,55 Cornelissen VA, Fagard RH, Coeckelberghs E, Vanhees L. Impact of resistance training on blood pressure and other cardiovascular risk factors: a meta-analysis of randomized, controlled trials. Hypertension. 2011;58(5):950-8.,66 Moraes MR, Bacurau RF, Casarini DE, Jara ZP, Ronchi FA, Almeida SS, et al. Chronic conventional resistance exercise reduces blood pressure in stage 1 hypertensive men. J Strength Cond Res. 2012;26(4):1122-9. which are important for health and quality of life,1010 Artero EG, Lee DC, Ruiz JR, Sui X, Ortega FB, Church TS, et al. A prospective study of muscular strength and all-cause mortality in men with hypertension. J Am Coll Cardiol. 2011;57(18):1831-7. there is a lack of data in literature regarding the role of the RT intensity on BP control.

Moreover, there is no consensus regarding the dose-response of RT intensity on BP of humans with SH.44 Cornelissen VA, Smart NA. Exercise training for blood pressure: a systematic review and meta-analysis. J Am Heart Assoc. 2013;2(1):e004473.,55 Cornelissen VA, Fagard RH, Coeckelberghs E, Vanhees L. Impact of resistance training on blood pressure and other cardiovascular risk factors: a meta-analysis of randomized, controlled trials. Hypertension. 2011;58(5):950-8. Thus, the resistance exercise mode and intensity to be tolerated by patients with hypertension that would optimize the hemodynamic benefits while avoiding musculoskeletal injuries and acute cardiac complications still remain to be determined.66 Moraes MR, Bacurau RF, Casarini DE, Jara ZP, Ronchi FA, Almeida SS, et al. Chronic conventional resistance exercise reduces blood pressure in stage 1 hypertensive men. J Strength Cond Res. 2012;26(4):1122-9.,77 Moraes MR, Bacurau RF, Simoes HG, Campbell CS, Pudo MA, Wasinski F, et al. Effect of 12 weeks of resistance exercise on post-exercise hypotension in stage 1 hypertensive individuals. J Hum Hypertens. 2012;26(9):533-9.,1414 de Souza Nery S, Gomides RS, da Silva GV, de Moraes Forjaz CL, Mion D Jr, Tinucci T. Intra-arterial blood pressure response in hypertensive subjects during low- and high-intensity resistance exercise. Clinics (Sao Paulo). 2010;65(3):271-7. Yet, there is no study investigating the effects of different intensities of RT in BP control for individuals with SH.55 Cornelissen VA, Fagard RH, Coeckelberghs E, Vanhees L. Impact of resistance training on blood pressure and other cardiovascular risk factors: a meta-analysis of randomized, controlled trials. Hypertension. 2011;58(5):950-8.

Spontaneously hypertensive rat (SHR) - a polygenic animal model for essential hypertension,33 Dornas WC, Silva ME. Animal models for the study of arterial hypertension. J Biosci. 2011;36(4):731-7. has been widely used to investigate the effects of AE on BP control.1515 Evenwel R, Struyker-Boudier H. Effect of physical training on the development of hypertension in the spontaneously hypertensive rat. Pflugers Arch. 1979;381(1):19-24.

16 Kohno H, Furukawa S, Naito H, Minamitani K, Ohmori D, Yamakura F. Contribution of nitric oxide, angiotensin II and superoxide dismutase to exercise-induced attenuation of blood pressure elevation in spontaneously hypertensive rats. Jpn Heart J. 2002;43(1):25-34.

17 Petriz BA, Almeida JA, Gomes CP, Ernesto C, Pereira RW, Franco OL. Exercise performed around MLSS decreases systolic blood pressure and increases aerobic fitness in hypertensive rats. BMC Physiol. 2015;15:1.
-1818 Umemura Y, Ishiko T, Aoki K, Gunji A. Effects of voluntary exercise on bone growth and calcium metabolism in spontaneously hypertensive rats. Int J Sports Med. 1992;13(6):476-80. They are normotensives at birth and become hypertensive throughout life, like some humans. Without treatment, these animals will develop SH.33 Dornas WC, Silva ME. Animal models for the study of arterial hypertension. J Biosci. 2011;36(4):731-7. However, studies regarding resistance exercise in SHR were conducted only under acute interventions.1919 Faria T de O, Targueta GP, Angeli JK, Almeida EA, Stefanon I, Vassallo DV, et al. Acute resistance exercise reduces blood pressure and vascular reactivity, and increases endothelium-dependent relaxation in spontaneously hypertensive rats. Eur J Appl Physiol. 2010;110(2):359-66.,2020 Lizardo JH, Silveira EA, Vassallo DV, Oliveira EM. Post-resistance exercise hypotension in spontaneously hypertensive rats is mediated by nitric oxide. Clin Exp Pharmacol Physiol. 2008;35(7):782-7.

Thus, the present study was designed to investigate the effects of two RT protocols, one prescribed relative to body weight (BW),2121 Cassilhas RC, Lee KS, Venancio DP, Oliveira MG, Tufik S, de Mello MT. Resistance exercise improves hippocampus-dependent memory. Braz J Med Biol Res. 2012;45(12):1215-20. and the other based on the maximal weight carried test (MWC)2222 Hornberger TA Jr, Farrar RP. Physiological hypertrophy of the FHL muscle following 8 weeks of progressive resistance exercise in the rat. Can J Appl Physiol. 2004;29(1):16-31. performed at different intensities, on BP and muscle strength in hypertensive rats with SH. We hypothesize that a higher intensity RT may be safe and would be more effective in reducing BP and increasing muscle strength in animals with SH.

Methods

Animals

All the procedures were approved by the Institutional Ethics Committee on Animal Use, Federal University of São Paulo-UNIFESP (CEUA: 922985/2014).

Five male Wistar-Kyoto (WKY) rats and fifteen SHR rats with 17 weeks of age were obtained from the CEDEME/UNIFESP. The animals were housed in collective cages (5 animals/cage) and were maintained at a 12-12h dark-light cycle at 22 ± 2°C and 55 ± 10% relative humidity, and fed standard chow (Nuvital® CR1, Sao Paulo, Brazil), receiving water ad libitum. The BP values of the SHR groups start to increase after the fourth week of life, and from the fifth to the seventh week hypertension is installed. From this period, if left untreated, these animals will develop SH - SBP ≥ 180 mmHg, according to the VI Brazilian Guidelines on Hypertension.2323 Sociedade Brasileira de Cardiologia; Sociedade Brasileira de Hipertensão; Sociedade Brasileira de Nefrologia. ENT#091;VI Brazilian Guidelines on HypertensionENT#093;. Arq Bras Cardiol. 2010;95(1 Suppl):1-51. Erratum in: Arq Bras Cardiol. 2010;95(4):553. This shows that, following 12 weeks of training (excluding the two weeks of training adaptation), the age of the studied animals was 31 weeks at the end of the intervention.

Experimental Groups

The animals were divided into four groups: sedentary WKY rats (SED-WKY), sedentary SHR (SED-SHR), SHR RT relative to BW (RT1) and SHR RT based on MWC (RT2). The animals in the trained groups completed 3 weekly sessions of RT for 12 weeks between 06:00 and 08:00 p.m. The SED groups were kept in a box with the same dimensions of the training apparatus for 10 min to simulate the stress of handling and the environmental conditions experienced by the trained groups.

Familiarization with the Vertical Ladder

Initially, all rats were adapted to the RT protocol by climbing a vertical ladder (110 cm high•18 cm wide, 2 cm grid, 80° incline) Figure 1. A housing chamber (L•W•H = 20•20•20 cm) was located at the top of the ladder and served as a shelter during the resting period. The familiarization consisted of climbing the ladder with the load apparatus without weight for two consecutive weeks, three times per week every other day with a total of six sessions for adaptation as has already been described.2222 Hornberger TA Jr, Farrar RP. Physiological hypertrophy of the FHL muscle following 8 weeks of progressive resistance exercise in the rat. Can J Appl Physiol. 2004;29(1):16-31.

Figure 1
Apparatus used to perform resistance training in the rats, adapted from Cassilhas et al. 2012. Ladder 110cm high, 18 cm wide, 2 cm between grid steps and 80° incline. Box (L × W × H = 20 × 20 × 20 cm) located centrally at the top of the ladder served as a shelter during the resting period for the exercising rats.

BP Measurement

The SBP was measured using the tail-cuff method with the rats under conscious condition with PowerLab system (ADInstruments, Inc., Sydney, Australia). This tail-cuff method (Figure 2) is a sensitive and accurate approach for the noninvasive measurement of BP in conscious SHR.2424 Kubota Y, Umegaki K, Kagota S, Tanaka N, Nakamura K, Kunitomo M, et al. Evaluation of blood pressure measured by tail-cuff methods (without heating) in spontaneously hypertensive rats. Biol Pharm Bull. 2006;29(8):1756-8. SBP was measured once a week at the same time each day (between 6:00- 8:00 p.m.) to allow the animals to become adapted to the procedure.2525 Passos CS, Carvalho LN, Pontes RB Jr, Campos RR, Ikuta O, Boim MA. Blood pressure reducing effects of Phalaris canariensis in normotensive and spontaneously hypertensive rats. Can J Physiol Pharmacol. 2012;90(2):201-8. The rate-pressure product (RPP) was calculated as the product of HR and SBP. SBP, HR and BW measurements were taken on a weekly basis by the same evaluator.

Figure 2
Blood pressure measured by the tail-cuff method with the rats under conscious condition.

Maximal Weight Carried Test (MWC)

Two days after the familiarization procedure, all animals of the training groups had their MWC determined. For the initial climb, the weight carried was 75% of the animal's BW. After this, an additional 30g of load was added, until a maximal load was reached when the rat could not climb the entire length of the ladder between 4-9 attempts. Failure was determined when the animal could not progress up the ladder after three consecutive stimuli in the tail (using tweezers), with a 60-s rest period between each climb. The heaviest load that the animal successfully carried over the entire length of the ladder was considered the rat's MWC for that test session. Then, the next test session consisted of a ladder climb with 50%, 75%, 90%, and 100% of the rat's previous MWC with a rest interval of 60 seconds between each climb. For the subsequent ladder climbs, a 30-g load was added until a new MWC was determined; the recovery period between each climb was 120 s.2222 Hornberger TA Jr, Farrar RP. Physiological hypertrophy of the FHL muscle following 8 weeks of progressive resistance exercise in the rat. Can J Appl Physiol. 2004;29(1):16-31. This procedure was applied in the first week and repeated every 15 days throughout the 12 weeks in both groups (RT1 and RT2) in order to determine the time-course adaptations of muscle strength and the prescription of the RT2 group training intensity.

RT Protocols

Following the MWC, both RT groups (RT1 and RT2) completed three sessions / week in non-consecutive days, between 6:00 and 8:00 p.m. for 12 weeks, totalizing 36 sessions consisting of 6-8 climbing sets of 10-12 repetitions, 1' pause between sets, with a mean duration of each training session of ~10-12 minutes. The load adjustments were performed every 15 days according to the animal's BW or the MWC test. The relative intensity of each training protocol is described in Table 1.

Table 1
Progression of the intensity and volume of training loads for both protocols of resistance training

RT1 Protocol: This protocol used the animal's BW to determine the intensity of the RT sessions. A progressively heavier load using conical tubes of 50 mL with weights inside and fixed to the proximal part of the animal's tail with a Coastlock Snap Swivel and Scotch Rubber Tape (Scotch 3 M, Sao Paulo, Brazil) was used as described by Cassilhas et al.2121 Cassilhas RC, Lee KS, Venancio DP, Oliveira MG, Tufik S, de Mello MT. Resistance exercise improves hippocampus-dependent memory. Braz J Med Biol Res. 2012;45(12):1215-20. RT2 Protocol: Rat's MWC test was used to calculate and prescribe intensity for RT; this protocol was adapted from Hornberger and Farrar.2222 Hornberger TA Jr, Farrar RP. Physiological hypertrophy of the FHL muscle following 8 weeks of progressive resistance exercise in the rat. Can J Appl Physiol. 2004;29(1):16-31.

Tissue Collection

Forty-eight hours after the last training session, the rats were euthanized by decapitation. The gastrocnemius and soleus muscles were removed and weighed immediately.2222 Hornberger TA Jr, Farrar RP. Physiological hypertrophy of the FHL muscle following 8 weeks of progressive resistance exercise in the rat. Can J Appl Physiol. 2004;29(1):16-31. Gastrocnemius was chosen because of its greater proportion of type-II muscle fibers, while soleus presents a higher amount of type-I fibers. Moreover, these muscles present almost all fibers across the middle belly of the muscle and are distributed from tendon to tendon.88 Prestes J, Leite RD, Pereira GB, Shiguemoto GE, Bernardes CF, Asano RY, et al. Resistance training and glycogen content in ovariectomized rats. Int J Sports Med. 2012;33(7):550-4.

Statistical Analysis

All results are expressed as means ± standard deviation of the mean (SD). To compare BP, strength gains, sum of all weight lifted, and the animal's BW values within and between sessions Split plot ANOVA (mixed ANOVA) with post hoc Bonferroni was used and the level of significance was p < 0.05.Statistical analysis was performed using the GraphPad Prism 6.0 software (GraphPad Software, Inc, CA, USA).

Results

Body and Muscle Weights

BW and wet weight of the gastrocnemius and soleus are presented in Table 2. Pre and post-training BW within all groups were significantly different (p < 0.05). There was no significant difference in gastrocnemius and soleus muscle weight (p > 0.05). Therefore it was not need to normalize muscle mass for differences in BW.

Table 2
Anthropometric and hemodynamic data for the WKY and SHR rats pre and post-resistance training

Cardiovascular Changes

The reproductibility of SBP measures was assessed by Pearson's coefficient of variation of BP data, which demonstrated a good reliability of BP data over the 12-week experimental period, SED-WKY 2 ± 1%, SED-SHR 1 ± 1%, RT1-SHR 3 ± 1% and RT2-SHR 2 ± 1%. The results of cardiovascular parameters are presented in Table 2. The baseline SBP of the SHR groups (206 ± 10, 199 ± 6, and 206 ± 13 mmHg, SED-SHR, RT1, and RT2 - respectively) were higher as compared with those of the SED-WKY group (119 ± 4 mmHg - p < 0.05). After twelve weeks, SBP of the SED-SHR increased by 9% (∆ = 19 mmHg, p < 0.05) as compared with baseline, while SHR RT1 and RT2 groups presented a decrease by 2.5% (∆ = -5 mmHg; p > 0.05) and 3.4% (∆ = -7 mmHg; p > 0.05) in BP at the end of training, respectively.

There was a decrease in HR for the group RT1 post-training (482 ± 15 vs. 430 ± 11 bpm; p < 0.05). In addition, there was no significant difference in HR in the higher-intensity RT2 group (445 ± 27 vs. 407 ± 50; p > 0.05). The baseline RPP of the hypertensive rats (SED-SHR, RT1, and RT2) assessed throughout the training was higher when compared with that of the normotensive rats (SED-WKY, p < 0.05). The RT1 group presented a decrease in RPP pre vs. post-training (959 ± 41 vs. 834 ± 28 (mmHg•bpm)/100; p < 0.05), while there was no significant difference for the RT2 group on RPP pre vs. post-training (917 ± 26 vs 810 ± 101 (mmHg•bpm)/100; p > 0.05).

Time course BP

There was no difference in SBP within groups (pre-training vs post; p > 0.05; Figure 3), except in the SED-SHR group (p < 0.05). The SBP in the SED-SHR group increased at week 8 of protocol as compared with the trained groups; this response remained until the end of the study (p < 0.05).

Figure 3
Behavior of systolic blood pressure in WKY rats and SHR. a, p < 0.05 vs. pre (1st week); b, p < 0.05 vs. RT1; c, p < 0.05 vs. RT2; d, p < 0.05 vs. SHR groups. All values are presented as means ± SD.

Muscle Strength

SHR RT2 group presented a progressive increase in muscle strength compared with the first week (p < 0.05), while the muscle strength of the RT1 group did not increase throughout the intervention (p > 0.05). Considering both training protocols, the RT2 group had a muscle strength gain of 140 ± 16.6%, while the SHR RT1 group increased strength by 11 ± 4.8% (p < 0.05) (Figure 4). Although BW of the hypertensive rats remained unchanged during the study, the RT2 group showed a progressive increase in muscle strength relative to BW (p < 0.05). The RT2 group exhibited a muscle strength gain relative to BW of 118 ± 28.3 %, and this increase was significantly different as compared with the RT1 group in which the increase was of only 0.1 ± 3.4% (p < 0.05).

Figure 4
Delta strength gain seen by maximum weight carried in two different protocols for 12 weeks. a, p < 0.05 vs. pre (1st week); b, p < 0.05 VS. RT1. All values are presented as means ± SD.

Total Overload

The total overload consisted of the sets•repetitions•weight performed throughout the training weeks (i.e., all climbing sets held in the week added), and is presented in Figure 5 for the studied groups. The RT1 group displayed an increase in total load carried from the second week and the remaining weeks as compared to the first week (p < 0.05). The RT2 group also displayed a significant increase in this variable from the second week, and this difference was maintained throughout the experimental protocol compared with the first week (p < 0.05). In the 3rd week of training the RT2 group had a significant increase as compared with the RT1 group, and this pattern was maintained until the 12th week of training (4337 ± 280 vs. 9659 ± 928 g, RT1 and RT2 respectively; p < 0.05).

Figure 5
Total overload in grams for the 12 weeks of resistance training. a, p < 0.05 VS. pre (1st week); b, p < 0.05 vs. RT1 group. All values are presented as means ± SD.

Discussion

The effects of the intensity of RT (as % of MWC) on BP and muscle strength of SHR were evaluated. The results indicated that, although the heavier RT protocol had elicited higher muscle strength gains, the chronic benefits of both protocols on controlling BP in animals with SH were similar. While some studies have demonstrated the benefits of AE in untreated severely hypertensive rats2626 Boissiere J, Eder V, Machet MC, Courteix D, Bonnet P. Moderate exercise training does not worsen left ventricle remodeling and function in untreated severe hypertensive rats. J Appl Physiol (1985). 2008;104(2):321-7. and humans under medication.1111 Kokkinos PF, Narayan P, Fletcher RD, Tsagadopoulos D, Papademetriou V. Effects of aerobic training on exaggerated blood pressure response to exercise in African-Americans with severe systemic hypertension treated with indapamide +/- verapamil +/- enalapril. Am J Cardiol. 1997;79(10):1424-6.,1212 Kokkinos PF, Narayan P, Colleran J, Fletcher RD, Lakshman R, Papademetriou V. Effects of moderate intensity exercise on serum lipids in African-American men with severe systemic hypertension. Am J Cardiol. 1998;81(6):732-5. Moraes et al showed that moderate-intensity RT also reduces BP in non-medicated men with stage 1 hypertension similarly to the AE, and in addition to gains in muscle strength.66 Moraes MR, Bacurau RF, Casarini DE, Jara ZP, Ronchi FA, Almeida SS, et al. Chronic conventional resistance exercise reduces blood pressure in stage 1 hypertensive men. J Strength Cond Res. 2012;26(4):1122-9.

To the best of our knowledge, this was the first study analyzing the efficacy of resistance exercise and the role of training intensity for SHR with SH. Other authors, such as Araujo et al.,2727 Araujo AJ, Santos AC, Souza K dos S, Aires MB, Santana-Filho VJ, Fioretto ET, et al. Resistance training controls arterial blood pressure in rats with L-NAME- induced hypertension. Arq Bras Cardiol. 2013;100(4):339-46. already had demonstrated the efficacy of RT on BP control in animals with stage-1 hypertension (drug-induced) trained at moderate-intensity RT (50% of one-repetition maximum for four weeks). In the present study it was possible to prevent the BP increase in SHR undergoing 12 weeks of RT, regardless of the training intensity, suggesting that both intensities of RT protocols (i.e.~40% and 70% MWC) were effective as an antihypertensive nonpharmacological therapy. Furthermore, intensities of approximately 40-70% 1RM are considered suitable as a safe recommendation for hypertensive patients.44 Cornelissen VA, Smart NA. Exercise training for blood pressure: a systematic review and meta-analysis. J Am Heart Assoc. 2013;2(1):e004473.

5 Cornelissen VA, Fagard RH, Coeckelberghs E, Vanhees L. Impact of resistance training on blood pressure and other cardiovascular risk factors: a meta-analysis of randomized, controlled trials. Hypertension. 2011;58(5):950-8.

6 Moraes MR, Bacurau RF, Casarini DE, Jara ZP, Ronchi FA, Almeida SS, et al. Chronic conventional resistance exercise reduces blood pressure in stage 1 hypertensive men. J Strength Cond Res. 2012;26(4):1122-9.
-77 Moraes MR, Bacurau RF, Simoes HG, Campbell CS, Pudo MA, Wasinski F, et al. Effect of 12 weeks of resistance exercise on post-exercise hypotension in stage 1 hypertensive individuals. J Hum Hypertens. 2012;26(9):533-9.

Maintaining BP levels is very important, since each 10 mmHg increase in BP levels is associated with a 25% increase in the risk of myocardial infarction and stroke.2626 Boissiere J, Eder V, Machet MC, Courteix D, Bonnet P. Moderate exercise training does not worsen left ventricle remodeling and function in untreated severe hypertensive rats. J Appl Physiol (1985). 2008;104(2):321-7. Furthermore, it has been demonstrated that 12 weeks of RT induce changes in the cardiovascular risk factors, such as decreased lipid content in the liver, mesenteric and retroperitoneal fat depot, blood lipids and atherogenic index in ovariectomized rats.2828 Leite RD, Prestes J, Bernardes CF, Shiguemoto GE, Pereira GB, Duarte JO, et al. Effects of ovariectomy and resistance training on lipid content in skeletal muscle, liver, and heart; fat depots; and lipid profile. Appl Physiol Nutr Metab. 2009;34(6):1079-86.

By the end of the training protocols, RT1 and RT2 groups showed a downward trend on SBP by 5 mmHg and 7 mmHg (p > 0.05), respectively. These results reflect a low cardiac overload demonstrated by the evaluation of the RPP. In contrast, in the SED-SHR group there was a significant increase by 19 mmHg in BP, with a high RPP (p < 0.05). It has been shown that the decrease in HR, as observed in our RT1 group (lower intensity), may be explained by a modulation of baroreflex sensitivity leading to a decreased sympathetic tone.2929 Shimojo GL, Palma RK, Brito JO, Sanches IC, Irigoyen MC, De Angelis K. Dynamic resistance training decreases sympathetic tone in hypertensive ovariectomized rats. Braz J Med Biol Res. 2015;48(6):523-7.

When we compared our data to those of other studies using AE in SHR also with elevated BP,1616 Kohno H, Furukawa S, Naito H, Minamitani K, Ohmori D, Yamakura F. Contribution of nitric oxide, angiotensin II and superoxide dismutase to exercise-induced attenuation of blood pressure elevation in spontaneously hypertensive rats. Jpn Heart J. 2002;43(1):25-34.,3030 Agarwal D, Haque M, Sriramula S, Mariappan N, Pariaut R, Francis J. Role of proinflammatory cytokines and redox homeostasis in exercise-induced delayed progression of hypertension in spontaneously hypertensive rats. Hypertension. 2009;54(6):1393-400.,3131 Lee YI, Cho JY, Kim MH, Kim KB, Lee DJ, Lee KS. Effects of exercise training on pathological cardiac hypertrophy related gene expression and apoptosis. Eur J Appl Physiol. 2006;97(2):216-24. a similar result was found in terms of inhibition of the resting BP elevation throughout the experimental period. In view of these findings, a moderate-intensity RT also appeared to be promising in a severe condition of hypertension. Faria et al.1919 Faria T de O, Targueta GP, Angeli JK, Almeida EA, Stefanon I, Vassallo DV, et al. Acute resistance exercise reduces blood pressure and vascular reactivity, and increases endothelium-dependent relaxation in spontaneously hypertensive rats. Eur J Appl Physiol. 2010;110(2):359-66. e Lizardo et al.2020 Lizardo JH, Silveira EA, Vassallo DV, Oliveira EM. Post-resistance exercise hypotension in spontaneously hypertensive rats is mediated by nitric oxide. Clin Exp Pharmacol Physiol. 2008;35(7):782-7. found that moderate-intensity acute resistance exercises lower BP and increase the production of nitric oxide in SHR. In this sense, probably this mechanism is involved in the decrease of BP in hypertensive rats.

On the other hand, when a higher intensity was applied (70% MWC), a higher increase of muscle strength (approximately 140% and 118% relative to BW) was elicited for the RT2 group. However, the RT1 group (40% MWC) showed a little but not negligible increase in absolute strength (11%). When these values were adjusted to BW gain in this low power disappeared (0.1%). There is evidence showing that the increase in muscle strength is essential for individuals with hypertension,1010 Artero EG, Lee DC, Ruiz JR, Sui X, Ortega FB, Church TS, et al. A prospective study of muscular strength and all-cause mortality in men with hypertension. J Am Coll Cardiol. 2011;57(18):1831-7. probably because of a lower cardiovascular overload presented during activities of the daily living, mainly those in which strength performance is needed, such as carrying shopping bags, climbing stairs or dragging furniture.99 Vescovi J, Fernhall B. Cardiac rehabilitation and resistance training: are they compatible? J Strength Condit Res. 2000;14(3):350-8. Additionally, RT may increase muscle mass, which may be beneficial for the resting metabolic rate, improvement of the immune system, and prevention of falls in the elderly.55 Cornelissen VA, Fagard RH, Coeckelberghs E, Vanhees L. Impact of resistance training on blood pressure and other cardiovascular risk factors: a meta-analysis of randomized, controlled trials. Hypertension. 2011;58(5):950-8. Likewise, a recent study conducted, for two decades, in 1,506 men with hypertension suggested that high levels of muscular strength seem to protect these individuals from all-cause mortality.1010 Artero EG, Lee DC, Ruiz JR, Sui X, Ortega FB, Church TS, et al. A prospective study of muscular strength and all-cause mortality in men with hypertension. J Am Coll Cardiol. 2011;57(18):1831-7.

In our study, the weight of the soleus and gastrocnemius muscles did not increase in the trained groups in comparison to SED-SHR (p > 0.05). Hornberger and Farrar2222 Hornberger TA Jr, Farrar RP. Physiological hypertrophy of the FHL muscle following 8 weeks of progressive resistance exercise in the rat. Can J Appl Physiol. 2004;29(1):16-31. found the weight of the flexor hallucis longus muscle to be increased after 8 weeks of RT, but not the weight of the soleus, plantar, gastrocnemius and quadriceps muscles. Corroborating our findings, Duncan et al.3232 Duncan ND, Williams DA, Lynch GS. Adaptations in rat skeletal muscle following long-term resistance exercise training. Eur J Appl Physiol Occup Physiol. 1998;77(4):372-8. also did not find muscle hypertrophy gains in the extensor digitorum longus or soleus muscles after a heavy RT model in Wistar rats. Possibly, both the intensities used, duration of the training, muscles assessed, animal model, and training may explain these distinct results.

Study limitations

The lack of measurements such as morphological, biochemical and molecular parameters are a limitation of this study, and should be addressed in further investigations. For the present, however, the initial idea was to demonstrate that RT appears to be safe, even in extreme conditions of arterial hypertension. Throughout the training no deaths or incidents with animals were observed. This absence of complications in the study may be linked to the sample size.

Conclusion

In summary, these findings suggest that different intensities of RT prevent the rise of BP in rats with SH. Moreover, an important result was that the greater-intensity RT induced more expressive gain in muscle strength, without raising the resting BP levels. Thus, RT may function as an adjuvant to pharmacological treatment to prevent BP elevation at rest, in addition to benefiting the muscle strength of hypertensive patients attending a rehabilitation program.

  • Sources of Funding
    This study was funded by Capes and CNPq.
  • Study Association
    This article is part of the thesis of master submitted by Rodrigo Vanerson Passos Neves, from Universidade Federal de São Paulo.

Acknowledgments

The authors thank Prof. Ricardo Cardosos Cassilhas, Ph.D. for support with training apparatus. We would like to thank the CAPES and CNPq for the financial support for the development of this study. The authors declare that there are no conflicts of interest.

References

  • 1
    Basu S, Millett C. Social epidemiology of hypertension in middle-income countries: determinants of prevalence, diagnosis, treatment, and control in the WHO SAGE study. Hypertension. 2013;62(1):18-26.
  • 2
    Mancia G, Fagard R, Narkiewicz K, Redon J, Zanchetti A, Bohm M, et al; Task Force for the Management of Arterial Hypertension of the European Society of Hypertension, the European Society of Cardiology. 2013 ESH/ESC Practice Guidelines for the Management of Arterial Hypertension. Blood Press. 2014;23(1):3-16.
  • 3
    Dornas WC, Silva ME. Animal models for the study of arterial hypertension. J Biosci. 2011;36(4):731-7.
  • 4
    Cornelissen VA, Smart NA. Exercise training for blood pressure: a systematic review and meta-analysis. J Am Heart Assoc. 2013;2(1):e004473.
  • 5
    Cornelissen VA, Fagard RH, Coeckelberghs E, Vanhees L. Impact of resistance training on blood pressure and other cardiovascular risk factors: a meta-analysis of randomized, controlled trials. Hypertension. 2011;58(5):950-8.
  • 6
    Moraes MR, Bacurau RF, Casarini DE, Jara ZP, Ronchi FA, Almeida SS, et al. Chronic conventional resistance exercise reduces blood pressure in stage 1 hypertensive men. J Strength Cond Res. 2012;26(4):1122-9.
  • 7
    Moraes MR, Bacurau RF, Simoes HG, Campbell CS, Pudo MA, Wasinski F, et al. Effect of 12 weeks of resistance exercise on post-exercise hypotension in stage 1 hypertensive individuals. J Hum Hypertens. 2012;26(9):533-9.
  • 8
    Prestes J, Leite RD, Pereira GB, Shiguemoto GE, Bernardes CF, Asano RY, et al. Resistance training and glycogen content in ovariectomized rats. Int J Sports Med. 2012;33(7):550-4.
  • 9
    Vescovi J, Fernhall B. Cardiac rehabilitation and resistance training: are they compatible? J Strength Condit Res. 2000;14(3):350-8.
  • 10
    Artero EG, Lee DC, Ruiz JR, Sui X, Ortega FB, Church TS, et al. A prospective study of muscular strength and all-cause mortality in men with hypertension. J Am Coll Cardiol. 2011;57(18):1831-7.
  • 11
    Kokkinos PF, Narayan P, Fletcher RD, Tsagadopoulos D, Papademetriou V. Effects of aerobic training on exaggerated blood pressure response to exercise in African-Americans with severe systemic hypertension treated with indapamide +/- verapamil +/- enalapril. Am J Cardiol. 1997;79(10):1424-6.
  • 12
    Kokkinos PF, Narayan P, Colleran J, Fletcher RD, Lakshman R, Papademetriou V. Effects of moderate intensity exercise on serum lipids in African-American men with severe systemic hypertension. Am J Cardiol. 1998;81(6):732-5.
  • 13
    Santana HA, Moreira SR, Asano RY, Sales MM, Cordova C, Campbell CS, et al. Exercise intensity modulates nitric oxide and blood pressure responses in hypertensive older women. Aging Clin Exp Res. 2013;25(1):43-8.
  • 14
    de Souza Nery S, Gomides RS, da Silva GV, de Moraes Forjaz CL, Mion D Jr, Tinucci T. Intra-arterial blood pressure response in hypertensive subjects during low- and high-intensity resistance exercise. Clinics (Sao Paulo). 2010;65(3):271-7.
  • 15
    Evenwel R, Struyker-Boudier H. Effect of physical training on the development of hypertension in the spontaneously hypertensive rat. Pflugers Arch. 1979;381(1):19-24.
  • 16
    Kohno H, Furukawa S, Naito H, Minamitani K, Ohmori D, Yamakura F. Contribution of nitric oxide, angiotensin II and superoxide dismutase to exercise-induced attenuation of blood pressure elevation in spontaneously hypertensive rats. Jpn Heart J. 2002;43(1):25-34.
  • 17
    Petriz BA, Almeida JA, Gomes CP, Ernesto C, Pereira RW, Franco OL. Exercise performed around MLSS decreases systolic blood pressure and increases aerobic fitness in hypertensive rats. BMC Physiol. 2015;15:1.
  • 18
    Umemura Y, Ishiko T, Aoki K, Gunji A. Effects of voluntary exercise on bone growth and calcium metabolism in spontaneously hypertensive rats. Int J Sports Med. 1992;13(6):476-80.
  • 19
    Faria T de O, Targueta GP, Angeli JK, Almeida EA, Stefanon I, Vassallo DV, et al. Acute resistance exercise reduces blood pressure and vascular reactivity, and increases endothelium-dependent relaxation in spontaneously hypertensive rats. Eur J Appl Physiol. 2010;110(2):359-66.
  • 20
    Lizardo JH, Silveira EA, Vassallo DV, Oliveira EM. Post-resistance exercise hypotension in spontaneously hypertensive rats is mediated by nitric oxide. Clin Exp Pharmacol Physiol. 2008;35(7):782-7.
  • 21
    Cassilhas RC, Lee KS, Venancio DP, Oliveira MG, Tufik S, de Mello MT. Resistance exercise improves hippocampus-dependent memory. Braz J Med Biol Res. 2012;45(12):1215-20.
  • 22
    Hornberger TA Jr, Farrar RP. Physiological hypertrophy of the FHL muscle following 8 weeks of progressive resistance exercise in the rat. Can J Appl Physiol. 2004;29(1):16-31.
  • 23
    Sociedade Brasileira de Cardiologia; Sociedade Brasileira de Hipertensão; Sociedade Brasileira de Nefrologia. ENT#091;VI Brazilian Guidelines on HypertensionENT#093;. Arq Bras Cardiol. 2010;95(1 Suppl):1-51. Erratum in: Arq Bras Cardiol. 2010;95(4):553.
  • 24
    Kubota Y, Umegaki K, Kagota S, Tanaka N, Nakamura K, Kunitomo M, et al. Evaluation of blood pressure measured by tail-cuff methods (without heating) in spontaneously hypertensive rats. Biol Pharm Bull. 2006;29(8):1756-8.
  • 25
    Passos CS, Carvalho LN, Pontes RB Jr, Campos RR, Ikuta O, Boim MA. Blood pressure reducing effects of Phalaris canariensis in normotensive and spontaneously hypertensive rats. Can J Physiol Pharmacol. 2012;90(2):201-8.
  • 26
    Boissiere J, Eder V, Machet MC, Courteix D, Bonnet P. Moderate exercise training does not worsen left ventricle remodeling and function in untreated severe hypertensive rats. J Appl Physiol (1985). 2008;104(2):321-7.
  • 27
    Araujo AJ, Santos AC, Souza K dos S, Aires MB, Santana-Filho VJ, Fioretto ET, et al. Resistance training controls arterial blood pressure in rats with L-NAME- induced hypertension. Arq Bras Cardiol. 2013;100(4):339-46.
  • 28
    Leite RD, Prestes J, Bernardes CF, Shiguemoto GE, Pereira GB, Duarte JO, et al. Effects of ovariectomy and resistance training on lipid content in skeletal muscle, liver, and heart; fat depots; and lipid profile. Appl Physiol Nutr Metab. 2009;34(6):1079-86.
  • 29
    Shimojo GL, Palma RK, Brito JO, Sanches IC, Irigoyen MC, De Angelis K. Dynamic resistance training decreases sympathetic tone in hypertensive ovariectomized rats. Braz J Med Biol Res. 2015;48(6):523-7.
  • 30
    Agarwal D, Haque M, Sriramula S, Mariappan N, Pariaut R, Francis J. Role of proinflammatory cytokines and redox homeostasis in exercise-induced delayed progression of hypertension in spontaneously hypertensive rats. Hypertension. 2009;54(6):1393-400.
  • 31
    Lee YI, Cho JY, Kim MH, Kim KB, Lee DJ, Lee KS. Effects of exercise training on pathological cardiac hypertrophy related gene expression and apoptosis. Eur J Appl Physiol. 2006;97(2):216-24.
  • 32
    Duncan ND, Williams DA, Lynch GS. Adaptations in rat skeletal muscle following long-term resistance exercise training. Eur J Appl Physiol Occup Physiol. 1998;77(4):372-8.

Publication Dates

  • Publication in this collection
    02 Feb 2016
  • Date of issue
    Mar 2016

History

  • Received
    05 Sept 2015
  • Reviewed
    12 Nov 2015
  • Accepted
    13 Nov 2015
Sociedade Brasileira de Cardiologia - SBC Avenida Marechal Câmara, 160, sala: 330, Centro, CEP: 20020-907, (21) 3478-2700 - Rio de Janeiro - RJ - Brazil, Fax: +55 21 3478-2770 - São Paulo - SP - Brazil
E-mail: revista@cardiol.br