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Effect of aerobic exercise training on cGMP levels and blood pressure in treated hypertensive postmenopausal women

Abstract

The second messenger cGMP has been largely studied as a therapeutic target in a variety of disorders such as erectile dysfunction, arterial hypertension and heart failure. Evidence has shown thatcGMP activators are less efficient in estrogen-deficiency animals, but no studies exist involving non-pharmacological approacheson NO/cGMP signaling pathway in hypertensive postmenopausal women. The aim of this study is to examine NO/cGMP pathway, redox state and blood pressure in trained treatedhypertensive (HT) postmenopausal women comparing with normotensive (NT) group. The rationale for that is most of HT patients is encouraged by physician to perform exercise associated with pharmacological treatments.Aerobic exercise training (AET) consisted of 24 sessions, 3 times/week.Parameters were evaluated at baseline and after AET for both groups (HT=28; NT=33).In treatedHT group, AET was significantly effective in increasing cGMP concentrations (28%) accompanied by an up-regulation of SOD (97%) and catalase activity (37%). In NT group, we found an increasein SOD activity (58%). TreatedHT postmenopausal women were still responsive to AET increasing cGMP levels and up-regulating antioxidant system. It should also be emphasized that these findings provide information on the circulating biomarkers that might delay the developing of cardiovascular events in this particular population.

Keywords
hypertension; postmenopause; aerobic exercise, cGMP, redox state

Introduction

The second messenger cyclic guanosine 3’5’monophosphate (cGMP) has been largely studied as a therapeutic target in a variety of disorders such as erectile dysfunction, arterial hypertension, atherosclerosis and heart failure. Indeed, agents that increase cGMP generation or decrease its degradation,such as inhibitors of phosphodiesterase 5 (PDE5) and activators of soluble guanylylcyclase, have been investigated by different laboratories(11 Stasch JP, Pacher P, Evgenov OV. Soluble guanylatecyclase as an emerging therapeutic target in cardiopulmonary disease. Circulation. 2011;24;123(20):2263-73.,22 Buglioni A, Burnett JC Jr. New Pharmacological Strategies to Increasec GMP. Annu Rev Med.2016;67:229-43.). Strategies to enhance cGMPlevels would be useful in managementcardiovascular diseases (CVD) or in preventing their complications. Of note, it was recently demonstrated that the efficacy of PDE5 inhibition in cardiac diseases is dependent of estrogen levels in female mice(33 Sasaki H, Nagayama T, Blanton RM, Seo K, Zhang M, Zhu G, et al. PDE5 inhibitor efficacy is estrogen dependent in female heart disease. J Clin Invest 2014;124(6):2464-71. ). Thus, clinical trials examining some biomarkers in women after menopause are extremely relevant.

It has been shown that aerobic exercise training (AET) is an important approach to prevent or to mitigate the complications of CVDpromoting an improvement of eNOS/NO signaling pathway in both humans and laboratory animals(44 Zanesco A, Antunes E. Effects of exercisetraining on the cardiovascular system: pharmacologicalapproaches. Pharmacol Ther. 2007;114(3):307-17.,55 Claudino MA, Franco-Penteado CF, Priviero FB, Camargo EA, Teixeira SA, Muscará MN, et al. Upregulation of gp91phox subunit of NAD(P)H oxidase contributes to erectile dysfunction caused by long-term nitric oxide inhibition in rats: reversion by regular physical training. Urology. 2010;75(4):961-7.). Interestingly, only two studies exist evaluating the effects of AET on cGMP levels in women after menopause; however, the number of the participants were too small and no age-matched group was studied(66 Maeda S, Tanabe T, Otsuki T, Sugawara J, Iemitsu M, Miyauchi T, et al. Moderate regular exercise increases basal production of nitric oxide in elderly women. Hypertens Res. 2004;27(12):947-53.,77 Jarrete AP, Novais IP, Nunes HA, Puga GM, Delbin MA, Zanesco A.Influence of aerobic exercise training on cardiovascular and endocrine-inflammatory biomarkers in hypertensive postmenopausal women. J Clin Transl Endocrinol. 2014;1(3):108-14. ). The objective of this study was to examine the effects of AET on cGMP levels in hypertensive postmenopausal women treated with antihypertensive therapy. The rationale for that is most of hypertensive patients isencouraged by physician to perform physical exercise associated with pharmacological treatments. Therefore, it would be feasible to evaluate treatedparticipants in an attempting to detect additional effects of both interventions (AET plus antihypertensive drugs). We also compared treated hypertensive postmenopausal women with normotensive and the effects of AET on blood pressure and its association with cardiovascular biomarkers.

Materials and Methods

Participants

Sixty-one postmenopausal womenwere enrolled in the study, normotensive group (NT, n=33) and treatedhypertensive group(HT, N=28) according to previous medical diagnosis.The inclusion criteria for the participants were: reported absence of menses for at least 1 year at recruitment, body mass index ≤ 30 kg/m(22 Buglioni A, Burnett JC Jr. New Pharmacological Strategies to Increasec GMP. Annu Rev Med.2016;67:229-43.), and physically inactivity (< 150 minutes of moderate physical activity per week or < 60 minutes of vigorous physical activity per week). Exclusion criteria were: menopausal hormone therapy use, smoking, individuals with diabetes (type 1 or 2), previous CVD (stroke, heart failure), renal dysfunction, inability to perform physical exercise, poorly controlled hypertension(88 James PA, Oparil S, Carter BL, Cushman WC, Dennison-Himmelfarb C, Handler J, et al. 2014 evidence-based guideline for the management of high blood pressure in adults: report from the panel members appointed to the Eighth Joint National Committee (JNC 8). JAMA. 2014; 311: 507-20.).

The study was approved by the Ethical Committee of the Bioscience Institute of the University of São Paulo State (Ref.4395/2010) and each participant signeda written informed consent.

Experimental Design

Participants of the study underwent to 24-session ofAET, see Figure 1 for more details. Anthropometric assessment (height, weight, body mass index), aerobic capacity test, biochemical analyses were performed at baseline and after AET. The participants were instructed to maintain their habitual diet routine during the protocol.

Figure 1
Study design

Anthropometric and cardiovascular assessments

Body weight (kg) and height (cm) were determined using a scale and stadiometer (Toledo® 2096 PP) and body mass index was calculated (BMI in kg/m2). Blood pressure (BP) was performed using a semi-automatic equipment (Microlife® MIB-P3BTOA) and three BP measurements were taken. Resting BP was determined as the average of the measurements. Heart rate (HR) was assessed using a heart rate monitor (Polar® FT1 TRQ). Both BP and HR were evaluated after 20 minutes in the sitting position. All measurements were taken following the Brazilian Guidelines of Hypertension(99 Sociedade Brasileira de Cardiologia. ENT#091;VII Brazilian Guidelineson Hypertension ENT#093;. Arq Bras Cardiol.2016;107(3).).

Aerobic Capacity Test

Before the exercise tests and training program, women were familiarized to the treadmill by walking during 2-3 days, depending on each participant.After that, all participants performed 2-5 tests to determine the maximal lactate steady state (MLSS)to be used for the intensity of AET prescription. Each constant workload test with fixed walking speed (5.5 Km/h) on a treadmill (Movement® RT 250 PRO) lasted 30 min according to previousstudy(1010 Benecke R. Anaerobic thre shold, individual anaerobic thres hold, and maximal lactateste adystate in rowing. Med Sci Sports Exerc. 1995;27(6):863-7.). The exercise intensity was controlled by the inclination of the treadmill (measured in %), with the grade adjusted according to the aerobic capacity of the participant in each session. The inclination ranged between 2% and 10% during the test sessions. Capillary blood samples (25 μL) were collected by micropuncture(earlobe) at tenth and thirtieth minutes for the determination of blood lactate concentration (ENT#091;LacENT#093;)(1111 Engel PC, Jones JB.Causes and elimination of erratic blanks in enzymatic metabolite assays involving the use of NAD+ in alkaline hydrazine buffers: improved conditions for the assay of L-glutamate, L-lactate, and other metabolites.Anal Biochem. 1978;88(2):475-84.). The MLSS workload (anaerobic threshold) was defined as the highest power intensity(treadmill inclination) at which blood lactate concentration did not increase by more than 1 nmol/Lbetween the tenth and thirtiethminutes of the constant load test(1212 Beneke R. Methodo logical aspects of maximal lactates teadystate-implications for performance testing. Eur J Appl Physiol. 2003;89(1):95-9.).

Blood collection and biochemical analyses

Blood samples were collected at 07h30 a.m. in two different days: after 12 hours of overnight fast (fasting) and after daily breakfast (postprandial). Blood samples were immediately centrifuged at 3000 rpm during 10 min, and the supernatant (plasma and serum) was separated into several aliquots and stored at -80 °C for biochemicalanalyses.

Nitrite/Nitrate (NOx -) and cGMPlevels

Plasma concentrations of NOx - were measured to evaluate nitric oxide (NO) production by commercial available kit (Cayman Chemical®, Ann Arbor, MI, USA). Before starting this assay, samples were ultra-filtered through micro filter (Microcon® Centrifugal Filter Units, 10 kDa, Millipore, Bedford, MA).Plasma concentrations of cGMP were measured by ELISA method using a commercial available kit (Cayman Chemical®, Ann Arbor, MI, USA).

Antioxidant enzyme activities and lipid peroxidation

Superoxide Dismutase (SOD) and catalase (CAT) activity were measured by ELISA method using a commercial available kit (Cayman Chemical®, Ann Arbor, MI, USA). SOD’s assay detects radicals superoxide generated by xanthine oxidase and hypoxanthine, revealing the plasmatic activity of this enzyme. Catalase’s assay is based on the reaction of the enzyme with methanol in an optimal H2O2 concentration. Levels of Thiobarbituric Acid Reactive Substances (TBARS) were determined by using the TBARS assay kit again from Cayman Chemical® (Ann Arbor, MI, USA) in which the MDA-TBA adduct formed by the reaction of malondialdehyde (MDA) and thiobarbituric acid (TBA) under high temperature (90-100ºC) and acidic conditions is measured colorimetrically at 530-540nm. This method reflects lipid peroxidation andwas expressed in μM MDA.

Aerobic exercise training (AET)

The AET program began with appropriate warmup (5 min speed walking 4 km/h on a treadmill without inclination) under supervision. Participants performed the exercise session on a treadmill in a quiet room with environment-controlled temperature ((25°C) and humidity ((50%). Physical exercise was performed 3 days/week, for a total of 8 weeks (24 sessions), and each session consisting of 30 min (first 3 weeks), 35 min (following 3 weeks), and 40 min (last 2 weeks). Theintensity (treadmill inclination) was prescribed according to previous individual MLSS test. Heart rate and the rate of perceived exertion (Borg's scale) were also recorded every 10 min in each session.

Statistical analysis

Data are presented as mean ± standard error mean. Before applying statistical methods, the normality of the data was tested by the Kolmogorov-Smirnov’s test. Two-way analysis of variance (ANOVA) was used comparing the effect of AET and difference between groups (NT and HT). Bonferroni correction was used as a post hoc test. The power of the study was 95% for both groups. Statistical analysis was performed using the GraphpadPrism® version 5 software package (California, USA),and the level of significance was set at p < 0.05.

Results

Both groups were homogenous in terms of time after menopause (NT: 8.0 ± 0.9; HT: 10.3 ± 1.2 yrs). Approximately 70% of treated hypertensive women were on angiotensin system inhibition plus diuretics and 30% were on beta blocker/calcium channel blocker.

Anthropometric and cardiovascular parameters, lipid profile, and blood glucose were similar between NT and HT postmenopausal women at baseline. Exercise training did not modify these parameters(Table 1).

Table 1
Effects of aerobic exercise training on anthropometric, cardiovascular, biochemical parameters and aerobic capacity test in hypertensive postmenopausal women comparing with normotensive

Exercise training for 24 sessions was effective in increasing the exercise intensitywithout changes in blood lactate concentration, approximately 38% and 35% for NT and HT women, respectively, showing the efficacy of the AET in improving aerobic capacity.

Given that experimental studies have attributed to the greater prevalence of arterial hypertension in women after menopause to endothelial dysfunction, we evaluated NO/cGMP signaling pathway in both groups. We found no differences in the concentrations of NOx - and cGMP between NT and HT women at baseline. In fasting state, a marked increase in the concentration of NOx - was found in trained HT group, approximately 42%, as compared with trained NT group. At postprandial state, trained hypertensive group had an increase in cGMP concentration (28%), but no changes in NOx - levels were observed. Figure 2 illustrates these data.

We also examined fasting redox state by measuring TBARS concentration and antioxidant enzymes in plasma. At baseline, no differences were found between the groups and exercise training did not change TBARS concentration that reflects lipid peroxidation. In contrast, SOD activity was significantly increased in both groups (58 and 97% for NT and HT women, respectively). Moreover, trained HT group presented higher SOD activity as compared with NT women, approximately 27%. Interestingly, catalase activity was significantly increased in HT group, approximately 73% (Figure 3).

Figure 2
Effects of aerobic exercise training on NOx - and cGMPinnormotensive and hypertensivepostmenopausal women at baseline and post aerobic exercise training.

Figure 3
Fasting redox state in normotensive and hypertensive postmenopausal women at baseline and post aerobic exercise training.

Discussion

Our findings show that treatedHT postmenopausal women are still responsive to AET with increase incGMPlevelsand up-regulation of the antioxidant system even though BP was well-controlled.

Arterial hypertension is a chronic disease that maylead to a variety of complications such as vascular remodeling, heart attack, stroke and heart failure(1313 Borlaug BA, Paulus WJ. Heart failure with preserved ejection fraction: pathophysiology, diagnosis, and treatment. EurHeart J. 2011;32(6):670-9. ). The Global Burden of Disease Study identified that uncontrolled BP is the leading risk factor for death and disability-adjusted life-years lost(1414 Lim SS, Vos T, Flaxman AD, Danaei G, Shibuya K, Adair-Rohani H,et al. A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2001;380:2224-60. ). Moreover, it has shown that the incidence of CVD in women increases after menopause(1515 Mozaffarian D, Benjamin EJ, Go AS, Arnett DK, Blaha MJ, Cushman M, et al. Heart disease and stroke statistics-2015 update: a report from the American Heart Association. Circulation. 2015.27;131(4):e29-322.). It is believed that sex hormones play a major role and estrogen deficiency might be the primary cause of this phenomenon in women in climacteric period; however, most of studies are based on experimental studies, using ovariectomized animals or isolated cells(1616 Maranon R, Reckelhoff JF. Sex and gender differences in control of blood pressure. ClinSci (Lond) 2013;125:311-18.).

Although no changes in blood pressure values were found in trained HT group, AET was effective in promoting increase in cardiovascular biomarkers that play a crucial role on BP regulation or oxidative stress modulation. Accordingly, it has been demonstrated that exercise training is more effective in lowering blood pressure in uncontrolled hypertensive subjects(1717 Fagard RH. Exercise is good for your blood pressure: effects of endurance training and resistance training. Clin Exp Pharmacol Physiol. 2006;33(9):853-6.). Moreover, epidemiological studies have systematically reportedthat higher fitness levels could delay the developing of arterial hypertension or its complications, showing the beneficial effects of physical activity/exercise on CVD(1818 Blair SN, Kohl HW 3rd, Paffenbarger RS Jr, Clark DG, Cooper KH, Gibbons LW. Physical fitness and all-cause mortality. A prospective study of healthy men and women. JAMA. 1989;262(17):2395-401.,1919 Liu J, Sui X, Lavie CJ, Zhou H, Park YM, Cai B, et al. Effects of cardiorespiratoryfitness on bloodpressuretrajectory with aging in a cohort of healthymen. J Am Coll Cardiol. 2014;64(12):1245-53.). Thus, our findings are clinically relevant since most of HT patients are encouraged to get involved in physical activities or in exercise training under supervision.

Of note, greatinterest exists regarding new pharmacological targetsto increase cGMPlevels,either increasing cGMP generation or decreasing its degradation mainly in patients with heart failure(22 Buglioni A, Burnett JC Jr. New Pharmacological Strategies to Increasec GMP. Annu Rev Med.2016;67:229-43.). Nevertheless, recent clinical data were disappointing mainly because of up-regulation of PDE5 during long-term inhibition treatment(2020 Redfield MM, Chen HH, Borlaug BA, Semigran MJ, Lee KL, Lewis G, et al. Effect of phosphodiesterase-5 inhibition on exercise capacity and clinical status in heart failure with preserved ejection fraction: a randomized clinical trial. JAMA. 2013;309(12):1268-77.).Interestingly, our study shows that HT postmenopausal women are responsive in increasingcGMP levels after AET that would prevent or, so far, delay the developing of heart failure during climacteric period.

Only one study evaluated postmenopausal women andfound no differences in cGMP levels between the control group and patients with unstable coronary artery disease (CAD) (Nielsen et al, 1999). Indeed, patients with signs of ischaemia in the form of ST-depression during an exercise test had higher levels of cGMP than those without signs of ischaemia.Another study found no differences in basal plasma cGMP levels between healthy physically active, healthy inactive, and in patients withcoronary artery disease, however, short-term aerobic exercise increased cGMP urinary concentrations in healthy subjects and in CAD patients, if measured during and soon after termination of the exercise (Alfieri et al, 2000). Nevertheless, the participants were men up to 49 years old and there is no data available in hypertensive postmenopausal women.

The possible mechanism for that may be related to the effect of shear stress induced by physical exercise. Indeed, physical exercise is a powerful stimulus to promote vascular shear stress activating mechanosensors present in endothelial cells. These mechanosensors are coupled to complex biochemical signaling pathways, such as Ras/MEK/ERK, c-Src, G proteins, ion channel, VE-cadherin, and PI3K/Akt, which in turn, regulate NO/cGMP pathway(2121 Balligand JL, Feron O, Dessy C. eNOS activation by physical forces: from short-term regulation of contraction to chronic remodeling of cardiovascular tissues. Physiol Rev. 2009;89(2):481-534.). Accordingly, the beneficial effects of physical training on cardiovascular system are strongly associated with increased blood flow(44 Zanesco A, Antunes E. Effects of exercisetraining on the cardiovascular system: pharmacologicalapproaches. Pharmacol Ther. 2007;114(3):307-17.).

Differently from experimental studies, no difference was found in TBARS levels and antioxidant enzymes activity between the two groups at baseline. Indeed, few studies exist examining this issue in human population. A previous study showed an increase in oxidative stress in obese postmenopausal women(2222 Uppoor RB, Rajesh A, Srinivasan MP, Unnikrishnan B, Holla R. Oxidative Stress in Obese Postmenopausal Women: An Additive Burden for Atherosclerosis. J Clin Diagn Res. 2015;9(12):OC03-OC05.) whereas another study demonstrated a decrease in antioxidant defense in older population as compared to young in healthy women and men(2323 Singh K, Kaur S, Kumari K, Singh G, Kaur A.Alterations in Lipid Peroxidation and Certain Antioxidant Enzymes in Different Age Groups under Physiological Conditions. J Hum Ecol. 2009;27(2):143-147.). Regarding the effect of physical exercise, we found an up-regulation of SOD activity in both groups and this effect was greater in hypertensive group. Accordingly, a cross-sectional study evaluating postmenopausal women demonstrated increased total SOD, cytosolic SOD and CAT activities in physically active group in comparisonto sedentary(2424 Farinha J, De Carvalho N, Steckling F, De Vargas S, Courtes A, Stefanello S, Martins C, Bresciani G, Dos Santos D, Soares F. An active lifestyle induces positive antioxidant enzyme modulation in peripheral blood mononuclear cells of overweight/obese postmenopausal women. Life Sci. 2015;121:152-7. ). Another study reported increased SOD activity in overweight and obese postmenopausal women after a 4-month program of 1-hour low- intensity physical activity for 2 days per week(2525 Merino J,Ferré R, Girona J, Aguas D, Cabré A, Plana N, et al. Evenlow physical activity levels improve vascular function in overweight and obesepostmenopausalwomen. Menopause. 2013;20(10):1036-42. ). Collectively, AET is an important approach to promote up-regulation antioxidant enzymes in postmenopausal women that might result in beneficial effect in cardiovascular system. However, more studies are necessary to examine the exercise-related oxidative stress in this population in an attempt toprovide new approachesfor health care and preventing the deleterious effects of CVD in women.

Conclusion

In conclusion, our findings show that AET is an effective non-pharmacological approach in increasing cGMP levels as well as up-regulating antioxidant enzymes in treatedHT postmenopausal women. It should also be emphasized that these findings provide information on the circulating biomarkers that might delay the developing of cardiovascular events in this population.

References

  • 1
    Stasch JP, Pacher P, Evgenov OV. Soluble guanylatecyclase as an emerging therapeutic target in cardiopulmonary disease. Circulation. 2011;24;123(20):2263-73.
  • 2
    Buglioni A, Burnett JC Jr. New Pharmacological Strategies to Increasec GMP. Annu Rev Med.2016;67:229-43.
  • 3
    Sasaki H, Nagayama T, Blanton RM, Seo K, Zhang M, Zhu G, et al. PDE5 inhibitor efficacy is estrogen dependent in female heart disease. J Clin Invest 2014;124(6):2464-71.
  • 4
    Zanesco A, Antunes E. Effects of exercisetraining on the cardiovascular system: pharmacologicalapproaches. Pharmacol Ther. 2007;114(3):307-17.
  • 5
    Claudino MA, Franco-Penteado CF, Priviero FB, Camargo EA, Teixeira SA, Muscará MN, et al. Upregulation of gp91phox subunit of NAD(P)H oxidase contributes to erectile dysfunction caused by long-term nitric oxide inhibition in rats: reversion by regular physical training. Urology. 2010;75(4):961-7.
  • 6
    Maeda S, Tanabe T, Otsuki T, Sugawara J, Iemitsu M, Miyauchi T, et al. Moderate regular exercise increases basal production of nitric oxide in elderly women. Hypertens Res. 2004;27(12):947-53.
  • 7
    Jarrete AP, Novais IP, Nunes HA, Puga GM, Delbin MA, Zanesco A.Influence of aerobic exercise training on cardiovascular and endocrine-inflammatory biomarkers in hypertensive postmenopausal women. J Clin Transl Endocrinol. 2014;1(3):108-14.
  • 8
    James PA, Oparil S, Carter BL, Cushman WC, Dennison-Himmelfarb C, Handler J, et al. 2014 evidence-based guideline for the management of high blood pressure in adults: report from the panel members appointed to the Eighth Joint National Committee (JNC 8). JAMA. 2014; 311: 507-20.
  • 9
    Sociedade Brasileira de Cardiologia. ENT#091;VII Brazilian Guidelineson Hypertension ENT#093;. Arq Bras Cardiol.2016;107(3).
  • 10
    Benecke R. Anaerobic thre shold, individual anaerobic thres hold, and maximal lactateste adystate in rowing. Med Sci Sports Exerc. 1995;27(6):863-7.
  • 11
    Engel PC, Jones JB.Causes and elimination of erratic blanks in enzymatic metabolite assays involving the use of NAD+ in alkaline hydrazine buffers: improved conditions for the assay of L-glutamate, L-lactate, and other metabolites.Anal Biochem. 1978;88(2):475-84.
  • 12
    Beneke R. Methodo logical aspects of maximal lactates teadystate-implications for performance testing. Eur J Appl Physiol. 2003;89(1):95-9.
  • 13
    Borlaug BA, Paulus WJ. Heart failure with preserved ejection fraction: pathophysiology, diagnosis, and treatment. EurHeart J. 2011;32(6):670-9.
  • 14
    Lim SS, Vos T, Flaxman AD, Danaei G, Shibuya K, Adair-Rohani H,et al. A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2001;380:2224-60.
  • 15
    Mozaffarian D, Benjamin EJ, Go AS, Arnett DK, Blaha MJ, Cushman M, et al. Heart disease and stroke statistics-2015 update: a report from the American Heart Association. Circulation. 2015.27;131(4):e29-322.
  • 16
    Maranon R, Reckelhoff JF. Sex and gender differences in control of blood pressure. ClinSci (Lond) 2013;125:311-18.
  • 17
    Fagard RH. Exercise is good for your blood pressure: effects of endurance training and resistance training. Clin Exp Pharmacol Physiol. 2006;33(9):853-6.
  • 18
    Blair SN, Kohl HW 3rd, Paffenbarger RS Jr, Clark DG, Cooper KH, Gibbons LW. Physical fitness and all-cause mortality. A prospective study of healthy men and women. JAMA. 1989;262(17):2395-401.
  • 19
    Liu J, Sui X, Lavie CJ, Zhou H, Park YM, Cai B, et al. Effects of cardiorespiratoryfitness on bloodpressuretrajectory with aging in a cohort of healthymen. J Am Coll Cardiol. 2014;64(12):1245-53.
  • 20
    Redfield MM, Chen HH, Borlaug BA, Semigran MJ, Lee KL, Lewis G, et al. Effect of phosphodiesterase-5 inhibition on exercise capacity and clinical status in heart failure with preserved ejection fraction: a randomized clinical trial. JAMA. 2013;309(12):1268-77.
  • 21
    Balligand JL, Feron O, Dessy C. eNOS activation by physical forces: from short-term regulation of contraction to chronic remodeling of cardiovascular tissues. Physiol Rev. 2009;89(2):481-534.
  • 22
    Uppoor RB, Rajesh A, Srinivasan MP, Unnikrishnan B, Holla R. Oxidative Stress in Obese Postmenopausal Women: An Additive Burden for Atherosclerosis. J Clin Diagn Res. 2015;9(12):OC03-OC05.
  • 23
    Singh K, Kaur S, Kumari K, Singh G, Kaur A.Alterations in Lipid Peroxidation and Certain Antioxidant Enzymes in Different Age Groups under Physiological Conditions. J Hum Ecol. 2009;27(2):143-147.
  • 24
    Farinha J, De Carvalho N, Steckling F, De Vargas S, Courtes A, Stefanello S, Martins C, Bresciani G, Dos Santos D, Soares F. An active lifestyle induces positive antioxidant enzyme modulation in peripheral blood mononuclear cells of overweight/obese postmenopausal women. Life Sci. 2015;121:152-7.
  • 25
    Merino J,Ferré R, Girona J, Aguas D, Cabré A, Plana N, et al. Evenlow physical activity levels improve vascular function in overweight and obesepostmenopausalwomen. Menopause. 2013;20(10):1036-42.

Publication Dates

  • Publication in this collection
    Mar 2017

History

  • Received
    11 Dec 2016
  • Accepted
    12 Dec 2016
Universidade Estadual Paulista Universidade Estadual Paulista, Av. 24-A, 1515, 13506-900 Rio Claro, SP/Brasil, Tel.: (55 19) 3526-4330 - Rio Claro - SP - Brazil
E-mail: motriz.rc@unesp.br