Concurrent exercise training potentiates the effects of angiotensin-converting enzyme inhibitor on regulatory systems of blood pressure control in ovariectomized hypertensive rats

被引:0
|
作者
Ferreira, Maycon Junior [1 ]
Dias, Danielle da Silva [2 ,3 ]
Silva, Gabriel do Carmo [1 ]
de Araujo, Amanda Aparecida [1 ]
Dutra, Marina Rascio Henriques [3 ]
Bernardes, Nathalia [4 ]
Irigoyen, Maria-Claudia [5 ]
De Angelis, Katia [1 ,3 ,6 ]
机构
[1] Univ Fed Sao Paulo UNIFESP, Exercise Physiol Lab, Sao Paulo, SP, Brazil
[2] Univ Fed Maranhao UFMA, Postgrad Program Phys Educ, Sao Luis, MA, Brazil
[3] Univ Nove Julho UNINOVE, Translat Physiol Lab, Sao Paulo, Brazil
[4] Univ Sao Judas Tadeu USJT, Human Movement Lab, Sao Paulo, Brazil
[5] Univ Sao Paulo, Heart Inst InCor, Hypertens Unit, Sao Paulo, SP, Brazil
[6] Univ Fed Sao Paulo, UNIFESP, BR-04023901 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
arterial hypertension; baroreflex sensitivity; concurrent exercise training; enalapril; CARDIOVASCULAR AUTONOMIC CONTROL; OXIDATIVE STRESS; RISK PROFILE; METABOLIC SYNDROME; HYDROGEN-PEROXIDE; SKELETAL-MUSCLE; MENOPAUSE; ENALAPRIL; AGE; ANTIOXIDANT;
D O I
10.1097/HJH.0000000000003670
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Objective: Enalapril has shown satisfactory potential in controlling increased and sustained blood pressure (BP). However, multiple dysregulated mechanisms that interact with each other and are involved in the pathophysiology of arterial hypertension may not be affected, contributing to the remaining cardiovascular risk. Using an exercise training protocol, we investigated whether adding both approaches to arterial hypertension management could promote higher modulation of regulatory mechanisms of BP in postmenopausal rats. Methods: Spontaneously hypertensive rats were allocated into sedentary (S) and ovariectomized groups: sedentary (OS), sedentary treated with enalapril maleate (OSE) and trained treated with enalapril maleate (OTE). Both the pharmacological and exercise training protocols lasted for 8 weeks. The BP was directly recorded. Inflammation and oxidative stress were evaluated in the cardiac tissue. Results: Although BP reduction was similar between OSE and OTE, trained group showed lower vasopressor systems outflow after sympathetic ganglion blocking by hexamethonium (mean BP) (OTE: -53.7 +/- 9.86 vs. OS: -75.7 +/- 19.2 mmHg). Bradycardic and tachycardic response were increased in OTE group (-1.4 +/- 0.4 and -2.6 +/- 0.4 vs. OS: -0.6 +/- 0.3 and -1.3 +/- 0.4 bpm/mmHg, respectively), as well as BP variability. In addition, the combination of approaches induced an increase in interleukin 10, antioxidant defense (catalase and glutathione peroxidase) and nitrite levels compared with the OS group. Conclusion: Despite similar BP, the inclusion of exercise training in antihypertensive drug treatment exacerbates the positive adaptations induced by enalapril alone on autonomic, inflammatory and oxidative stress profiles, probably affecting end-organ damage and remaining risk.
引用
收藏
页码:650 / 661
页数:12
相关论文
共 50 条
  • [1] Effects of exercise training on the expression of angiotensin-converting enzyme in the kidney of spontaneously hypertensive rats
    Sakuyama, A.
    Ito, O.
    Cao, P.
    Rong, R.
    Ito, D.
    Kohzuki, M.
    6TH WORLD CONGRESS OF THE INTERNATIONAL SOCIETY OF PHYSICAL AND REHABILITATION MEDICINE, 2011, : 143 - 144
  • [2] Effect of estrogen and angiotensin-converting enzyme inhibitor on vascular remodeling in ovariectomized spontaneously hypertensive rats
    Garcia, Maria P.
    Gimenez, Jose
    Serna, Mar
    Salom, Miguel G.
    Bonacasa, Barbara
    Carbonell, Luis F.
    Quesada, Tomas
    Hernandez, Isabel
    MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY, 2006, 13 (03): : 397 - 403
  • [3] Additional salutary effects of the combination of exercise training and an angiotensin-converting enzyme inhibitor on the left ventricular function of spontaneously hypertensive rats
    Ziada, Amal M.
    JOURNAL OF HYPERTENSION, 2009, 27 (06) : 1309 - 1316
  • [4] Effects of angiotensin-converting enzyme inhibitor and exercise training on exercise capacity and skeletal muscle
    Minami, Naoyoshi
    Li, Yingyu
    Guo, Qi
    Kawamura, Takayuki
    Mori, Nobuyoshi
    Nagasaka, Makoto
    Ogawa, Mika
    Ito, Osamu
    Kurosawa, Hajime
    Kanazawa, Masayuki
    Kohzuki, Masahiro
    JOURNAL OF HYPERTENSION, 2007, 25 (06) : 1241 - 1248
  • [5] Effects of angiotensin-converting enzyme inhibitor and exercise training on exercise capacity and skeletal muscle
    Minami, Naoyoshi
    Ito, Osamu
    Kanazawa, Masayuki
    Kohzuki, Masahiro
    JOURNAL OF HYPERTENSION, 2006, 24 : 300 - 300
  • [6] Effects of oestrogen treatment and angiotensin-converting enzyme inhibition on the microvasculature of ovariectomized spontaneously hypertensive rats
    Giménez, J
    Garcia, PM
    Bonacasa, B
    Carbonell, LF
    Quesada, T
    Hernández, I
    EXPERIMENTAL PHYSIOLOGY, 2006, 91 (01) : 261 - 268
  • [7] Effects of benazepril, an angiotensin-converting enzyme inhibitor, combined with CGS 35066, a selective endothelin-converting enzyme inhibitor, on arterial blood pressure in normotensive and spontaneously hypertensive rats
    Battistini, B
    Ayach, B
    Molez, S
    Blouin, A
    Jeng, AY
    CLINICAL SCIENCE, 2002, 103 : 363S - 366S
  • [8] Effects of an angiotensin-converting enzyme inhibitor and a β-blocker on cerebral arteriolar dilatation in hypertensive rats
    Chillon, JM
    Baumbach, GL
    HYPERTENSION, 2001, 37 (06) : 1388 - 1393
  • [9] Effects of Estradiol, Angiotensin-Converting Enzyme Inhibitor and Exercise Training on Exercise Capacity and Skeletal Muscle in Old Female Rats
    Guo, Qi
    Minami, Naoyoshi
    Mori, Nobuyoshi
    Nagasaka, Makoto
    Ito, Osamu
    Kurosawa, Hajime
    Kanazawa, Masayuki
    Kohzuki, Masahiro
    CLINICAL AND EXPERIMENTAL HYPERTENSION, 2010, 32 (02) : 76 - 83
  • [10] EFFECTS OF ENALAPRIL ON THE EXPRESSION OF CARDIAC ANGIOTENSIN-CONVERTING ENZYME AND ANGIOTENSIN-CONVERTING ENZYME 2 IN SPONTANEOUSLY HYPERTENSIVE RATS
    Yang Zhen
    Yu Xin
    Jiang Wenping
    HEART, 2013, 99 : E190 - E190