Effects of PDE type 5 inhibitors on Left Ventricular Diastolic Dysfunction in Resistant Hypertension

被引:1
作者
Cabral de Faria, Ana Paula [1 ]
Modolo, Rodrigo [1 ]
Domingues Moreno, Beatriz Vaz [1 ]
Moreno, Heitor [1 ]
机构
[1] Univ Estadual Campinas FCM UNICAMP, Fac Ciencias Med, Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
B-NATRIURETIC PEPTIDE; HEART-FAILURE; NITRIC-OXIDE; IN-VIVO; L-NAME; SILDENAFIL; RELAXATION; PHOSPHODIESTERASE-5; HYPERTROPHY; PREVALENCE;
D O I
10.5935/abc.20140159
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Resistant hypertension (RHTN) is a multifactorial disease characterized by blood pressure (BP) levels above goal (140/90 mmHg) in spite of the concurrent use of three or more antihypertensive drugs of different classes. Moreover, it is well known that RHTN subjects have high prevalence of left ventricular diastolic dysfunction (LVDD), which leads to increased risk of heart failure progression. This review gathers data from studies evaluating the effects of phosphodiesterase-5 (PDE-5) inhibitors (administration of acute sildenafil and short-term tadalafil) on diastolic function, biochemical and hemodynamic parameters in patients with RHTN. Acute study with sildenafil treatment found that inhibition of PDE-5 improved hemodynamic parameters and diastolic relaxation. In addition, short-term study with the use of tadalafil demonstrated improvement of LVDD, cGMP and BNP-32 levels, regardless of BP reduction. No endothelial function changes were observed in the studies. The findings of acute and short-term studies revealed potential therapeutic effects of IPDE-5 drugs on LVDD in RHTN patients.
引用
收藏
页码:85 / 89
页数:5
相关论文
共 36 条
[1]   CARDIAC WEIGHT IN HYPERTENSION INDUCED BY NITRIC-OXIDE SYNTHASE BLOCKADE [J].
ARNAL, JF ;
ELAMRANI, AI ;
CHATELLIER, G ;
MENARD, J ;
MICHEL, JB .
HYPERTENSION, 1993, 22 (03) :380-387
[2]   Sildenafil and B-Type Natriuretic Peptide Acutely Phosphorylate Titin and Improve Diastolic Distensibility In Vivo [J].
Bishu, Kalkidan ;
Hamdani, Nazha ;
Mohammed, Selma F. ;
Kruger, Martina ;
Ohtani, Tomohito ;
Ogut, Ozgur ;
Brozovich, Frank V. ;
Burnett, John C., Jr. ;
Linke, Wolfgang A. ;
Redfield, Margaret M. .
CIRCULATION, 2011, 124 (25) :2882-U299
[3]   Sildenafil inhibits β-adrenergic-stimulated cardiac contractility in humans [J].
Borlaug, BA ;
Melenovsky, V ;
Marhin, T ;
Fitzgerald, P ;
Kass, DA .
CIRCULATION, 2005, 112 (17) :2642-2649
[4]   DIASTOLIC FAILURE - PATHOPHYSIOLOGY AND THERAPEUTIC IMPLICATIONS [J].
BRUTSAERT, DL ;
SYS, SU ;
GILLEBERT, TC .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1993, 22 (01) :318-325
[5]   Phenotypic Characteristics of Resistant Hypertension in the Brazilian Population [J].
Cabral de Faria, Ana Paula ;
Sabbatini, Andrea Rodrigues ;
Coca, Antonio ;
Moreno, Heitor .
ARQUIVOS BRASILEIROS DE CARDIOLOGIA, 2013, 100 (06) :579-582
[6]   Resistant hypertension: Diagnosis, evaluation, and treatment - A Scientific Statement from the American Heart Association Professional Education Committee of the Council for High Blood Pressure Research [J].
Calhoun, David A. ;
Jones, Daniel ;
Textor, Stephen ;
Goff, David C. ;
Murphy, Timothy P. ;
Toto, Robert D. ;
White, Anthony ;
Cushman, William C. ;
White, William ;
Sica, Domenic ;
Ferdinand, Keith ;
Giles, Thomas D. ;
Falkner, Bonita ;
Carey, Robert M. .
HYPERTENSION, 2008, 51 (06) :1403-1419
[7]   Intensive Monitoring of Adherence to Treatment Helps to Identify "True" Resistant Hypertension [J].
de Souza, Walneia Aparecida ;
Sabha, Maricene ;
Favero, Fabricio de Faveri ;
Bergsten-Mendes, Gun ;
Yugar-Toledo, Juan Carlos ;
Moreno, Heitor, Jr. .
JOURNAL OF CLINICAL HYPERTENSION, 2009, 11 (04) :183-191
[8]   Sildenafil reduces cardiovascular remodeling associated with hypertensive cardiomyopathy in NOS inhibitor-treated rats [J].
Ferreira-Melo, Silvia Elaine ;
Yugar-Toledo, Juan Carlos ;
Coelho, Otavio Rizzi ;
De Luca, Iara M. ;
Tanus-Santos, Jose Eduardo ;
Hyslop, Stephen ;
Irigoyen, Mania Claudia ;
Moreno, Heitor, Jr. .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2006, 542 (1-3) :141-147
[9]   Sildenafil preserves diastolic relaxation after reduction by L-NAME and increases phosphodiesterase-5 in the intercalated discs of cardiac myocytes and arterioles [J].
Ferreira-Melo, Silvia Elaine ;
Demacq, Caroline ;
Lacchini, Silvia ;
Krieger, Jose Eduardo ;
Irigoyen, Maria Claudia ;
Moreno, Heitor .
CLINICS, 2011, 66 (07) :1253-1258
[10]   cGMP-Dependent Protein Kinases and cGMP Phosphodiesterases in Nitric Oxide and cGMP Action [J].
Francis, Sharron H. ;
Busch, Jennifer L. ;
Corbin, Jackie D. .
PHARMACOLOGICAL REVIEWS, 2010, 62 (03) :525-563