Effects of conjugated oestrogen and droloxifene on the renin-angiotensin system, blood pressure and renal blood flow in postmenopausal women

被引:34
作者
Seely, EW
Brosnihan, KB
Jeunemaitre, X
Okamura, K
Williams, GH
Hollenberg, NK
Herrington, DM
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Endocrine Hypertens, Boston, MA 02115 USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med, Boston, MA 02115 USA
[3] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Radiol, Boston, MA 02115 USA
[4] Wake Forest Univ, Sch Med, Hypertens & Vasc Dis Ctr, Winston Salem, NC 27109 USA
[5] Hop Europeen Georges Pompidou, Paris, France
[6] Wake Forest Univ, Sch Med, Dept Internal Med Cardiol, Winston Salem, NC 27109 USA
关键词
D O I
10.1046/j.1365-2265.2004.01980.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE The aim of this study was to evaluate the effect of conjugated equine oestrogen (CEE), and droloxifene, a selective oestrogen receptor modulator (SERM) on individual components of renin-angiotensin-aldosterone (RAAS) and blood pressure (BP) in postmenopausal women. DESIGN AND PATIENTS Twenty-one normotensive (NT) and 10 hypertensive (HT) postmenopausal women received either CEE (0.625 mg/day) or droloxifene (60 mg/day) for 6 weeks and, after a 4-week washout, were restudied on the alternate medication. MEASUREMENTS Hormones of the RAAS and supine BP were measured prior to and at the end of each drug treatment in all subjects. In a subgroup of the NT (n = 10), 24 h ambulatory BP was performed and renal blood flow was determined by PAH clearance both basally and in response to 45-min angiotensin II (Ang II) infusion (3 ng/kg/min). RESULTS CEE significantly increased angiotensinogen, decreased active renin and angiotensin-converting enzyme (ACE), and maintained plasma immunoreactive (ir) angiotensin I (Ang I) levels compared to baseline. With droloxifene, angiotensinogen, active renin and Ang I remained unchanged. Both CEE and droloxifene significantly increased plasma ir-Ang II levels (pmol/l) in NT (baseline: 25.7 +/- 2.5, CEE: 36.6 +/- 3.4, droloxifene: 33.3 +/- 3.1, P < 0.002) and HT women (baseline: 17.9 +/- 2.3, CEE: 27.9 +/- 3.2, droloxifene: 25.9 +/- 4.9, P < 0.005). Renal blood flow was lower on CEE (P = 0.02) compared with baseline. Systemic BP (supine and 24-h ambulatory) was unchanged during both treatments. CONCLUSION This study demonstrates higher circulating levels of ir-Ang II with CEE and droloxifene.
引用
收藏
页码:315 / 321
页数:7
相关论文
共 38 条
[1]   Differing responses in blood pressure over 24 hours in normotensive women receiving oral or transdermal estrogen replacement therapy [J].
Akkad, AA ;
Halligan, AWF ;
Abrams, K ;
AlAzzawi, F .
OBSTETRICS AND GYNECOLOGY, 1997, 89 (01) :97-103
[2]  
Arakawa K, 1996, J HYPERTENS, V14, pS3
[3]   Bi-directional actions of estrogen on the renin-angiotensin system [J].
Brosnihan, KB ;
Senanayake, PS ;
Li, P ;
Ferrario, CM .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 1999, 32 (04) :373-381
[4]   PLASMA RENIN ACTIVITY AND ALDOSTERONE EXCRETION RATE IN NORMAL SUBJECTS .I. EFFECT OF ETHINYL ESTRADIOL AND MEDROXYPROGESTERONE ACETATE [J].
CRANE, MG ;
HARRIS, JJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1969, 29 (04) :550-+
[5]   Both raloxifene and estrogen reduce major cardiovascular risk factors in healthy postmenopausal women - A 2-year, placebo-controlled study [J].
de Valk-de Roo, GW ;
Stehouwer, CDA ;
Meijer, P ;
Mijatovic, V ;
Kluft, C ;
Kenemans, P ;
Cohen, F ;
Watts, S ;
Netelenbos, C .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (12) :2993-3000
[6]   IMMUNOREACTIVE RENIN, PRORENIN, AND ENZYMATICALLY ACTIVE RENIN IN PLASMA DURING PREGNANCY AND IN WOMEN TAKING ORAL-CONTRACEPTIVES [J].
DERKX, FHM ;
STUENKEL, C ;
SCHALEKAMP, MPA ;
VISSER, W ;
HUISVELD, IH ;
SCHALEKAMP, MADH .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1986, 63 (04) :1008-1015
[7]   Estrogen regulation of angiotensin-converting enzyme mRNA [J].
Gallagher, PE ;
Li, P ;
Lenhart, JR ;
Chappell, MC ;
Brosnihan, KB .
HYPERTENSION, 1999, 33 (01) :323-328
[8]   Gender affects renal vasoconstrictor response to Ang I and Ang II [J].
Gandhi, SK ;
Gainer, J ;
King, D ;
Brown, NJ .
HYPERTENSION, 1998, 31 (01) :90-96
[9]   THE LONG-TERM EFFECT OF ORAL AND PERCUTANEOUS ESTRADIOL ON PLASMA-RENIN SUBSTRATE AND BLOOD-PRESSURE [J].
HASSAGER, C ;
RIIS, BJ ;
STROM, V ;
GUYENE, TT ;
CHRISTIANSEN, C .
CIRCULATION, 1987, 76 (04) :753-758
[10]   Cardiovascular effects of droloxifene, a new selective estrogen receptor modulator, in healthy postmenopausal women [J].
Herrington, DM ;
Pusser, BE ;
Riley, WA ;
Thuren, TY ;
Brosnihan, KB ;
Brinton, EA ;
MacLean, DB .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (06) :1606-1612