Effects of intranasal estradiol treatment on serum paraoxonase and lipids in healthy, postmenopausal women

被引:9
作者
Fenkci, Ibrahim Veysel
Serteser, Mustafa
Fenkci, Semin
Akyol, Ahmet Melih
机构
[1] Afyon Kocatepe Univ, Sch Med, Dept Obstet & Gynecol, Afyon, Turkey
[2] Afyon Kocatepe Univ, Sch Med, Dept Biochem, Afyon, Turkey
[3] Pamukkale Univ, Sch Med, Dept Internal Med, Div Endocrinol & Metab, Denizli, Turkey
关键词
paraoxonase; 1; intranasal; 17; beta-estradiol; menopause;
D O I
10.1159/000091418
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
Background/Aims: Serum lipid concentrations worsen after the menopause because of estrogen deficiency, leading to an increased atherogenic pattern. It is known that serum paraoxonase (PON1) activity prevents the development of atherosclerosis. The aim of this cross-sectional study was to observe the effects of intranasal 17 beta-estradiol (300 mu g/day) on serum PON1 and lipid levels in healthy postmenopausal women. Methods: 48 healthy, postmenopausal women were enrolled into this cross-sectional study. 28 subjects without an intact uterus and ovaries were using single-dose (300 mu g/day) intranasal 17 beta-estradiol and 20 subjects with spontaneous natural menopause were not on any hormone therapy. Body mass index (BMI), blood pressure, serum follicle-stimulating hormone, estradiol, fasting glucose, insulin, lipid fractions and PON1 levels were measured. Homeostasis model assessment (HOMA-R) was used to estimate insulin resistance. Results:The higher estradiol, high-density lipoprotein and salt-stimulated paraoxonase (SSP) levels were observed in intranasal 17 beta-estradiol users in comparison with non-users. There were no statistically significant differences in BMI, blood pressures, other lipid fractions, basal paraoxonase, arylesterase, fasting glucose and insulin levels, HOMA-R between the groups. SSP was inversely associated with fasting insulin levels and HOMA-R. Conclusion: These observations may suggest that intranasal 17 beta-estradiol does not have harmful effects on the PON1 activity and lipid metabolism. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:203 / 207
页数:5
相关论文
共 42 条
[1]
Does paraoxonase play a role in susceptibility to cardiovascular disease? [J].
Aviram, M .
MOLECULAR MEDICINE TODAY, 1999, 5 (09) :381-386
[2]
Paraoxonase inhibits high-density lipoprotein oxidation and preserves its functions - A possible peroxidative role for paraoxonase [J].
Aviram, M ;
Rosenblat, M ;
Bisgaier, CL ;
Newton, RS ;
Primo-Parmo, SL ;
La Du, BN .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (08) :1581-1590
[3]
Serum paraoxonase after myocardial infarction [J].
Ayub, A ;
Mackness, MI ;
Arrol, S ;
Mackness, B ;
Patel, J ;
Durrington, PN .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (02) :330-335
[4]
PLASMA-LIPOPROTEIN LEVELS AS PREDICTORS OF CARDIOVASCULAR DEATH IN WOMEN [J].
BASS, KM ;
NEWSCHAFFER, CJ ;
KLAG, MJ ;
BUSH, TL .
ARCHIVES OF INTERNAL MEDICINE, 1993, 153 (19) :2209-2216
[5]
What is oxidative stress? [J].
Betteridge, DJ .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2000, 49 (02) :3-8
[6]
Serum paraoxonase is reduced in type 1 diabetic patients compared to non-diabetic, first degree relatives; influence on the ability of HDL to protect LDL from oxidation [J].
Boemi, M ;
Leviev, I ;
Sirolla, C ;
Pieri, C ;
Marra, M ;
James, RW .
ATHEROSCLEROSIS, 2001, 155 (01) :229-235
[7]
New targets for medical treatment of lipid disorders. [J].
Brousseau M.E. ;
Schaefer E.J. .
Current Atherosclerosis Reports, 2002, 4 (5) :343-349
[8]
Serum paraoxonase: effect of the apolipoprotein composition of HDL and the acute phase response [J].
Cabana, VG ;
Reardon, CA ;
Feng, N ;
Neath, S ;
Lukens, J ;
Getz, GS .
JOURNAL OF LIPID RESEARCH, 2003, 44 (04) :780-792
[9]
Comparison of transdermal and oral estrogen-progestin replacement therapy: effects on cardiovascular risk factors [J].
Chen, FP ;
Lee, N ;
Soong, YK ;
Huang, KE .
MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY, 2001, 8 (05) :347-352
[10]
Glycaemic control and plasma lipoproteins in menopausal women with Type 2 diabetes treated with oral and transdermal combined hormone replacement therapy [J].
Darko, DA ;
Dornhorst, A ;
Kennedy, G ;
Mandeno, RC ;
Seed, M .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2001, 54 (03) :157-164