Published online before print August 22, 2002, doi: 10.1161/01.ATV.0000034929.42459.0D
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
© 2002 American Heart Association, Inc.
Vascular Biology |
In Vivo Estrogen Manipulations on Coronary Capillary Network and Angiogenic Molecule Expression in Middle-Aged Female Rats
From the Departments of Cardiovascular Medicine (S.J., I.S., A.K.) and Pharmacology (Y.H.), Hokkaido University School of Medicine, Sapporo, Japan.
Correspondence to Ichiro Sakuma, MD, PhD, Department of Cardiovascular Medicine, Hokkaido University School of Medicine, Sapporo 060-8638, Japan. E-mail sakuichi{at}seagreen.ocn.ne.jp
 |
Abstract |
|---|
 Top Abstract IntroductionMethodsResultsDiscussionReferences |
|---|
Objective— Estrogen replacement therapy (ERT) ameliorates symptoms in postmenopausal women with syndrome X. We hypothesized that estrogen deprivation and replacement may modulate coronary expressions of angiogenic molecules, thereby modifying the coronary capillary network in perimenopausal women.
Methods and Results— Middle-aged (40-week-old) female rats were subjected to sham surgery, ovariectomy, or ovariectomy with ERT. Using immunohistochemical and in situ hybridization techniques, we showed that protein and gene expressions of estrogen receptor ß, but not 
, in coronary vessels were regulated by in vivo estrogen manipulations. Morphometric analysis showed a reduction in total coronary capillary density with decreased arteriolar capillaries after ovariectomy. ERT resulted in normalization of total capillary number with increased venular capillaries. Coronary expressions of vascular endothelial growth factor (VEGF) and its angiogenic receptor (fetal liver kinase-1) were diminished after ovariectomy, and ERT restored it to intact levels. Higher expressions of VEGF and fetal liver kinase-1 in middle-aged compared with young female rats were associated with an accumulation of hypoxia-inducible factor-1 protein, which was highly expressed in middle-aged female rats.
Conclusions— The coronary capillary network in middle-aged women may be regulated by physiological angiogenesis via VEGF, and reduction in coronary VEGF expression by estrogen deficiency could play a role as a molecular pathogenesis in the development of coronary heart disease in postmenopausal women.
Key Words: angiogenesis • coronary capillary network • estrogen • vascular endothelial growth factors • middle-aged female rats
|
Introduction |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
It is widely held that the incidence of coronary heart disease in women dramatically increases after menopause.1 Many postmenopausal women with typical chest pain and ischemic changes on the exercise test are less likely than men to have atherosclerotic coronary lesions. Syndrome X is a term now frequently used to indicate a diagnostic level for patients with exertional angina, a positive response to exercise testing, and angiographically normal coronary arteries.2 Although syndrome X is heterogeneous with multiple pathogenic entities, an increased prevalence of the syndrome in postmenopausal women postulates a possible link between estrogen deficiency and this syndrome.3 This hypothesis could be supported by a significant reduction in the frequency of chest pain in estrogen-deficient women with syndrome X receiving estrogen replacement therapy (ERT).4
The potential mechanism(s) for the symptomatic benefits of ERT in syndrome X remains poorly understood. Reduced coronary vasodilator reserve is proposed to explain syndrome X.5,6 Furthermore, some investigators have invoked a disturbance of coronary microvascular function as a central feature of this syndrome.7 Although the direct effects of estrogen on the vasculature are now well recognized, among the vascular effects of estrogen, one of the most important is its angiogenic property.8 Thus, it is possible that the presence of estrogen may play an important role in the development of the coronary capillary network in association with the regulation of physiological angiogenesis, which would be expected to bring about normalization of coronary blood flow reserve with ameliorated microvascular function.
In the present study, we used an experimental model of estrogen deficiency induced by ovariectomy (OVX) in middle-aged female rats, which can be expected to exhibit the same changes in coronary capillary network of the heart as observed in postmenopausal women. Our working design was to determine whether in vivo estrogen manipulations affect the cardiac expressions of several kinds of molecules that are pertinent as possible mediators of angiogenesis. In part, the hormonal influences were also investigated with the use of male and young female rats. The present experiments should contribute to an understanding of the molecular mechanisms that may involve cardiac alterations occurring in the setting of estrogen deficiency in elderly women.
|
Methods |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
See supplementary Methods section for details (which can be accessed online at http://atvb.ahajournals.org).
Animal Models
Male and female Wistar rats, aged 12 and 44 weeks, were used. Female rats aged 8 or 40 weeks were anesthetized by an intraperitoneal injection of ketamine (100 mg/kg) under aseptic conditions. Some female rats were ovariectomized by making a small incision in the lower abdomen and removing both ovaries, as previously described.9 Sham-operated (intact) female rats received only laparotomy. Some OVX rats were given 17ß-estradiol (3 and 10 µg/d for middle-aged and young rats, respectively) subcutaneously through an osmotic pump that was implanted in the back.9 Female rats were euthanized 4 weeks after surgery. Blood samples were collected from the inferior cava, and the plasma 17ß-estradiol level was determined by radioimmunoassay.9 Only young female rats that were in the proestrus to the estrus stage (based on vaginal smear findings)9 when they were killed were used as controls. Middle-aged female rats did not exhibit an obvious estrous cycle, as confirmed by vaginal smears. On the day of the experiments, rats were anesthetized with diethyl ether and killed by exsanguination (20 animals for each group). The heart was removed quickly after the opening of the chest.
Staining of Capillary Morphology
Serial sections (16 µm thick) were cut from the frozen left ventricle (LV). Double staining of sections was carried out to discriminate arteriolar and venular capillaries, as previously described.10 Arteriolar capillaries were stained blue because they contained alkaline phosphatase; venular capillaries were stained red because they contained dipeptidylpeptidase IV.
Capillary density was assessed light-microscopically on 6-µm-thick deparaffinized tissue sections that were immunostained by anti–von Willebrand factor (factor VIII) antibody (Dako). The antibody was made visible by a secondary exposure of the sections to Cy3-conjugated AffiniPure donkey anti-rabbit IgG (Jackson Immunoresearch Laboratories).
Immunohistochemistry
Five- to 8-µm-thick frozen cryostat sections were fixed in acetone and air-dried. The sections were incubated with primary antibodies, followed by exposure to a suitable secondary antibody coupled to horseradish peroxidase. Immunostains were visualized by light microscopy with diaminobenzidine. The specificity of the immunoreaction was compared with that of the negative control specimen in which nonimmune IgG was used instead of the primary antibodies. Quantification of immunoreactivity by pixel intensity was analyzed by image-analyzing software, as previously described.10
Immunofluorescence and Confocal Analysis
Immunodetection of target proteins was also performed with the use of fluorescence secondary antibodies, as previously described.10 For double-label immunofluorescent staining of the 2 estrogen receptor (ER) subtypes, ER and ERß, the sections were incubated with ER rabbit polyclonal antibody, followed by Cy3-conjugated anti-rabbit IgG, and then incubated with ERß mouse monoclonal antibody, followed by fluorescein-conjugated anti-mouse IgG. Immunofluorescent images were observed by a laser scanning confocal imaging system.10
In Situ Hybridization
In situ hybridization was performed on 10- to 15-µm-thick tissue sections with the use of 35S-labeled synthetic oligonucleotides, as previously described.10 The specificity of in situ hybridization was confirmed by the disappearance of signals when excessive doses of the corresponding cold oligonucleotides were added to the hybridization fluid. The mRNA grains per blood vessel were quantified by using image-analyzing software.10
Statistical Analysis
Data are shown as mean±SEM. Means were compared by ANOVA, followed by the Fisher protected least significance t test for multiple comparisons. Differences were considered significant at a value of P<0.05.
|
Results |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Plasma 17ß-Estradiol Levels
The plasma 17ß-estradiol levels of middle-aged female rats were essentially low (12.5±3.0 pg/mL). Further reduction in plasma 17ß-estradiol levels was found after OVX (1.8±0.3 pg/mL, P<0.01). ERT in OVX rats markedly increased the levels to 20.0±6.1 pg/mL, levels that were not significantly different from those observed in intact female rats. The average value of plasma 17ß-estradiol levels was much higher in young female rats (179±9 pg/mL, P<0.001) than in middle-aged female rats. Plasma 17ß-estradiol levels in young rats after OVX were markedly reduced (to 39±3 pg/mL, P<0.001), and ERT in OVX rats maintained the control level of plasma 17ß-estradiol (194±8 pg/mL).
Expression of ER and ERß
Double-label immunofluorescent staining for ER and ERß in LV cross sections from middle-aged female rats showed the presence of the 2 ER subtypes in coronary vessels and cardiac myocytes (Figure 1A). Immunohistochemical analysis confirmed that the nuclei of cells stained positively for ERs. In coronary vessels of sham-operated intact female rats, ER and ERß were expressed almost equivalently, resulting in an ER/ERß ratio of 0.95±0.06. When females were subjected to OVX, coronary ERß expression was evidently diminished, and the ER/ERß ratio was changed to a significantly higher level (1.41±0.03, P<0.01). Treatment of OVX rats with 17ß-estradiol enhanced coronary ERß expression, as seen in intact female rats, and reversed the ER/ERß ratio (0.91±0.05, P<0.01). In situ hybridization studies showed that ERß mRNA was decreased in middle-aged rats after OVX (Figure 1B). When the numbers of mean mRNA grains per section of coronary vessel were calculated (10 fieldsx20 samples), OVX reduced the numbers of grains per section from 62±3 to 31±1 (P<0.01). The OVX-induced reduction in the number of mRNA grains was significantly prevented by ERT (68±3 grains per section, P<0.001). There was no significant difference in the level of ER gene expression among the 3 groups (57±3 grains per section for intact rats, 55±4 grains per section for OVX rats, and 58±3 grains per section for OVX+ERT rats; Figure 1C).
|
Positive staining for ERß in coronary vessels was observed more strongly in young female rats than in middle-aged female rats (please refer to Figure I, which can be accessed at http://atvb.ahajournals.org). Because quantification of immunoreactivity was assessed by pixel intensity, the value for coronary ERß in young female rats (3.67±0.21) was significantly higher than that in middle-aged female rats (2.57±0.10, P<0.001), but the values for coronary ER did not differ between young and middle-aged female rats (2.49±0.11 versus 2.45±0.11, respectively). Thus, young female rats exhibited a significantly lower ER/ERß ratio (0.68±0.05, P<0.05). OVX caused a marked reduction in coronary ERß expression, resulting in a significant increase in the ER/ERß ratio (1.49±0.06, P<0.001).
Compared with middle-aged female rats, male rats showed essentially the same coronary expressions of ER and ERß (please refer to online Figure I, which can be accessed at http://atvb.ahajournals.org). The ER/ERß ratio was 0.93±0.06. No age difference was found in coronary expressions of ER and ERß in male rats.
Morphometric Changes
Micrographs of coronary capillaries in LV sections by the double-staining method showed that the arteriolar capillary portion, which was stained blue, was evidently abundant in intact middle-aged female rats (Figure 2A). There was a marked reduction in arteriolar capillaries after OVX. Thus, OVX significantly diminished the proportion of arteriolar capillaries without changing the venular capillary proportion (Figure 2B). This resulted in a remarkable decrease in the density of labeled capillaries (Figure 2C). After OVX, the total capillary density was reduced to 76% of that in intact middle-aged female rats (Figure 2D). ERT in OVX rats significantly improved the total capillary density to the intact level (Figure 2C and 2D). However, the venular capillary portion, which was stained red, became evident in OVX+ERT rats (Figure 2A). Thus, ERT caused a 2-fold increase in the proportion of venular capillaries, and the arteriolar capillary proportion remained at the reduced level (Figure 2B). As a result of the capillary morphometric changes, the capillary domain area (an area where 1 capillary provides oxygen) was significantly (P<0.01) increased (from 468±8 to 595±6 µm2) after OVX, and this increase was reversed by ERT (458±7 µm2).
|
P<0.001 vs OVX females. C, Photomicrographs of LV sections where capillaries were stained by antibodies directed against the endothelium constituent factor VIII. Original magnification x400. D, Bar graph showing the total capillary density in LV sections. Total capillary density is expressed as the number per millimeter squared. Data are mean±SEM (30 fieldsx20 samples). *P<0.001 vs intact females; In young female rats, the total capillary density (1765±4/mm2) was significantly lower than that in middle-aged female rats (75%, P<0.001). This was associated with a lower proportion of arteriolar capillaries, but a higher venular proportion was evident (see online Figure IIB). In young female rats, OVX reduced the total coronary capillary density, with decreases in arteriolar and venular capillaries, and ERT resulted in restoration of the total number of capillaries with an increased venular proportion. Young and middle-aged male rats also exhibited a low value of the total capillary density (1920±6/mm2, 87% of that in middle-aged female rats), and the venular capillary portion was found to be much pronounced (see online Figure IIB).
Expression of VEGF and Its Receptors
Immunofluorescent staining for vascular endothelial growth factor (VEGF) showed that its expression was evident in coronary vessels of LV sections from middle-aged female rats (Figure 3A). VEGF was weakly stained after OVX, and its expression was reduced to the same level found in male rats (Figure 3B). The reduced VEGF expression level seen in OVX female rats was completely reversed by ERT (Figure 3A and 3B). VEGF expression was less pronounced in young female rats compared with middle-aged female rats, but OVX caused a further reduction in its expression (Figure 3B). VEGF mRNA was evidently decreased in middle-aged female rats after OVX (Figure 3C). When the numbers of mean mRNA grains per section of coronary vessel were calculated (10 fieldsx20 samples), VEGF mRNA was decreased to 40% of that in intact female rats by OVX (P<0.001). The OVX-induced decrease in VEGF mRNA was significantly prevented by ERT (P<0.001).
|
P<0.01 vs intact young female rats. C, In situ hybridization analysis showing gene expression for VEGF in LV sections from intact, OVX, and OVX+ERT middle-aged female rats. Original magnification x400.Reduced immunofluorescent staining for fetal liver kinase-1 (Flk-1) was detected in LV sections from OVX compared with intact middle-aged female rats (Figure 4A). Positive staining for Flk-1 was primarily in coronary vessels. ERT increased the expression of Flk-1 protein in coronary vessels to the level obtained in intact female rats (Figure 4A and 4B). Male rats exhibited a level of Flk-1 expression similar to that in OVX females (Figure 4B). Flk-1 was less abundantly expressed in young female rats than in middle-aged female rats, although its expression was significantly reduced after OVX (Figure 4B). The decrease in positive staining for Flk-1 protein in coronary vessels of OVX middle-aged female rats was correlated with a decrease in Flk-1 mRNA, which was obtained from in situ hybridization experiments (Figure 4C). The results of quantitative analysis showed a 53% decrease in Flk-1 mRNA expression after OVX (P<0.001). ERT significantly increased its gene expression nearly to the level obtained in intact middle-aged female rats (P<0.001). The expression of another VEGF receptor, fms-like tyrosine kinase-1 (Flt-1), was moderately detected in coronary vessels of rat LV sections. In contrast to the Flk-1 level, the expression level of Flt-1 was not significantly affected by OVX, sex, and age.
|
Expression of HIF Family
Immunofluorescent staining for 2 hypoxia-inducible factor-1 (HIF-1) subunits, HIF-1 and HIF-1ß, showed that their protein expressions were markedly enhanced in coronary vessels of LV sections from middle-aged female rats compared with young female rats (Figure 5A and 5B). Although HIF-1 and HIF-1ß proteins were present in the nucleus in young female rats, these proteins were increased at nuclear and cytoplasmic levels in middle-aged female rats, as analyzed by immunohistochemistry. As assessed by the quantification of immunoreactivity with the use of pixel intensity, HIF-1 and HIF-1ß proteins were both increased 2-fold in middle-aged female rats compared with young female rats (P<0.001). The increased expression levels of HIF-1 and HIF-1ß in middle-aged female rats were unmodified by OVX (see online Figure IIIA, which can be accessed at http://atvb.ahajournals.org). In middle-aged male rats, HIF-1 and HIF-1ß protein expressions were maintained at the same levels as found in young male and female rats (see online Figure IIIA). HIF-2 protein expression levels did not significantly differ among middle-aged female rats (intact and OVX), middle-aged male rats, and young female rats (Figure 5C; see online Figure IIIA).
|
In situ hybridization studies showed no difference in HIF-1 and HIF-1ß mRNAs between middle-aged and young female rats (see online Figure IIIB). Also, the gene expression of HIF-2 remained unchanged with age.
|
Discussion |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Estrogen has been shown to regulate ER expression in tissues relevant to gonadal function, such as breast and uterus.11,12 Radioligand binding studies indicate that ERs are also expressed in tissues not classically defined as estrogen targets, including the vasculature.13 To date, 2 ERs have been described, ER
and ERß,14 but their physiological relevance in vasculature is incompletely understood. We found the presence of ER and ERß in the coronary vessels of rat hearts at mRNA and protein levels by using immunofluorescence and in situ hybridization. OVX resulted in a marked decrease in coronary ERß in middle-aged female rats. ERT restored coronary ERß in OVX rats to levels similar to those in sham-operated rats. A notable reduction in coronary ERß was also obtained when young female rats were subjected to OVX. These results suggest that gene and protein expression of ERß in coronary vessels can be strongly regulated by circulating estrogen. This idea is consistent with the finding that young female rats, compared with middle-aged female rats, exhibit more abundant expression of coronary ERß, with a much higher level of circulating estrogen. No significant changes were seen in gene and protein expression levels of ER in coronary vessels after estrogen deprivation or treatment compared with intact levels regardless of whether the animals were young or middle-aged. This result agrees with the reported findings that reverse transcription–PCR has shown no significant differences in the expression levels of ER mRNA in the hearts of sham-operated, OVX, and OVX+ERT rats.15
Among the many roles of estrogen, one of the most important is its angiogenic property. Our findings that the total density of coronary capillaries in middle-aged female rats significantly declined after OVX and returned to intact levels with ERT are interpreted to indicate that estrogen participates in promoting the formation of new capillaries from preexisting coronary vessels in middle-aged female rat hearts. The role of estrogen in uterine angiogenesis, mediated by ER, has been suggested by the demonstration that angiogenesis is impaired in ER knockout mice.16 However, the striking changes in ERß expression in parallel with the total capillary density after in vivo estrogen manipulations raise the possibility that ERß may mediate coronary angiogenesis in response to estrogen. Recent research using endometrial adenocarcinoma cells transfected with VEGF luciferase vectors and expression vectors encoding either ER or ERß has demonstrated that estrogen-regulated VEGF gene transcription is dependent on ER and ERß.17 The contribution of each ER subtype to the angiogenic effect of estrogen may be tissue specific. The recent development of ERß-specific antagonists and the ERß knockout mouse would allow the crucial role of ERß in mediating coronary angiogenesis by estrogen to be studied directly.
The ratio of venular to total coronary capillaries was much lower in middle-aged female rats than in young female rats, and arteriolar capillary portions were markedly increased in middle-aged female rats. As a result of the decreased total capillary density after OVX, the capillary domain area was increased, indicating low LV perfusion. Although ERT significantly improved the decreased total capillary density in middle-aged female rats after OVX, this resulted from an increase in venular capillaries. Thus, the ratio of arteriolar to total capillaries remained low even after ERT in OVX middle-aged female rats. However, such a change in the capillary proportion was essentially similar to that seen in intact young female rats. It may be stated that ERT could result in a trend of rejuvenation rather than normalization of the capillary network. Because capillary angiogenesis is usually initiated from the venular site, the increased venular capillary density would reduce the intercapillary distance, leading to facilitation of the oxygen supply to the surrounding tissues.
The possibility that the angiogenic action of estrogen is mediated indirectly, via the production of VEGF, has been suggested by the finding that VEGF expression in the endometrium is increased by estrogen.18 The mRNA and protein expression levels of VEGF in coronary vessels were significantly decreased with estrogen deprivation, but with estrogen replacement, these levels increased to levels similar to those seen in the control group, supporting the suggestion that estrogen directly regulates VEGF gene transcription.18 Expression of Flk-1, a receptor that mediates the angiogenic effect of VEGF,19 was significantly downregulated at mRNA and protein levels after OVX in coronary vessels, and ERT prevented the OVX-induced change in Flk-1 expression. On the other hand, no significant changes were seen in the expression of another VEGF receptor, Flt-1, which is devoid of angiogenic activities,19 in coronary vessels after estrogen deprivation or treatment. This specific regulation of Flk-1 expression by estrogen deprivation or treatment suggests that expression of the VEGF angiogenic receptor is a contributory factor to estrogen-regulated VEGF-dependent angiogenesis. Interestingly, despite the fact that the circulating estrogen level in middle-aged female rats was much lower than that in young female rats, expressions of VEGF and Flk-1 were significantly higher in middle-aged female rats, implying that alterations in circulating estrogen cannot totally account for the mechanisms responsible for VEGF and Flk-1 expressions in middle-aged female rats.
HIF-1 and HIF-1ß proteins were highly expressed in the coronary vessels of middle-aged compared with young female rat hearts regardless of whether the animals were subjected to OVX. HIF-1 and HIF-1ß are the subunits of HIF-1, which is a transcriptional factor under hypoxic conditions.20 Whereas HIF-1ß is constitutively expressed, HIF-1 is a specific factor responsible for hypoxic responses. Under hypoxic conditions, HIF-1 protein is stabilized without being degraded through oxygen-dependent proteolysis and initiates a multistep pathway of activation, including dimerization with its partner, HIF-1ß.21 Thus, HIF-1 activities are not regulated at the mRNA level but at the level of protein stability.22 This could explain the lack of HIF-1 and HIF-1ß mRNA induction in middle-aged female rats. Because coronary expressions of HIF-1 and HIF-1ß proteins remained unchanged in middle-aged male rats, the female heart might be rendered ischemic from the perimenopausal stage, leading to increased HIF-1 expression. However, there could be factors other than hypoxia involved that are able to induce HIF-1 protein expression. Recent work has demonstrated that HIF-1 protein is present in the nuclei of different tissues, including the heart, under normoxic conditions.23 Furthermore, we did not detect any increase in coronary expression of HIF-2 protein, which is also subject to oxygen-dependent proteosomal destruction,24 in middle-aged female rats. The activation of HIF-1 regulates the VEGF gene by its binding to a hypoxia-responsive element in the 5'-flanking region of the VEGF gene.25 Thus, HIF-1 is a strong inducer of VEGF mRNA expression. Therefore, it seems likely that the increased expression levels of HIF-1 and HIF-1ß proteins in middle-aged female rats may have contributed to increased VEGF expression.
In conclusion, to the best of our knowledge, this is the first report demonstrating that the effects of in vivo estrogen manipulations on the coronary capillary network in middle-aged female rats are strictly associated with VEGF expression in coronary vessels. We propose that VEGF may be a critical regulatory molecule for physiological coronary angiogenesis that constitutes a naturally occurring, compensatory change under the hypoestrogenic condition with aging. The dramatic reduction in VEGF expression in middle-aged female rats after OVX suggests that subtle changes from critical concentrations of estrogen at this age could affect the expression level of VEGF. Moreover, the transcription factor HIF-1, whose expression level greatly increases in middle-aged female rats, appears to lead to an additive action on VEGF expression. The findings observed in our animal models of hypoestrogenic female rats may have clinical implications for postmenopausal women with syndrome X. The understanding of the regulation by estrogen deprivation or replacement of the coronary VEGF expression mechanisms in middle-aged women deserves consideration and can lead to a potential therapeutic strategy for this clinical setting.
|
Acknowledgments |
|---|
This work was supported in part by a grant-in-aid for scientific research from the Ministry of Education, Science, Sports, and Culture of Japan and by Health Sciences Research grants for comprehensive research on aging and health from the Ministry of Health, Welfare, and Labor of Japan. We thank Dr Tomiyasu Koyama for his kind advice and suggestions.
Received June 2, 2002; accepted August 11, 2002.
|
References |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
1. Colditz GA, Willett WC, Stamfer MJ, Rosner B, Speizer FE, Hennekens CH. Menopause and the risk of coronary heart disease in women. N Engl J Med. 1987; 316: 1105–1110.[Abstract]
2. Kaski JC, Crea F, Nihoyannopoulos P, Hackett D, Maseri A. Transient myocardial ischemia during daily life in patients with syndrome X. Am J Cardiol. 1986; 58: 1242–1247.[CrossRef][Medline] [Order article via Infotrieve]
3. Kaski JC, Rosano GMC, Collins P, Nihoyannopoulos P, Maseri A, Poole-Wilson PA. Cardiac syndrome X: clinical characteristics and left ventricular function: long-term follow-up study. J Am Coll Cardiol. 1995; 25: 807–814.[Abstract]
4. Rosano GMC, Peters FN, Lefroy D, Lindsay DC, Sarrel PM, Collins P, Poole-Wilson PA. 17-Beta-estradiol therapy lessens angina in postmenopausal women with syndrome X. J Am Coll Cardiol. 1996; 28: 1500–1505.[Abstract]
5. Opherk D, Mall G, Zebe H, Schwartz F, Weihe E, Manthey J, Kubler W. Reduction of coronary reserve: a mechanism for angina pectoris in patients with arterial hypertension and normal coronary arteries. Circulation. 1984; 69: 1–7.
6. Cannon RO, Epstein SE. "Microvascular angina" as a cause of chest pain with angiographically normal coronary arteries. Am J Cardiol. 1988; 61: 1338–1343.[CrossRef][Medline] [Order article via Infotrieve]
7. Operk D, Schuler G, Wetterauer K, Manthey J, Schwartz F, Kubler W. Four year follow up study in patients with angina pectoris and normal coronary arteriograms (syndrome X). Circulation. 1989; 80: 1610–1616.
8. Losordo DW, Isner JM. Estrogen and angiogenesis: a review. Arterioscler Thromb Vasc Biol. 2001; 21: 6–12.
9. Liu M-Y, Hattori Y, Fukao M, Sato A, Sakuma I, Kanno M. Alterations in EDHF-mediated hyperpolarization and relaxation in mesenteric arteries of female rats in long-term deficiency of oestrogen and during oestrus cycle. Br J Pharmacol. 2001; 132: 1035–1046.[CrossRef][Medline] [Order article via Infotrieve]
10. Jesmin S, Sakuma I, Hattori Y, Fujii S, Kitabatake A. Long-acting calcium channel blocker benidipine suppresses expression of angiogenic growth factors and prevents cardiac remodeling in a type II diabetic rat model. Diabetologia. 2002; 45: 402–415.[CrossRef][Medline] [Order article via Infotrieve]
11. Saceda M, Lippman ME, Chambon P, Lindsey RL, Ponglikitmongkol M. Regulation of the estrogen receptor in MCF-7 cells by estradiol. Mol Endocrinol. 1988; 2: 1157–1162.
12. Yamashita S, Newbold PR, McLachlan JA, Korach KS. The role of estrogen receptor in uterine epithelial proliferation and cytodifferentiation in neonatal mice. Endocrinology. 1990; 127: 2456–2463.
13. McGill HC, Sheridan PJ. Nuclear uptake of sex steroid hormones in the cardiovascular system of the baboon. Circ Res. 1981; 48: 238–244.
14. Gustafsson J-Å. Estrogen receptor ß: a new dimension in estrogen mechanism of action. J Endocrinol. 1999; 163: 379–383.[CrossRef][Medline] [Order article via Infotrieve]
15. Mohamed MK, Abdel-Rahman AA. Effect of long-term ovariectomy and estrogen replacement on the expression of estrogen gene in female rats. Eur J Endocrinol. 2000; 142: 307–314.[Abstract]
16. Johns A, Freay AD. Fraser W, Korach KS, Rubanyi GM. Disruption of estrogen receptor gene prevents 17 beta estradiol-induced angiogenesis in transgenic mice. Endocrinology. 1996; 137: 4511–4513.[Abstract]
17. Mueller MD, Vigne J-L, Minchenko A, Lebovic DI, Leitman DC, Taylor RN. Regulation of vascular endothelial growth factor (VEGF) gene transcription by estrogen receptor and ß. Proc Natl Acad Sci U S A. 2000; 97: 10972–10977.
18. Greb RR, Heikinheimo O, Williams RF, Hodgen GD, Goodman AL. Vascular endothelial growth factor in primate endometrium is regulated by oestrogen-receptor and progesterone-receptor ligands in vivo. Hum Reprod. 1997; 12: 1280–1292.
19. Ferrara N. Role of vascular endothelial growth factor in regulation of physiological angiogenesis. Am J Physiol. 2001; 280: C1358–C1366.
20. Wang GL, Jiang BH, Rue EA, Semenza GL. Hypoxia-inducible factor 1 is a basic-helix-loop-helix-PAS heterodimer regulated by cellular O2 tension. Proc Natl Acad Sci U S A. 1995; 92: 5510–5514.
21. Wenger RH, Gassmann M. Oxygen(es) and hypoxia-inducible factor-1. Biol Chem. 1997; 378: 609–616.[Medline] [Order article via Infotrieve]
22. Wenger RH, Kvietikova I, Rolfs A, Gassmann M. Hypoxia-inducible factor-1 is regulated at the post-mRNA level. Kidney Int. 1997; 51: 560–563.[Medline]
[Order article via Infotrieve]
23. Stroka DM, Burkhardt T, Desballets I, Wenger RH, Neil DPH. HIF-1 is expressed in normoxic tissue and displays an organ-specific regulator under systemic hypoxia. FASEB J. 2001; 15: 2445–2453.
24. Wiesener M, Turley H, Allen W, William C, Eckardt K, Maxwell P. Induction of endothelial PAS domain protein-1 by hypoxia: characterization and comparison with hypoxia-inducible factor-1alpha. Blood. 1998; 92: 2260–2268.
25. Forsythe JA, Jiang B-H, Iyer NV, Agani F, Leung SW, Koos RD, Semenza GL. Activation of vascular endothelial growth factor gene transcription by hypoxia-inducible factor 1. Mol Cell Biol. 1996; 16: 4604–4613.[Abstract]
This article has been cited by other articles:
 |
|
 |
|
  S. Jesmin, S. Zaedi, N. Shimojo, M. Iemitsu, K. Masuzawa, N. Yamaguchi, C. N. Mowa, S. Maeda, Y. Hattori, and T. Miyauchi Endothelin antagonism normalizes VEGF signaling and cardiac function in STZ-induced diabetic rat hearts Am J Physiol Endocrinol Metab, April 1, 2007; 292(4): E1030 - E1040. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. Gimenez, P. M Garcia, B. Bonacasa, L. F Carbonell, T. Quesada, and I. Hernandez Effects of oestrogen treatment and angiotensin-converting enzyme inhibition on the microvasculature of ovariectomized spontaneously hypertensive rats Exp Physiol, January 1, 2006; 91(1): 261 - 268. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 S. Jesmin, H. Togashi, I. Sakuma, C. N. Mowa, K.-I. Ueno, T. Yamaguchi, M. Yoshioka, and A. Kitabatake Gonadal Hormones and Frontocortical Expression of Vascular Endothelial Growth Factor in Male Stroke-Prone, Spontaneously Hypertensive Rats, a Model for Attention-Deficit/Hyperactivity Disorder Endocrinology, September 1, 2004; 145(9): 4330 - 4343. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 K. G. Lamping, L. P. Christensen, and R. J. Tomanek Estrogen therapy induces collateral and microvascular remodeling Am J Physiol Heart Circ Physiol, November 1, 2003; 285(5): H2039 - H2044. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||