Effects of short-term administration of estradiol on reperfusion arrhythmias in rats of different ages.

Little is known about age-related differences in short-term effects of estradiol on ischemia-reperfusion (I/R) insults. The present study was designed to evaluate the effects of short-term treatment with estradiol on reperfusion arrhythmias in isolated hearts of 6-7-week-old and 12-14-month-old female rats. Wistar rats were sham-operated, ovariectomized and treated with vehicle or ovariectomized and treated with 17β-estradiol (E2; 5 µg·100 g-1·day-1) for 4 days. Hearts were perfused by the Langendorff technique. Reperfusion arrhythmias, i.e., ventricular tachycardia and/or ventricular fibrillation, were induced by 15 min of left coronary artery ligation and 30 min of reperfusion. The duration and incidence of I/R arrhythmias were significantly higher in young rats compared to middle-aged rats (arrhythmia severity index: 9.4 ± 1.0 vs 3.0 ± 0.3 arbitrary units, respectively, P < 0.05). In addition, middle-aged rats showed lower heart rate, systolic tension and coronary flow. Four-day E2 treatment caused an increase in uterine weight. Although E2 administration had no significant effect on the duration of I/R arrhythmias in middle-aged rats, it induced a marked reduction in the rhythm disturbances of young rats accompanied by a decrease in heart rate of isolated hearts. Also, this reduction was associated with an increase in QT interval. No significant changes were observed in the QT interval of middle-aged E2-treated rats. These data demonstrate that short-term estradiol treatment protects against I/R arrhythmias in hearts of young female rats. The anti-arrhythmogenic effect of estradiol might be related to a lengthening of the QT interval.

Introduction

Premenopausal women are less susceptible to heart diseases and sudden cardiac death than men at a similar age (1). The incidence of coronary diseases in women increases substantially after menopause (2). Animal models of heart diseases clearly support the cardioprotective effects of estrogen supplementation. Basic experiments have revealed that estrogen could attenuate ischemia- or reperfusion-induced ventricular arrhythmias, thereby suggesting that sex hormones may have protective effects against cardiac arrhythmias (3). Patten et al. (4) showed that ovariectomized rats supplemented with 17β-estradiol (E2) presented reduced cardiomyocyte apoptosis in vitro and in vivo. Additionally, E2 had an antiarrhythmic activity and reduced the L-type calcium current (ICaL) in female and male rats; however, approximately 10-fold less hormone was required to produce these effects in female rats (5). The natural cardioprotection observed in female rats is absent after ovariectomy (OVX) and E2 supplementation of estrogen-deficient animals provides protection of myocardial function against ischemia/reperfusion (I/R) injury by decreasing inflammation and apoptotic signaling (6).

Although the effects of chronic administration of estrogen have been widely explored in the last few decades, especially in studies involving postmenopausal hormone replacement therapy (7-11), the short-term actions of estrogen have not been fully evaluated. In spite of this, short-term estrogen therapy might be an important strategy to treat cardiovascular diseases. Indeed, short-term administration of E2 to ovariectomized spontaneously hypertensive rats (SHR) causes a significant reduction in blood pressure on the fourth day of treatment (12), suggesting that the beneficial effects of E2 on the cardiovascular system can be already observed after a few days of hormonal supplement. Thus, the aim of the present study was to investigate the effects of short-term estrogen administration on cardiac reperfusion arrhythmias in young and middle-aged rats since age-related differences might change the cardiovascular responses to the administration of E2.

Material and Methods

Ethical approval

All experimental protocols were performed in accordance with the guidelines for the humane use of laboratory animals of our Institute and approved by the local authority, the Ethics Committee in Animal Experimentation (CETEA), protocol #017/07.

Animals

Female Wistar rats [6-7 weeks old, 200-250 g (young, N = 28) and 12-14 months old, 350-400 g (middle-aged, N = 29)] were obtained from the animal facility of the Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (CEBIO-UFMG). The animals were housed in a temperature- and humidity-controlled room maintained on a 14:10-h light-dark cycle with free access to food and water.

Surgical ovariectomy

Rats underwent surgical ovariectomy by standard procedures. Briefly, each ovary was removed and the animals were allowed to recover from the surgery for 18 days before experimentation. Successful OVX was confirmed by a reduction in the uterine weight, which was expressed by the ratio between uterine weight (mg) and body weight (g). Control animals (control group: young, N = 10, middle-aged, N = 12) were left with intact ovaries. OVX rats received daily injections of E2 (E2 group: 5 µg·100 g−1·day−1, SARSA, Hoechst Marion Roussel, France; young, N = 11, middle-aged, N = 7) or vehicle (vehicle group: 0.1 mL corn oil·100 g−1·day−1; young, N = 7, middle-aged, N = 10) for 4 days. We chose the dose and duration of treatment with E2 (4 days) based on a previous study by Belo et al. (12). In the cited study, the authors showed that short-term E2 treatment (5 µg·100 g−1·day−1 for 4 days) reduced the arterial pressure of ovariectomized animals. Also, this effect was correlated with an increase in plasma atrial natriuretic peptide levels (12). Thus, these results suggest that only 4 days of administration of E2 can induce beneficial cardiovascular effects in female rats.

Isolated heart preparation

After a 4-day period of treatment, the rats were decapitated 10 to 15 min after intraperitoneal injection of 400 IU heparin. The thorax was immediately opened and the heart was carefully dissected and perfused with Krebs-Ringer solution (118.4 mM NaCl, 4.7 mM KCl, 1.2 mM KH2PO4, 1.2 mM MgSO4.7H2O, 2.5 mM CaCl2.2H2O, 11.7 mM glucose, and 26.5 mM NaHCO3) through a 1.0 ± 0.3-cm aortic stump. The perfusion fluid was maintained at 37 ± 1°C with a constant pressure of 65 mmHg and constant oxygenation (5% CO2-95% O2). A force transducer was attached through a heart clip to the apex of the ventricles to record the contractile force (tension, g) in a computer equipped with a data-acquisition system (Biopac System, USA). A diastolic tension of 1.0 ± 0.2 g was applied to the hearts. Electrical activity was recorded with an electrocardiogram (Nihon Kohden, Japan) with the aid of 2 cotton wicks placed directly on the surface of the right atrium and left ventricle. Coronary flow was measured by collecting the perfusate over a period of 1 min at regular intervals. The systolic tension and coronary flow parameters were normalized to the heart mass. Because a diastolic tension of 1.0 ± 0.2 g was applied to the hearts, diastolic tension was not normalized to heart mass. After the equilibration period (approximately 30 min), the left anterior descending coronary artery was completely occluded by the method described by Lubbe et al. (13), beneath the left auricular appendage together with the adjacent veins. The ligature was released after 15 min and reperfusion was performed for an additional 30 min. Cardiac arrhythmias were defined as the presence of ventricular tachycardia and/or ventricular fibrillation after the ligature of the coronary artery was released. To obtain a quantitative measurement, the arrhythmias were graded arbitrarily by their duration, with the duration of 30 min considered to be irreversible arrhythmias. Therefore, the occurrence of cardiac arrhythmias for 0 to 3 min was assigned a factor of 2; 3 to 6 min was assigned a factor of 4; 6 to 10 min was assigned a factor of 6; 10 to 15 min was assigned a factor of 8; 15 to 20 min was assigned a factor of 10; 20 to 25 min was assigned a factor of 11, and 25 to 30 min was assigned a factor of 12. A value of 0 to 12 was thus obtained in each experiment and was denoted as arrhythmia severity index (ASI) (14).

Statistical analysis

Data are reported as mean ± SEM. Statistical analysis was performed by the Student t-test or one- or two-way ANOVA followed by the Bonferroni test. P < 0.05 was considered to be significant (GraphPad Prism 4.0, USA).

Results

As depicted in Figure 1, ventricular tachycardia and/or ventricular fibrillation were observed in young and middle-aged groups during the reperfusion period. However, the duration of I/R arrhythmias was significantly longer in young rats compared to middle-aged rats (ASI: 9.4 ± 1.0 vs 3.0 ± 0.3 arbitrary units in young and middle-aged rats, respectively; Figure 2A). In addition, 50% of the hearts from young rats presented irreversible arrhythmias while none of the hearts from middle-aged animals showed irreversible arrhythmias during the reperfusion period. Thus, the incidence of irreversible arrhythmias was markedly higher in young rats compared to older rats (Figure 2B).

Figure 1.

Original raw traces of contraction force (tension, g) of representative experiments conducted on (A) young and (B) middle-aged rats. Arrhythmias were produced by 15-min occlusion of the left anterior descending coronary artery in isolated rat hearts followed by reperfusion for 30 min. Insets demonstrate ventricular fibrillation during the reperfusion period. Arrhythmia severity index (ASI) = 12 for the young rat and ASI = 4 for the middle-aged rat.

Figure 2.

Effect of age on ischemia/reperfusion arrhythmias in female rats. Arrhythmias were produced by 15-min occlusion of the left anterior descending coronary artery in isolated rat hearts followed by reperfusion. A, Averaged arrhythmia severity index (ASI) and B, percentage of irreversible arrhythmias. N = 8-10 rats. *P < 0.05 vs young group (Student t-test).

The success of the OVX procedure and of E2 treatment was confirmed by the analysis of uterine weight. OVX caused a significant reduction of the uterine weight of both young and middle-aged rats, which was reversed by 4-day E2 administration (Figure 3). No significant changes in body weight were observed when comparing the young groups (control: 179.8 ± 4.8 g; vehicle: 173.8 ± 4.9 g; E2: 172.0 ± 6.8 g) or when comparing the middle-aged groups (control: 351.4 ± 15.8 g; vehicle: 332.0 ± 13.3 g; E2: 356.4 ± 12.8 g).

Figure 3.

Effects of ovariectomy (OVX) and hormonal treatment (estradiol) on uterine weight. Uterine weight is reported as the ratio between uterine weight (mg) and body weight (g). N = 4-6 rats. *P < 0.05 vs control of the same age, #P < 0.05 vs vehicle-treated group of the same age (two-way ANOVA followed by the Bonferroni test).

We next determined if short-term administration of E2 might modify the duration and incidence of I/R arrhythmias in young and middle-aged rats. Short-term E2 administration induced a significant reduction in the rhythm disturbances of young rats (ASI: 6.6 ± 1.7 in vehicle group vs 3.8 ± 0.8 in E2 group; Figure 4A). On the other hand, treatment with E2 did not cause any significant effect on the duration of I/R arrhythmias in middle-aged rats (Figure 4B).

Figure 4.

Effects of estradiol on ischemia/reperfusion arrhythmias in isolated hearts from (A) young and (B) middle-aged female rats. Arrhythmias were produced by 15-min occlusion of the left anterior descending coronary artery in isolated rat hearts followed by reperfusion. ASI = arrhythmia severity index; OVX = ovariectomy. N = 7-12 rats. *P < 0.05 vs control group (one-way ANOVA followed by the Bonferroni test).

In terms of cardiac function, control and ovariectomized E2-treated middle-aged rats presented lower coronary flow compared to young rats. In ovariectomized E2-untreated rats no significant differences were observed between young and middle-aged animals (Figure 5A). The systolic tension was lower in control and in ovariectomized E2-untreated and -treated middle-aged animals compared to young rats. However, systolic tension was significantly higher in vehicle-treated rats than in control middle-aged animals (Figure 5B). No significant differences in diastolic tension were observed in any of the groups (Figure 5C). Heart rate was lower only in control middle-aged animals compared to young rats. In OVX-untreated and OVX + E2-treated rats, no significant differences were observed between young and middle-aged animals. However, the heart rate of young E2-treated rats was significantly lower than that of young control animals (Figure 5D). In addition, E2 administration induced a significant increase in QT and PR intervals in young rats compared to control. No significant changes in QT or PR intervals were observed in middle-aged E2-treated rats (Table 1).

Figure 5.

Effects of estradiol on coronary flow (A), systolic tension (B), diastolic tension (C), and heart rate (D) of isolated perfused hearts from young and middle-aged female rats during the basal period. OVX = ovariectomy. N = 5-11 rats. *P < 0.05 (two-way ANOVA followed by the Bonferroni test).

Table 1.

Effects of estradiol on PR and QT intervals of hearts isolated from young and middle-aged female rats during the basal period.

	Young rats (6-7 weeks old)		Middle-aged rats (12-14 months old)
	PR (ms)	QT (ms)	PR (ms)	QT (ms)
Control	33.15 ± 1.41	75.95 ± 2.37	37.76 ± 0.52	79.10 ± 3.55
OVX + Veh	34.74 ± 1.82	70.51 ± 4.56	36.53 ± 2.06	73.91 ± 2.91
OVX + E2	39.67 ± 1.87+	87.65 ± 3.12+*	37.32 ± 2.20	77.05 ± 1.74

Data are reported as mean ± SEM for 5-7 animals/group. ms = millisecond; OVX = ovariectomy; E2 = estradiol.

P < 0.05 vs control at the same age;

P < 0.05 vs vehicle (Veh) at the same age (one-way ANOVA followed by the Bonferroni test).

Discussion

The results obtained in this study show that E2 treatment was less effective in attenuating cardiac reperfusion arrhythmias in middle-aged female rats compared to young female rats, thereby suggesting that the protective effects of estrogen on I/R insults are age-dependent. One possible explanation for this observation is that aging influences the cellular regulation of cardiac estrogen receptors (ERs). The cardiac effects of E2 are mediated, at least in part, by two distinct receptors: ER-alpha and ER-beta (15-17). Vornehm et al. (18) found that both ER-alpha and ER-beta are involved in mediating E2-induced rapid cardioprotection after I/R injury. Additionally, a membrane-bound G protein-coupled estrogen receptor (GPER) with high affinity for estrogen has been identified in the heart (19,20). Activation of GPER improves the functional recovery and reduces the infarct size in isolated rat hearts following I/R through a PI3K-dependent and gender-independent mechanism (21). Although we did not evaluate cardiac ER expression in the current study, Jazbutyte et al. (22) demonstrated that ER-alpha expression in hearts was significantly lower in sham-operated and in ovariectomized senescent (24 months old) SHR compared to young animals (3 months old). On the other hand, the expression of ER-beta was detected at comparable levels in hearts of young and senescent rats. Taken together, these findings suggest that cardiac ER expression decreases with age and may influence the responses to E2 treatment. Consequently, this leads to a reduction in the cardioprotective effects of E2.

One may argue that 4-day E2 treatment could not be sufficient to modulate the cardiovascular system. However, as shown by Belo et al. (12), short-term E2 administration resulted in intense reduction of SHR blood pressure with a concomitant increase in the synthesis and release of atrial natriuretic peptide, which is mainly synthesized, stored and secreted by cardiac atria (23). Also, many studies have demonstrated the effects of estrogen infusion on cardiac activity in rats (5,24). We found that the efficiency of short-term E2 treatment was demonstrated by the increase in uterine weight observed in ovariectomized E2-treated young and middle-aged rats. These latter data suggest that estrogen metabolism is similar in young and middle-aged rats, thereby indicating that aging did not interfere with the metabolism of E2.

In keeping with previous reports, we observed that, in addition to the antiarrhythmogenic effect induced by estrogen treatment, young animals had an increased QT interval. Indeed, Burke et al. (25) have reported that the QT interval tends to be longer in women than in men. Also, Philp et al. (5) have shown that E2 induces a blockade of Ca2+ channels in female rats. Ca2+ channel blockers possess antiarrhythmogenic actions in animal models of myocardial ischemia (26) and may contribute to the longer QT interval observed in females (27). Additionally, the ICaL transmural gradient together with lower IK and IK1 densities in female than in male rabbit ventricles (28) could result in prolonged repolarization and greater transmural dispersion of repolarization (27). Thus, our findings suggest that prolongation of the QT interval might be involved in the antiarrhythmogenic effects observed in ovariectomized young rats treated with estrogen.

Although there is evidence that E2 can contribute to the reduction of arrhythmias as a consequence of vasore-laxation (29,30), in our study this possibility is an unlikely mechanism since E2-treated rats presented no alterations in coronary flow.

Also, it is important to note that, although we did not measure the plasma E2 levels of the animals, Belo et al. (12) demonstrated that treatment with E2 for 4 days induces a sustained increase in plasma E2 levels, reaching 40-50 pg/mL. These levels are higher than the plasma concentration of E2 in female control rats, whose values range between 5 and 40 pg/mL during the estrous cycle (12,31). It is likely that estrogen levels were higher in the OVX + E2-treated group compared to both the OVX + vehicle and the intact control group. Thus, estrogen treatment producing blood concentrations exceeding endogenous levels might be required to reduce ASI in young animals.

The current study demonstrated that short-term E2 treatment protects against I/R arrhythmias in hearts of young females rats, but not of middle-aged rats, thereby indicating that the anti-arrhythmogenic effect of E2 is dependent on age. This cardioprotective effect might be related to a lengthening of the QT interval. However, further experiments are needed to clearly identify the mechanisms underlying the anti-arrhythmogenic effects of aging and of E2 in young female rats.