Myocardial contractility is preserved early but reduced late after ovariectomy in young female rats
© Paigel et al; licensee BioMed Central Ltd. 2011
Received: 3 January 2011
Accepted: 23 April 2011
Published: 23 April 2011
Ovarian sex hormones (OSHs) are implicated in cardiovascular function. It has been shown that OSHs play an important role in the long term regulation of cardiac sarcoplasmic reticulum (SR) function and contractility, although early effects of OSHs deprivation on myocardial contractility have not yet been determined. This study evaluated the early and late effects of OSHs deficiency on left ventricular contractility in rats after ovariectomy.
Young female Wistar rats were divided into 3 groups (n = 9-15): sham operated (Sham), ovariectomized (Ovx) and Ovx treated with estradiol (1 mg/kg, i.m., once a week) (Ovx+E2). After 7, 15, 30 and 60 days post Ovx, left ventricle papillary muscle was mounted for isometric tension recordings. The inotropic response to Ca2+ (0.62 to 3.75 mM) and isoproterenol (Iso 10-8 to 10-2 M) and contractility changes in response to rate changes (0.25 to 3 Hz) were assessed. Protein expression of SR Ca2+-ATPase (SERCA2a) and phospholamban (PLB) in the heart was also examined.
The positive inotropic response to Ca2+ and Iso at 7, 15, and 30 days after Ovx was preserved. However, at 60 days, the Ovx group had decreased myocardial contractility which was subsequently restored with E2 replacement. The reduction in SERCA2a and increase in PLB expression observed at 60 days after Ovx were restored with E2 replacement.
This study demonstrated that myocardial contractility and expression of key Ca2+ handling proteins were preserved in the early phase and reduced at long-term during OSHs deprivation.
Cardiovascular disease is a major contributor to morbidity and mortality among post-menopausal women in the western world . Interestingly, pre-menopausal women have a reduced risk of mortality from cardiovascular disease while post-menopausal women have a similar or even increased risk for cardiovascular disease as compared to men . It has been suggested that ovarian sex hormones (OSHs) have a protective effect on the cardiovascular system [2, 3]. However, the effects of estrogen replacement therapy on the cardiovascular risk only account for about 50% of the reduction seen in cardiovascular disease suggesting that there must be additional mechanisms whereby estrogen exerts its cardioprotective effects . Though observational and experimental studies have suggested that ovarian sex hormones (OSHs) replacement therapy may be cardioprotective [5, 6], large trials utilizing oral conjugated estrogen and medroxyprogesterone acetate did not confirm these findings .
In the last few years, the main ovarian hormone, estrogen (E2), has received special attention for its protective effects against atherosclerosis [8, 9]. Several studies have also indicated that E2 directly protective of cardiac muscle contractility [10, 11]. However, though studies have indicated that OSHs therapy restore contractile performance in post-menopausal women [12–14], short-term of cardiac effects of ovariectomy and E2 replacement have not been demonstrated.
Recent studies further suggest that mechanical functioning and proteomic profiles in ventricular myocytes are directly regulated by E2 [15–18]. However, those studies only investigated cardiac performance and proteins involved in Ca2+ homeostasis at 4 to 10 weeks after OSHs deprivation leaving short-term effects of OSHs deprivation on myocardial contractility poorly understood. Thus, our aim was to study the inotropic response of left ventricular papillary muscles short and long-term (7, 15, 30 and 60 days) after ovariectomy in young female rats. We also investigated the expression of cardiac regulatory proteins sarcoplasmic reticulum (SR) Ca2+-ATPase (SERCA2a), phospholamban (PLB) and sodium-calcium exchanger (NCX) at 7, 15, 30 and 60 days after Ovx. We studied the expression of these proteins primarily due the fact that PLB regulates the Ca2+-affinity of SERCA2a, facilitating calcium uptake into the SR and muscle relaxation, which is considered an important intracellular mechanism involved in myocardial contractility [19, 20].
The care and use of the laboratory animals were in accordance with National Institutes of Health (NIH) guidelines and were approved by the local animal ethics committee. All rats had free access to water and were fed with food ad libitum.
Experimental groups, surgical procedures and E2 replacement. Eight-week-old female Wistar rats weighting 185g approximately were randomly divided into two groups. One group underwent bilateral ovariectomy (Ovx) as described previously . Briefly, a dorsal midline skin incision was made under anesthesia caudal to the posterior border of the ribs. The posterior abdominal muscle wall was bluntly dissected, the abdominal cavity was opened and the ovary was gently exteriorized and removed. The uterine horn was returned into the abdomen. The skin incision was closed with sterile nylon sutures, and the process was repeated on the other side. At 1 week after Ovx, a subgroup of the ovariectomized rats (Ovx+E2) started treatment with estradiol valerate (E2) 1 mg/Kg injected, i.m., once a week for 8 weeks. The second group underwent a sham operation and served as normal controls (sham). Left ventricle papillary muscle contractility was studied at 7, 15, 30 and 60 days after surgery. E2 replacement was carried out only in the 60 day ovariectomized subgroup because it was the only group that showed a reduction in myocardial contractility. At the time of sacrifice, adequacy of the ovariectomy was determined grossly by the absence of ovarian tissue and marked atrophy of the uterus . We also determined the weight of the entire animal, as well as the weight of the left and right ventricles and the uterus.
Isometric tension and myocardial contractility
Rats received 500 units of heparin intraperitoneal (i.p.) and then were anesthetized 10 minutes later with 45 mg/kg sodium pentobarbital, i.p., (Cristália, SP, Brazil). Hearts were rapidly removed and perfused through the aortic stump and the left ventricle papillary muscles were dissected. Muscle preparations were mounted for isometric tension recording and maintained in a 20 mL glass-bath containing Krebs-Henseleit solution (in mM: NaCl 118, KCl 4.7, CaCl2 1.25, KH2PO4 1.2, MgSO4 1.2, NaHCO3 23 and glucose 11) at 30°C and pH = 7.4, which was continuously aerated with 95% O2 and 5% CO2. Resting tension was adjusted to produce maximal contractile force (Lmax). The twitch contraction rate was controlled by isolated rectangular pulses (10 to 15 V, 12 ms duration) through a pair of platinum electrodes. The standard stimulation rate was 0.5 Hz (steady-state). Isometric force development was measured with an isometric force transducer (TSD105A, Biopac) and normalized to muscle weight (g/g). Recording started after 60 minutes to permit the muscle to adapt to the new environmental conditions. Myocardial contractility was tested by the following protocol. First, we measured the inotropic response to changes in extracellular calcium concentration (Ca2+, 0.62 to 3.75 mM). Next, the positive inotropic response, produced by increasing isoproterenol concentrations added to the bath (10-8 - 10-2 M), was analyzed. Finally, we evaluated the isometric force development relationship at stimulation rates of 0.25 to 3.0 Hz. At the end of the experiment, the papillary muscle was removed and weighed for force normalization (g/g).
Serum estrogen level
Blood samples were collected in tubes with anticoagulant from group at 60 days after surgery. Blood samples were centrifuged at 1,500 g for 15 min at 4°C. The resulting serum was kept at -80°C until used to determine estrogen levels. The E2 levels in the serum were measured using ELISA technique according to the manufacturer's instruction.
Western blot analysis of SERCA2a, NCX and PLB
Proteins from homogenized hearts (100 μg) were separated by 7.5% (SERCA2a and NCX) or 15% (PLB) SDS-PAGE. Proteins were transferred to nitrocellulose membranes for SERCA2a and NCX and polyvinyl difluoride membranes for PLB and were incubated with mouse monoclonal antibodies for SERCA2a (1:1000, Affinity BioReagents, CO, USA), NCX (1:200, Abcam Cambridge, MA, USA) and PLB (1 μg/ml, Affinity BioReagents, CO, USA). After washing, membranes were incubated with anti-mouse (1:5000, StressGen, Victoria, Canada) immunoglobulin antibody conjugated to horseradish peroxidase. After thorough washing, immunocomplexes were detected using an enhanced horseradish peroxidase/luminal chemiluminescence system (ECL Plus, Amersham International, Little Chalfont, UK) and film (Hyperfilm ECL International). Signals on the immunoblot were quantified with the National Institutes of Health Image V1.56 computer program. The same membrane was used to determine GAPDH expression using a mouse monoclonal antibody (1:5000, Abcam Cambridge, MA, USA).
All values are expressed as mean ± SEM. Differences among groups were analyzed using the two way ANOVA test followed by the Tukey post hoc test for multiple comparisons. A p value < 0.05 was considered statistically significant. For protein expression, data are expressed as the ratio between protein and GAPDH signals.
Drugs and chemicals
All chemicals, unless specified in the text, were purchased from Sigma Chemical (St. Louis, MO).
Weight data from sham, ovariectomized (Ovx) and estrogen replacement
195 ± 3
201 ± 5
204 ± 3
232 ± 8*
233 ± 3
274 ± 5*
256 ± 5
310 ± 9*
251 ± 9#
2.25 ± 0.06
2.12 ± 0.07
2.21 ± 0.07
2.07 ± 0.05
2.25 ± 0.09
2.09 ± 0.06
2.0 ± 0.03
1.9 ± 0.04
1.93 ± 0.05
0.57 ± 0.02
0.55 ± 0.02
0.52 ± 0.02
0.53 ± 0.01
0.54 ± 0.01
0.58 ± 0.04
0.48 ± 0.03
0.49 ± 0.02
0.54 ± 0.02
2.09 ± 0.14
0.70 ± 0.04*
2.40 ± 0.17
0.60 ± 0.05*
1.96 ± 0.07
0.47 ± 0.04*
2.60 ± 0.16
0.45 ± 0.04*
2.56 ± 0.19#
Papillary Muscle (mg)
5.5 ± 0.46
5.6 ± 0.56
4.9 ± 0.35
6.1 ± 0.51
4.11 ± 0.36
5.0 ± 0.4
5.2 ± 0.47
5.7 ± 0.33
5.9 ± 0.5
Isometric contractility response to calcium
Force increases with increasing myocardial mass, characterizing a positive correlation between theses variables. Assuming the 60 days group is older and the papillary muscles are heavier, we expected to find higher values for all parameter in the 60 days groups. As the OVX group has a contractility dysfunction, the force did not increase as expected.
Isometric contractile response to β-adrenergic receptor stimulation
Effect of ovariectomy on maximum positive and negative force derivatives
Estrogen replacement therapy
Western blot analysis of SERCA2a, NCX and PLB
This study examines the effects of OSHs deprivation on cardiac contractility in rats at both short and late-term periods after ovariectomy. Our results demonstrated myocardial contractility was preserved short-term. However, at long-term, deficiency in OSHs reduced cardiac contractility which was associated with changes in expression of key contractile proteins, SERCA2a and PLB. The long-term ovariectomy-induced reduction in myocardial contractility corroborates data previously described [15–18]. The novel finding in this study is that changes in contractility due to ovariectomy were not evident until 60 days after hormone loss. Interestingly, myocardial contractility, analyzed at 7, 15 and 30 days, was preserved during basal conditions and even under positive inotropic stimuli. Besides, at 60 days the Sham group showed an increasing in myocardial contractility response to calcium and Isoproterenol corroborating data previously described .
Our results demonstrated that the PLB to SERCA2a ratio was increased at 60 days in the Ovx group by approximately 1.6-fold and was normalized after E2 treatment. The protein expression of NCX remained unchanged. Based on transgenic and gene-targeted mouse model studies, alterations to the PLB to SERCA2a ratio has been suggested to be a major regulator of cardiac contractility [25, 27]. In vivo studies using transgenic mice which overexpress cardiac specific PLB suggested that the "functional stoichiometry" of PLB/SERCA2 is less than 1:1 in native cardiac sarcoplasmic reticulum membranes . Two-fold higher PLB protein levels in these transgenic mice as compared to WT, resulted in greater inhibition of Ca2+-ATPase affinity for Ca2+, which was associated with decreases in contractility and Ca2+ transport in cardiomyocytes.
This suggests that changes observed in SR protein expression at 60 days in Ovx rats may be responsible for the reduced contractility observed. Further, because E2 replacement restored SR protein expression and myocardial contractility, it is plausible that OSHs participate in the long-term regulation of cardiac contractility. In fact, a previous study observed thyroid hormone regulation of SR protein expression and cardiac contractility . These authors also observed enhanced cardiac PLB expression which was associated with decreased rates of cardiac SR Ca2+ uptake which is consistent with increased inhibition of the cardiac SR Ca2+ pump and decreased contractility in hypothyroid rats.
Long-term studies demonstrated the influence of OSHs on rat cardiac contractility  through impaired left ventricular function. Impaired function was characterized by decreases in cardiac output, peak systolic pressure and ejection fraction at all preloads in the hearts of rat ovariectomized before puberty. These contractile changes were further associated with a decrease in myosin ATPase activity. Another study  demonstrated the same changes in cardiac function which were reversed by E2 replacement. Further studies reporting changes in intracellular Ca2+ homeostasis in cardiomyocytes suggest a possible modulating effect of OSH deficiency on the Ca2+ responsiveness of cardiac myofilament activation by induction of myofilament Ca2+ hypersensitivity but suppression of maximum myofibrillar ATPase activity [28, 16], which may underlie the cardiac dysfunction observed in OSHs deficiency. These findings support our results. The regulatory role of OSHs in the calcium uptake activity of cardiac SR was also demonstrated in 10 week ovariectomized rat hearts . These authors demonstrated that estrogen and progesterone supplementation were equally effective in preventing changes in ovariectomized hearts.
In our study, 30 days after Ovx, myocardial isometric contractility in response to extracellular Ca2+ and β-adrenergic agonist as well as the rate-force development relationship were preserved. In another study, hormone status did not affect levels of SERCA2a, PLB, ryanodine receptor and the mRNA encoding for β1-adrenoreceptor at 4 weeks post ovariectomy in rat . Chu et al. further demonstrated that there was no difference in the isoproterenol-elicited increase in developed force though the abundance of β1-adrenoreceptor was over 2-fold higher in the Ovx group compared with Sham.
We also conducted our study at an early stage after ovariectomy. Rat hearts were studied at 7 and 15 days post ovariectomy. Clear evidence of OSH absence was observed as early as 7 days after ovariectomy with a close to 3-fold reduction in uterus weight compared to sham animals. In addition, there was an increase in body weight in the Ovx rats at 15 days. However, myocardial contractility was preserved in these animals.
E2 receptor signaling in the cardiovascular system is a complex process that is not completely understood. Its effects on the vascular system have been demonstrated in normal rats  and after myocardial infarction . It is well recognized that E2 has genomic and non-genomic actions. The long-term effects of estrogen are mediated by different nuclear hormone receptors, ER α and ER β, which are encoded by different genes and act as ligand-dependent transcription factors . To date, a number of mechanisms have been proposed to decipher the cardio protective effects of E2. E2 alters the expression of ventricular ß1-adrenoreceptor [17, 33], intracellular calcium homeostasis related to the L-type Ca2+ channel , cardiac SR Ca2+ uptake  and Ca2+ sensitivity of cardiac myofilaments in ovariectomized rats , which are important mediators of cardiac contractility. Although a cardiac transcriptional regulation of estrogen is well described, there is little direct evidence of membrane cardiac estrogen receptors. Data reporting on the non-genomic signal transduction in cardiomyocytes have demonstrated that 17β estradiol has a negative inotropic effect on guinea-pig single ventricular myocytes by inhibiting ICa and so reducing systolic Ca2+ .
Furthermore, in isolated rat ventricular cardiomyocytes, it was demonstrated that E2 exerts opposite effects on intracellular myocyte pH, which is associated with pro-and anti-hypertrophic effects .
A question raised by the results presented here is whether OSHs affects the myocardium directly or by secondary mechanisms involving other hormones modulated by E2. Also, as contractility was altered so late after loss of OSHs, does E2 act only by genomic mechanisms, or are compensatory mechanisms involved in the short term? Further studies are necessary to clarify these questions. Taken together, our results suggest that changes in Ca2+ handling due to abnormal SR function may contribute to reduced myocardial contractility in chronically OSH-deficient rats. Further studies would be beneficial to determine the importance of these findings in humans, as there are significant species-dependent differences in PLB regulation of SERCA2a . Further, long-term rather than short-term estrogen suppression lead to contractile dysfunction which was subsequently reversed with estrogen replacement.
In conclusion, the most novel aspect demonstrated in this study is the long delay in development of cardiac dysfunction after ovariectomy in young female rats.
This work was supported by grants from The National Council for Scientific and Technological Development (CNPq, Brazil) and by Espírito Santo Research Foundation (FAPES/FUNCITEC, ES, Brazil). We thank Dr Erinne Dabkowski for editorial assistance.
- The ESHRE Capri Workshop Group: Hormones and cardiovascular health in women. Hum Reprod Update. 2006, 12: 483-497.View ArticleGoogle Scholar
- Mosca L, Manson JE, Sutherland SE, Langer RD, Manolio T, Barrett-Connor E: Cardiovascular disease in women: a statement for healthcare professionals from the American Heart Association. Circulation. 1997, 96: 2468-2482.View ArticlePubMedGoogle Scholar
- Mosca L, Banka CL, Benjamin EJ, Berra K, Bushnell C, Lolor RJ, Ganiats TG, et al: Evidence-based guidelines for cardiovascular disease prevention in women: 2007 update. JACC. 2007, 49: 1230-1250.View ArticlePubMedGoogle Scholar
- Kuroski de Bold ML: Estrogen, natriuretic peptides and the renin-angiotensin system. Cardiovasc Res. 1999, 41: 524-531. 10.1016/S0008-6363(98)00324-1.View ArticlePubMedGoogle Scholar
- Wenger NK, Speroff L, Packard B: Cardiovascular health and disease in women. N Engl J Med. 1993, 22: 247-256.View ArticleGoogle Scholar
- Hayward CS, Kalnis WV, Kelly RP: Acute effects of 17B- estradiol on ventricular and vascular hemodynamics in postmenopausal women. Am J Physiol. 2000, 279: H2277-H2284.Google Scholar
- Grady D, Herrington D, Bittner V, Blumenthal R, Davidson M, Hlatky M, Hsia J, Hulley S, Herd A, Khan S, Newby LK, Waters D, Vittinghoff E, Wenger N: HERS Research Group Cardiovascular disease outcomes during 6.8 years of hormone therapy: Heart and Estrogen/progestin Replacement Study follow-up (HERS II). JAMA. 2002, 3: 49-57.View ArticleGoogle Scholar
- Bush TL, Barrett-Connor E, Cowan LD, Criqui MH, Wallace RB, Suchindran CM, Tyroler Hayward CS, Kalnis WV, Kelly RP: Acute effects of 17B- estradiol on ventricular and vascular hemodynamics in postmenopausal women. Am J Physiol. 2000, 279: H2277-H2284.Google Scholar
- Guetta V, Cannon RO: Cardiovascular effects of estrogen and lipid-lowering therapies in postmenopausal women. Circulation. 1996, 93: 1928-1937.View ArticlePubMedGoogle Scholar
- Grohé C, Kahlert S, Löbbert K, Stimpel M, Karas RH, Vetter H, Neyses L: Cardiac myocytes and fibroblasts contain functional estrogen receptors. FEBS Letters. 1997, 13: 107-112.View ArticleGoogle Scholar
- Grohé C, Kahlert S, Löbbert K, Vetter H: Expression of oestrogen receptor alpha and beta in rat heart: role of local oestrogen synthesis. J Endocrinol. 1998, 156: R1-7. 10.1677/joe.0.156R001.View ArticlePubMedGoogle Scholar
- Alecrin IN, Aldrighi JM, Caldas MA, Gebara OC, Lopes NH, Ramires JA: Acute and chronic effects of oestradiol on left ventricular diastolic function in hypertensive postmenopausal women with left ventricular diastolic dysfunction. Heart. 2004, 90: 777-781. 10.1136/hrt.2003.016493.PubMed CentralView ArticlePubMedGoogle Scholar
- Schaible TF, Malhotra A, Ciambrone G, Scheuer J: The effects of gonadectomy on left ventricular function and cardiac contractile proteins in male and female rats. Circ Res. 1984, 54: 38-49.View ArticlePubMedGoogle Scholar
- Scheuer J, Malhotra A, Schaible TF, Capasso J: Effects of gonadectomy and hormonal replacement on rat hearts. Circ Res. 1987, 61: 12-19.View ArticlePubMedGoogle Scholar
- Ren J, Hintz KK, Roughead ZKF, Duan J, Colligan PB, Ren BH, Lee KJ, Zeng H: Impact of estrogen replacement on ventricular myocyte contractile function and protein kinase B/Akt activation. Am J Physiol. 2003, 284: H1800-H1807.Google Scholar
- Bupha-Intr T, Wattanapermpool J: Regulatory role of ovarian sex hormones in calcium uptake activity of cardiac sarcoplasmic reticulum. Am J Physiol. 2006, 291: H1101-H1108. 10.1152/ajpcell.00481.2006.View ArticleGoogle Scholar
- Chu SH, Goldspink P, Kowalski J, Beck J, Schwertz DW: Effect of estrogen on calcium-handling proteins, beta-adrenergic receptors, and function in rat heart. Life Sci. 2006, 79: 1257-1267. 10.1016/j.lfs.2006.03.037.View ArticlePubMedGoogle Scholar
- Kravtsov GM, Kam KWL, Liu J, Wu Song, Wong TM: Altered Ca2+ handling by ryanodine receptor and Na+-Ca2+ Exchange in the heart from ovariectomized rats: role of protein kinase A. Am J Physiol. 2007, 292: 1625-1635.View ArticleGoogle Scholar
- Simmerman HK, Jones LR: Phospholamban: Protein Structure, Mechanism of Action and Role in Cardiac Function. Physiol Rev. 1998, 78: 921-947.PubMedGoogle Scholar
- Brittsan AG, Kranias EG: Phospholamban and cardiac contractile function. J Mol Cell Cardiol. 2000, 32: 2131-2139. 10.1006/jmcc.2000.1270.View ArticlePubMedGoogle Scholar
- Waynforth HB, Flecknell PA: Specific surgical operations. Experimental and Surgical Technique in the rat. Academic, San Diego, CA. 1998, 276-278.Google Scholar
- Bers DM, Perez-Reyes E: Ca channels in cardiac myocytes: structure and function in Ca influx and intracellular Ca release. Cardiovasc Res. 1999, 42: 339-60. 10.1016/S0008-6363(99)00038-3.View ArticlePubMedGoogle Scholar
- Brodde OE, Michel MC: Adrenergic and muscarinic receptors in the human heart. Pharmacol Rev. 1999, 51: 651-690.PubMedGoogle Scholar
- Sonnenblick EH: Determinants of active state in heart muscle: Force, velocity, instantaneous muscle length and time. Fed Proc. 24 (suppl): 1396-1965.Google Scholar
- Koss KL, Kranias EG: Phospholamban: a prominent regulator of myocardial contractility. Circ Res. 1996, 79: 1059-1063.View ArticlePubMedGoogle Scholar
- Bocalini DS, Tucci PJ: Developed Force of Papillary Muscle What Index Correctly Indicates Contractile Capacity?. Int Heart J. 2009, 5: 643-652.View ArticleGoogle Scholar
- Kadambi VJ, Ponniah S, Harrer J, Hoit B, Dorn GW, Walsh RA, Kranias EG: Cardiac-specific overexpression of phospholamban alters calcium kinetics and resultant cardiomyocyte mechanics in transgenic mice. J Clin Invest. 1996, 97: 533-539. 10.1172/JCI118446.PubMed CentralView ArticlePubMedGoogle Scholar
- Kiss E, Jakab G, Kranias EG, Edes I: Thyroid hormone-induced alterations in phospholamban protein expression. Regulatory effects on sarcoplasmic reticulum Ca2+ transport and myocardial relaxation. Circ Res. 1994, 75: 245-251.View ArticlePubMedGoogle Scholar
- Wattanapermpool J: Increase in calcium responsiveness of cardiac myofilament activation in ovariectomized rats. Life Sci. 1998, 63: 955-964. 10.1016/S0024-3205(98)00353-1.View ArticlePubMedGoogle Scholar
- Miller VM, Duckles SP: Vascular actions of estrogens: functional implications. Pharmacol Rev. 2008, 60: 210-241. 10.1124/pr.107.08002.PubMed CentralView ArticlePubMedGoogle Scholar
- Bianchi PR, Gumz BP, Giuberti K, Stefanon I: Myocardial infarction increases reactivity to phenylephrine in isolated aortic rings of ovariectomized rats. Life Sci. 2006, 78: 875-881. 10.1016/j.lfs.2005.05.086.View ArticlePubMedGoogle Scholar
- Mendelsohn ME, Karas RH: Molecular and cellular basis of cardiovascular gender differences. Science. 2005, 308: 1583-1587. 10.1126/science.1112062.View ArticlePubMedGoogle Scholar
- Thawornkaiwong A, Preawnim S, Wattanapermpool J: Upregulation of beta 1-adrenergic receptors in ovariectomized rat hearts. Life Scis. 2003, 72: 1813-1824. 10.1016/S0024-3205(02)02473-6.View ArticleGoogle Scholar
- Johnson BD, Zheng W, Korach KS, Scheuer T, Catterall WA, Rubanyi GM: Increased expression of the cardiac L-type calcium channel in estrogen receptor-deficient mice. J Gen Physiol. 1997, 110: 135-140. 10.1085/jgp.110.2.135.PubMed CentralView ArticlePubMedGoogle Scholar
- Jiang C, Poole-Wilson PA, Sarrel PM, Mochizuki S, Collins P, MacLeod KT: Effect of 17 beta-oestradiol on contraction, Ca2+ current and intracellular free Ca2+ in guinea-pig isolated cardiac myocytes. Br J Pharmacol. 1992, 106: 739-745.PubMed CentralView ArticlePubMedGoogle Scholar
- Kilic A, Javadov S, Karmazyn M: Estrogen exerts concentration-dependent pro-and anti-hyperthophic effects on adult cultured ventricular myocytes. Role of NHE-1 in estrogen-induced hyperthophy. J Mol Cell Cardiol. 2009, 46: 360-369. 10.1016/j.yjmcc.2008.11.018.View ArticlePubMedGoogle Scholar
- Waggoner JR, Ginsburg KS, Mitton BA, Haghighi K, Robbins J, Bers DM, Kranias EG: Phospholamban overexpression in rabbit ventricular myocytes does not alter sarcoplasmic reticulum calcium transport. Am J Physiol. 2009, 296: H698-703.Google Scholar
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