University of Miami, Miller School of Medicine, Miami, Florida, USA.
Clin Transl Sci. 2009 Apr;2(2):134-42. doi: 10.1111/j.1752-8062.2009.00094.x.
Aldosterone receptor antagonism reduces mortality and improves post-myocardial infarction (MI) remodeling. Because aldosterone and estrogen signaling pathways interact, we hypothesized that aldosterone blockade is sex-specific. Therefore, we investigated the impact of eplerenone on left ventricular (LV) remodeling and gene expression of male infarcted rats versus female infarcted rats. MI and Sham animals were randomized to receive eplerenone (100 mg/kg/day) or placebo 3 days post-surgery for 4 weeks and assessed by echocardiography. In the MI placebo group, left ventricular end-diastolic dimension (LVEDD) increased from 7.3 +/- 0.4 mm to 10.2 +/- 1.0 mm (p < 0.05) and ejection fraction (EF) decreased from 82.3 +/- 4% to 45.5 +/- 11% (p < 0.05) in both sexes (p = NS between groups). Eplerenone attenuated LVEDD enlargement more effectively in females (8.8 +/- 0.2 mm, p < 0.05 vs. placebo) than in males (9.7 +/- 0.2 mm, p = NS vs. placebo) and improved EF in females (56.7 +/- 3%, p < 0.05 vs. placebo) but not in males (50.6 +/- 3%, p = NS vs. placebo). Transcriptomic analysis using Rat_230-2.0 microarrays (Affymetrix) revealed that in females 19% of downregulated genes and 44% of upregulated genes post-MI were restored to normal by eplerenone. In contrast, eplerenone only restored 4% of overexpressed genes in males. Together, these data suggest that aldosterone blockade reduces MI-induced cardiac remodeling and phenotypic alterations of gene expression preferentially in females than in males. The use of transcriptomic signatures to detect greater benefit of eplerenone in females has potential implications for personalized medicine.
醛固酮受体拮抗剂可降低死亡率并改善心肌梗死后(MI)的重构。因为醛固酮和雌激素信号通路相互作用,我们假设醛固酮阻断是有性别特异性的。因此,我们研究了依普利酮对雄性和雌性梗死大鼠的左心室(LV)重构和基因表达的影响。MI 和假手术(Sham)动物在手术后 3 天随机接受依普利酮(100mg/kg/天)或安慰剂治疗 4 周,并通过超声心动图进行评估。在 MI 安慰剂组中,雄性和雌性的 LVEDD 从 7.3+/-0.4mm 增加到 10.2+/-1.0mm(p<0.05),EF 从 82.3+/-4%降低到 45.5+/-11%(p<0.05)(两组间无统计学差异,p=NS)。依普利酮更有效地抑制 LVEDD 扩大,在雌性(8.8+/-0.2mm,p<0.05 vs.安慰剂)比在雄性(9.7+/-0.2mm,p=NS vs.安慰剂)更有效,并改善雌性的 EF(56.7+/-3%,p<0.05 vs.安慰剂),但对雄性没有影响(50.6+/-3%,p=NS vs.安慰剂)。使用 Rat_230-2.0 微阵列(Affymetrix)进行的转录组分析显示,在雌性中,19%的 MI 后下调基因和 44%的上调基因被依普利酮恢复正常。相比之下,依普利酮仅在雄性中恢复了 4%的过度表达基因。这些数据表明,醛固酮阻断可降低 MI 引起的心脏重构,并优先在雌性中恢复基因表达的表型改变,而在雄性中则不然。使用转录组特征来检测依普利酮在雌性中的更大益处可能对个性化医疗具有潜在意义。