Department of Anesthesiology, Division of Molecular Medicine, Cardiovascular Research Laboratories, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, CA, USA.
Hypertension. 2012 Aug;60(2):425-30. doi: 10.1161/HYPERTENSIONAHA.112.191445. Epub 2012 Jul 2.
Pretreatment with a phytoestrogen genistein has been shown to attenuate the development of pulmonary hypertension (PH). Because PH is not always diagnosed early, we examined whether genistein could also reverse preexisting established PH and prevent associated right heart failure (RHF). PH was induced in male rats by 60 mg/kg of monocrotaline. After 21 days, when PH was well established, rats received daily injection of genistein (1 mg/kg per day) for 10 days or were left untreated to develop RHF by day 30. Effects of genistein on human pulmonary artery smooth muscle cell and endothelial cell proliferation and neonatal rat ventricular myocyte hypertrophy were assessed in vitro. Severe PH was evident 21 days after monocrotaline, as peak systolic right ventricular pressure increased to 66.35±1.03 mm Hg and right ventricular ejection fraction reduced to 41.99±1.27%. PH progressed to RHF by day 30 (right ventricular pressure, 72.41±1.87 mm Hg; RV ejection fraction, 29.25±0.88%), and mortality was ≈75% in RHF rats. Genistein therapy resulted in significant improvement in lung and heart function as right ventricular pressure was significantly reduced to 43.34±4.08 mm Hg and right ventricular ejection fraction was fully restored to 65.67±1.08% similar to control. Genistein reversed PH-induced pulmonary vascular remodeling in vivo and inhibited human pulmonary artery smooth muscle cell proliferation by ≈50% in vitro likely through estrogen receptor-β. Genistein also reversed right ventricular hypertrophy (right ventricular hypertrophy index, 0.35±0.029 versus 0.70±0.080 in RHF), inhibited neonatal rat ventricular myocyte hypertrophy, and restored PH-induced loss of capillaries in the right ventricle. These improvements in cardiopulmonary function and structure resulted in 100% survival by day 30. Genistein restored PH-induced downregulation of estrogen receptor-β expression in the right ventricle and lung. In conclusion, genistein therapy not only rescues preexisting severe PH but also prevents the progression of severe PH to RHF.
植物雌激素金雀异黄素预处理已被证明可减轻肺动脉高压 (PH) 的发展。由于 PH 并不总是早期诊断,我们研究了金雀异黄素是否也能逆转已存在的 PH 并预防相关的右心衰竭 (RHF)。雄性大鼠通过给予 60mg/kg 的单环素来诱导 PH。21 天后,当 PH 已完全建立时,大鼠每天接受金雀异黄素 (1mg/kg/天) 注射 10 天,或不治疗至第 30 天发展为 RHF。金雀异黄素对人肺动脉平滑肌细胞和内皮细胞增殖以及新生大鼠心室肌细胞肥大的影响在体外进行评估。单环素 21 天后出现严重 PH,表现为收缩期右心室压力升高至 66.35±1.03mmHg,右心室射血分数降低至 41.99±1.27%。第 30 天 PH 进展为 RHF(右心室压力,72.41±1.87mmHg;RV 射血分数,29.25±0.88%),RHF 大鼠的死亡率约为 75%。金雀异黄素治疗可显著改善肺和心脏功能,右心室压力显著降低至 43.34±4.08mmHg,右心室射血分数完全恢复至 65.67±1.08%,与对照组相似。金雀异黄素在体内逆转 PH 诱导的肺血管重塑,并在体外抑制约 50%的人肺动脉平滑肌细胞增殖,可能通过雌激素受体-β。金雀异黄素还逆转右心室肥大(右心室肥大指数,0.35±0.029 与 RHF 中的 0.70±0.080),抑制新生大鼠心室肌细胞肥大,并恢复 PH 诱导的右心室毛细血管丢失。这些心肺功能和结构的改善导致第 30 天的 100%存活率。金雀异黄素恢复 PH 诱导的右心室和肺中雌激素受体-β表达的下调。总之,金雀异黄素治疗不仅挽救了已存在的严重 PH,而且还预防了严重 PH 进展为 RHF。