Laboratory of Pathological and Molecular Pharmacology, Osaka University of Pharmaceutical Sciences, Takatsuki, Japan.
J Cardiovasc Pharmacol. 2012 Sep;60(3):269-75. doi: 10.1097/FJC.0b013e31825e2e57.
The purpose of this study is to elucidate the relationship between sex difference and norepinephrine (NE) release in the pathogenesis of myocardial ischemia/reperfusion (I/R) injury. Isolated male and female rat hearts were subjected to 40-minute global ischemia followed by 30-minute reperfusion. Compared with male hearts, I/R-induced cardiac dysfunction, such as decreased left ventricular developed pressure and dP/dtmax and increased left ventricular end diastolic pressure, was significantly attenuated in female hearts. An excessive NE overflow in the coronary effluent from the postischemic heart in females was much less than that in males. These sex differences were abolished by ovariectomy, but in vivo treatment with 17β-estradiol recovered it. This ameliorating effect of 17β-estradiol was not observed in the presence of nitric oxide (NO) synthase inhibitor N-nitro-L-arginine. When NOx (NO2/NO3) levels in the coronary effluent after onset of reperfusion were measured, reversed correlated relationships between NOx production and I/R-induced cardiac dysfunction, and NE overflow, were observed. These findings suggest that sex differences in the postischemic cardiac dysfunction are closely related to the NE overflow from the postischemic heart and that estrogen plays a key role in the cardioprotective effect against I/R injury in female rats, by suppressing NE release via the enhancement of NO production.
本研究旨在阐明性别差异与去甲肾上腺素(NE)释放在心肌缺血/再灌注(I/R)损伤发病机制中的关系。将雄性和雌性大鼠的离体心脏分别进行 40 分钟的整体缺血,随后进行 30 分钟的再灌注。与雄性心脏相比,雌性心脏的 I/R 诱导的心脏功能障碍(如左心室发展压和 dp/dtmax 的降低以及左心室舒张末期压的升高)明显减轻。在雌性心脏中,缺血后心脏冠状流出液中的 NE 过度溢出比雄性心脏少得多。这些性别差异在卵巢切除术后被消除,但体内用 17β-雌二醇处理可恢复这些差异。在存在一氧化氮(NO)合酶抑制剂 N-硝基-L-精氨酸的情况下,17β-雌二醇没有观察到这种改善作用。当测量再灌注开始后冠状流出液中的 NOx(NO2/NO3)水平时,观察到 NOx 产生与 I/R 诱导的心脏功能障碍和 NE 溢出之间呈反向相关关系。这些发现表明,缺血后心脏功能障碍的性别差异与缺血后心脏的 NE 溢出密切相关,雌激素通过增强 NO 产生来抑制 NE 释放,从而在雌性大鼠的 I/R 损伤保护作用中发挥关键作用。