Sun Dong, Yan Changdong, Jacobson Azita, Jiang Houli, Carroll Mairead A, Huang An
Department of Physiology, New York Medical College, Valhalla, NY 10595, USA.
Am J Physiol Regul Integr Comp Physiol. 2007 Sep;293(3):R1239-46. doi: 10.1152/ajpregu.00185.2007. Epub 2007 Jul 18.
We studied the roles of estrogen receptors (ER) and aromatase in the mediation of flow-induced dilation (FID) in isolated arteries of male ERalpha-knockout (ERalpha-KO) and wild-type (WT) mice. FID was comparable between gracilis arteries of WT and ERalpha-KO mice. In WT arteries, inhibition of NO and prostaglandins eliminated FID. In ERalpha-KO arteries, N(omega)-nitro-L-arginine methyl ester (L-NAME) inhibited FID by approximately 26%, whereas indomethacin inhibited dilations by approximately 50%. The remaining portion of the dilation was abolished by additional administration of 6-(2-proparglyoxyphenyl)hexanoic acid (PPOH) or iberiotoxin, inhibitors of epoxyeicosatrienoic acid (EET) synthesis and large-conductance potassium channels, respectively. By using an electrophysiological technique, we found that, in the presence of 10 dyne/cm(2) shear stress, perfusate passing through donor vessels isolated from gracilis muscle of ERalpha-KO mice subjected to L-NAME and indomethacin elicited smooth muscle hyperpolarization and a dilator response of endothelium-denuded detector vessels. These responses were prevented by the presence of iberiotoxin in detector or PPOH in donor vessels. Gas chromatography-mass spectrometry (GC-MS) analysis indicated a significant increase in arterial production of EETs in ERalpha-KO compared with WT mice. Western blot analysis showed a significantly reduced endothelial nitric oxide synthase expression but enhanced expressions of aromatase and ERbeta in ERalpha-KO arteries. Treatment of ERalpha-KO arteries with specific aromatase short-interfering RNA for 72 h, knocked down the aromatase mRNA and protein associated with elimination of EET-mediation of FID. Thus, FID in male ERalpha-KO arteries is maintained via an endothelium-derived hyperpolarizing factor/EET-mediated mechanism compensating for reduced NO mediation due, at least in part, to estrogen aromatized from testosterone.
我们研究了雌激素受体(ER)和芳香化酶在雄性ERα基因敲除(ERα-KO)小鼠和野生型(WT)小鼠离体动脉血流诱导性扩张(FID)介导中的作用。WT和ERα-KO小鼠的股薄肌动脉FID相当。在WT动脉中,一氧化氮(NO)和前列腺素的抑制消除了FID。在ERα-KO动脉中,N(ω)-硝基-L-精氨酸甲酯(L-NAME)抑制FID约26%,而吲哚美辛抑制扩张约50%。通过额外给予6-(2-炔丙氧基苯基)己酸(PPOH)或iberiotoxin(分别为环氧二十碳三烯酸(EET)合成抑制剂和大电导钾通道抑制剂),消除了剩余部分的扩张。通过使用电生理技术,我们发现,在10达因/平方厘米的剪切应力下,通过从接受L-NAME和吲哚美辛处理的ERα-KO小鼠股薄肌分离的供体血管的灌注液,引起内皮剥脱的检测血管平滑肌超极化和扩张反应。这些反应在检测血管中iberiotoxin或供体血管中PPOH存在时被阻止。气相色谱-质谱(GC-MS)分析表明,与WT小鼠相比,ERα-KO小鼠动脉中EETs的产生显著增加。蛋白质免疫印迹分析显示,ERα-KO动脉中内皮型一氧化氮合酶表达显著降低,但芳香化酶和ERβ表达增强。用特异性芳香化酶短发夹RNA处理ERα-KO动脉72小时,敲低了与消除FID的EET介导相关的芳香化酶mRNA和蛋白质。因此,雄性ERα-KO动脉中的FID通过内皮衍生超极化因子/EET介导的机制维持,该机制至少部分补偿了由于睾酮芳香化产生的雌激素减少导致的NO介导减少。