Department of Physiology, Medical College of Georgia, Augusta, GA 30912-3000, USA.
Vascul Pharmacol. 2010 May-Jun;52(5-6):236-42. doi: 10.1016/j.vph.2010.02.003. Epub 2010 Mar 1.
High soy (HS) diets are neuroprotective and promote vascular dilatation in the periphery. We hypothesized that an HS diet would promote vascular dilatation in the cerebrovasculature by mimicking estradiol's actions on the endothelial nitric oxide synthase (eNOS) system including increasing eNOS expression and decreasing caveolin-1 expression to increase nitric oxide (NO) production. Ovariectomized rats were fed HS or a soy-free diet (SF)+/-low physiological estradiol (E2) for 4weeks. Neither E2 nor HS altered middle cerebral artery (MCA) structure or vascular responses to acetylcholine, serotonin, or phenylephrine. Estradiol enhanced bradykinin-induced relaxation in an eNOS-dependent manner. Although E2 and HS increased eNOS mRNA expression in the brain and cerebrovasculature, they had no effect on eNOS protein expression or phosphorylation in the MCA. However, E2 decreased caveolin-1 protein in the MCA. In MCAs neither E2 nor HS altered estrogen receptor (ER) alpha expression, but E2 did reduce ER beta levels. These data suggest that HS diets have no effect on vascular NO production, and that E2 may modulate basal NO production by reducing the expression of caveolin-1, an allosteric inhibitor of NOS activity. However, the effects of E2 and HS on the cerebrovasculature are small and may not underlie their protective actions in pathological states.
高大豆(HS)饮食具有神经保护作用,并促进外周血管扩张。我们假设 HS 饮食通过模拟雌二醇对内皮型一氧化氮合酶(eNOS)系统的作用,包括增加 eNOS 表达和减少 caveolin-1 表达,从而增加一氧化氮(NO)的产生,促进脑血管扩张。给去卵巢大鼠喂食 HS 或不含大豆的饮食(SF)+/-低生理雌二醇(E2)4 周。E2 和 HS 均未改变大脑中动脉(MCA)的结构或对乙酰胆碱、5-羟色胺或苯肾上腺素的血管反应。雌二醇以依赖于 eNOS 的方式增强缓激肽诱导的松弛。尽管 E2 和 HS 增加了大脑和脑血管中的 eNOS mRNA 表达,但它们对 MCA 中的 eNOS 蛋白表达或磷酸化没有影响。然而,E2 减少了 MCA 中的 caveolin-1 蛋白。在 MCA 中,E2 和 HS 均未改变雌激素受体(ER)α的表达,但 E2 确实降低了 ERβ的水平。这些数据表明 HS 饮食对血管 NO 的产生没有影响,而 E2 可能通过减少作为 NOS 活性变构抑制剂的 caveolin-1 的表达来调节基础 NO 的产生。然而,E2 和 HS 对脑血管的作用较小,并且可能不是它们在病理状态下的保护作用的基础。