Van Kempen Tracey A, Narayan Ankita, Waters Elizabeth M, Marques-Lopes Jose, Iadecola Costantino, Glass Michael J, Pickel Virginia M, Milner Teresa A
Feil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, New York, 10065.
Weill Cornell Graduate School of Medical Sciences. Weill Cornell Medicine, New York, New York, 10021.
J Comp Neurol. 2016 Aug 1;524(11):2251-65. doi: 10.1002/cne.23944. Epub 2015 Dec 23.
At younger ages, women have a lower risk for hypertension than men, but this sexual dimorphism declines with the onset of menopause. These differences are paralleled in rodents following "slow-pressor" angiotensin II (AngII) administration: young male and aged female mice, but not young females, develop hypertension. There is also an established sexual dimorphism both in the cardiovascular response to the neurohypophyseal hormone arginine vasopressin (AVP) and in the expression of oxidative stress. We examined the relationship between AngII-mediated hypertension and the cellular distribution of the superoxide generating NADPH oxidase (NOX) in AVP-expressing hypothalamic paraventricular nucleus (PVN) neurons in "menopausal" female mice. Dual-labeling immunoelectron microscopy was used to determine whether the subcellular distribution of the organizer/adapter NOX p47(phox) subunit is altered in PVN dendrites following AngII administered (14 days) during the "postmenopausal" stage of accelerated ovarian failure (AOF) in young female mice treated with 4-vinylcyclohexene diepoxide. Slow-pressor AngII elevated blood pressure in AOF females and induced a significant increase in near plasmalemmal p47(phox) and a decrease in cytoplasmic p47(phox) in PVN AVP dendrites. These changes are the opposite of those observed in AngII-induced hypertensive male mice (Coleman et al. [2013] J. Neurosci. 33:4308-4316) and may be ascribed in part to baseline differences between young females and males in the near plasmalemmal p47(phox) on AVP dendrites seen in the present study. These findings highlight fundamental differences in the neural substrates of oxidative stress in the PVN associated with AngII hypertension in postmenopausal females compared with males. J. Comp. Neurol. 524:2251-2265, 2016. © 2015 Wiley Periodicals, Inc.
在较年轻的时候,女性患高血压的风险低于男性,但这种性别差异会随着更年期的到来而减小。在给予“缓升压型”血管紧张素II(AngII)后,啮齿动物中也存在类似的差异:年轻雄性和老年雌性小鼠会出现高血压,而年轻雌性小鼠不会。在对神经垂体激素精氨酸加压素(AVP)的心血管反应以及氧化应激的表达方面,也存在既定的性别差异。我们研究了在“更年期”雌性小鼠中,AngII介导的高血压与表达AVP的下丘脑室旁核(PVN)神经元中产生超氧化物的NADPH氧化酶(NOX)的细胞分布之间的关系。采用双标记免疫电子显微镜来确定,在用4-乙烯基环己烯二环氧化物处理的年轻雌性小鼠的加速卵巢衰竭(AOF)“绝经后”阶段给予AngII(14天)后,组织/衔接蛋白NOX p47(phox)亚基在PVN树突中的亚细胞分布是否发生改变。缓升压型AngII使AOF雌性小鼠的血压升高,并导致PVN AVP树突中靠近质膜的p47(phox)显著增加,细胞质中的p47(phox)减少。这些变化与在AngII诱导的高血压雄性小鼠中观察到的变化相反(Coleman等人,[2013]《神经科学杂志》33:4308 - 4316),并且可能部分归因于本研究中在AVP树突上年轻雌性和雄性之间靠近质膜的p47(phox)的基线差异。这些发现突出了绝经后女性与男性相比,与AngII高血压相关的PVN氧化应激神经基质的根本差异。《比较神经学杂志》524:2251 - 2265,2016。©2015威利期刊公司。