Department of Neuroscience and Experimental Therapeutics, Albany Medical College, 47 New Scotland Ave, Albany, NY 12208, United States.
Brain Res. 2019 May 1;1710:43-60. doi: 10.1016/j.brainres.2018.12.030. Epub 2018 Dec 20.
Sex differences exist in how cerebral blood vessels function under both physiological and pathological conditions, contributing to observed sex differences in risk and outcomes of cerebrovascular diseases (CBVDs), such as vascular contributions to cognitive impairment and dementia (VCID) and stroke. Throughout most of the lifespan, women are protected from CBVDs; however, risk increases following menopause, suggesting sex hormones may play a significant role in this protection. The cerebrovasculature is a target for sex hormones, including estrogens, progestins, and androgens, where they can influence numerous vascular functions and pathologies. While there is a plethora of information on estrogen, the effects of progestins and androgens on the cerebrovasculature are less well-defined. Estrogen decreases cerebral tone and increases cerebral blood flow, while androgens increase tone. Both estrogens and androgens enhance angiogenesis/cerebrovascular remodeling. While both estrogens and androgens attenuate cerebrovascular inflammation, pro-inflammatory effects of androgens under physiological conditions have also been demonstrated. Sex hormones exert additional neuroprotective effects by attenuating oxidative stress and maintaining integrity and function of the blood brain barrier. Most animal studies utilize young, healthy, gonadectomized animals, which do not mimic the clinical conditions of aging individuals likely to get CBVDs. This is also concerning, as sex hormones appear to mediate cerebrovascular function differently based on age and disease state (e.g. metabolic syndrome). Through this review, we hope to inspire others to consider sex as a key biological variable in cerebrovascular research, as greater understanding of sex differences in cerebrovascular function will assist in developing personalized approaches to prevent and treat CBVDs.
在生理和病理条件下,大脑血管的功能存在性别差异,这导致了脑血管疾病(CBVD)风险和结局的性别差异,如血管性认知障碍和痴呆(VCID)和中风。在大多数生命周期中,女性免受 CBVD 的影响;然而,绝经后风险增加,表明性激素可能在这种保护中发挥重要作用。脑血管系统是性激素的靶标,包括雌激素、孕激素和雄激素,它们可以影响许多血管功能和病理。虽然有大量关于雌激素的信息,但孕激素和雄激素对脑血管的影响还不太明确。雌激素降低大脑张力并增加脑血流量,而雄激素增加张力。雌激素和雄激素都增强血管生成/脑血管重塑。虽然雌激素和雄激素都能减轻脑血管炎症,但在生理条件下雄激素也具有促炎作用。性激素通过减轻氧化应激和维持血脑屏障的完整性和功能发挥额外的神经保护作用。大多数动物研究都使用年轻、健康、去势的动物,这些动物不能模拟可能患上 CBVD 的老年个体的临床状况。这也令人担忧,因为性激素似乎根据年龄和疾病状态(例如代谢综合征)以不同的方式调节脑血管功能。通过这篇综述,我们希望激发其他人将性别视为脑血管研究中的一个关键生物学变量,因为更好地了解脑血管功能的性别差异将有助于制定预防和治疗 CBVD 的个性化方法。