Department of Biomedical Sciences, School of Medicine and Health Sciences, University of Barcelona, 08036 Barcelona, Spain.
Department of Medicine and Life Sciences, University Pompeu Fabra, 08003 Barcelona, Spain.
Int J Mol Sci. 2023 Feb 7;24(4):3261. doi: 10.3390/ijms24043261.
Williams-Beuren syndrome (WBS) is a rare disorder caused by a recurrent microdeletion with hallmarks of cardiovascular manifestations, mainly supra-valvular aortic stenosis (SVAS). Unfortunately, there is currently no efficient treatment. We investigated the effect of chronic oral treatment with curcumin and verapamil on the cardiovascular phenotype of a murine model of WBS harbouring a similar deletion, CD (complete deletion) mice. We analysed systolic blood pressure in vivo and the histopathology of the ascending aorta and the left ventricular myocardium to determine the effects of treatments and their underlying mechanism. Molecular analysis showed significantly upregulated xanthine oxidoreductase (XOR) expression in the aorta and left ventricular myocardium of CD mice. This overexpression is concomitant with increased levels of nitrated proteins as a result of byproduct-mediated oxidative stress damage, indicating that XOR-generated oxidative stress impacts the pathophysiology of cardiovascular manifestations in WBS. Only the combined therapy of curcumin and verapamil resulted in a significant improvement of cardiovascular parameters via activation of the nuclear factor erythroid 2 (NRF2) and reduction of XOR and nitrated protein levels. Our data suggested that the inhibition of XOR and oxidative stress damage could help prevent the severe cardiovascular injuries of this disorder.
威廉姆斯-贝伦综合征(WBS)是一种由复发性微缺失引起的罕见疾病,其特征为心血管表现,主要为主动脉瓣上狭窄(SVAS)。不幸的是,目前尚无有效的治疗方法。我们研究了慢性口服姜黄素和维拉帕米治疗对携带类似缺失的 WBS 小鼠模型(CD 小鼠)心血管表型的影响。我们分析了体内收缩压和升主动脉及左心室心肌的组织病理学,以确定治疗效果及其潜在机制。分子分析显示,CD 小鼠的主动脉和左心室心肌中黄嘌呤氧化还原酶(XOR)的表达显著上调。这种过表达伴随着由于副产物介导的氧化应激损伤导致的硝化蛋白水平的增加,表明 XOR 产生的氧化应激影响 WBS 心血管表现的病理生理学。只有姜黄素和维拉帕米的联合治疗通过激活核因子红细胞 2(NRF2)和降低 XOR 和硝化蛋白水平,才能显著改善心血管参数。我们的数据表明,抑制 XOR 和氧化应激损伤可能有助于预防这种疾病的严重心血管损伤。