脉冲波速
医学
血压
内科学
脉冲压力
动脉硬化
心脏病学
舒张期
内分泌学
作者
Marc Isabelle,Stefano Chimenti,Hélène Beaussier,Denis Gransagne,Nicole Villeneuve,Michel E. Safar,Véronique Duchatelle,Jean‐Paul Vilaine,Christine Vayssettes‐Courchay,Yvonnick Bézie
标识
DOI:10.1097/hjh.0000000000000838
摘要
Enhanced aortic stiffness and blood pressure variability (BPV) are independent risk factors for cardiovascular disease and all-cause mortality in man. They are also correlated with increased blood pressure (BP) and/or arterial remodeling. However, the interplay between BP and BPV on the stiffening process is still unclear. Our objectives were to determine the temporal evolution of both BPV and pulse wave velocity (PWV), a surrogate measure of arterial stiffness, using an animal model of remodeling-dependent aortic stiffening.We thus, developed a new telemetric technique allowing continuous measurement of PWV in conscious, unrestrained rats. Studies were performed in spontaneously hypertensive rats (SHR) treated for 2 weeks with N-nitro-L-arginine methyl ester, a nitric oxide synthase inhibitor (SHR-LN). BPV was evaluated conventionally or with a new device composed of two pressure transducers in two different sets of rats. This allowed a continuous monitoring of telemetered PWV, systolic (SPV), diastolic (DPV), and pulse pressure variability (PPV). Aortic structure was then characterized by immunohistochemical analysis.SPV, DPV, and PPV were increased in SHR-LN, when calculated by 24-h SD or using average real variability a parameter used to assess short-term variability in man. We observed rapid and simultaneous increases in BP, SPV, and PWV. Interestingly, PPV was the most increased parameter resulting mainly from different time course of SPV and DPV. Structural alterations of the aortic wall were observed, with a eutrophic inward remodeling and accumulation of fibronectin and its two main receptors (α5 and αv integrins).This offers unequivocal evidence of a significant relationship between PWV, BPV, and arterial structure.
科研通智能强力驱动
Strongly Powered by AbleSci AI