Department of Basic Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi, Jiangsu, P.R. China.
J Cell Biochem. 2018 Jan;119(1):926-937. doi: 10.1002/jcb.26258. Epub 2017 Aug 23.
Sympathetic overdrive, activation of renin angiotensin systems (RAS), and oxidative stress are vitally involved in the pathogenesis of hypertension and cardiovascular remodeling. We recently identified that vaccarin protected endothelial cell function from oxidative stress or high glucose. In this study, we aimed to investigate whether vaccarin attenuated hypertension and cardiovascular remodeling. Two-kidney one-clip (2K1C) model rats were used, and low dose of vaccarin (10 mg/kg), high dose of vaccarin (30 mg/kg), captopril (30 mg/kg) were intraperitoneally administrated. Herein, we showed that 2K1C rats exhibited higher systolic blood pressure (SBP), diastolic blood pressure (DBP), mean arterial pressure (MAP), left ventricular mass/body weight ratio, myocardial hypertrophy or fibrosis, media thickness, and media thickness to lumen diameter, which were obviously alleviated by vaccarin and captopril. In addition, both vaccarin and captopril abrogated the increased plasma renin, angiotensin II (Ang II), norepinephrine (NE), and the basal sympathetic activity. The AT1R protein expressions, NADPH oxidase subunit NOX-2 protein levels and malondialdehyde (MDA) content were significantly increased, whereas superoxide dismutase (SOD) and catalase (CAT) activities were decreased in myocardium, aorta, and mesenteric artery of 2K1C rats, both vaccarin and captopril treatment counteracted these changes in renovascular hypertensive rats. Collectively, we concluded that vaccarin may be a novel complementary therapeutic medicine for the prevention and treatment of hypertension. The mechanisms for antihypertensive effects of vaccarin may be associated with inhibition of sympathetic activity, RAS, and oxidative stress.
交感神经过度兴奋、肾素-血管紧张素系统(RAS)激活和氧化应激在高血压和心血管重构的发病机制中起着至关重要的作用。我们最近发现,蝙蝠葛苏林碱可保护内皮细胞功能免受氧化应激或高糖的影响。在这项研究中,我们旨在研究蝙蝠葛苏林碱是否可减轻高血压和心血管重构。使用双肾一夹(2K1C)模型大鼠,腹腔内给予低剂量蝙蝠葛苏林碱(10mg/kg)、高剂量蝙蝠葛苏林碱(30mg/kg)和卡托普利(30mg/kg)。结果表明,2K1C 大鼠的收缩压(SBP)、舒张压(DBP)、平均动脉压(MAP)、左心室质量/体重比、心肌肥大或纤维化、中膜厚度和中膜厚度与管腔直径均升高,而蝙蝠葛苏林碱和卡托普利可明显减轻这些变化。此外,蝙蝠葛苏林碱和卡托普利均减弱了血浆肾素、血管紧张素 II(Ang II)、去甲肾上腺素(NE)和基础交感神经活性的增加。AT1R 蛋白表达、NADPH 氧化酶亚基 NOX-2 蛋白水平和丙二醛(MDA)含量在 2K1C 大鼠的心肌、主动脉和肠系膜动脉中显著增加,而超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性降低,而蝙蝠葛苏林碱和卡托普利治疗可逆转这些变化。总之,我们得出结论,蝙蝠葛苏林碱可能是预防和治疗高血压的一种新型补充治疗药物。蝙蝠葛苏林碱的降压作用机制可能与抑制交感神经活性、RAS 和氧化应激有关。