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首页> 外文期刊>Journal of the American Society of Hypertension : >Effects of carvedilol or amlodipine on target organ damage in L-NAME hypertensive rats: their relationship with blood pressure variability
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Effects of carvedilol or amlodipine on target organ damage in L-NAME hypertensive rats: their relationship with blood pressure variability

机译:Carvedilol或氨氯地平对L型高血压大鼠靶器官损伤的影响:与血压变异性的关系

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The aim of the study was to compare the effects of chronic oral treatment with carvedilol or amlodipine on blood pressure, blood pressure variability and target organ damage in N-nitro-l-arginine methyl ester (L-NAME) hypertensive rats. Wistar rats were treated with L-NAME administered in the drinking water for 8 weeks together with oral administration of carvedilol 30 mg/kg (n = 6), amlodipine 10 mg/kg (n = 6), or vehicle (n = 6). At the end of the treatment, echocardiographic evaluation, blood pressure, and short-term variability measurements were performed. Left ventricular and thoracic aortas were removed to assess activity of metalloproteinase 2 and 9 and expression levels of transforming growth factor beta, tumor necrosis factor a, and interleukin 6. Histological samples were prepared from both tissues. Carvedilol and amlodipine induced a comparable reduction of systolic and mean arterial pressure and its short-term variability in L-NAME rats. The expression of transforming growth factor beta, tumor necrosis factor alpha, and interleukin 6 decreased in both organs after carvedilol or amlodipine treatment and the activity of metalloproteinase was reduced in aortic tissue. Treatment with carvedilol or amlodipine completely prevented left ventricular collagen deposition and morphometric alterations in aorta. Oral chronic treatment with carvedilol or amlodipine significantly attenuates blood pressure variability and reduces target organ damage and biomarkers of tissue fibrosis and inflammation in L-NAME hypertensive rats. (C) 2017 American Society of Hypertension. All rights reserved.
机译:该研究的目的是将慢性口服治疗与卡维地洛或氨氯地平对血压,血压变异性和靶器官损伤的血压,血压变异性和靶器官损伤的影响进行比较。 Wistar大鼠用饮用水中施用的L-NAME治疗8周,加上甲络合物30mg / kg(n = 6),氨氯嗪10mg / kg(n = 6)或载体(n = 6) 。在治疗结束时,进行超声心动图评估,血压和短期可变性测量。除去左心室和胸部主动脉以评估金属蛋白酶2和9的活性,以及​​转化生长因子β,肿瘤坏死因子A和白细胞介素6的表达水平。组织学样品由两种组织制备。 Carvedilol和氨氯堇他诱导收缩性和平均动脉压的相当降低及其在L型大鼠中的短期变异性。在卡维地洛或氨氯地平治疗后,在两种器官中转化生长因子β,肿瘤坏死因子α和白细胞介素6的表达,并且在主动脉组织中降低了金属蛋白酶的活性。用Carvedilol或氨氯地平治疗完全防止左心室胶原沉积和主动脉的形态学改变。用卡维地洛或氨氯嘧啶的口服慢性处理显着衰减血压变异性,并降低了L-Name高血压大鼠组织纤维化和炎症的靶器官损伤和生物标志物。 (c)2017年美国高血压学会。版权所有。

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