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Ameliorated biomechanical properties of carotid arteries by puerarin in spontaneously hypertensive rats

机译:葛根素在自发性高血压大鼠中改善生物力学性质

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An emerging body of evidence indicates that puerarin (PUE) plays an important role in the treatment of angina pectoris, myocardial ischemia-reperfusion injury, hypertension and other cardiovascular diseases, but how PUE affects the vascular remodeling of hypertensive rats has not been reported yet. This study aimed to investigate the effect and mechanism of PUE on carotid arteries of spontaneously hypertensive rats (SHR) to provide the basis for the clinical application of PUE. Thirty male SHR and six male Wistar Kyoto rats (WKY) aged 3?months were used in this study, SHR rats were randomly divided into 5 groups, PUE(40 or 80?mg/kg/d, ip) and telmisartan (TELMI) (30?mg/kg/d, ig) were administrated for 3?months. We use DMT myography pressure-diameter system to investigate biomechanical properties of carotid arteries, 10?μM pan-classical transient receptor potential channels (TRPCs) inhibitor SKF96365, 200?nM specific TRPC6 inhibitor SAR7334 and 100?μM Orai1 inhibitor ANCOA4 were used in the mechanical test. PUE can significantly decrease systolic and diastolic blood pressure, long-term administration of PUE resulted in a mild reduction of thickness and inner diameter of carotid artery. PUE ameliorate NE-response and vascular remodeling mainly through inhibiting TRPCs channel activities of VSMC. PUE can ameliorate biomechanical remodeling of carotid arteries through inhibiting TRPCs channel activities of VSMC in spontaneously hypertensive rats.
机译:新兴的证据表明,葛根素(Pue)在治疗心绞痛,心肌缺血再灌注损伤,高血压和其他心血管疾病中起重要作用,但是提出的影响尚未报告高血压大鼠的血管重塑。本研究旨在探讨坪对自发性高血压大鼠(SHR)颈动脉的疗效和机制为临床应用的临床应用依据。三十只男性shr和六个男性wistar kyoto大鼠(Wky)在本研究中使用了3个月,将ShR大鼠随机分为5组,扁平(40或80×Mg / kg / d,IP)和Telmisartan(Telmi) (30?mg / kg / d,Ig)施用3个月。我们使用DMT界面压力直径系统来研​​究颈动脉的生物力学性质,10?μm泛古瞬态受体潜在通道(TRPCS)抑制剂SKF96365,200β特异性TRPC6抑制剂SAR7334和100?μmORAI1抑制剂ANCOA4机械测试。扁平可以显着降低收缩性和舒张血压,长期施用扁平,导致颈动脉厚度和内径的轻度降低。 PUE主要通过抑制VSMC的TRPCS频道活动来改善NE响应和血管改造。 Pue可以通过抑制VSMC在自发性高血压大鼠中的TRPCS信道活动来改善颈动脉的生物力学重塑。

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