首页> 美国卫生研究院文献>Antioxidants >Butterfly Pea Flower (Clitoria ternatea Linn.) Extract Ameliorates Cardiovascular Dysfunction and Oxidative Stress in Nitric Oxide-Deficient Hypertensive Rats
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Butterfly Pea Flower (Clitoria ternatea Linn.) Extract Ameliorates Cardiovascular Dysfunction and Oxidative Stress in Nitric Oxide-Deficient Hypertensive Rats

机译:蝴蝶豌豆花(Clitoria Ternatea Linn。)提取物改善了一氧化氮缺乏高血压大鼠的心血管功能障碍和氧化应激

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摘要

In this study, we examine whether Clitoria ternatea Linn. (CT) can prevent Nω-nitro-L-arginine methyl ester hydrochloride (L-NAME)-induced cardiac and vascular dysfunction in rats. Male Sprague Dawley rats were given L-NAME (40 mg/kg, drinking water) and orally administered with CT extract (300 mg/kg/day) or lisinopril (2.5 mg/kg/day) for 5 weeks. The main phytochemical components of the CT extract were found to be flavonoids. The CT extract alleviated the high blood pressure in rats receiving L-NAME. Decreased vasorelaxation responses to acetylcholine and enhanced contractile responses to sympathetic nerve stimulation in aortic rings and mesenteric vascular beds of L-NAME treated rats were ameliorated by CT extract supplementation. Left ventricular hypertrophy and dysfunction were developed in L-NAME rats, which were partially prevented by CT extract treatment. The CT extract alleviated upregulated endothelial nitric oxide synthase expression, decreased plasma nitrateitrite levels, and increased oxidative stress in L-NAME rats. It suppressed high levels of serum angiotensin-converting enzyme activity, plasma angiotensin II, and cardiac angiotensin II type 1 receptor, NADPH oxidases 2, nuclear factor-kappa B, and tumor necrosis factor-alpha expression. The CT extract, therefore, partially prevented L-NAME-induced hypertension and cardiovascular alterations in rats. These effects might be related to a reduction in the oxidative stress and renin–angiotensin system activation due to L-NAME in rats.
机译:在这项研究中,我们检查Clitoria Ternatea Linn。 (CT)可以预防Nω-Nitro-L-精氨酸甲酯盐酸盐(L-NAME) - 大鼠的心脏和血管功能障碍。给予雄性Sprague Dawley大鼠L-Name(40mg / kg,饮用水),口服用Ct提取物(300mg / kg /天)或丽思诺普利(2.5mg / kg /天)5周。发现CT提取物的主要植物化学成分是黄酮类化合物。 CT提取物缓解了接受L-NAME的大鼠的高血压。通过CT提取物补充,减少对乙酰胆碱对乙酰胆碱的反应和增强对同性恋神经刺激的增强的合成响应,并通过CT提取物来改善L-NAME处理的大鼠的肠系膜血管床。左心室肥大和功能障碍在L型大鼠中开发,通过CT提取物处理部分预防。 CT提取物缓解了上调的内皮一氧化氮合酶表达,降低了氮酸盐/亚硝酸盐水平,并增加了L-名称大鼠的氧化胁迫。它抑制了高水平的血清血管紧张素转化酶活性,血浆血管紧张素II和心血管素II型1受体,NADPH氧化酶2,核因子-Kappa B和肿瘤坏死因子-α表达。因此,CT提取物,部分地防止了L名诱导的大鼠的高血压和心血管改变。由于L-NAME在大鼠中,这些效果可能与氧化应激和肾素 - 血管紧张素系统活化的减少有关。

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