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首页> 外文期刊>Alternative medicine review: a journal of clinical therapeutic >A Clinical Trial Testing the Safety and Efficacy of a Standardized Eucommia ulmoides Oliver Bark Extract to Treat Hypertension
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A Clinical Trial Testing the Safety and Efficacy of a Standardized Eucommia ulmoides Oliver Bark Extract to Treat Hypertension

机译:临床试验测试标准杜仲奥利弗树皮提取物治疗高血压的安全性和有效性

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摘要

BACKGROUND: A tea made from Eucommia ulmoides leaves and bark is part of the Japanese diet. Eucommia is an herbal medicine that, by increasing nitric oxide, reduced blood pressure (BP) in rats and humans in an uncontrolled clinical trial. OBJECTIVE: A controlled clinical trial was conducted to evaluate an aqueous bark extract of Eucommia standardized to eight percent pinoresinol di-beta-D-glucoside (PG) for BP reduction in humans. METHODS: Study 1: Twenty-four healthy adult subjects with a BP between 120-160/80-100 mmHg were randomized to Eucommia extract 500 mg three times daily for eight weeks. Automatic 24-hour ambulatory blood pressure monitoring (24-h ABPM) was utilized at baseline and after eight weeks. Study 2: The effect of the Eucommia extract on isoproterenol-stimulated lipolysis was evaluated in a human fat cell assay to determine whether Eucommia was a beta-adrenergic blocker. Study 3: Thirty healthy adult subjects with a BP between 120-160/80-100 mmHg were randomized to 1 g Eucommia extract three times daily for two weeks with 24-h ABPM at baseline and after two weeks. RESULTS: Study 1: There was no toxicity or any difference in BP between the two groups. Study 2: Eucommia at 0.5% w/v reduced isoproterenol-stimulated lipolysis from 2.67 to 1.4 times the buffer control (p<0.001). Study 3: The Eucommia extract was well-tolerated and reduced BP by an average of 7.5/3.9 mmHg (p<0.008). CONCLUSION: The standardized Eucommia extract reduced BP and has beta-adrenergic blocking activity. Eucommia may be an appropriate nutraceutical intervention for prehypertension.
机译:背景:由杜仲叶和树皮制成的茶是日本饮食的一部分。杜仲是一种草药,通过增加一氧化氮,在一项未经控制的临床试验中,可以降低大鼠和人体的血压(BP)。目的:进行了一项对照临床试验,以评估杜仲的水树皮提取物标准化为8%的松脂醇二β-D-葡萄糖苷(PG)来降低人的血压。方法:研究1:将24名BP在120-160 / 80-100 mmHg之间的健康成人受试者随机分为三天,每天500次注射杜仲提取物500 mg。在基线和八周后使用自动24小时动态血压监测(24小时ABPM)。研究2:在人体脂肪细胞分析中评估了杜仲提取物对异丙肾上腺素刺激的脂解的影响,以确定杜仲是否为β-肾上腺素能阻滞剂。研究3:将30名BP在120-160 / 80-100 mmHg之间的健康成人受试者随机分为1 g杜仲提取物,每天两次,持续两周,基线时为24小时ABPM,两周后。结果:研究1:两组之间无毒性或血压差异。研究2:0.5%w / v的杜仲将异丙肾上腺素刺激的脂解作用从缓冲液对照的2.67降至1.4倍(p <0.001)。研究3:杜仲提取物耐受性良好,血压平均降低7.5 / 3.9 mmHg(p <0.008)。结论:标准杜仲提取物可降低血压,并具有β-肾上腺素阻断活性。杜仲可能是高血压前的适当营养保健干预措施。

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