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Effect of Onopordon acanthium L. as Add on Antihypertensive Therapy in Patients with Primary Hypertension Taking Losartan: a Pilot Study

机译:先天性高血压对服用氯沙坦的原发性高血压患者降压治疗的影响

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Purpose: Onopordon acanthium L. is known for its medicinal properties. Our recent study showed that its seed extract is a novel natura angiotensin-converting-enzyme inhibitor (ACEI). This study was carried out to investigate its possible antihypertensive effects in patients receiving losartan. Methods: This uncontrolled clinical trial was carried out among 20 patients (30-60y) with uncontrolled hypertension despite receiving 50 mg losartan (stage I & II) in two hospitals in Iran. After completing informed consent, patients were treated by 2 capsules [each 1g of Onopordon acanthium seed extract (OSE)] as add-on therapy, two times per day. Results: 18 patients completed the study (50.94 ±8.37y). Mean systolic blood pressure (SBP) at the baseline was 151.9 ± 13.74mmHg and at the end of the study, it was 134.6 ± 18.25 mmHg and mean diastolic blood pressure (DBP) was 97.41 ± 10.36 at the baseline and was 85.71 ± 7.481 after 8 weeks. OSE significantly reduced SBP and DBP at the end of 8 weeks (P=0.003, 95% CI: -19.7, -15.1; P=0.0006, 95% CI: -10.23, -13.15; respectively). No evidence of hepatic or renal toxicity was detected. Conclusion: Based on the results of this study OSE has antihypertensive property with no significant adverse effects. However, because of the low number of samples, this medication may be not safely administered. The results of this study could be the basis for further studies with larger sample size. IRCT registration number: IRCT2013020712391N.
机译:目的:Onopordon acanthium L.以其药用特性而闻名。我们最近的研究表明,其种子提取物是一种新型的自然界血管紧张素转化酶抑制剂(ACEI)。进行这项研究以研究其在接受氯沙坦治疗的患者中可能的降压作用。方法:尽管在伊朗的两家医院接受了50 mg氯沙坦治疗(I和II期),但仍对20例(30-60岁)高血压患者进行了这项不受控制的临床试验。在获得知情同意后,患者需每天2次服用2粒胶囊[每片1克Onopordon acanthium种子提取物(OSE)]作为附加疗法。结果:18位患者完成了研究(50.94±8.37y)。基线时的平均收缩压(SBP)为151.9±13.74mmHg,研究结束时为基线的平均收缩压(SBP)为134.6±18.25 mmHg,舒张压的平均舒张压(DBP)在基线时为97.41±10.36,之后为85.71±7.481 8个星期。 OSE在8周结束时显着降低了SBP和DBP(分别为P = 0.003、95%CI:-19.7,-15.1; P = 0.0006、95%CI:-10.23,-13.15)。没有发现肝或肾毒性的证据。结论:根据这项研究的结果,OSE具有降压作用,且无明显不良反应。但是,由于样品数量少,这种药物可能无法安全使用。这项研究的结果可能是进行更大样本量进一步研究的基础。 IRCT注册号:IRCT2013020712391N。

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