Ghods Roshanak, Gharouni Manouchehr, Amanlou Massoud, Sharifi Niusha, Ghobadi Ali, Amin Gholamreza
Research Institute for Islamic and Complementary Medicine, Iran University of Medical Sciences, Tehran, Iran.
School of Persian Medicine, Iran University of Medical Sciences, Tehran, Iran.
Adv Pharm Bull. 2018 Mar;8(1):69-75. doi: 10.15171/apb.2018.009. Epub 2018 Mar 18.
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. 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. 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. 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.
刺苞菜蓟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天然血管紧张素转换酶抑制剂(ACEI)。本研究旨在调查其对接受氯沙坦治疗的患者可能产生的降压作用。这项非对照临床试验在伊朗的两家医院对20名年龄在30至60岁之间、尽管服用了50毫克氯沙坦(I期和II期)但高血压仍未得到控制的患者进行。在获得知情同意后,患者接受2粒胶囊[每粒含1克刺苞菜蓟种子提取物(OSE)]作为附加治疗,每天两次。18名患者完成了研究(年龄50.94±8.37岁)。基线时平均收缩压(SBP)为151.9±13.74毫米汞柱,研究结束时为134.6±18.25毫米汞柱;基线时平均舒张压(DBP)为97.41±10.36,8周后为85.71±7.481。8周结束时,OSE显著降低了SBP和DBP(P = 0.003,95%置信区间:-19.7,-15.1;P = 0.0006,95%置信区间:-10.23,-13.15;)。未检测到肝毒性或肾毒性证据。基于本研究结果,OSE具有降压特性且无明显不良反应。然而,由于样本数量较少,这种药物可能无法安全给药。本研究结果可为进一步开展更大样本量的研究奠定基础。IRCT注册号:IRCT2013020712391N。