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人参根提取物的安全性和耐受性:一项在健康韩国志愿者中进行的随机、安慰剂对照、临床试验。

Safety and tolerability of Panax ginseng root extract: a randomized, placebo-controlled, clinical trial in healthy Korean volunteers.

机构信息

Liver and Immunology Research Center, Daejeon Oriental Hospital of Oriental Medical College of Daejeon University, Daejeon, Republic of Korea.

出版信息

J Altern Complement Med. 2012 Nov;18(11):1061-9. doi: 10.1089/acm.2011.0591. Epub 2012 Aug 21.

Abstract

OBJECTIVES

Panax ginseng has been extensively used as an adaptogen and is among the top 10 selling herbal supplements in the United States over the past decade. However, there have been few reports about the toxicity of P. ginseng in human studies. Given the lack of toxicological studies in human, this study investigated whether P. ginseng administration causes any noticeable toxic effects in healthy volunteers.

METHODS

This study was designed as a randomized, double-blind, placebo-controlled, and parallel group trial in healthy volunteers. The subjects were required to be healthy, free from any significant disease, as assessed at screening by physical examination, medical history, and laboratory (hematological and biochemical) tests. Eligible subjects received P. ginseng extract (1 g/day or 2 g/day) or placebo over a 4-week period.

RESULTS

Although mild adverse events, such as dyspepsia, hot flash, insomnia, and constipation, were reported in both P. ginseng and placebo group, no serious untoward reactions were reported following P. ginseng administration. Nonsignificant changes were observed in hematological and biochemical tests.

CONCLUSIONS

P. ginseng administration for 4 weeks was shown to be safe, tolerable, and free of any untoward toxic effect in healthy male and female volunteers. Future results from ongoing multicenter collaborative efforts to evaluate short- and long-term effects of P. ginseng may contribute to our current understanding of safety and tolerability of this herbal product.

摘要

目的

人参被广泛用作适应原,在过去十年中,它是美国销量排名前十的草本补充剂之一。然而,在人体研究中,关于人参毒性的报道很少。鉴于缺乏人体毒理学研究,本研究调查了人参给药是否会对健康志愿者造成任何明显的毒副作用。

方法

本研究设计为健康志愿者的随机、双盲、安慰剂对照、平行组试验。要求受试者健康,无任何重大疾病,在筛选时通过体检、病史和实验室(血液和生化)检查进行评估。合格的受试者在 4 周内接受人参提取物(1 克/天或 2 克/天)或安慰剂治疗。

结果

尽管人参和安慰剂组均报告了轻度不良反应,如消化不良、热潮红、失眠和便秘,但在人参给药后未报告严重不良反应。血液和生化检查未见明显变化。

结论

人参给药 4 周显示安全、耐受,且在健康男性和女性志愿者中无任何不良毒性作用。正在进行的多中心合作努力评估人参的短期和长期效果的未来结果可能有助于我们目前对这种草药产品的安全性和耐受性的理解。

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