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灵芝在健康受试者中的安全性和耐受性:一项双盲随机安慰剂对照试验。

Safety and tolerability of Ganoderma lucidum in healthy subjects: a double-blind randomized placebo-controlled trial.

作者信息

Wicks Sheila M, Tong Robin, Wang Chong-Zhi, O'Connor Michael, Karrison Theodore, Li Shang, Moss Jonathan, Yuan Chun-Su

机构信息

Tang Center for Herbal Medicine Research, The Pritzker School of Medicine, University of Chicago, Chicago, IL 60637, USA.

出版信息

Am J Chin Med. 2007;35(3):407-14. doi: 10.1142/S0192415X07004928.

Abstract

Ganoderma lucidum is a herbal medicine commonly used in oriental countries as a remedy for treating various medical conditions. In this controlled study, we evaluated the safety and tolerance of oral administration of Ganoderma lucidum in 16 human volunteers who received 2 grams of the extract or placebo twice daily for 10 consecutive days. During the study, information from subjective questionnaires were obtained, electrocardiograms, complete blood counts, blood chemistry analysis and urinalysis were performed. In addition, blood tests reflecting immunity were done. Our data showed that compared to placebo group, no adverse effects were observed after the extract intake. Although there were no obvious changes in CD4, CD8, and CD19 levels after the extract, CD56 cell count increased during the study and returned to baseline 10 days after the herbal intake. However, due to relatively high variability and small sample size, this CD56 increase did not achieve statistical significance, and remains to be re-evaluated in the future. It appears that an additional long-term safety and tolerance trial with herbal dose-escalating design is warranted.

摘要

灵芝是一种在东方国家常用于治疗各种疾病的草药。在这项对照研究中,我们评估了16名人类志愿者口服灵芝的安全性和耐受性,这些志愿者连续10天每天两次服用2克提取物或安慰剂。在研究期间,获取了主观问卷信息,进行了心电图、全血细胞计数、血液化学分析和尿液分析。此外,还进行了反映免疫的血液检测。我们的数据显示,与安慰剂组相比,摄入提取物后未观察到不良反应。尽管提取物摄入后CD4、CD8和CD19水平没有明显变化,但研究期间CD56细胞计数增加,并在摄入草药10天后恢复到基线水平。然而,由于变异性相对较高且样本量较小,这种CD56的增加未达到统计学意义,有待未来重新评估。看来有必要进行一项额外的采用草药剂量递增设计的长期安全性和耐受性试验。

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