Okano Masato, Sato Mitsuhiko, Kageyama Shinji
Anti-Doping Laboratory, LSI Medience Corporation, 3-30-1 Shimura, Itabashi-ku, Tokyo, 174-8555, Japan.
Drug Test Anal. 2017 Nov;9(11-12):1788-1793. doi: 10.1002/dta.2258. Epub 2017 Sep 15.
Higenamine is a key component of traditional Chinese herbal medicine. The fruit of Nandina domestica (which contains this component) is available as an ingredient in the so-called Nanten-nodo-ame throat lozenge found on the Japanese market, which is an over-the-counter pharmaceutical and is easy to purchase for Japanese athletes. However, higenamine is a non-selective β2-agonist, which is exemplified in the prohibited list of the World Anti-Doping Agency (WADA). Therefore, some have raised a concern regarding the potential cause of increased unintentional higenamine doping cases in the Asian region. This study aimed to investigate components of throat lozenges and develop a mass-spectrometry method for the quantification of higenamine and coclaurine in human urine. Moreover, a population study of Japanese subjects (n = 246) and an excretion study (n = 4) of the corresponding throat-lozenge recipients were performed to test the applicability of the current reporting threshold (i.e., 10 ng/mL) of higenamine set by WADA. The estimates of higenamine and coclaurine were 2.2 ± 0.1 μg/drop (mean of n = 12) and 0.5 ± 0.01 μg/drop (mean of n = 12), respectively. The maximum concentrations of higenamine and coclaurine were 0.2-0.4 and 0.3-1.0 ng/mL, respectively, at 10-12 h after administration of higenamine (nine drops); however, the concentrations in all four volunteers did not reach the positivity criterion of 10 ng/mL. No higenamine and coclaurine could be detected in the Japanese subjects. Therefore, there is no risk of detecting unintentional higenamine doping when the WADA reporting threshold is used.
去甲乌药碱是传统中草药的关键成分。南天竹(含有该成分)的果实作为一种成分,存在于日本市场上所谓的南天竹润喉糖中,这是一种非处方药,日本运动员很容易买到。然而,去甲乌药碱是一种非选择性β2激动剂,已被列入世界反兴奋剂机构(WADA)的禁用清单。因此,有人对亚洲地区无意中使用去甲乌药碱导致兴奋剂检测呈阳性的潜在原因表示担忧。本研究旨在调查润喉糖的成分,并开发一种质谱方法来定量测定人尿中的去甲乌药碱和去甲劳丹碱。此外,对246名日本受试者进行了群体研究,并对相应润喉糖服用者进行了4例排泄研究,以测试WADA设定的当前去甲乌药碱报告阈值(即10 ng/mL)的适用性。去甲乌药碱和去甲劳丹碱的估计含量分别为2.2±0.1μg/滴(n = 12的平均值)和0.5±0.01μg/滴(n = 12的平均值)。服用去甲乌药碱(9滴)后10 - 12小时,去甲乌药碱和去甲劳丹碱的最高浓度分别为0.2 - 0.4 ng/mL和0.3 - 1.0 ng/mL;然而,所有4名志愿者的浓度均未达到10 ng/mL的阳性标准。在日本受试者中未检测到去甲乌药碱和去甲劳丹碱。因此,使用WADA报告阈值时,不存在无意中检测出去甲乌药碱兴奋剂的风险。