He Yufei, Wang Ze, Wu Weidang, Xie Ying, Wei Zihong, Yi Xiulin, Zeng Yong, Li Yazhuo, Liu Changxiao
Shenyang Pharmaceutical University No. 103 Wenhua Road, Shenhe District Shenyang City Liaoning Province China
Tianjin University of Traditional Chinese Medicine China.
RSC Adv. 2019 May 23;9(28):16136-16146. doi: 10.1039/c9ra00393b. eCollection 2019 May 20.
Aconite as a commonly used herb has been extensively applied in the treatment of rheumatoid arthritis, as pain relief, as well as for its cardiotonic actions. Aconitum alkaloids have been shown to be the most potent ingredients in aconite, in terms of efficacy against disease, but they are also highly toxic. Apart from neurological and cardiovascular toxicity exposed, the damage to hepatocytes and nephrocytes with long-term use of aconitum alkaloids should also be carefully considered. This study attempted to investigate the critical role of uptake transporters mediating the transport of aconitum alkaloids into the liver and the kidneys. The resulting data revealed that hOATP1B1, 1B3, hOCT1 and hOAT3 were mainly involved in the uptake of aconitum alkaloids. Additionally, the inhibitory effects of bioactive ingredients of liquorice on uptake transporters were screened and further confirmed by determining the IC values. The study suggested that liquorice might lower the toxicity of aconite by reducing its exposure in the liver and/or kidneys through inhibition of uptake transporters. Eventually, the study was indicative of detoxification of liquorice by decreasing the exposure of aconitine as representative compound in liver after co-administration, even though the exposure in kidney altered was less significant. In summary, hOATP1B1, 1B3, hOCT1 and hOCT3 were determined as the key uptake transporters mediating the transport process of aconitum alkaloids into the liver and/or kidneys, and liquorice may alleviate the toxicity caused by reduction of exposure through inhibition of those key uptake transporters.
附子作为一种常用草药,已广泛应用于类风湿性关节炎的治疗、止痛以及强心作用。乌头生物碱已被证明是附子中最有效的成分,就疾病疗效而言,但它们也具有高毒性。除了已知的神经和心血管毒性外,长期使用乌头生物碱对肝细胞和肾细胞的损害也应予以仔细考虑。本研究试图探究摄取转运体在介导乌头生物碱转运至肝脏和肾脏过程中的关键作用。所得数据表明,hOATP1B1、1B3、hOCT1和hOAT3主要参与乌头生物碱的摄取。此外,通过测定IC值筛选并进一步证实了甘草生物活性成分对摄取转运体的抑制作用。该研究表明,甘草可能通过抑制摄取转运体来减少附子在肝脏和/或肾脏中的暴露,从而降低其毒性。最终,该研究表明,联合给药后,甘草通过减少作为代表性化合物的乌头碱在肝脏中的暴露而起到解毒作用,尽管在肾脏中的暴露变化不太显著。总之,hOATP1B1、1B3、hOCT1和hOCT3被确定为介导乌头生物碱转运至肝脏和/或肾脏过程的关键摄取转运体,甘草可能通过抑制这些关键摄取转运体减少暴露来减轻毒性。