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Toxicity of daphnane-type diterpenoids from Genkwa Flos and their pharmacokinetic profile in rat

机译:Genkwa Flos中达芙烷型二萜的毒性及其在大鼠体内的药代动力学

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Daphnane-type diterpenoids (DDs) are the main types of plant diterpene orthoesters known and have remarkable biological activities. However, the in vivo toxicity and pharmacokinetic profile of DDs remains unkonwn. The aim of this study was to investigate the toxicity and pharmacokinetic profile of DDs from Genkwa Flos (Thymelaeaceae). The toxicity of diterpenoids was evaluated after oral administration of total diterpenoids extract from Genkwa Flos to rats, and the blood concentration of diterpenoids was analyzed by ultra performance liquid chromatography tandem triple-quadrupole mass spectrometry (UPLC-TQ-MS). The diterpenoids were confirmed to be the toxic components of Genkwa Flos. The pharmacokinetic profile of these diterpenoids was quite different due to their different structures. Although the contents of yuanhuafine and yuanhuapine were low in the extract, the blood concentrations were extremely high. In contrary, the contents of genkwanine F and Wikstroemia factor M1 in the extract were much higher, but they could not be detected in the blood. This result implied that yuanhuafine and yuanhuapine but not genkwanine F and Wikstroemia factor M1 were the potentail toxic components of Genkwa Flos in vivo. This paper shows for the first time the toxicity of diterpenoids from Genkwa Flos was correlated with their blood concentration and when DDs were used for medicinal purposes, their contents in herb as well as their blood concentrations should be considered.
机译:达芙烷型二萜类化合物(DDs)是已知的植物二萜原酸酯的主要类型,并具有显着的生物活性。但是,DDs的体内毒性和药代动力学特征仍然未知。这项研究的目的是调查Genkwa Flos(百里香科)DDs的毒性和药代动力学特征。口服Genkwa Flos提取的总二萜类化合物后,评估其对大鼠的毒性,并通过超高效液相色谱串联三重四极杆质谱(UPLC-TQ-MS)分析其血药浓度。确认二萜是Genkwa Flos的有毒成分。这些二萜类化合物的药代动力学特征因结构不同而有很大差异。尽管提取物中的原花粉和原花粉含量较低,但血药浓度却很高。相反,提取物中的Genkwanine F和Wikstroemia因子M1的含量高得多,但在血液中无法检测到。该结果表明,元华芬和元华平而不是Genkwanine F和Wikstroemia因子M1是Genkwa Flos在体内的潜在毒性成分。本文首次显示了Genkwa Flos的二萜类化合物的毒性与它们的血药浓度相关,当DDs用于药物用途时,应考虑其在草药中的含量以及其血药浓度。

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