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毛冬青总三萜皂苷给药后人脐静脉内皮细胞中冬青素A和冬青皂苷B1的吸收特性

Absorption characteristics of ilexgenin A and ilexsaponin B1 in human umbilical vein endothelial cells after administration of the total triterpenoid saponins from Ilex pubescens.

作者信息

Qiu Jingwen, Shang Xueying, Chen Bingying, Bai Rongyu, Wu Yurong, Wang Ying, Wan Xin, Zhou Yuan, Zhu Chenchen, Zhang Ren, Zhang Juan, Zhao Zhongxiang, Zhang Lei

机构信息

School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, China.

Guangzhou Baiyunshan Chenliji Pharmaceutical Co., Guangzhou, China.

出版信息

Biomed Chromatogr. 2022 Oct;36(10):e5438. doi: 10.1002/bmc.5438. Epub 2022 Aug 5.

Abstract

Ilex pubescens is a famous Chinese herbal medicine, frequently used to treat cardiovascular disease in South China. In this study, we aim to explore the absorption properties of ilexgenin A (C1) and ilexsaponin B1 (C3) in vascular endothelial cells after administration of the total triterpenoid saponins from Ilex pubescens (IPTS) and clarify the possible transport mechanisms. A UPLC-qTOF-MS/MS system was used to identify the components in IPTS that could be intracellularly transported by human umbilical vein endothelial cells (HUVECs). Afterwards, a rapid, highly selective and sensitive method was established to simultaneously quantify the concentration of C1 and C3 in HUVECs after administration of IPTS. The results demonstrate that pretreatment with IPTS could promote the survival of HUVECs and reduce the damage caused by TNF-α to HUVECs. Among the main 11 components in IPTS, eight components could be absorbed by HUVECs, including seven triterpenoids and one phenolic acid. The uptake of C1 and C3 by HUVECs occurred in a time-, temperature- and concentration-dependent manner, indicating the participation of passive diffusion and active transportation mechanisms. The two triterpenoid saponins all exhibited rapid absorption and a bimodal phenomenon in their concentration-time profiles, and equilibrium could be achieved after 6 h. Furthermore, C1 and C3 intracellular transportation was regulated by serum proteins, sodium-dependent glucose transporter 1 and P-glycoprotein. The current research for the first time demonstrates the in vitro pharmacokinetics characteristics of C1 and C3 in HUVECs lines, which could supply a new way of understanding the treatment of cardiovascular diseases.

摘要

毛冬青是一种著名的中药材,在华南地区常用于治疗心血管疾病。在本研究中,我们旨在探讨毛冬青总三萜皂苷(IPTS)给药后,冬青素A(C1)和冬青皂苷B1(C3)在血管内皮细胞中的吸收特性,并阐明可能的转运机制。采用超高效液相色谱-四极杆飞行时间串联质谱(UPLC-qTOF-MS/MS)系统鉴定IPTS中可被人脐静脉内皮细胞(HUVECs)细胞内转运的成分。之后,建立了一种快速、高选择性和灵敏的方法,用于同时定量给药IPTS后HUVECs中C1和C3的浓度。结果表明,IPTS预处理可促进HUVECs的存活,并减少TNF-α对HUVECs造成的损伤。在IPTS的11种主要成分中,有8种成分可被HUVECs吸收,包括7种三萜类化合物和1种酚酸。HUVECs对C1和C3的摄取呈现时间、温度和浓度依赖性,表明被动扩散和主动转运机制均参与其中。这两种三萜皂苷在其浓度-时间曲线上均表现出快速吸收和双峰现象,6小时后可达到平衡。此外,C1和C3的细胞内转运受血清蛋白、钠依赖性葡萄糖转运蛋白1和P-糖蛋白的调节。目前这项研究首次证明了C1和C3在HUVECs细胞系中的体外药代动力学特征,这可为理解心血管疾病的治疗提供新的途径。

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