Xin Zhang, Li-Fang Wang, Jia-Qi Chen, Bo-Lin Zou, Xiu-Hong Chen, Jun L I, Peng-Fei T U, Jin-Ling Wang
Modern Research Center for Traditional Chinese Medicine, School of Chinese Materia Medica,Beijing University of Chinese Medicine Beijing 100029, China.
Zhongguo Zhong Yao Za Zhi. 2020 Oct;45(20):4889-4895. doi: 10.19540/j.cnki.cjcmm.20200914.301.
The purpose of this study was to study the absorption characteristics of eight main components from dragon's blood phenolic extracts in Caco-2 cells based on the humancolon cancer cell Caco-2 model, and to clarify the oral absorption mechanism of such phenolic extracts. UPLC-MS/MS was used in this study to determine the content of 8 active ingredients including thevetiaflavone, 7,4'-dihydroxyflavone, 7,4'-dihydroxy-5-methoxyhomoisoflavanone, 7,4'-dihydroxyhomoisoflavanone, loureirin C, loureirin A, loureirin B and pterostilbene from dragon's blood phenolic extracts, and Caco-2 cells were used to investigate the effects of incubation time, concentration, temperature, P-gp inhibitor, MRP inhibitor, OCTN1 inhibitor and OCTN2 inhibitor on the absorption of each component. In addition, the transport experiment was conducted to measure the apparent permeability coefficient P_(app) and transport rate of the eight main components to predict the oral absorption mechanism of dragon's blood phenolic extracts. The experimental results showed that the cell uptake of the eight main components in dragon's blood phenolic extracts was time-dependent and concentration dependent, and the uptake of each component did not need to consume energy, which was consistent with the passive diffusion process. P-gp inhibitor, MRP inhibitor and OCTN1 inhibitor had no effect on the cell uptake of each component, only the addition of OCTN2 inhibitor significantly reduced the uptake of pterostilbene(P<0.05). In the transport results, the ER values of the outflow rates of the eight components were all less than 1.5. The above results show that the absorption mechanism of the eight components in Draconis resina phenolic extract may be passive diffusion, and pterostilbene may be the substrate of OCTN2.
本研究旨在基于人结肠癌细胞Caco-2模型,研究血竭酚提取物中8种主要成分在Caco-2细胞中的吸收特性,阐明此类酚提取物的口服吸收机制。本研究采用超高效液相色谱-串联质谱法(UPLC-MS/MS)测定血竭酚提取物中8种活性成分的含量,包括黄夹次苷黄酮、7,4'-二羟基黄酮、7,4'-二羟基-5-甲氧基高异黄酮、7,4'-二羟基高异黄酮、龙血素C、龙血素A、龙血素B和紫檀芪,并利用Caco-2细胞研究孵育时间、浓度、温度、P-糖蛋白抑制剂、多药耐药相关蛋白抑制剂、有机阳离子转运体1抑制剂和有机阳离子转运体2抑制剂对各成分吸收的影响。此外,进行转运实验以测定8种主要成分的表观渗透系数P_(app)和转运速率,预测血竭酚提取物的口服吸收机制。实验结果表明,血竭酚提取物中8种主要成分的细胞摄取具有时间依赖性和浓度依赖性,各成分的摄取不需要消耗能量,这与被动扩散过程一致。P-糖蛋白抑制剂、多药耐药相关蛋白抑制剂和有机阳离子转运体1抑制剂对各成分的细胞摄取无影响,仅添加有机阳离子转运体2抑制剂显著降低了紫檀芪的摄取(P<0.05)。在转运结果中,8种成分流出率的ER值均小于1.5。上述结果表明,血竭树脂酚提取物中8种成分的吸收机制可能为被动扩散,紫檀芪可能是有机阳离子转运体2的底物。