Wang Kuilong, Liu Lian, Huang Jianyu, Yu Hongli, Wu Hao, Duan Yu, Cui Xiaobing, Zhang Xingde, Liu Liping, Wang Wei
School of pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
Jiangsu Key Laboratory of Chinese Medicine Processing, Nanjing University of Chinese Medicine, Nanjing 210023, China.
Molecules. 2017 Mar 14;22(3):465. doi: 10.3390/molecules22030465.
This study was designed to evaluate the toxic effects of total diterpenoids extracted from the roots of Euphorbia pekinensis (TDEP) on the mouse colon and to clarify the mechanism. Dried powdered roots of E. pekinensis were extracted with chloroform, and then the extract (6.7 g) was subjected to column chromatography and preparative TLC, giving TDEP. Using the HPLC-DAD method, the purity of TDEP was determined as 85.26%. Mice were orally administered with TDEP (3.942, 19.71 and 39.42 mg/kg), after which fecal water content and colon water content were examined. Both of them increased over time after TDEP administration, accompanied by severe diarrhea. Three hours after TDEP administration, the animals were sacrificed to obtain their colons. The mRNA and protein expression levels of aquaporin 1 (AQP1), AQP3 and AQP4 in the colon were measured using real-time RT-PCR and Western blotting, respectively. TDEP significantly increased the levels of AQP3 and AQP4, but decreased that of AQP1 in dose-dependent manners. Similarly, Pekinenin C, a casbane diterpenoid, significantly increased AQP3 protein and mRNA expressions in human intestinal epithelial cells (HT-29). Histopathological examination revealed that the colon was not significantly damaged. The laxative effects of E. pekinensis were associated with the alterations of AQPs in the colon by TDEP.
本研究旨在评估大戟根中提取的总二萜类化合物(TDEP)对小鼠结肠的毒性作用并阐明其机制。将大戟干燥的根粉用氯仿提取,然后将提取物(6.7 g)进行柱色谱和制备型薄层色谱,得到TDEP。采用高效液相色谱-二极管阵列检测法(HPLC-DAD)测定TDEP的纯度为85.26%。给小鼠口服TDEP(3.942、19.71和39.42 mg/kg),之后检测粪便含水量和结肠含水量。给予TDEP后,两者均随时间增加,同时伴有严重腹泻。给予TDEP 3小时后,处死动物获取其结肠。分别采用实时逆转录聚合酶链反应(real-time RT-PCR)和蛋白质免疫印迹法检测结肠中aquaporin 1(AQP1)、AQP3和AQP4的mRNA和蛋白表达水平。TDEP以剂量依赖的方式显著增加AQP3和AQP4的水平,但降低AQP1的水平。同样,一种蓖麻二萜类化合物pekinenin C显著增加人肠上皮细胞(HT-29)中AQP3蛋白和mRNA的表达。组织病理学检查显示结肠未受到明显损伤。大戟的泻下作用与TDEP引起的结肠中水通道蛋白(AQPs)的改变有关。