Tang Qian, Zhang Mei, Hong Zexuan, Chen Yao, Wang Pan, Wang Jian, Wang Zili, Fang Rendong, Jin Meilan
Laboratory of Veterinary Pathology, Department of Veterinary Medicine, College of Animal Science and Technology, Southwest University, 1-13-4 Hongyuhuayuan, No. 196 Beinan Road, BeiBei District, Chongqing 400700, P.R. China.
J Toxicol Pathol. 2019 Jul;32(3):155-164. doi: 10.1293/tox.2019-0006. Epub 2019 Apr 15.
To clarify the suppressive effects of astragalus injection (AI) on different stages of early hepatocarcinogenesis induced by weak promotion, SD rats initiated with a single intraperitoneal (i.p.) injection of -diethylnitrosamine (DEN) at 200 mg/kg body weight and promoted with 0.5% piperonyl butoxide (PBO) in diet were repeatedly administered AI at 5 ml/kg body weight/day in the early postinitiation (EPI) or late postinitiation (LPI) period for 2 or 8 weeks, respectively. The number and area of glutathione -transferase placental form (GST-P)-immunoreactive foci tended to increase in the DEN+PBO group compared with the DEN-alone group. Among the PBO-promoted groups, number and area of GST-P foci did not visibly change in the DEN+PBO+AI-EPI group compared with the DEN+PBO group. In contrast, number and area of GST-P foci tended to decrease in the DEN+PBO+AI-LPI group compared with the DEN+PBO group. Number of Ki67 cells was increased in the DEN+PBO group compared with the DEN-alone group and was decreased in both AI-administered groups compared with the DEN+PBO group. Gene expression analysis revealed that the DEN+PBO+AI-LPI group showed increased transcript levels of , , , , , and compared with the DEN+PBO group; however, the DEN+PBO+AI-EPI group did not show changes in the transcript levels of any genes examined compared with the DEN+PBO. These results suggest that AI administration during the LPI period caused weak suppression of hepatocarcinogenesis under weak promotion with a low PBO dose by the mechanism involving facilitation of cell cycle suppression causing G1/S arrest and apoptosis via the mitochondrial pathway. In addition, the results suggest that AI administration during the EPI period has no effect on weakly promoted hepatocarcinogenesis.
为阐明黄芪注射液(AI)对弱促癌诱导的早期肝癌发生不同阶段的抑制作用,将体重200 mg/kg的SD大鼠单次腹腔注射二乙基亚硝胺(DEN)启动肝癌发生,并用含0.5%胡椒基丁醚(PBO)的饲料进行促癌,在启动后早期(EPI)或启动后晚期(LPI)分别以5 ml/kg体重/天的剂量重复给予AI 2周或8周。与单独给予DEN的组相比,DEN+PBO组中谷胱甘肽-S-转移酶胎盘型(GST-P)免疫反应灶的数量和面积有增加趋势。在PBO促癌组中,与DEN+PBO组相比,DEN+PBO+AI-EPI组中GST-P灶的数量和面积无明显变化。相反,与DEN+PBO组相比,DEN+PBO+AI-LPI组中GST-P灶的数量和面积有减少趋势。与单独给予DEN的组相比,DEN+PBO组中Ki67细胞数量增加,与DEN+PBO组相比,两个给予AI的组中Ki67细胞数量均减少。基因表达分析显示,与DEN+PBO组相比,DEN+PBO+AI-LPI组中、、、、、和的转录水平升高;然而,与DEN+PBO组相比,DEN+PBO+AI-EPI组中所检测的任何基因的转录水平均无变化。这些结果表明,在LPI期给予AI通过涉及促进细胞周期抑制导致G1/S期阻滞和通过线粒体途径诱导凋亡的机制,对低剂量PBO弱促癌条件下的肝癌发生有微弱抑制作用。此外,结果表明在EPI期给予AI对弱促癌的肝癌发生无影响。