中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
In vitro assessment of the glucose-lowering effects of berberrubine-9-O-beta-D-glucuronide, an active metabolite of berberrubine

文献类型:期刊论文

作者Yang, Na1; Sun, Run-Bin1; Chen, Xing-Long2; Zhen, Le1; Ge, Chun1; Zhao, Yu-Qing1; He, Jun1; Geng, Jian-Liang1; Guo, Jia-Hua1; Yu, Xiao-Yi1
刊名ACTA PHARMACOLOGICA SINICA
出版日期2017-03-01
卷号38期号:3页码:351-361
关键词hyperglycemia glucose-lowering effect berberine berberrubine glucuronide alpha-glycosidase HFD-induced hyperglycemia model of C57BL/6 mice human normal liver cell line L-O2 pharmacokinetics
英文摘要Berberrubine (BRB) is the primary metabolite of berberine (BBR) that has shown a stronger glucose-lowering effect than BBR in vivo. On the other hand, BRB is quickly and extensively metabolized into berberrubine-9-O-beta-D-glucuronide (BRBG) in rats after oral administration. In this study we compared the pharmacokinetic properties of BRB and BRBG in rats, and explored the mechanisms underlying their glucose-lowering activities. C57BL/6 mice with HFD-induced hyperglycemia were administered BRB (50 mg . kg-1 . d-1, ig) for 6 weeks, which caused greater reduction in the plasma glucose levels than those caused by BBR (120 mg . kg(-1) . d(-1)) or BRB (25 mg . kg(-1) . d(-1)). In addition, BRB dose-dependently decreased the activity of alpha-glucosidase in gut of the mice. After oral administration of BRB in rats, the exposures of BRBG in plasma at 3 different dosages (10, 40, 80 mg/kg) and in urine at different time intervals (0-4, 4-10, 10-24 h) were dramatically greater than those of BRB. In order to determine the effectiveness of BRBG in reducing glucose levels, we prepared BRBG from the urine pool of rats, and identified and confirmed it through LC-MS-IT-TOF and NMR spectra. In human normal liver cell line L-O2 in vitro, treatment with BRB or BRBG (5, 20, 50 ae mol/L) increased glucose consumption, enhanced glycogenesis, stimulated the uptake of the glucose analog 2-NBDG, and modulated the mRNA levels of glucose-6-phosphatase and hexokinase. However, both BBR and BRB improved 2-NBDG uptake in insulin-resistant L-O2 cells, while BRBG has no effect. In conclusion, BRB exerts a stronger glucose-lowering effect than BBR in HFD-induced hyperglycemia mice. Although BRB significantly stimulated the insulin sensitivity and glycolysis in vitro, BRBG may have a greater contribution to the glucose-lowering effect because it has much greater system exposure than BRB after oral administration of BRB. The results suggest that BRBG is a potential agent for reducing glucose levels.
类目[WOS]Chemistry, Multidisciplinary ; Pharmacology & Pharmacy
研究领域[WOS]Chemistry ; Pharmacology & Pharmacy
关键词[WOS]INSULIN-RESISTANCE ; BERBERINE ; GLUCURONIDATION ; IDENTIFICATION ; OBESITY ; ACID ; ADIPOGENESIS ; ALKALOIDS ; PROTECTS ; MORPHINE
收录类别SCI
语种英语
WOS记录号WOS:000395792800006
源URL[http://ir.kib.ac.cn/handle/151853/51006]  
专题昆明植物研究所_植物化学与西部植物资源持续利用国家重点实验室
作者单位1.China Pharmaceut Univ, Key Lab Drug Metab & Pharmacokinet, Jiangsu Key Lab Drug Design & Optimizat, Nanjing 210009, Peoples R China
2.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Peoples R China
3.Jiangsu Prov Hosp Tradit Chinese Med, Clin Res Inst, Dept Pharmacol, Nanjing 210009, Peoples R China
4.Yantai Univ, Sch Pharm, Collaborat Innovat Ctr Adv Drug Delivery Syst & B, Yantai 264005, Peoples R China
推荐引用方式
GB/T 7714
Yang, Na,Sun, Run-Bin,Chen, Xing-Long,et al. In vitro assessment of the glucose-lowering effects of berberrubine-9-O-beta-D-glucuronide, an active metabolite of berberrubine[J]. ACTA PHARMACOLOGICA SINICA,2017,38(3):351-361.
APA Yang, Na.,Sun, Run-Bin.,Chen, Xing-Long.,Zhen, Le.,Ge, Chun.,...&Wang, Guang-Ji.(2017).In vitro assessment of the glucose-lowering effects of berberrubine-9-O-beta-D-glucuronide, an active metabolite of berberrubine.ACTA PHARMACOLOGICA SINICA,38(3),351-361.
MLA Yang, Na,et al."In vitro assessment of the glucose-lowering effects of berberrubine-9-O-beta-D-glucuronide, an active metabolite of berberrubine".ACTA PHARMACOLOGICA SINICA 38.3(2017):351-361.

入库方式: OAI收割

来源:昆明植物研究所

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