Yang Jing-Ming, Jiang Hua, Dai Hong-Liang, Wang Zi-Wei, Jia Gui-Zhi, Meng Xiang-Cai
College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin, China; College of Pharmacy, Jinzhou Medical University, Jinzhou, China.
School of Nursing, Jinzhou Medical University, Jinzhou, China.
Pharmacogn Mag. 2017 Jan-Mar;13(49):168-174. doi: 10.4103/0973-1296.197637.
4'-O-β-D-glucosyl-5-O-methylvisamminol (GML) is a conventional marker compound for quality control of Radix Saposhnikoviae. Despite that, neither pharmacodynamic or pharmacokinetic information is available with regard to GML. As such, the aim of thisstudy was to assess the conventional evaluation indices for the quality of Radix Saposhnikoviae.
Pyretic animal model, hot plate test, and ear edema model were established to evaluate and compare the antipyretic, analgesic, and anti-inflammatory effect of the chromone derivativescimifugin, prime-O-glucosylcimifugin (PGCN), and GML in Radix Saposhnikoviae. High performance liquid chromatography separation and analysis was used to obtain pharmacokinetic parameters. Simulated gastric fluid and simulated intestinal fluid was used to investigate the metabolite profiles of PGCN and GML in gastrointestinal tract.
Cimifugin exerted a marked dose-dependent antipyretic, analgesic, and anti-inflammatory effect, whereas the effects of PGCN were relatively lower. GML had feeble pharmacodynamic effects. Pharmacokinetic study showed that only cimifugin was detected in the plasma sample of cimifugin and PGCN-treated animals, with drug concentration in the former much higher than the latter. No components were traced in the plasma samples from GML-treated rats. Stability study showed that PGCN and GML was predominantly biotransformed into cimifugin and 5-O-methyvisammiol, respectively. The latter was proven to be extremely unstable in liver tissue homogenate and plasma.
A feeble antipyretic, analgesic, and anti-inflammatory activities was observed when GML was orally delivered. Given that Radix Saposhnikoviae extract is generally administered orally, we speculate that this compound might be a nonpharmacolagically active agent in real usage. Thus, it might be unscientific to evaluate the quality of Radix Saposhnikoviae based on the content of GML.
GML-derived cimifugin, which represents the potential pharma codynamic component of Radix Saposhnikoviae chromones, in plasma was almost nil in contrast to cimifugin and PGCN. And thus, feeble antipyretic, analgesic, and anti-inflammatory activities were found with GML. AUC:area under concentration-time curve, DNP:2,4-Dinitrophenol, HPLC:high performance liquid chromatography, HPLC-MS:high performance liquid chromatography- mass spectrography, GML:4'-O-β-D-glucosyl-5-O-methylvisamminol, MVL:5-O-methyvisammiol, PGCN:prime-O-glucosylcimifugin, SGF:alkaline phosphatase. SIF:simulated intestinal fluid.
4'-O-β-D-葡萄糖基-5-O-甲基维斯阿米醇(GML)是防风质量控制的传统标志性化合物。尽管如此,关于GML的药效学或药代动力学信息均未可知。因此,本研究的目的是评估防风质量的传统评价指标。
建立发热动物模型、热板试验和耳部水肿模型,以评价和比较防风中色酮衍生物升麻素、升麻素苷(PGCN)和GML的解热、镇痛和抗炎作用。采用高效液相色谱分离分析获得药代动力学参数。用模拟胃液和模拟肠液研究PGCN和GML在胃肠道中的代谢产物谱。
升麻素具有显著的剂量依赖性解热、镇痛和抗炎作用,而PGCN的作用相对较弱。GML的药效作用微弱。药代动力学研究表明,在升麻素和PGCN处理动物的血浆样品中仅检测到升麻素,前者的药物浓度远高于后者。在GML处理大鼠的血浆样品中未检测到任何成分。稳定性研究表明,PGCN和GML分别主要生物转化为升麻素和5-O-甲基维斯阿米醇。后者在肝组织匀浆和血浆中极不稳定。
口服GML时观察到微弱的解热、镇痛和抗炎活性。鉴于防风提取物通常口服给药,我们推测该化合物在实际应用中可能是一种无药理活性的物质。因此,基于GML的含量来评价防风的质量可能是不科学的。
与升麻素和PGCN相比,血浆中由GML衍生的升麻素几乎为零,而升麻素是防风色酮潜在的药效学成分。因此,GML的解热、镇痛和抗炎活性较弱。AUC:浓度-时间曲线下面积,DNP:2,4-二硝基苯酚,HPLC:高效液相色谱,HPLC-MS:高效液相色谱-质谱,GML:4'-O-β-D-葡萄糖基-5-O-甲基维斯阿米醇,MVL:5-O-甲基维斯阿米醇,PGCN:升麻素苷,SGF:碱性磷酸酶,SIF:模拟肠液