Lau D T, Gumbleton M, Labisch C, Benet L Z
Department of Pharmacy, School of Pharmacy, University of California, San Francisco 94143-0446.
Biopharm Drug Dispos. 1991 Apr;12(3):215-22. doi: 10.1002/bdd.2510120306.
1,2- and 1,3-glyceryl dinitrates (1,2-GDN and 1,3-GDN) are the primary metabolites of glyceryl trinitrate, a commonly used anti-anginal agent. The goal of this study was to examine the pharmacokinetic properties of these metabolites in rats. Sprague-Dawley rats were infused intravenously with 0.25 or 2.0 micrograms min-1 of either 1,2- or 1,3-GDN for 70 min, during which steady state blood concentrations were achieved. Post-infusion blood samples were collected for 30 min. 1,2-GDN was found to possess slightly higher clearance (32.3 vs 20.8 ml min-1 kg-1) and volume of distribution (695 vs 454 ml kg-1) than 1,3-GDN; however, the two metabolites exhibited similar mean residence times (22.0 vs 21.8 min). Upon an 8-fold increase in the infusion rate, the pharmacokinetic parameters were not significantly altered for either 1,2- or 1,3-GDN. When each GDN was co-infused with an 8-fold higher dose of the other GDN, there were also no significant changes in the parameters.
1,2-二硝酸甘油酯和1,3-二硝酸甘油酯(1,2-GDN和1,3-GDN)是常用抗心绞痛药物硝酸甘油的主要代谢产物。本研究的目的是检测这些代谢产物在大鼠体内的药代动力学特性。将Sprague-Dawley大鼠静脉输注0.25或2.0微克/分钟的1,2-GDN或1,3-GDN,持续70分钟,在此期间达到稳态血药浓度。输注后采集血样30分钟。结果发现,1,2-GDN的清除率(32.3对20.8毫升/分钟·千克-1)和分布容积(695对454毫升/千克-1)略高于1,3-GDN;然而,这两种代谢产物的平均驻留时间相似(22.0对21.8分钟)。当输注速率增加8倍时,1,2-GDN和1,3-GDN的药代动力学参数均未发生显著改变。当每种GDN与另一种GDN以高8倍的剂量共同输注时,参数也没有显著变化。