Bachmann K A, Sullivan T J, Jauregui L, Reese J, Miller K, Levine L
Center for Applied Pharmacology, University of Toledo College of Pharmacy, St Vincent Medical Center, Ohio 43606.
Scand J Gastroenterol Suppl. 1994;206:14-9. doi: 10.3109/00365529409091415.
Three drug interactions of nizatidine and of other antisecretory agents were studied comparatively. First, the effects of nizatidine, cimetidine and ranitidine on the dispositional kinetics of theophylline were evaluated in chronic obstructive pulmonary disease (COPD) patients. Second, the effect of magnesium/aluminium hydroxide on the relative bioavailability of nizatidine, famotidine, cimetidine and ranitidine was evaluated in healthy volunteers. Finally, the effects of nizatidine and omeprazole on the dispositional kinetics of phenytoin were evaluated in healthy volunteers. Only cimetidine altered the steady-state kinetics of oral theophylline, slowing theophylline clearance by 25%. Each of the H2-receptor antagonists exhibited a modest decline in relative bioavailability when ingested with antacid. Antacid ingestion decreased the bioavailability of famotidine, ranitidine and cimetidine by 20-25%, and the bioavailability of nizatidine by 12%. Each of these effects was statistically significant. Finally, it was found that neither omeprazole nor nizatidine affected the single dose kinetics of phenytoin.
对尼扎替丁与其他抗分泌剂的三种药物相互作用进行了比较研究。首先,在慢性阻塞性肺疾病(COPD)患者中评估了尼扎替丁、西咪替丁和雷尼替丁对茶碱处置动力学的影响。其次,在健康志愿者中评估了氢氧化镁/氢氧化铝对尼扎替丁、法莫替丁、西咪替丁和雷尼替丁相对生物利用度的影响。最后,在健康志愿者中评估了尼扎替丁和奥美拉唑对苯妥英处置动力学的影响。只有西咪替丁改变了口服茶碱的稳态动力学,使茶碱清除率减慢了25%。当与抗酸剂一起服用时,每种H2受体拮抗剂的相对生物利用度都有适度下降。服用抗酸剂使法莫替丁、雷尼替丁和西咪替丁的生物利用度降低了20% - 25%,尼扎替丁的生物利用度降低了12%。这些影响均具有统计学意义。最后,发现奥美拉唑和尼扎替丁均未影响苯妥英的单剂量动力学。