Nielsen-Kudsk J E, Buhl J S, Johannessen A C
Department of Internal Medicine, Silkeborg General Hospital.
Pharmacol Toxicol. 1990 Feb;66(2):101-3. doi: 10.1111/j.1600-0773.1990.tb00713.x.
The interaction between theophylline and verapamil was investigated in 7 healthy volunteers. Oral administration of verapamil in a dose of 120 mg t.i.d. for 7 days caused a significant inhibition of the elimination of theophylline (5 mg/kg intravenously). Theophylline clearance was reduced from 45.2 to 36.1 ml/hr/kg (20.1%; P less than 0.005). The apparent steady-state volume of distribution of the drug was not influenced. The terminal half-life of theophylline was increased from 6.80 to 8.23 hr (21.0%; P less than 0.001). Increased steady-state plasma theophylline concentrations may thus be expected when verapamil is added to a drug regimen which includes theophylline.
在7名健康志愿者身上研究了茶碱与维拉帕米之间的相互作用。以每日3次、每次120毫克的剂量口服维拉帕米,持续7天,可导致对静脉注射5毫克/千克茶碱消除的显著抑制。茶碱清除率从45.2毫升/小时/千克降至36.1毫升/小时/千克(20.1%;P<0.005)。该药物的表观稳态分布容积未受影响。茶碱的终末半衰期从6.80小时增加到8.23小时(21.0%;P<0.001)。因此,当在包含茶碱的药物治疗方案中添加维拉帕米时,预计稳态血浆茶碱浓度会升高。