Coleman A L, Robin A L, Pollack I P, Rudikoff M T, Enger C, Mayer P R
Glaucoma Service, Wilmer Ophthalmological Institute, Johns Hopkins University School of Medicine, Baltimore, Md.
Arch Ophthalmol. 1990 Sep;108(9):1264-7. doi: 10.1001/archopht.1990.01070110080029.
We performed a double-masked, crossover study comparing the cardiovascular and intraocular pressure effects of 0.5% and 0.25% topical apraclonidine hydrochloride and 0.5% timolol maleate in 20 healthy female volunteers. The contralateral effects of unilateral apraclonidine and the plasma concentrations of apraclonidine were also assessed. All measurements were done 2, 5, and 8 hours after drop instillation. A 15-minute treadmill test was performed after the 2-hour measurements. All three active medications lowered intraocular pressure comparably. There was no significant contralateral intraocular pressure effect seen with apraclonidine. The apraclonidine plasma concentrations were variable and unrelated to the amount of intraocular pressure lowering and cardiovascular parameters measured. Apraclonidine did not affect blood pressure or heart rate any differently than placebo. Timolol, however, blunted exercise-induced tachycardia. There were no significant differences in pupillary diameters or interpalpebral fissure widths among treatment groups.
我们对20名健康女性志愿者进行了一项双盲交叉研究,比较0.5%和0.25%的局部用盐酸阿可乐定以及0.5%的马来酸噻吗洛尔对心血管和眼压的影响。还评估了单侧阿可乐定的对侧效应以及阿可乐定的血浆浓度。所有测量均在滴眼后2小时、5小时和8小时进行。在2小时测量后进行了15分钟的跑步机测试。所有三种活性药物降低眼压的效果相当。阿可乐定未观察到明显的对侧眼压效应。阿可乐定的血浆浓度各不相同,且与所测量的眼压降低量和心血管参数无关。阿可乐定对血压或心率的影响与安慰剂无异。然而,噻吗洛尔抑制了运动诱发的心动过速。各治疗组之间瞳孔直径和睑裂宽度无显著差异。