Everitt D E, Boike S C, Piltz-Seymour J R, VanCoevorden R, Audet P, Zariffa N, Jorkasky D
SmithKline Beecham Clinical Research Unit, Presbyterian Medical Center, Philadelphia, PA 19104, USA.
J Clin Pharmacol. 1997 Apr;37(4):312-20. doi: 10.1002/j.1552-4604.1997.tb04308.x.
Intravenous fenoldopam, a selective dopamine-1 receptor agonist, was compared with placebo in this randomized, double-blind, two-period crossover study to evaluate its effects on intraocular pressure, aqueous dynamics, and macular blood flow in patients with elevated intraocular pressure or primary open-angle glaucoma. Doses of fenoldopam were titrated up to a maximum of 0.5 microgram/kg/min. Intraocular pressure, measured by pneumotonometry, was the primary outcome variable. Other outcomes included macular blood flow assessed by blue field examination, visual field examined by automated perimetry, aqueous outflow facility measured by tonography, and aqueous humor production determined by fluorophotometry. During infusions of fenoldopam, intraocular pressure increased from a mean baseline level of 29.2 mmHg to a mean maximum level of 35.7 mmHg. During the placebo infusions, pressure increased from a mean baseline of 28.4 mmHg to a mean of 29.0 mmHg at the time point that corresponded to the mean maximum intraocular pressure on the day intravenous fenoldopam was administered, to yield a mean difference in pressure between study days of 6.7 mmHg (P < 0.05). There were no apparent changes in macular blood flow, visual fields, or production or outflow of aqueous humor associated with fenoldopam infusion. The increase in intraocular pressure seen in this population of patients with ocular hypertension during infusions of fenoldopam is consistent with fenoldopam-associated increases in intraocular pressure reported in previous studies of healthy volunteers and of patients with accelerated systemic hypertension. These results further suggest that dopamine-1 receptors play a role in the regulation of intraocular pressure.
在这项随机、双盲、两阶段交叉研究中,将静脉注射非诺多泮(一种选择性多巴胺 -1 受体激动剂)与安慰剂进行比较,以评估其对眼压升高或原发性开角型青光眼患者的眼压、房水动力学和黄斑血流的影响。非诺多泮的剂量滴定至最大 0.5 微克/千克/分钟。通过眼压计测量的眼压是主要结局变量。其他结局包括通过蓝域检查评估的黄斑血流、通过自动视野计检查的视野、通过眼压描记法测量的房水流出率以及通过荧光光度法测定的房水生成量。在输注非诺多泮期间,眼压从平均基线水平 29.2 mmHg 升高至平均最高水平 35.7 mmHg。在输注安慰剂期间,在与静脉注射非诺多泮当天的平均最高眼压相对应的时间点,眼压从平均基线 28.4 mmHg 升高至平均 29.0 mmHg,研究日之间的平均压差为 6.7 mmHg(P < 0.05)。与非诺多泮输注相关的黄斑血流、视野或房水生成或流出均无明显变化。在这群高眼压患者中,输注非诺多泮期间眼压升高与先前健康志愿者和加速性系统性高血压患者研究中报道的非诺多泮相关眼压升高一致。这些结果进一步表明多巴胺 -1 受体在眼压调节中起作用。