Taniguchi T, Kitazawa Y
Department of Ophthalmology, Gifu University School of Medicine, Japan.
Curr Opin Ophthalmol. 1997 Apr;8(2):55-8. doi: 10.1097/00055735-199704000-00010.
Although topical beta-blockers are generally tolerated, they can produce significant systemic side effects. The systemic side effects of nonselective beta-blockers (eg, timolol, carteolol) are primarily related to the cardiovascular (beta 1-adrenergic) and respiratory (beta 2-adrenergic) systems. Carteolol has intrinsic sympathomimetic activity, which theoretically reduces the risk of adverse effects through beta blockade. It has been reported that topical timolol and carteolol unfavorably alter the lipid profile and that the effects of carteolol are less pronounced than those of timolol. Topical beta-blockers are associated with systemic events, not only acting by themselves, but also interacting with other drugs (eg, quinidine) administered orally or intravenously. To reduce systemic absorption and adverse effects, new preparations of beta-blockers, such as timolol gellan, have been developed. We should always bear in mind the potential systemic effects of topically applied beta-blockers in glaucoma therapy.
虽然局部用β受体阻滞剂一般耐受性良好,但它们可产生显著的全身副作用。非选择性β受体阻滞剂(如噻吗洛尔、卡替洛尔)的全身副作用主要与心血管系统(β1肾上腺素能)和呼吸系统(β2肾上腺素能)有关。卡替洛尔具有内在拟交感活性,理论上可通过β受体阻滞降低不良反应风险。据报道,局部用噻吗洛尔和卡替洛尔会不利地改变血脂谱,且卡替洛尔的作用不如噻吗洛尔明显。局部用β受体阻滞剂与全身事件有关,不仅自身起作用,还会与口服或静脉给予的其他药物(如奎尼丁)相互作用。为减少全身吸收和不良反应,已开发出β受体阻滞剂的新制剂,如吉兰糖醛酸噻吗洛尔。在青光眼治疗中,我们应始终牢记局部应用β受体阻滞剂的潜在全身效应。