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青光眼治疗中的眼部β受体阻滞剂。临床药理学方面。

Ocular beta-blockers in glaucoma management. Clinical pharmacological aspects.

作者信息

Brooks A M, Gillies W E

机构信息

Glaucoma Investigation and Research Unit, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.

出版信息

Drugs Aging. 1992 May-Jun;2(3):208-21. doi: 10.2165/00002512-199202030-00005.

Abstract

Topical beta-blockers reduce the intraocular pressure (IOP) by blockade of sympathetic nerve endings in the ciliary epithelium causing a fall in aqueous humour production. Two types of topical beta-blockers are available for use in glaucoma: nonselective, which block both beta 1- and beta 2-adrenoceptors; and cardioselective, which block only beta 1-receptors. Of the beta-Blockers commercially available, timolol, levobunolol, metipranolol and carteolol are nonselective, and betaxolol is cardioselective. Twice-daily timolol is probably the most effective agent in lowering IOP, although levobunolol is equally effective and can be used once daily with little difference in effect. Carteolol is used twice daily and any theoretical advantage in diminished side effects conferred by its partial beta-agonist activity compared with timolol has not been fully substantiated. Metipranolol is effective twice daily and does not have partial beta-agonist activity. Betaxolol has an effect comparable to timolol in lowering IOP, but is less effective in some patients. beta-Blockers can be used with other antiglaucoma medications, but their combined action with epinephrine (adrenaline) is suspect, particularly in the case of the nonselective beta-blockers, and the effect should be assessed in patients on an individual basis. Local stinging can be a problem in some patients with betaxolol. The most serious side effects of beta-blockers are the exacerbation of chronic obstructive airways disease with nonselective agents and the precipitation of bronchospasm in some patients. Betaxolol seems relatively free of adverse respiratory effects, although this may be dose-related and extreme caution should still be exercised in patients with any history of respiratory illness. Because of the lower risk of precipitating side effects, betaxolol is probably the beta-blocker of first choice for use in glaucoma; timolol or levobunolol are reserved for patients who do not respond satisfactorily to betaxolol and are quite free of respiratory disease.

摘要

局部用β受体阻滞剂通过阻断睫状体上皮中的交感神经末梢来降低眼压(IOP),从而使房水生成减少。有两种类型的局部用β受体阻滞剂可用于青光眼治疗:非选择性的,可阻断β1和β2肾上腺素能受体;以及心脏选择性的,仅阻断β1受体。在市售的β受体阻滞剂中,噻吗洛尔、左布诺洛尔、美替洛尔和卡替洛尔是非选择性的,而倍他洛尔是心脏选择性的。每日两次使用噻吗洛尔可能是降低眼压最有效的药物,尽管左布诺洛尔同样有效且可每日使用一次,效果差异不大。卡替洛尔每日使用两次,与噻吗洛尔相比,其部分β激动剂活性在减少副作用方面的任何理论优势尚未得到充分证实。美替洛尔每日使用两次有效,且不具有部分β激动剂活性。倍他洛尔在降低眼压方面的效果与噻吗洛尔相当,但在某些患者中效果较差。β受体阻滞剂可与其他抗青光眼药物联合使用,但其与肾上腺素的联合作用存在疑问,尤其是非选择性β受体阻滞剂的情况,应根据个体情况对患者进行评估。局部刺痛在一些使用倍他洛尔的患者中可能是个问题。β受体阻滞剂最严重的副作用是使用非选择性药物会加重慢性阻塞性气道疾病,以及在某些患者中诱发支气管痉挛。倍他洛尔似乎相对没有不良呼吸影响,尽管这可能与剂量有关,对于有任何呼吸道疾病史的患者仍应极其谨慎使用。由于引发副作用的风险较低,倍他洛尔可能是青光眼治疗中首选的β受体阻滞剂;噻吗洛尔或左布诺洛尔则留给对倍他洛尔反应不佳且无呼吸道疾病的患者。

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