Chu T C, Ogidigben M J, Potter D E
Department of Pharmacology and Toxicology, Morehouse School of Medicine, Atlanta, Ga 30310-1495, USA.
Pharmacology. 1996 Oct;53(4):259-70. doi: 10.1159/000139438.
Oxymetazoline, an alpha 2 agonist, was active in lowering intraocular pressure in normal and sympathetically denervated rabbit eyes. Ocular hypotension was accompanied by decreased aqueous humor inflow. Topical pretreatment with rauwolscine, an alpha 2 antagonist, reduced the oxymetazoline-induced hypotensive effect more in contralateral than in ipsilateral eyes indicating the possible involvement of central alpha 2 adrenoceptors. Efaroxan, a relatively selective imidazoline antagonist, and diclofenac, a cyclooxygenase inhibitor, failed to inhibit the oxymetazoline-induced ocular hypotensive response. Oxymetazoline induced mydriasis in treated eyes at all doses. In in vitro studies, oxymetazoline inhibited isoproterenol-stimulated cAMP production in rabbit iris-ciliary bodies and cultured rabbit nonpigmented ciliary epithelial cells. The inhibition of cAMP accumulation induced by oxymetazoline was antagonized by rauwolscine or by BRL-44408, a relatively selective alpha 2A-adrenoceptor antagonist. These data indicate that oxymetazoline lowered intraocular pressure by activating alpha 2A receptors (ciliary epithelium) and that the ocular hypotensive effect was not totally dependent on intact sympathetic nerves. Results suggest that mechanisms involving centrally mediated effects of oxymetazoline are probable and this possibility is currently under investigation.
羟甲唑啉是一种α2激动剂,能降低正常兔眼和交感神经去支配兔眼的眼压。眼压降低伴随着房水流入减少。用α2拮抗剂萝芙辛进行局部预处理,对侧眼比同侧眼更能降低羟甲唑啉诱导的降压作用,这表明中枢α2肾上腺素能受体可能参与其中。相对选择性的咪唑啉拮抗剂依酚氯铵和环氧化酶抑制剂双氯芬酸未能抑制羟甲唑啉诱导的眼压降低反应。所有剂量的羟甲唑啉均可使用药眼瞳孔散大。在体外研究中,羟甲唑啉抑制异丙肾上腺素刺激的兔虹膜睫状体和培养的兔非色素睫状上皮细胞中cAMP的产生。羟甲唑啉诱导的cAMP积累抑制作用可被萝芙辛或相对选择性的α2A肾上腺素能受体拮抗剂BRL-44408拮抗。这些数据表明,羟甲唑啉通过激活α2A受体(睫状体上皮)降低眼压,且眼压降低作用并不完全依赖于完整的交感神经。结果提示,羟甲唑啉涉及中枢介导作用的机制是可能的,目前正在对此可能性进行研究。