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肾上腺素和α-甲基肾上腺素二特戊酸酯的眼部效应。

Ocular effects of dipivalyl esters of epinephrine and alpha-methylepinephrine.

作者信息

Gherezghiher T, Koss M C

机构信息

Dean A. McGee Eye Institute, University of Oklahoma, Oklahoma City 73104.

出版信息

Exp Eye Res. 1990 Nov;51(5):537-43. doi: 10.1016/0014-4835(90)90084-8.

Abstract

The intraocular pressure (IOP) and pupillary effects of dipivalyl esters of epinephrine and alpha-methylepinephrine were compared after topical application in conscious rabbits. Both dipivalyl-alpha-methylepinephrine (DP alpha meE) and dipivalylepinephrine (DPE) produced a dose-dependent pupillary dilation (PD) and decrease in IOP. The onset of PD was approximately 30 min for both agents and reached maximal plateau within 1 and 2 hr for DPE and DP alpha meE, respectively. Duration of mydriatic effect was also dose-related, although more prolonged with DP alpha meE. This probably reflects differences in rate of inactivation of these compounds. The onset of IOP lowering effect of DP alpha meE was more rapid (35-45 min) when compared with DPE (1.5-2 hr) which may be due to the initial ocular hypertensive response seen with DPE. The initial rise in IOP was prevented by transection of three rectus muscles. DP alpha meE produced initial ocular hypertension only at the highest doses. The decrease of IOP lasted more than 6 hr for both drugs, returning to normal by 24 hr. No pupillary or IOP effects were seen in the contralateral eye. Denervation supersensitivity to both the pupillary and IOP responses to DP alpha meE was seen after superior cervical ganglionectomy. These findings are consistent with the hypothesis that the pupillary and IOP responses to DP alpha meE do not require intact adrenergic innervation to the eye, and that these effects are mediated by activation of postjunctional alpha-adrenoceptors. It is concluded that DP alpha meE is a potent adrenergic ocular hypotensive agent.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在清醒兔局部应用后,比较了肾上腺素和α-甲基肾上腺素二特戊酸酯的眼内压(IOP)和瞳孔效应。二特戊酰-α-甲基肾上腺素(DPαmeE)和二特戊酰肾上腺素(DPE)均产生剂量依赖性瞳孔散大(PD)和IOP降低。两种药物的PD起效时间约为30分钟,DPE和DPαmeE分别在1小时和2小时内达到最大平台期。散瞳效应的持续时间也与剂量相关,尽管DPαmeE的持续时间更长。这可能反映了这些化合物失活速率的差异。与DPE(1.5 - 2小时)相比,DPαmeE的IOP降低效应起效更快(35 - 45分钟),这可能是由于DPE出现的初始眼内压升高反应。横断三条直肌可防止IOP的初始升高。DPαmeE仅在最高剂量时产生初始眼内压升高。两种药物的IOP降低持续超过6小时,24小时后恢复正常。对侧眼未观察到瞳孔或IOP效应。颈上神经节切除术后,对DPαmeE的瞳孔和IOP反应出现去神经超敏反应。这些发现与以下假设一致,即对DPαmeE的瞳孔和IOP反应不需要完整的眼肾上腺素能神经支配,并且这些效应是由节后α-肾上腺素能受体的激活介导的。结论是DPαmeE是一种有效的肾上腺素能性降眼压药物。(摘要截断于250字)

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