首页> 外文期刊>Journal of ocular pharmacology and therapeutics: The official journal of the Association for Ocular Pharmacology and Therapeutics >Comparison of effects of topical ibopamine and epinephrine on the circadian rhythm of intraocular pressure of the rabbit eye as measured by telemetry.
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Comparison of effects of topical ibopamine and epinephrine on the circadian rhythm of intraocular pressure of the rabbit eye as measured by telemetry.

机译:遥测法测定局部用伊巴明和肾上腺素对兔眼眼压昼夜节律影响的比较。

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The purpose of this study was to measure the effect of topical ibopamine and epinephrine on intraocular pressure in undisturbed rabbits. Six pigmented rabbits were outfitted with a telemetric transducer system connected via catheter to the vitreous cavity of one eye for continuous monitoring of intraocular pressure. After entrainment to a 12 hour light, 12 hour dark cycle and after stabilization of the circadian rhythm of intraocular pressure, the animals were tested with 2% ibopamine and 2% epinephrine. Each drug was instilled during the light phase and during the dark phase of the circadian cycle. When administered during the light phase, both drugs caused a transient pressure rise followed by prolonged hypotension. When administered during the dark phase, neither drug caused a pressure rise but both drugs caused prolonged hypotension. It was concluded that ibopamine and epinephrine cause identical intraocular pressure changes in the normal rabbit eye. The effect was dependent on the timing of administration during the circadian cycle. Since ibopamine is a pro-drug of deoxyepinephrine (N-methyl dopamine, epinine), its effects are assumed to be due to this metabolite, a metabolite that is structurally similar to epinephrine.
机译:这项研究的目的是测量局部ibopamine和肾上腺素对未受干扰的兔眼压的影响。六只有色兔子配备了遥测换能器系统,该系统通过导管连接到一只眼睛的玻璃体腔,以连续监测眼内压。进入12小时光照,12小时黑暗周期并稳定眼压的昼夜节律后,用2%的ibopamine和2%的肾上腺素测试动物。在昼夜节律周期的明亮阶段和黑暗阶段滴入每种药物。当在轻度阶段给药时,两种药物均会引起短暂的压力升高,然后持续低血压。在黑暗期给药时,两种药物均不会引起压力升高,但两种药物均会导致长时间的低血压。结论是,ibopamine和肾上腺素在正常兔眼中引起相同的眼内压变化。效果取决于生理周期中的给药时间。由于依巴帕明是脱氧肾上腺素的前药(N-甲基多巴胺,表必宁),因此其作用被认为是由于这种代谢产物而引起的,这种代谢产物在结构上类似于肾上腺素。

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