...
首页> 外文期刊>Acta ophthalmologica Scandinavica >Intrinsic vasomotricity and adrenergic effects in a model of isolated rabbit eye
【24h】

Intrinsic vasomotricity and adrenergic effects in a model of isolated rabbit eye

机译:在离体兔眼模型中的内在血管收缩和肾上腺素能作用

获取原文
获取原文并翻译 | 示例
           

摘要

Purpose: We aimed to investigate the responsiveness of the ocular arteries to adrenergic drugs in a model of perfused isolated rabbit eye. Methods: Rabbit external ophthalmic arteries (? = 15) in a head-mounted preparation were cannulated and the retinal and uveal vasculature perfused at a constant flow with warmed tyrode. The three-way polypropylene catheter was further connected to a pressure transducer and intraluminal pressure was taken as a measure of vascular resistance. Effects of intra-arterial injections of phenylephrine (group A, ? = 5), prazosin (group B, n = 5) and phentol-amine (group C, n = 5) on the recorded pressure were obtained. Student's paired-t test and one-way analysis of variance were used for statistical analysis (p < 0.05).Results: Intrinsic vasomotricity was observed in all preparations prior to any drug administration. Phenylephrine produced an increase in total vascular resistance. Intrinsic vasomotricity became more evident, showing a lower frequency but higher amplitude of oscillations. Evoked vasomotor responses with phenylephrine (250 mug/ml) were inhibited by intra-arterial administration of the selective alpha_1-adrenergic antagonist, prazosin (0.5 mg/ml), as well as the non-selective alpha-adrenergic antagonist phentolamine (6 mg/ml). Conclusions: Rabbit external ophthalmic arteries showed spontaneous contractions under constant perfusion. Phenylephrine elicited a vasoconstrictor response that was inhibited by adrenergic antagonists. In addition, the intrinsic vasomotricity was enhanced by phenylephrine and blocked by adrenergic antagonists. These results show that under in vitro perfusion the territory presents similar responses to adrenergic drugs to those observed in in vivo models and also provides evidence of myogenic autoregulatory properties in the rabbit ophthalmic artery and/or choroid.
机译:目的:我们旨在研究在离体灌注兔眼模型中眼动脉对肾上腺素能药物的反应性。方法:将头戴式制剂中的兔眼外动脉(?= 15)插管,并以恒定流量用加热的酪氨酸灌注视网膜和葡萄膜脉管系统。三通聚丙烯导管进一步连接到压力传感器,并以腔内压力作为血管阻力的量度。动脉内注射去氧肾上腺素(A组,α= 5),哌唑嗪(B组,n = 5)和苯酚-胺(C组,n = 5)对记录压力的影响。使用学生配对t检验和单向方差分析进行统计分析(p <0.05)。结果:在任何药物给药之前,所有制剂均观察到内在血管收缩。苯肾上腺素使总血管阻力增加。内在血管容积性变得更加明显,显示出较低的频率但较高的振荡幅度。动脉内施用选择性α_1-肾上腺素能拮抗药prazosin(0.5 mg / ml)和非选择性α-肾上腺素能芬妥拉明(6 mg / ml)可抑制苯肾上腺素(250杯/毫升)引起的血管舒缩反应。毫升)。结论:兔子的眼外动脉在持续灌注下表现出自发性收缩。苯肾上腺素引起血管收缩反应,被肾上腺素能拮抗剂抑制。此外,去氧肾上腺素增强了内在的血管舒张性,肾上腺素能拮抗剂阻断了其内在的血管舒张性。这些结果表明,在体外灌注下,该区域对肾上腺素能药物的反应与在体内模型中观察到的反应相似,并且还提供了兔眼动脉和/或脉络膜中肌原性自动调节特性的证据。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号