Department of Pharmacology & Toxicology, Morehouse School of Medicine, 720 Westview Dr., Atlanta, GA, 30310-1495, USA. address:
Exp Eye Res. 2009 Nov;89(5):660-4. doi: 10.1016/j.exer.2009.06.007. Epub 2009 Jun 23.
Considerable evidence suggests that the nitric oxide (NO)/cGMP signaling pathway plays an integral role in opioid receptor-mediated responses in the cardiovascular and immune systems. Previous studies in our laboratory and others have shown that nitric oxide (NO) plays a role in morphine-induced reduction of intraocular pressure (IOP) and pupil diameter (PD) in the New Zealand white (NZW) rabbit. The present study is designed to determine the effect of morphine on NO production in the isolated, iris-ciliary body (ICB), site of aqueous humor production, as this effect could be associated with morphine-stimulated changes in aqueous humor dynamics and iris function. ICBs obtained from normal NZW rabbits were utilized in these experiments. In some experiments, ICB samples were treated with morphine (1, 10 and 100 microM) for 1 h and later examined for changes in NO levels using a NO detection kit. In other experiments, tissue samples were pretreated with naloxone (non-selective opioid receptor antagonist), L-NAME (non-selective NO-synthase inhibitor) or GSH (sulfhydryl reagent) for 30 min, followed by treatment with morphine (10 muM). Morphine caused a concentration-dependent increase in the release of NO from ICBs. Levels of NO detected in the incubation medium of ICB samples increased from 1.49 +/- 0.19 (control) to 8.81 +/- 2.20 microM/mg protein (morphine-treated; 100 microM). Morphine-stimulated release of NO was significantly inhibited in tissues pretreated with 10 microM naloxone, L-NAME, or GSH. Results obtained from this study suggest that morphine stimulates NO release from the ICB through a mechanism that involves activation of NO-releasing opioid receptors. These results support the in vivo effects of morphine demonstrated in previous studies.
大量证据表明,一氧化氮(NO)/环鸟苷酸(cGMP)信号通路在心血管和免疫系统中阿片受体介导的反应中发挥着重要作用。我们实验室和其他实验室的先前研究表明,一氧化氮(NO)在吗啡引起的新西兰白兔(NZW)眼内压(IOP)和瞳孔直径(PD)降低中起作用。本研究旨在确定吗啡对分离的虹膜睫状体(ICB)中一氧化氮(NO)产生的影响,因为这种作用可能与吗啡刺激的房水动力学和虹膜功能变化有关。在这些实验中使用了来自正常 NZW 兔的 ICB。在一些实验中,用吗啡(1、10 和 100 μM)处理 ICB 样本 1 小时,然后使用一氧化氮检测试剂盒检查 NO 水平的变化。在其他实验中,组织样本用纳洛酮(非选择性阿片受体拮抗剂)、L-NAME(非选择性一氧化氮合酶抑制剂)或 GSH(巯基试剂)预处理 30 分钟,然后用吗啡(10 μM)处理。吗啡引起 ICB 释放的一氧化氮浓度依赖性增加。从 ICB 样本孵育培养基中检测到的 NO 水平从 1.49±0.19(对照)增加到 8.81±2.20 μM/mg 蛋白(吗啡处理;100 μM)。用 10 μM 纳洛酮、L-NAME 或 GSH 预处理的组织中,吗啡刺激的一氧化氮释放明显受到抑制。本研究结果表明,吗啡通过涉及激活释放一氧化氮的阿片受体的机制刺激 ICB 释放一氧化氮。这些结果支持了先前研究中显示的吗啡的体内作用。