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福司可林上调猪睫状体中一氧化氮合酶I蛋白表达:房水调节的新方面。

Forskolin upregulation of NOS I protein expression in porcine ciliary processes: a new aspect of aqueous humor regulation.

作者信息

Liu Rong, Flammer Josef, Haefliger Ivan O

机构信息

Laboratory of Ocular Pharmacology and Physiology, University Eye Clinic, Basel, Switzerland.

出版信息

Klin Monbl Augenheilkd. 2002 Apr;219(4):281-3. doi: 10.1055/s-2002-30643.

DOI:10.1055/s-2002-30643
PMID:12022018
Abstract

BACKGROUND

To determine whether nitric oxide synthase (NOS) protein expression can be modulated by forskolin in porcine ciliary processes.

METHOD

Western blot analysis using mouse monoclonal antibodies against NOS I (neuronal NOS or nNOS), NOS II (macrophage NOS or macNOS), and NOS III (endothelial NOS or eNOS) was performed in porcine ciliary processes. Expression of NOS I and II was also assessed in the presence or in the absence of 1 microM forskolin exposure (4 and 24 hours).

RESULTS

All three NOS isoforms could be detected in isolated porcine ciliary processes. Protein expression for NOS I was about 6 times higher than for NOS III and 15 times higher than for NOS II. In comparison to controls, after forskolin exposure, NOS I protein expression was increased by about 1.5-fold. No change could be observed in NOS II protein expression after forskolin exposure.

CONCLUSIONS

Nitric oxide is involved in transepithelial fluid transport of different organs (lung, kidney, colon, etc.) and is suspected to play a role in ciliary processes by modulating the aqueous humor production. The present study indicates that forskolin (which increases cAMP production) modulates NOS I protein expression in isolated porcine ciliary processes. These results suggest that selective inhibition of NOS I could be tried for reducing aqueous humor production. The clinical relevance requires further investigations.

摘要

背景

确定在猪睫状体中,一氧化氮合酶(NOS)蛋白表达是否可被福司可林调节。

方法

在猪睫状体中使用抗 NOS I(神经元型 NOS 或 nNOS)、NOS II(巨噬细胞型 NOS 或 macNOS)和 NOS III(内皮型 NOS 或 eNOS)的小鼠单克隆抗体进行蛋白质印迹分析。在有或没有 1 微摩尔福司可林暴露(4 小时和 24 小时)的情况下,也评估了 NOS I 和 II 的表达。

结果

在分离的猪睫状体中可检测到所有三种 NOS 同工型。NOS I 的蛋白表达比 NOS III 高约 6 倍,比 NOS II 高约 15 倍。与对照组相比,福司可林暴露后,NOS I 的蛋白表达增加了约 1.5 倍。福司可林暴露后,未观察到 NOS II 蛋白表达有变化。

结论

一氧化氮参与不同器官(肺、肾、结肠等)的跨上皮液体转运,并且被怀疑通过调节房水生成在睫状体过程中起作用。本研究表明,福司可林(可增加 cAMP 生成)可调节分离的猪睫状体中的 NOS I 蛋白表达。这些结果表明,可以尝试选择性抑制 NOS I 以减少房水生成。其临床相关性需要进一步研究。

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