Wiederholt M, Sturm A, Lepple-Wienhues A
Institut für Klinische Physiologie, Klinikum Steglitz, Freie Universität Berlin, Germany.
Invest Ophthalmol Vis Sci. 1994 Apr;35(5):2515-20.
Recent evidence suggests that nitric oxide (NO) is a major messenger molecule regulating smooth muscle contractility. A role for NO in aqueous humor dynamics, and thus regulation of intraocular pressure, has been postulated. Recently, we described contractile properties of isolated bovine trabecular meshwork and ciliary muscle strips. To assess whether vasodilators contribute to the regulation of trabecular meshwork and ciliary muscle contractility, we measured the effect of various substances known to induce vasodilation by increasing intracellular cGMP production.
Measurements of isometric tension were performed on isolated bovine ciliary muscle and trabecular meshwork strips using a custom-built electromagnetic force-length transducer. The effects of a membrane-permeable cGMP and an inhibitor of nitric oxide formation (L-nitroarginine = L-NAG) were investigated. Organic nitrate (isosorbide dinitrate = ISDN, isosorbide-5-mononitrate = 5-ISMN) and non-nitrate (sodium nitroprusside = SNP, S-nitroso-N-acetyl penicillamine = SNAP) vasodilators were tested.
Isolated strips were precontracted by carbachol 10(-6) mol/l for 30 minutes (100% carbachol maximal contraction). 8-bromo-cGMP 10(-4) mol/l evoked a relaxation to 86.7% +/- 1.4% (n = 8) in ciliary muscle and 58.6% +/- 5.4% (n = 7) in trabecular meshwork. Inhibition of NO-synthase by L-NAG increased the carbachol-induced contraction. The organic nitrovasodilators ISDN and 5-ISMN produced significant relaxations. The non-nitrates SNP and SNAP were the most potent relaxants. SNP 10(-4) mol/l relaxed the isolated ciliary muscle to 55.5% +/- 3.5% and the trabecular meshwork to 38.6% +/- 3.6%. ISDN and SNP were also tested on isolated strips without carbachol-induced precontraction. Both vasodilators had significant relaxing activity under these conditions.
The data indicate that an increase of intracellular cGMP by application of cGMP and organic nitrate or non-nitrate vasodilators induces relaxation of the bovine trabecular meshwork and ciliary muscle. Thus, nitric oxide is a cotransmitter of smooth muscle relaxation in the chamber angle and may be involved in the regulation of aqueous humor dynamics.
最近有证据表明,一氧化氮(NO)是调节平滑肌收缩性的主要信使分子。有人推测NO在房水动力学中发挥作用,进而调节眼压。最近,我们描述了分离的牛小梁网和睫状肌条带的收缩特性。为了评估血管舒张剂是否有助于调节小梁网和睫状肌的收缩性,我们测量了各种已知通过增加细胞内cGMP生成来诱导血管舒张的物质的作用。
使用定制的电磁力-长度换能器对分离的牛睫状肌和小梁网条带进行等长张力测量。研究了一种膜通透性cGMP和一氧化氮形成抑制剂(L-硝基精氨酸 = L-NAG)的作用。测试了有机硝酸盐(硝酸异山梨酯 = ISDN,5-单硝酸异山梨酯 = 5-ISMN)和非硝酸盐(硝普钠 = SNP,S-亚硝基-N-乙酰青霉胺 = SNAP)血管舒张剂。
分离的条带用10(-6) mol/l的卡巴胆碱预收缩30分钟(100%卡巴胆碱最大收缩)。10(-4) mol/l的8-溴-cGMP使睫状肌松弛至86.7%±1.4%(n = 8),小梁网松弛至58.6%±5.4%(n = 7)。L-NAG抑制一氧化氮合酶增加了卡巴胆碱诱导的收缩。有机硝基血管舒张剂ISDN和5-ISMN产生了显著的松弛作用。非硝酸盐SNP和SNAP是最有效的松弛剂。10(-4) mol/l的SNP使分离的睫状肌松弛至55.5%±3.5%,小梁网松弛至38.6%±3.6%。还在没有卡巴胆碱诱导预收缩的分离条带上测试了ISDN和SNP。在这些条件下,两种血管舒张剂都具有显著的松弛活性。
数据表明,通过应用cGMP和有机硝酸盐或非硝酸盐血管舒张剂增加细胞内cGMP可诱导牛小梁网和睫状肌松弛。因此,一氧化氮是房角平滑肌舒张的共同递质,可能参与房水动力学的调节。