Kitsiopoulou Eudoxia, Hatziefthimiou Apostolia A, Gourgoulianis Konstantinos I, Molyvdas Paschalis-Adam
Department of Physiology, Medical School, University of Thessaly, Papakiriazi 22, 41222 Larissa, Greece.
Mediators Inflamm. 2007;2007:24174. doi: 10.1155/2007/24174. Epub 2007 Mar 28.
The alteration of resting tension (RT) from 0.5 g to 2.5 g increased significantly airway smooth muscle contractions induced by acetylcholine (ACh) in rabbit trachea. The decrease in extracellular calcium concentration [Ca2+]o from 2 mM to 0.2 mM reduced ACh-induced contractions only at 2.5 g RT with no effect at 0.5 g RT. The nonselective inhibitor of nitric oxide synthase (NOS), N(G)-nitro-L-arginine methyl ester (L-NAME) increased ACh-induced contractions at 2.5 g RT. The inhibitor of inducible NOS, S-methylsothiourea or neuronal NOS, 7-nitroindazole had no effect. At 2.5 g RT, the reduction of [Ca2+]o from 2 mM to 0.2 mM abolished the effect of L-NAME on ACh-induced contractions. The NO precursor L-arginine or the tyrosine kinase inhibitors erbstatin A and genistein had no effect on ACh-induced contractions obtained at 2.5 g RT. Our results suggest that in airways, RT affects ACh-induced contractions by modulating the activity of epithelial NOS in a calcium-dependent, tyrosine-phosphorylation-independent way.
静息张力(RT)从0.5 g增加至2.5 g可显著增强兔气管中乙酰胆碱(ACh)诱导的气道平滑肌收缩。细胞外钙浓度[Ca2+]o从2 mM降至0.2 mM仅在RT为2.5 g时可降低ACh诱导的收缩,而在RT为0.5 g时无影响。一氧化氮合酶(NOS)的非选择性抑制剂N(G)-硝基-L-精氨酸甲酯(L-NAME)在RT为2.5 g时可增强ACh诱导的收缩。诱导型NOS抑制剂S-甲基异硫脲或神经元型NOS抑制剂7-硝基吲唑无作用。在RT为2.5 g时,[Ca2+]o从2 mM降至0.2 mM可消除L-NAME对ACh诱导收缩的作用。NO前体L-精氨酸或酪氨酸激酶抑制剂埃布他汀A和染料木黄酮对RT为2.5 g时获得的ACh诱导收缩无作用。我们的结果表明,在气道中,RT通过以钙依赖、酪氨酸磷酸化非依赖的方式调节上皮型NOS的活性来影响ACh诱导的收缩。