首页> 外文期刊>Pharmacology: International Journal of Experimental and Clinical Pharmacology >Effects of phosphodiesterase V inhibition on nitric oxide-mediated relaxation responses in guinea pig trachea.
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Effects of phosphodiesterase V inhibition on nitric oxide-mediated relaxation responses in guinea pig trachea.

机译:磷酸二酯酶V抑制对豚鼠气管中一氧化氮介导的舒张反应的影响。

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In the present study, we aimed to evaluate the effects of PDE V inhibition on NO-mediated relaxation responses in isolated guinea pig trachea. Under the NANC conditions, tracheal preparations were contracted with histamine (100 microm/l). When contraction had reached a plateau, relaxation responses to electrical field stimulation (EFS, 60 V, 0.5 ms, 5-10 Hz) were determined before and after incubation of the tracheal ring with L-NAME (1 mmol/l), a NO synthase inhibitor. L-NAME significantly inhibited the relaxation responses and this inhibitory effect was reversed by L-arginine (1 mmol/l), a precursor of NO, but was not affected by D-arginine. In addition, cumulative application of the NO donors, 3-morpholino-sydnonimine (SIN-1) and sodium nitroprusside (SNP), caused concentration-dependent relaxation of tissues precontracted with histamine. The selective PDE type V inhibitor zaprinast at EC50 concentration (30 micromol/l) significantly potentiated EFS-induced NANC relaxations and relaxant responses toSIN-1 and SNP. In conclusion, these data support the hypothesis that NO is a mediator of NANC relaxations of guinea pig tracheal rings and PDE V inhibition potentiates NO-mediated relaxation.
机译:在本研究中,我们旨在评估PDE V抑制对离体豚鼠气管中NO介导的舒张反应的影响。在NANC条件下,气管制剂与组胺(100 microm / l)收缩。当收缩达到平稳时,在气管环与L-NAME(1 mmol / l)孵育气管环之前和之后确定对电场刺激(EFS,60 V,0.5 ms,5-10 Hz)的弛豫响应合酶抑制剂。 L-NAME显着抑制了松弛反应,这种抑制作用被NO的前体L-精氨酸(1 mmol / l)逆转,但不受D-精氨酸影响。此外,NO施主3-吗啉代-亚砜亚胺(SIN-1)和硝普钠(SNP)的累积应用导致与组胺预收缩组织的浓度依赖性松弛。 EC50浓度(30微摩尔/升)的选择性PDE V型抑制剂扎普利斯特显着增强了EFS诱导的NANC松弛和对SIN-1和SNP的松弛反应。总之,这些数据支持以下假设:NO是豚鼠气管环NANC松弛的介体,PDE V抑制可增强NO介导的松弛。

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