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首页> 外文期刊>British Journal of Pharmacology >Nitric oxide synthase activity and non-adrenergic non-cholinergic relaxation in the rat gastric fundus
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Nitric oxide synthase activity and non-adrenergic non-cholinergic relaxation in the rat gastric fundus

机译:大鼠胃底一氧化氮合酶活性和非肾上腺素非胆碱能松弛

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1 In the presence of atropine (1 μM) and guanethidine (5 μM), electrical field stimulation (EFS, 120 mA, 1 ms, 0.5-16.0 Hz, trains of 2 min) induced frequency-dependent relaxations of 5-hydroxytryptamine (3 μM)-precontracted longitudinal muscle strips from the rat gastric fundus. 2 L-Citrulline concentrations were measured in the incubation medium of precontracted strips before and after EFS to investigate nitric-oxide (NO) synthase activity and its possible relation to non-adrenergic non-cholinergic (NANC) relaxation. 3 Basal NO synthase activity was reflected by the finding of prestimulation levels of L-citrulline of ≈30 nM. These levels were unaffected by tetrodotoxin (3 μM) and N~G-nitro-D-arginine methyl ester (D-NAME, 100 μM), slightly reduced by a calcium-free medium and halved by N~G-nitro-L-arginine methyl ester (L-NAME, 100 μM). 4 EFS evoked significant, frequency-dependent increases in bath levels of L-citrulline at all frequencies tested. The increases evoked by 16-Hz EFS were abolished by tetrodotoxin (3 μM), a calcium-free medium and L-NAME (100 μM) but not by D-NAME (100 μM). 5 L-NAME (0.1 μM-1.0 mM) produced significant reduction of 4-Hz EFS-induced L-citrulline production (100% inhibition at 10 μM), but had less marked effects on basal production (≈50% reduction at 100 μM) and 4-Hz EFS-induced NANC relaxation (≈50% reduction at 1 mM). 6 L-Arginine (1 mM), but not D-arginine (1 mM), increased basal L-citrulline levels and reversed the inhibitory effect of L-NAME (10 μM). 7 These findings represent clear biochemical evidence of both basal and EFS-stimulated NO synthase activity in the rat gastric fundus.
机译:1在存在阿托品(1μM)和胍乙啶(5μM)的情况下,电场刺激(EFS,120 mA,1 ms,0.5-16.0 Hz,2分钟的训练)诱导了5-羟基色胺的频率依赖性弛豫(3 (μM)从大鼠胃底预收缩的纵向肌肉条带。在EFS之前和之后,在预收缩试纸条的培养液中测量2 L-瓜氨酸浓度,以研究一氧化氮(NO)合酶活性及其与非肾上腺素非胆碱能(NANC)松弛的可能关系。 3基本的NO合酶活性反映在L-瓜氨酸的预刺激水平约为30 nM。这些水平不受河豚毒素(3μM)和N〜G-硝基-D-精氨酸甲酯(D-NAME,100μM)的影响,被无钙培养基略微降低,而被N〜G-硝基-L-半胱氨酸减半精氨酸甲酯(L-NAME,100μM)。 4 EFS诱发了在所有测试频率下L-瓜氨酸的浴液含量均随频率显着增加。河豚毒素(3μM),无钙培养基和L-NAME(100μM)消除了16 Hz EFS引起的增加,但D-NAME(100μM)没有消除。 5 L-NAME(0.1μM-1.0mM)显着降低了4-Hz EFS诱导的L-瓜氨酸生成(在10μM时抑制100%),但对基础生成的影响较小(在100μM时降低了约50%) )和4 Hz EFS诱导的NANC弛豫(在1 mM时降低约50%)。 6 L-精氨酸(1 mM)而不是D-精氨酸(1 mM)增加基础L-瓜氨酸水平并逆转L-NAME(10μM)的抑制作用。 7这些发现代表了大鼠胃底中基础和EFS刺激的NO合酶活性的明确生化证据。

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