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The presence of nitric oxide synthase in mucosal epithelial cells of the frog urinary bladder

机译:青蛙膀胱粘膜上皮细胞中一氧化氮合酶的存在

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In experiments on frog Rana temporaria L. urinary bladder, we investigated localization of NO-synthase (NOS) in urinary bladder slices and measured NOS activity in the suspension of mucosal epithelial cells. Intensive NADPH-diaphorase staining which is widely used as an indicator of NOS activity was found in mucosal epithelium. Almost all mucosal epithelial cells isolated in Ca2+ -free conditions demonstrated positive NADPH-diaphorase reactivity. Direct measurement of NOS activity in suspension of mucosal cells determined by the rate of conversion of L-arginine to L-citrullin showed that the enzyme activity was reduced in absence of external Ca2+ and was inhibited by L-NAME: non-specific NOS inhibitor, and 1400 W: a highly selective iNOS inhibitor (control: 754 +/- 184; L-NAME, 1 mM 329 +/- 87; 1400 W, 20 mM: 547 +/- 25; Ca2+ -free/EDTA: 490 +/- 184 cpm [3H]-citrullin/10(6) cells per 45 min, p < 0.05, n = 7-8). The data obtained demonstrate that frog urinary bladder mucosa epithelial cells provided antidiuretic hormone-induced increase of osmotic water permeability contain nitric oxide synthase. The presence of inducible (iNOS) as well as constitutive isoform(s) revealed in these cells allows to suggest involvement of NOS in intracellular signaling pathways regulated water transport across the epithelium. nauk
机译:在对青蛙Rana Temputaria L.膀胱的实验中,我们研究了尿膀胱切片中无合成酶(NOS)的定位,并测量了粘膜上皮细胞悬浮液中的NOS活性。在粘膜上皮内发现广泛用作NOS活性指示的强烈的NADPH-透明酶染色。几乎所有在CA2 + -FREE条件下分离的粘膜上皮细胞都显示出阳性NADPH-透明酶反应性。通过L-精氨酸转化率与L-柑橘蛋白确定的粘膜细胞悬浮液中的NOS活性的直接测量表明,在没有外部Ca2 +的情况下,酶活性降低,并被L-NAME抑制:非特异性NOS抑制剂, 1400 W:一种高度选择性的Inos抑制剂(控制:754 +/- 184;L名,1 mm 329 +/- 87; 1400 W,20 mm:547 +/- 25; CA2 + -Free / EDTA:490 + / - 184 CPM [3H] -Citrullin / 10(6)每45分钟细胞,P <0.05,n = 7-8)。所获得的数据表明,青蛙尿膀胱粘膜上皮细胞提供抗性激素诱导的渗透水渗透性升高含有一氧化氮合酶。在这些细胞中揭示的诱导型(InOS)以及组成型同种型的存在允许表明NoS在细胞内信号传导途径调节水上分布在上皮上的含量。 Nauk.

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