首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Differentiation by hydroquinone of relaxations induced by exogenous and endogenous nitrates in non-vascular smooth muscle: role of superoxide anions.
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Differentiation by hydroquinone of relaxations induced by exogenous and endogenous nitrates in non-vascular smooth muscle: role of superoxide anions.

机译:对苯二酚对非血管平滑肌中外源性和内源性硝酸盐引起的松弛的区分:超氧阴离子的作用。

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摘要

1. The influence of hydroquinone on relaxations induced by nitric oxide (NO), nitrovasodilator drugs, and non-adrenergic, non-cholinergic (NANC) field stimulation has been investigated in three tissues in which endogenous nitrates have been implicated in the NANC response; the mechanism of action of hydroquinone was also studied. 2. In mouse anococcygeus, hydroquinone (10-100 microM) produced a concentration-dependent inhibition of relaxations induced by 15 microM NO. Hydroquinone, 100 microM, which reduced responses to NO by 85%, had no effect on relaxations induced by NANC field stimulation (10 Hz; 20s trains), hydroxylamine (10 microM), sodium nitroprusside (1 microM) or sodium azide (20 microM). 3. In guinea-pig trachea, 100 microM hydroquinone reduced relaxations to 150 microM NO by 75%, but had no effect on those to NANC stimulation (10 Hz; 30 s trains) or sodium azide (5 microM). 4. In rat gastric fundus, 100 microM hydroquinone reduced relaxations to 1 microM NO by 85%, but had no effect on those to NANC stimulation (0.5 Hz; 15 s trains) or sodium azide (2 microM). 5. Superoxide dismutase (SOD; 50 u ml-1) had no effect on relaxations of the mouse anococcygeus in response to 15 microM NO or 10 Hz NANC stimulation. Further, the inhibition of responses to NO by hydroquinone was unaffected in the presence of SOD. 6. Hydroquinone (10-100 microM) failed to generate superoxide anions, as detected by a chemiluminescent assay. However, 100 microM hydroquinone, like SOD (50 u ml-1), produced almost complete inhibition of superoxide anion chemiluminescence induced by xanthine (500 microM): xanthine oxidase (0.07 u ml-1). 7. It is concluded that, in our system, hydroquinone inhibits NO by acting as a free radical scavenger rather than by generating superoxide anions. The ability of hydroquinone to block relaxations to NO, but not NANC stimulation, may suggest that the endogenous nitrate substance released by these NANC nerves may not be free NO, but may be an NO-containing, or NO-generating, molecule.
机译:1.研究了氢醌对一氧化氮(NO),硝基血管扩张药和非肾上腺素,非胆碱能(NANC)场刺激引起的弛豫的影响,其中三个组织均与内源硝酸盐有关。还研究了对苯二酚的作用机理。 2.在小鼠无球藻中,对苯二酚(10-100 microM)对15 microM NO诱导的松弛产生浓度依赖性抑制。对苯二酚(100 microM)对NO的响应降低了85%,对NANC场刺激(10 Hz; 20s列),羟胺(10 microM),硝普钠(1 microM)或叠氮化钠(20 microM)引起的弛豫没有影响)。 3.在豚鼠气管中,100 microM对苯二酚可将弛豫降至150 microM NO降低75%,但对NANC刺激(10 Hz; 30 s列)或叠氮化钠(5 microM)的弛豫没有影响。 4.在大鼠胃底中,100 microM对苯二酚可将松弛度降至1 microM NO降低85%,但对NANC刺激(0.5 Hz; 15 s训练)或叠氮化钠(2 microM)的松弛没有影响。 5.超氧化物歧化酶(SOD; 50 u ml-1)对响应15 microM NO或10 Hz NANC刺激的小鼠无球藻松弛没有影响。此外,在SOD的存在下,对苯二酚对NO响应的抑制作用不受影响。 6.如化学发光分析所检测,对苯二酚(10-100 microM)无法产生超氧阴离子。然而,像SOD(50 u ml-1)一样,100 microM对苯二酚几乎完全抑制了由黄嘌呤(500 microM)引起的超氧阴离子化学发光:黄嘌呤氧化酶(0.07 u ml-1)。 7.结论是,在我们的系统中,对苯二酚通过充当自由基清除剂而不是通过产生超氧阴离子来抑制NO。对苯二酚阻止松弛至NO的能力,但不能阻止NANC刺激,可能表明这些NANC神经释放的内源硝酸盐物质可能不是游离NO,而可能是含NO或生成NO的分子。

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