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对苯二酚对外源性和内源性硝酸盐在非血管平滑肌中诱导的舒张作用的分化:超氧阴离子的作用

Differentiation by hydroquinone of relaxations induced by exogenous and endogenous nitrates in non-vascular smooth muscle: role of superoxide anions.

作者信息

Hobbs A J, Tucker J F, Gibson A

机构信息

Biomedical Sciences Division, King's College London.

出版信息

Br J Pharmacol. 1991 Nov;104(3):645-50. doi: 10.1111/j.1476-5381.1991.tb12483.x.

Abstract
  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.
摘要
  1. 对苯二酚对一氧化氮(NO)、硝基血管舒张剂药物以及非肾上腺素能、非胆碱能(NANC)场刺激所诱导的舒张作用,已在三种内源性硝酸盐与NANC反应有关的组织中进行了研究;同时也研究了对苯二酚的作用机制。2. 在小鼠肛门尾骨肌中,对苯二酚(10 - 100微摩尔)对15微摩尔NO所诱导的舒张产生浓度依赖性抑制。100微摩尔的对苯二酚使对NO的反应降低了85%,但对NANC场刺激(10赫兹;20秒串刺激)、羟胺(10微摩尔)、硝普钠(1微摩尔)或叠氮化钠(20微摩尔)所诱导的舒张无影响。3. 在豚鼠气管中,100微摩尔对苯二酚使对150微摩尔NO的舒张降低了75%,但对NANC刺激(10赫兹;30秒串刺激)或叠氮化钠(5微摩尔)所诱导的舒张无影响。4. 在大鼠胃底中,100微摩尔对苯二酚使对1微摩尔NO的舒张降低了85%,但对NANC刺激(0.5赫兹;15秒串刺激)或叠氮化钠(2微摩尔)所诱导的舒张无影响。5. 超氧化物歧化酶(SOD;50单位/毫升)对小鼠肛门尾骨肌对15微摩尔NO或10赫兹NANC刺激的舒张无影响。此外,在有SOD存在的情况下,对苯二酚对NO反应的抑制作用不受影响。6. 通过化学发光测定法检测,对苯二酚(10 - 100微摩尔)未能产生超氧阴离子。然而,100微摩尔对苯二酚与SOD(50单位/毫升)一样,几乎完全抑制了黄嘌呤(500微摩尔):黄嘌呤氧化酶(0.07单位/毫升)所诱导的超氧阴离子化学发光。7. 结论是,在我们的系统中,对苯二酚通过作为自由基清除剂而非产生超氧阴离子来抑制NO。对苯二酚能够阻断对NO的舒张,但不影响对NANC刺激的舒张,这可能表明这些NANC神经释放的内源性硝酸盐物质可能不是游离的NO,而是可能是一种含NO或产生NO的分子。

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