Suppr超能文献

多胺对一氧化氮合酶诱导的抑制作用机制:醛代谢产物的作用

The mechanism of the inhibitory effect of polyamines on the induction of nitric oxide synthase: role of aldehyde metabolites.

作者信息

Szabó C, Southan G J, Thiemermann C, Vane J R

机构信息

William Harvey Research Institute, St. Bartholomew's Hospital Medical College, London.

出版信息

Br J Pharmacol. 1994 Nov;113(3):757-66. doi: 10.1111/j.1476-5381.1994.tb17058.x.

Abstract
  1. We have recently found that in the presence, but not in the absence, of foetal calf serum, spermine inhibits the production of nitric oxide (NO) in cultured J774.2 macrophages stimulated with bacterial endotoxin (lipopolysaccharide; LPS) or with gamma-interferon (IFN), showing that polyamines may act as suppressants of NO-mediated immune functions. Here, we have studied the mechanisms and the specificity of this inhibitory action. 2. Other polyamines, as well as spermine, inhibit the formation of NO in cultured J774.2 macrophages, with the order of potency being spermine > spermidine >> putrescine = cadaverine. This inhibition of NO formation is not due to any cytotoxic effect of these agents for they neither reduced mitochondrial respiration nor increased the release of lactate dehydrogenase into the supernatant. 3. Spermine is not a direct inhibitor of the activity of iNOS in induced J774.2 cells as measured by its lack of effect on the conversion of L-arginine to L-citrulline in homogenates. Neither spermine, nor its metabolites, interfere with the production of nitrite from NO or act as scavengers of NO. Thus, spermine is an inhibitor of the induction of iNOS. 4. Spermine inhibits nitrite formation in the presence of foetal, newborn or adult bovine serum, but not rat or human serum. 5. The effect of sper mine on nitrite production can be prevented by isoniazid, hydrazine or hydroxylamine, inhibitors of spermine oxidase, as well as by phenylhydrazine, an aldehyde inhibitor. We have, therefore, tested the effects of spermine dialdehyde or malon dialdehyde on the induction of iNOS. Spermine dialdehyde (SDA, 10(-5) M) inhibits nitrite formation by IFN-activated J774.2 cells in the absence of serum when given as a pretreatment but not when given 6 h after stimulation. In contrast, malon dialdehyde was ineffective. Thus, aldehyde metabolites of spermine, such as SDA, account for the inhibitory effect of polyamines on the induction of NOS in vitro. 6. The inhibitory effect of polyamines on iNOS induction appears to be fairly specific to iNOS, for spermine does not inhibit LPS-induced production of prostaglandin F2 alpha or tumour necrosis factor.
摘要
  1. 我们最近发现,在有胎牛血清存在的情况下(无胎牛血清时则不然),精胺可抑制经细菌内毒素(脂多糖;LPS)或γ干扰素(IFN)刺激的培养J774.2巨噬细胞中一氧化氮(NO)的产生,这表明多胺可能作为NO介导的免疫功能的抑制剂。在此,我们研究了这种抑制作用的机制和特异性。2. 其他多胺以及精胺均可抑制培养的J774.2巨噬细胞中NO的形成,其效力顺序为精胺>亚精胺>>腐胺 = 尸胺。这种对NO形成的抑制并非由于这些试剂的任何细胞毒性作用,因为它们既未降低线粒体呼吸作用,也未增加乳酸脱氢酶向上清液中的释放。3. 如通过其对匀浆中L-精氨酸向L-瓜氨酸转化缺乏影响所测定的那样,精胺不是诱导的J774.2细胞中诱导型一氧化氮合酶(iNOS)活性的直接抑制剂。精胺及其代谢产物均不干扰由NO产生亚硝酸盐,也不作为NO的清除剂。因此,精胺是iNOS诱导的抑制剂。4. 精胺在有胎牛、新生牛或成年牛血清存在的情况下抑制亚硝酸盐形成,但在有大鼠或人血清存在时则不然。5. 精胺对亚硝酸盐产生的作用可被精胺氧化酶抑制剂异烟肼、肼或羟胺以及醛抑制剂苯肼所阻止。因此,我们测试了精胺二醛或丙二醛对iNOS诱导的作用。精胺二醛(SDA,10⁻⁵ M)在无血清时作为预处理给予时可抑制IFN激活的J774.2细胞中亚硝酸盐的形成,但在刺激后6小时给予时则无效。相比之下,丙二醛无效。因此,精胺的醛代谢产物,如SDA,在体外解释了多胺对NOS诱导的抑制作用。6. 多胺对iNOS诱导的抑制作用似乎对iNOS相当特异,因为精胺不抑制LPS诱导的前列腺素F2α或肿瘤坏死因子的产生。

相似文献

3
Inhibition of the induction of nitric oxide synthase by spermine is modulated by aldehyde dehydrogenase.
Biochem Biophys Res Commun. 1994 Sep 30;203(3):1638-44. doi: 10.1006/bbrc.1994.2374.
7
Polyamines inhibit nitric oxide synthase in rat cerebellum.多胺抑制大鼠小脑一氧化氮合酶。
Neurosci Lett. 1994 Jul 4;175(1-2):41-5. doi: 10.1016/0304-3940(94)91073-1.

引用本文的文献

3
Arginine and Polyamines Fate in Infection.精氨酸和多胺在感染中的命运
Front Microbiol. 2018 Jan 15;8:2682. doi: 10.3389/fmicb.2017.02682. eCollection 2017.
9
Transcriptome changes in Mycoplasma hyopneumoniae during infection.猪肺炎支原体感染期间的转录组变化
Infect Immun. 2008 Feb;76(2):658-63. doi: 10.1128/IAI.01291-07. Epub 2007 Dec 10.

本文引用的文献

3
Nitric oxide--a new endogenous immunomodulator.一氧化氮——一种新的内源性免疫调节剂。
Transplantation. 1993 Jun;55(6):1205-12. doi: 10.1097/00007890-199306000-00001.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验