Suppr超能文献

肾上腺素能机制在肥大细胞释放组胺中(若有)起什么作用?

What - if any - is the role of adrenergic mechanisms in histamine release from mast cells?

作者信息

Alm P E, Bloom G D

出版信息

Agents Actions. 1981 Apr;11(1-2):60-6. doi: 10.1007/BF01991457.

Abstract

The effects of catecholamines on histamine release from rat peritoneal mast cells, was studied in an in vitro system. It was found that norepinephrine (10(-5)-101(-3) M) exerts a significant, dose related, repressive effect on compound 48/80-induced histamine release. This effect is greatly potentiated by beta-antagonists and is noticeable throughout the concentration range 10(-11)-10(-3) M norepinephrine. Phentolamine diminishes the repressive effect that norepinephrine shows at 10(-5) M. Norepinephrine (10(-5) M) totally inhibits the progressive histamine release induced by both compound 48/80 and strontium (10 muM) in non-Ca2+-depleted cells. The release that is dependent on extracellular calcium is inhibited by norepinephrine. The repressive effect of norepinephrine at 10(-3) is counteracted by 5.6 mM D-glucose, 2-deoxyglucose abolishes this effect. The repression of histamine release by 10(-5) M norepinephrine is not influenced by D-glucose. These results suggest that the effects on histamine release, observed within a low concentration range of norepinephrine (less than 10(-3) M), may be due to alpha-adrenoreceptor mechanisms and an interference in transmembrane calcium transport. Our data further suggest that norepinephrine at 10(-3) M may inhibit oxidative phosphorylation. Isoproterenol and epinephrine (10(-9)-10(-5) M) show little effect on 48/80-induced histamine release in a normal medium. However, when calcium is excluded from the medium, histamine release is potentiated. These results seem to indicate that isoproterenol and epinephrine act by displacing intracellular calcium, making it available for the exocytosis process.

摘要

在体外系统中研究了儿茶酚胺对大鼠腹膜肥大细胞组胺释放的影响。发现去甲肾上腺素(10⁻⁵ - 10⁻³ M)对化合物48/80诱导的组胺释放具有显著的、剂量相关的抑制作用。β-拮抗剂可大大增强这种作用,并且在10⁻¹¹ - 10⁻³ M去甲肾上腺素的整个浓度范围内都很明显。酚妥拉明可减弱去甲肾上腺素在10⁻⁵ M时表现出的抑制作用。去甲肾上腺素(10⁻⁵ M)完全抑制了在非Ca²⁺ 耗尽细胞中由化合物48/80和锶(10 μM)诱导的渐进性组胺释放。依赖细胞外钙的释放被去甲肾上腺素抑制。5.6 mM D-葡萄糖可抵消去甲肾上腺素在10⁻³ 时的抑制作用,2-脱氧葡萄糖可消除这种作用。10⁻⁵ M去甲肾上腺素对组胺释放的抑制不受D-葡萄糖的影响。这些结果表明,在去甲肾上腺素低浓度范围(小于10⁻³ M)内观察到的对组胺释放的影响可能是由于α-肾上腺素能受体机制和对跨膜钙转运的干扰。我们的数据进一步表明,10⁻³ M的去甲肾上腺素可能抑制氧化磷酸化。异丙肾上腺素和肾上腺素(10⁻⁹ - 10⁻⁵ M)在正常培养基中对48/80诱导的组胺释放几乎没有影响。然而,当培养基中不含钙时,组胺释放会增强。这些结果似乎表明,异丙肾上腺素和肾上腺素通过置换细胞内钙起作用,使其可用于胞吐过程。

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