儿茶酚胺研究的历史。

Chemical immunology and allergy Pub Date : 2014-01-01 Epub Date: 2014-05-23 DOI:10.1159/000359962
Klaus Starke
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引用次数: 3

摘要

儿茶酚胺及其同系物在过敏性疾病中的突出作用主要在于它们在哮喘和急性超敏反应(如过敏性反应)中的应用。它们通过激活α-和β-肾上腺素受体在这些适应症中起作用。肾上腺素是1893/1894年在肾上腺中发现的原型。1939年,多巴脱羧酶是第一个在儿茶酚胺生物合成中被描述的酶。后来,去甲肾上腺素和多巴胺等其他儿茶酚胺也有了特征。活性化学物质的鉴定伴随着儿茶酚胺受体的研究。直到1948年,人们才承认至少存在两种不同的受体来产生不同的效果。同时,所有哺乳动物儿茶酚胺受体的基因都已被克隆。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
History of catecholamine research.

The prominence of catecholamines and their congeners in allergic diseases rests chiefly on their use in asthma and acute hypersensitivity reactions, such as anaphylaxis. They act in these indications by activating both α- and β-adrenoceptors. Adrenaline, the prototype, was discovered in the adrenals in 1893/1894. In 1939, dopa decarboxylase was the first enzyme in the biosynthesis of catecholamines to be described. Later other catecholamines like noradrenaline and dopamine were characterized. The identification of the active chemicals went along with studies regarding catecholamine receptors. It took until 1948 before the existence of at least two different receptors for the different effects was accepted. Meanwhile, genes from all mammalian catecholamine receptors have been cloned.

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