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组胺在人肺组织和大鼠肥大细胞中的释放及前列腺素的形成。

Release of histamine and formation of prostaglandins in human lung tissue and rat mast cells.

作者信息

Strandberg K, Mathé A A, Yen S S

出版信息

Int Arch Allergy Appl Immunol. 1977;53(6):520-9. doi: 10.1159/000231794.

Abstract

Release of histamine and prostaglandins (PGs) from human lung tissue and rat mast cells was investigated. Passively sensitized lung fragments released PGE, PGF2alpha and the 15-ketodihydro metabolites into the media with time alone. Antigen challenge liberated 20% tissue histamine and there was a twofold increase in PGs. Twice as much PGF2alpha as PGE was found. beta-Adrenergic agonists inhibited the anaphylactic release of mediators and this action was blocked by propranolol. Both PGF2alpha and PGE were consistently found in the mast cell media, demonstrating that mast cells can synthesize PGs. Anaphylaxis induced a marked liberation of histamine but not of PGs. The results indicate that the release of histamine may precede the major release of PGs and suggest that the bulk of PGs may derive from cells in the proximity of the mast cells.

摘要

对人肺组织和大鼠肥大细胞中组胺和前列腺素(PGs)的释放进行了研究。仅随着时间的推移,被动致敏的肺组织碎片就会将前列腺素E(PGE)、前列腺素F2α(PGF2α)和15 - 酮二氢代谢产物释放到培养基中。抗原刺激释放出20%的组织组胺,并且PGs增加了两倍。发现PGF2α的量是PGE的两倍。β - 肾上腺素能激动剂抑制介质的过敏反应释放,且这种作用被普萘洛尔阻断。在肥大细胞培养基中始终能检测到PGF2α和PGE,这表明肥大细胞能够合成PGs。过敏反应诱导组胺大量释放,但PGs未大量释放。结果表明组胺的释放可能先于PGs的主要释放,并提示大部分PGs可能来源于肥大细胞附近的细胞。

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