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脂氧素A的生物活性包括体内肺条收缩和小动脉扩张。

Biological activities of lipoxin A include lung strip contraction and dilation of arterioles in vivo.

作者信息

Dahlén S E, Raud J, Serhan C N, Björk J, Samuelsson B

出版信息

Acta Physiol Scand. 1987 Aug;130(4):643-7. doi: 10.1111/j.1748-1716.1987.tb08187.x.

Abstract

Lipoxin A ([5S,6R,15S]-5,6,15-trihydroxy-7,9,13-trans-11-cis-eicosatetraenoic acid), a recently characterized lipoxygenation product of arachidonic acid, in submicromolar concentrations elicited long-lasting contractions of the guinea-pig lung strip. The response to lipoxin A was not due to release of acetylcholine, histamine, noradrenaline or cyclo-oxygenase products. 15-hydroperoxyeicosatetraenoic acid (15-HPETE), one precursor of lipoxin A, also contracted the lung strip, but 15-HPETE was less potent on the guinea-pig trachea whereas 15-HPETE relaxed this preparation. Lipoxin A was also inactive on the guinea-pig ileum. Intravital microscopy of the hamster cheek pouch disclosed that lipoxin A, as well as 15-HPETE, induced arteriolar dilation but had no effects on microvascular permeability or leucocyte adherence to venular endothelium. Taken together, the leucocyte product lipoxin A displayed a pattern of activity in spasmogenic assays and on the microvasculature that was distinct from those known for prostaglandins, thromboxanes and leukotrienes. The findings indicate that lipoxin A is an additional arachidonic acid derived autacoid with biological actions on smooth muscle in vitro and in vivo.

摘要

脂氧素A([5S,6R,15S]-5,6,15-三羟基-7,9,13-反式-11-顺式-二十碳四烯酸)是最近鉴定出的花生四烯酸的脂氧化产物,亚微摩尔浓度的脂氧素A可引起豚鼠肺条的持久收缩。对脂氧素A的反应并非由于乙酰胆碱、组胺、去甲肾上腺素或环氧化酶产物的释放。15-氢过氧二十碳四烯酸(15-HPETE)是脂氧素A的前体之一,也可使肺条收缩,但15-HPETE对豚鼠气管的作用较弱,而15-HPETE可使该制剂舒张。脂氧素A对豚鼠回肠也无活性。对仓鼠颊囊进行活体显微镜观察发现,脂氧素A以及15-HPETE可引起小动脉扩张,但对微血管通透性或白细胞与小静脉内皮的黏附无影响。综上所述,白细胞产物脂氧素A在致痉挛试验和微血管系统中表现出的活性模式与前列腺素、血栓素和白三烯已知的活性模式不同。这些发现表明,脂氧素A是另一种源自花生四烯酸的自分泌物质,在体外和体内对平滑肌具有生物学作用。

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