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前列腺素E1、E2和F2α对大鼠皮肤血管系统的影响。

The effects of prostaglandins E1, E2 and F2alpha on the cutaneous vasculature of the rat.

作者信息

Chahl L A, Ladd R J

出版信息

Br J Pharmacol. 1976 Mar;56(3):317-22. doi: 10.1111/j.1476-5381.1976.tb07645.x.

Abstract

1 The responses of the rat cutaneous vasculature to prostaglandins E1, E2 and F2alpha have been investigated by a photomicrographic technique. 2 Prostaglandin E1 produced transient arterial constriction which was blocked by local pretreatment of preparations with compound 48/80 or methysergide. It was concluded that prostaglandin E1 produced vasoconstriction by release of 5-hydroxytryptamine (5-HT) from mast cells. The magnitude of the vasoconstrictor response appeared to be subject to seasonal variation. 3 Prostaglandin F2alpha produced arterial constriction of longer duration which was not blocked by compound 48/80, methysergide or phenoxybenzamine. 4 Preparations pretreated with prostaglandin F2alpha were found to be more sensitive to the venous constrictor effect, and less sensitive to the arterial constrictor effect, of noradrenaline. 5 Prostaglandin E2 produced arterial constriction which was usually partially blocked by compound 48/80 and methysergide and it was concluded that a major component of the vasoconstrictor response to prostaglandin E2 was of the E1 type but some component was of the F2alpha type.

摘要
  1. 采用显微摄影技术研究了大鼠皮肤血管对前列腺素E1、E2和F2α的反应。2. 前列腺素E1引起短暂的动脉收缩,用化合物48/80或麦角新碱对标本进行局部预处理可阻断这种收缩。得出的结论是,前列腺素E1通过肥大细胞释放5-羟色胺(5-HT)产生血管收缩。血管收缩反应的程度似乎存在季节性变化。3. 前列腺素F2α引起持续时间更长的动脉收缩,化合物48/80、麦角新碱或酚苄明不能阻断这种收缩。4. 发现用前列腺素F2α预处理的标本对去甲肾上腺素的静脉收缩作用更敏感,而对其动脉收缩作用不太敏感。5. 前列腺素E2引起动脉收缩,通常部分被化合物48/80和麦角新碱阻断,得出的结论是,对前列腺素E2血管收缩反应的主要成分是E1型,但有些成分是F2α型。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f235/1666931/9e35c0f8111f/brjpharm00511-0076-a.jpg

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