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花生四烯酸氢过氧化物对离体胃肠组织的拮抗作用作为前列腺素生物合成抑制的一种衡量指标。

Antagonism of arachidonic acid hydroperoxide on isolated gastrointestinal tissues as a measure of the inhibition of prostaglandin biosynthesis.

作者信息

Van Nueten J M

出版信息

Adv Prostaglandin Thromboxane Res. 1976;1:139-45.

PMID:11650
Abstract

Arachidonic acid hydroperoxide (AAP)-induced contractions of the isolated guinea pig ileum and rat stomach fundus are inhibited by suprofen [alpha-methyl-4-(2-thienylcarbonyl) benzeneacetic acid], indomethacin, phenylbutazone, and acetylsalicyclic acid in descending order of activity. This effect is highly specific, since prostaglandins (PG) and various agonists of gastrointestinal smooth muscle are not, or only weakly antagonized by these four compounds, whereas various compounds, including narcotic analgesics, are inactive versus AAP. The antagonism of AAP-induced contractions of the isolated rat stomach fundus is a valuable test system for inhibitors of PG biosynthesis.

摘要

花生四烯酸氢过氧化物(AAP)诱导的离体豚鼠回肠和大鼠胃底收缩,被舒洛芬[α-甲基-4-(2-噻吩基羰基)苯乙酸]、吲哚美辛、保泰松和乙酰水杨酸以活性递减的顺序所抑制。这种作用具有高度特异性,因为前列腺素(PG)和各种胃肠道平滑肌激动剂不会被这四种化合物拮抗,或仅被其微弱拮抗,而包括麻醉性镇痛药在内的各种化合物对AAP则无活性。AAP诱导的离体大鼠胃底收缩的拮抗作用,是PG生物合成抑制剂的一个有价值的测试系统。

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