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合成前列腺素1类似物:对人中性粒细胞的体外研究

Synthetic prostaglandin1 analogue: in vitro studies on human neutrophils.

作者信息

Spisani S, Vicenzi E, Traniello S, Pollini G P, Barco A

出版信息

Immunopharmacology. 1982 Aug;4(4):323-30. doi: 10.1016/0162-3109(82)90053-4.

Abstract

Prostaglandin (PG) E1 and chemically related compounds 15 alpha-11-deoxy-8-azaPGE1 and 15 epi-11-deoxy-8-azaPGE1 were examined in vitro for their capacity to modulate some physiological functions of human polymorphonuclear leukocytes (PMN). PGE1 was completely devoid of chemotactic activity and did not affect leukocyte phagocytosis. On the contrary, 15 alpha-11-deoxy-8-azaPGE1 showed a potent leukotactic activity. In addition, this synthetic substance significantly depressed the phagocytic activity and the concomitant NBT reduction by leukocytes. The analogue 15 epi-11-deoxy-8-azaPGE1 did not exert any of these effects. From these results it appeared that the substitution of the carbon-8 by the nitrogen and the lack of hydroxyl group at the position 11 into the PGE1 structure, make the compound active towards human neutrophils.

摘要

对前列腺素(PG)E1以及化学相关化合物15α-11-脱氧-8-氮杂PGE1和15表-11-脱氧-8-氮杂PGE1进行了体外研究,以考察它们调节人多形核白细胞(PMN)某些生理功能的能力。PGE1完全没有趋化活性,且不影响白细胞吞噬作用。相反,15α-11-脱氧-8-氮杂PGE1表现出强大的白细胞趋化活性。此外,这种合成物质显著降低了白细胞的吞噬活性以及伴随的NBT还原。类似物15表-11-脱氧-8-氮杂PGE1没有产生这些作用中的任何一种。从这些结果看来,在PGE1结构中用氮取代碳-8以及在11位缺少羟基,使得该化合物对人中性粒细胞具有活性。

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