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金盐和保泰松对前列腺素生物合成的选择性抑制作用。

Selective inhibition of prostaglandin biosynthesis by gold salts and phenylbutazone.

作者信息

Stone K J, Mather S J, Gibson P P

出版信息

Prostaglandins. 1975 Aug;10(2):241-51. doi: 10.1016/0090-6980(75)90043-x.

Abstract

Gold salts and phenylbutazone selectively inhibit the synthesis of PGF2alpha and PGE2 respectively. Lowered production of one prostaglandin species is accompanied by an increased production of the other. Selective inhibition by these drugs was observed in the presence of adrenaline, reduced glutathione and copper sulphate under conditions when most anti-inflammatory compounds inhibited PGE2 and PGF2alpha syntheses equally. It is postulated that selective inhibitors may have a different mode of action in vivo and beneficial effects may be related to the endogenous ratio of PGE to PGF required for normal function.

摘要

金盐和保泰松分别选择性抑制前列腺素F2α(PGF2α)和前列腺素E2(PGE2)的合成。一种前列腺素生成量的降低伴随着另一种前列腺素生成量的增加。在大多数抗炎化合物同等程度抑制PGE2和PGF2α合成的条件下,在肾上腺素、还原型谷胱甘肽和硫酸铜存在时观察到了这些药物的选择性抑制作用。据推测,选择性抑制剂在体内可能具有不同的作用方式,其有益作用可能与正常功能所需的PGE与PGF的内源性比例有关。

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