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冠状动脉扩张剂对前列腺素E、F2α、I2和腺苷代谢的影响。

Influence of coronary vasodilators on prostaglandin E, F2alpha, I2, and adenosine metabolism.

作者信息

Förster W, Mentz P, Pönicke K, Zehl U

出版信息

Acta Biol Med Ger. 1978;37(5-6):755-63.

PMID:369257
Abstract

We investigated the influence of oxyfedrine, verapamil, prenylamine, sodium nitrite, nitroglycerin, papaverine and carbochromen on the release of prostaglandins (PG) and adenosine from Langendorff heart preparations of guinea pigs and rabbits and on the PG biosynthesis in the heart and renal medulla of rabbits, in the bovine seminal vesicle homogenate, and in the rat stomach fundus. Oxyfedrine stimulated the release of PGE and PGF2alpha from the Langendorff hearts and increased the PG biosynthesis in all organs investigated. Compared with the other drugs, oxyfedrine showed the strongest stimulation of PGI2-synthesis in the rat stomach fundus. Prenylamine depressed the PG biosynthesis in all organs investigated but increased the PGE release from Langendorff hearts. Nitroglycerin, verapamil and, to some degree, also carbochromen increased the PGI2 synthesis in rat stomach fundus. Sodium nitrite was without influence on the PG release from Langendorff hearts and on the PG biosynthesis. Papaverine did not influence the PGI2 synthesis. Independently of the PG release, oxyfedrine, prenylamine and sodium nitrite increased the adenosine efflux from the rabbit hearts.

摘要

我们研究了奥昔非君、维拉帕米、普尼拉明、亚硝酸钠、硝酸甘油、罂粟碱和卡波铬对豚鼠和家兔Langendorff心脏标本中前列腺素(PG)和腺苷释放的影响,以及对家兔心脏和肾髓质、牛精囊匀浆和大鼠胃底中PG生物合成的影响。奥昔非君刺激Langendorff心脏释放PGE和PGF2α,并增加所有研究器官中的PG生物合成。与其他药物相比,奥昔非君对大鼠胃底中PGI2合成的刺激作用最强。普尼拉明抑制所有研究器官中的PG生物合成,但增加Langendorff心脏中PGE的释放。硝酸甘油、维拉帕米以及在一定程度上卡波铬增加大鼠胃底中PGI2的合成。亚硝酸钠对Langendorff心脏中PG的释放和PG生物合成无影响。罂粟碱不影响PGI2的合成。与PG释放无关,奥昔非君、普尼拉明和亚硝酸钠增加家兔心脏中腺苷的流出。

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