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前列腺素E2、I2和F2α、花生四烯酸及吲哚美辛对清醒大鼠去甲肾上腺素升压反应的影响

Effects of prostaglandins E2, I2 and F2 alpha, arachidonic acid and indomethacin on pressor responses to norepinephrine in conscious rats.

作者信息

Okuno T, Kondo K, Suzuki H, Saruta T

出版信息

Prostaglandins. 1980 Jun;19(6):855-64. doi: 10.1016/0090-6980(80)90119-7.

Abstract

The effects of prostaglandins E2 (PGE2), I2 (PGI2) and F2 alpha (PGF2 alpha), arachidonic acid and indomethacin on pressor responses to norepinephrine were examined in conscious rats. Intravenously infused PGE2, (0.3, 1.25 micrograms/kg/min), PGI2 (50, 100 ng/kg/min), PGF2 alpha (1.8, 5.4 micrograms/kg/min) and arachidonic acid (0.7, 1.4 mg/kg/min) did not change the basal blood pressure. Both PGE2 and PGI2 significantly attenuated pressor responses to norepinephrine, whereas PGF2 alpha significantly potentiated them. Arachidonic acid, a precursor of the prostaglandings (PGs), significantly attenuated pressor responses to norepinephrine. Since the attenuating effect of arachidonic acid was completely abolished by the pretreatment with indomethacin (5 mg/kg), arachidonic acid is thought to exert an effect through its conversion to PGs. On the contrary, intravenously injected indomethacin (0.2--5.0 mg/kg) facilitated pressor responses to norepinephrine in a dose-related manner without any direct effect on the basal blood pressure. These results suggest that endogenous PGs may participate in the regulation of blood pressure by modulating pressor responses to norepinephrine in conscious rats.

摘要

在清醒大鼠中研究了前列腺素E2(PGE2)、I2(PGI2)和F2α(PGF2α)、花生四烯酸和吲哚美辛对去甲肾上腺素升压反应的影响。静脉输注PGE2(0.3、1.25微克/千克/分钟)、PGI2(50、100纳克/千克/分钟)、PGF2α(1.8、5.4微克/千克/分钟)和花生四烯酸(0.7、1.4毫克/千克/分钟)均未改变基础血压。PGE2和PGI2均显著减弱对去甲肾上腺素的升压反应,而PGF2α则显著增强该反应。花生四烯酸作为前列腺素(PGs)的前体,显著减弱对去甲肾上腺素的升压反应。由于吲哚美辛(5毫克/千克)预处理可完全消除花生四烯酸的减弱作用,因此认为花生四烯酸通过转化为PGs发挥作用。相反,静脉注射吲哚美辛(0.2 - 5.0毫克/千克)以剂量相关方式促进对去甲肾上腺素的升压反应,且对基础血压无任何直接影响。这些结果表明,内源性PGs可能通过调节清醒大鼠对去甲肾上腺素的升压反应参与血压调节。

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