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吲哚美辛对清醒家兔中肼苯哒嗪诱导的肾素和儿茶酚胺释放的影响。

Effect of indomethacin on hydralazine-induced renin and catecholamine release in the conscious rabbit.

作者信息

Campbell W B, Graham R M, Jackson E K, Loisel D P, Pettinger W A

出版信息

Br J Pharmacol. 1980;71(2):529-31. doi: 10.1111/j.1476-5381.1980.tb10968.x.

Abstract
  1. The effects of hydralazine on mean arterial pressure (MAP) heart rate (HR), plasma renin activity (PRA) and plasma catecholamines were examined in conscious rabbits before and after prostaglandin synthesis inhibition with indomethacin. 2. Hydralazine (3 mg/kg. i.v.) produced a 12% decrease in MAP and significant increases in HR, PRA and plasma noradrenaline and adrenaline. 3. Indomethacin (5 mg/kg, s.c.) failed to alter significantly the control MAP, HR, PRA or plasma catecholamines but inhibited renal venous prostaglandin E2 by 56% (P less than 0.02). 4. Indomethacin inhibited the hydralazine-induced tachycardia by 24% and augmented its hypotensive effects by 6%. 5. The hydralazine-stimulated increase in PRA was also inhibited 75% (P less than 0.001) by indomethacin whereas noradrenaline and adrenaline concentrations were not significantly reduced. 6. Indomethacin inhibits hydralazine-induced renin release in the presence of elevated concentrations of plasma catecholamines; these findings suggest that renal prostaglandins function as important mediators of sympathetically-induced renin release.
摘要
  1. 在使用吲哚美辛抑制前列腺素合成之前和之后,研究了肼屈嗪对清醒家兔平均动脉压(MAP)、心率(HR)、血浆肾素活性(PRA)和血浆儿茶酚胺的影响。2. 肼屈嗪(3毫克/千克,静脉注射)使MAP降低了12%,并使HR、PRA、血浆去甲肾上腺素和肾上腺素显著增加。3. 吲哚美辛(5毫克/千克,皮下注射)未能显著改变对照的MAP、HR、PRA或血浆儿茶酚胺,但使肾静脉前列腺素E2降低了56%(P<0.02)。4. 吲哚美辛使肼屈嗪诱导的心动过速降低了24%,并使其降压作用增强了6%。5. 吲哚美辛还使肼屈嗪刺激的PRA增加受到75%的抑制(P<0.001),而去甲肾上腺素和肾上腺素浓度没有显著降低。6. 在血浆儿茶酚胺浓度升高的情况下,吲哚美辛抑制肼屈嗪诱导的肾素释放;这些发现表明,肾前列腺素作为交感神经诱导的肾素释放的重要介质发挥作用。

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