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吲哚美辛可减弱卡托普利的急性血流动力学和激素效应。

Acute haemodynamic and hormonal effects of captopril are diminished by indomethacin.

作者信息

Witzgall H, Hirsch F, Scherer B, Weber P C

出版信息

Clin Sci (Lond). 1982 Jun;62(6):611-5. doi: 10.1042/cs0620611.

Abstract
  1. The acute haemodynamic and hormonal effects of 100 mg of captopril (SQ 14.225) orally were tested in twelve healthy men in the sodium replete state before and after indomethacin pretreatment. 2. Without indomethacin, mean arterial blood pressure was reduced at 30 and 60 min after captopril (P less than 0.02). Heart rate did not change during the whole experiment. Although plasma renin activity (PRA) increased (P less than 0.002), plasma and urinary aldosterone and plasma 18-hydroxycorticosterone (18-OH-B) decreased after captopril (P less than 0.02). Prostaglandin (PG) E2, sodium and potassium excretion rates remained constant after captopril. 3. Under indomethacin pretreatment, the fall in mean arterial blood pressure was less than without indomethacin at 30 and 60 min after captopril (P less than 0.05). Heart rate was constantly lower than without indomethacin during the whole experiment (P less than 0.05). Indomethacin pretreatment decreased basal PGE2 excretion (P less than 0.02) and baseline PRA as well as the increase in PRA after captopril (P less than 0.05). Control mineralocorticoid levels were significantly lower than without indomethacin. In indomethacin-pretreated subjects, aldosterone did not further decrease after captopril, and 18-OH-B fell only slightly. 4. Without indomethacin pretreatment a significant, positive correlation was found between PRA values before captopril and the maximum decrease of mean arterial blood pressure after captopril. Under indomethacin pretreatment this correlation was no longer demonstrable. The results suggest that prostaglandins may contribute to the haemodynamic and hormonal actions of captopril.
摘要
  1. 对12名处于钠充足状态的健康男性,在吲哚美辛预处理前后口服100毫克卡托普利(SQ 14.225),测试其急性血液动力学和激素效应。2. 未用吲哚美辛时,卡托普利给药后30和60分钟平均动脉血压降低(P<0.02)。整个实验过程中心率未变。虽然血浆肾素活性(PRA)升高(P<0.002),但卡托普利给药后血浆和尿醛固酮以及血浆18 - 羟皮质酮(18 - OH - B)降低(P<0.02)。卡托普利给药后前列腺素(PG)E2、钠和钾排泄率保持恒定。3. 在吲哚美辛预处理下,卡托普利给药后30和60分钟平均动脉血压的下降幅度小于未用吲哚美辛时(P<0.05)。整个实验过程中心率持续低于未用吲哚美辛时(P<0.05)。吲哚美辛预处理降低了基础PGE2排泄(P<0.02)以及基线PRA和卡托普利给药后PRA的升高幅度(P<0.05)。对照盐皮质激素水平显著低于未用吲哚美辛时。在吲哚美辛预处理的受试者中,卡托普利给药后醛固酮未进一步降低,18 - OH - B仅略有下降。4. 未用吲哚美辛预处理时,发现卡托普利给药前的PRA值与卡托普利给药后平均动脉血压的最大下降幅度之间存在显著正相关。在吲哚美辛预处理下,这种相关性不再明显。结果表明,前列腺素可能参与了卡托普利的血液动力学和激素作用。

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