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通过无线电遥测法测定,非肽类血管紧张素Ⅱ 1型受体拮抗剂KT3 - 671重复给药对易卒中型自发性高血压大鼠血压、心率和运动活动昼夜变化的影响。

Effect of repeated administration of KT3-671, a nonpeptide AT1 receptor antagonist, on diurnal variation in blood pressure, heart rate, and locomotor activity in stroke-prone spontaneously hypertensive rats as determined by radiotelemetry.

作者信息

Kawashima K, Amano H, Fujimoto K, Suzuki T, Fujii T, Mochizuki S, Tomiyama A

机构信息

Department of Pharmacology, Kyoritsu College of Pharmacy, Minato-ku, Tokyo, Japan.

出版信息

J Cardiovasc Pharmacol. 1996 Mar;27(3):411-6. doi: 10.1097/00005344-199603000-00014.

DOI:10.1097/00005344-199603000-00014
PMID:8907803
Abstract

KT3-671, a nonpeptide AT1 receptor antagonist, was administered to 20-week-old stroke-prone spontaneously hypertensive rats (SHRSP) daily for 3 weeks. Its effects on systolic, mean, and diastolic arterial blood pressure (SAP, MAP, DAP), heart rate and locomotor activity were investigated with radiotelemetry. A clear diurnal variation in blood pressure, heart rate, and locomotor activity was observed in synchrony with the light cycle. KT3-671 at a daily dose of 10 mg/kg orally (p.o), produced a significant and consistent reduction in blood pressure, preventing the development of hypertension. KT3-671 reduced SAP more than DAP, suggesting that it may affect both vascular tone and cardiac output. Although KT3-671 did not affect diurnal rhythms in heart rate and locomotor activity, it did cause a slight but significant reduction in heart rate. The MAP determined 23 h after the administration of KT3-671 showed a significant reduction from the day 2 of therapy to the day 3 after discontinuation of therapy, suggesting a long duration of antihypertensive action. There was no rebound increase in blood pressure after discontinuation of KT3-671 therapy. These results suggest that KT3-671 may be potentially useful in the therapy of hypertension.

摘要

非肽类血管紧张素 II 1 型受体拮抗剂 KT3-671 连续 3 周每日给予 20 周龄的易中风自发性高血压大鼠(SHRSP)。通过无线电遥测技术研究其对收缩压、平均动脉压和舒张压(SAP、MAP、DAP)、心率和运动活动的影响。观察到血压、心率和运动活动存在明显的昼夜变化,与光周期同步。每日口服(p.o)剂量为 10 mg/kg 的 KT3-671 可显著且持续降低血压,预防高血压的发展。KT3-671 降低 SAP 的幅度大于 DAP,表明它可能同时影响血管张力和心输出量。虽然 KT3-671 不影响心率和运动活动的昼夜节律,但确实导致心率略有但显著降低。在给予 KT3-671 后 23 小时测定的 MAP 显示,从治疗第 2 天到停药后第 3 天有显著降低,表明降压作用持续时间长。停药后血压没有反跳性升高。这些结果表明,KT3-671 可能对高血压治疗有潜在用途。

相似文献

1
Effect of repeated administration of KT3-671, a nonpeptide AT1 receptor antagonist, on diurnal variation in blood pressure, heart rate, and locomotor activity in stroke-prone spontaneously hypertensive rats as determined by radiotelemetry.通过无线电遥测法测定,非肽类血管紧张素Ⅱ 1型受体拮抗剂KT3 - 671重复给药对易卒中型自发性高血压大鼠血压、心率和运动活动昼夜变化的影响。
J Cardiovasc Pharmacol. 1996 Mar;27(3):411-6. doi: 10.1097/00005344-199603000-00014.
2
Antihypertensive effect of repeatedly administered YM358, an angiotensin AT1-receptor antagonist, in stroke-prone spontaneously hypertensive rats.血管紧张素AT1受体拮抗剂YM358反复给药对易卒中型自发性高血压大鼠的降压作用
Jpn J Pharmacol. 1997 Jan;73(1):83-91. doi: 10.1254/jjp.73.83.
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Antihypertensive effect of chronic KT3-671, a structurally new nonpeptide angiotensin AT1-receptor antagonist, in stroke-prone spontaneously hypertensive rats.新型结构非肽类血管紧张素AT1受体拮抗剂慢性KT3-671对易卒中型自发性高血压大鼠的降压作用
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Pharmacological properties of KT3-671, a novel nonpeptide angiotensin II receptor antagonist.新型非肽类血管紧张素II受体拮抗剂KT3-671的药理特性
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KT3-671, an angiotensin AT1 receptor antagonist, attenuates vascular but not cardiac responses to sympathetic nerve stimulation in pithed rats.血管紧张素AT1受体拮抗剂KT3-671可减弱去大脑大鼠对交感神经刺激的血管反应,但不影响心脏反应。
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Circadian rhythms of blood pressure, heart rate, and locomotor activity in spontaneously hypertensive rats as measured with radio-telemetry.通过无线电遥测技术测量自发性高血压大鼠的血压、心率和运动活动的昼夜节律。
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引用本文的文献

1
The effects of KT3-671, a new angiotensin II (AT 1) receptor blocker in mild to moderate hypertension.新型血管紧张素II(AT1)受体阻滞剂KT3 - 671对轻至中度高血压的影响。
Br J Clin Pharmacol. 2003 Nov;56(5):513-9. doi: 10.1046/j.1365-2125.2003.01932.x.