首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Haemodynamic effects of dicentrine a novel alpha 1-adrenoceptor antagonist: comparison with prazosin in spontaneously hypertensive and normotensive Wistar-Kyoto rats.
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Haemodynamic effects of dicentrine a novel alpha 1-adrenoceptor antagonist: comparison with prazosin in spontaneously hypertensive and normotensive Wistar-Kyoto rats.

机译:Dicentrine(一种新型的α1肾上腺素能受体拮抗剂)的血流动力学效应:与自发性高血压和正常血压Wistar-Kyoto大鼠的哌唑嗪比较。

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摘要

1. The haemodynamic effects of dicentrine, an aporphine derivative isolated from the plant Lindera megaphylla, were investigated and compared with prazosin in rats. 2. In anaesthetized normotensive Wistar-Kyoto (WKY) rats, i.v. administration of dicentrine (0.1, 0.5, 1.0 mg kg-1) and prazosin (0.01, 0.05, 0.1 mg kg-1) induced a dose-related reduction of mean arterial pressure (MAP) which reached a maximal effect 5-10 min after injection and persisted for 2 h. 3. In anaesthetized WKY rats, a higher dose of dicentrine (1.0 mg kg-1, i.v.) did not cause any significant changes in heart rate (HR), cardiac output (CO) and stroke volume (SV) but markedly increased tail blood flow. In contrast, a higher dose of prazosin (0.1 mg kg-1, i.v.) produced a decrease in HR which paralleled the time course of the hypotensive response. 4. The hypotensive activity of dicentrine was completely abolished by alpha-adrenoceptor blockade. Both dicentrine and prazosin significantly attenuated pressor responses to noradrenaline but failed, even at maximal hypotensive doses, to impair the pressor effects of angiotensin II or vasopressin. These observations suggest that dicentrine appears to exert its hypotensive action through alpha 1-adrenoceptor blockade. 5. In conscious normotensive and spontaneously hypertensive (SH) rats, dicentrine (0.5-2.0 mg kg-1, i.v.) and prazosin (0.05-0.2 mg kg-1, i.v.) also evoked dose-related decreases in MAP which were of greater magnitude in SH rats. Oral administration of dicentrine (5 and 8 mg kg-1) to conscious SH rats caused a hypotensive effect which persisted for over 15 h.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.研究了从植物大叶菩提树中分离出的一种海豚碱衍生物Dicentrine对大鼠的血流动力学作用,并将其与哌唑嗪进行了比较。 2.在麻醉的血压正常的Wistar-Kyoto(WKY)大鼠中,静脉注射。施用dicentrine(0.1,0.5,1.0 mg kg-1)和prazosin(0.01,0.05,0.1 mg kg-1)引起剂量相关的平均动脉压(MAP)降低,在5-10分钟后达到最大作用注射并持续2 h。 3.在麻醉的WKY大鼠中,较高剂量的百安定(1.0 mg kg-1,iv)不会引起心率(HR),心输出量(CO)和中风量(SV)的任何显着变化,但尾血显着增加流。相反,更高剂量的哌唑嗪(0.1mg kg-1,i.v。)导致HR降低,这与降压反应的时间过程平行。 4.α-肾上腺素受体阻滞剂完全消除了Dicentrine的降压活性。 dicentrine和prazosin都显着减弱了对去甲肾上腺素的升压反应,但即使在最大降压剂量下也未能减弱血管紧张素II或加压素的升压作用。这些观察结果表明,敌草碱似乎通过α1-肾上腺素受体的阻滞发挥其降压作用。 5.在有意识的血压正常和自发性高血压(SH)大鼠中,地辛那汀(0.5-2.0 mg kg-1,iv)和哌唑嗪(0.05-0.2 mg kg-1,iv)也引起MAP的剂量相关性降低,这更大SH大鼠的数量级。对清醒的SH大鼠口服给予dicentrine(5和8 mg kg-1)会引起降压作用,持续15小时以上(摘要截断为250个单词)

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