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新型α1肾上腺素能受体拮抗剂双苄基异喹啉的血流动力学效应:与哌唑嗪在自发性高血压和正常血压Wistar-Kyoto大鼠中的比较

Haemodynamic effects of dicentrine, a novel alpha 1-adrenoceptor antagonist: comparison with prazosin in spontaneously hypertensive and normotensive Wistar-Kyoto rats.

作者信息

Yu S M, Hsu S Y, Ko F N, Chen C C, Huang Y L, Huang T F, Teng C M

机构信息

Pharmacological Institute, College of Medicine, National Taiwan University, Taipei.

出版信息

Br J Pharmacol. 1992 Aug;106(4):797-801. doi: 10.1111/j.1476-5381.1992.tb14415.x.

Abstract
  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.6. These results suggest that dicentrine may have therapeutic potential as an oral antihypertensive drug via alpha-adrenoceptor blockade.
摘要
  1. 研究了从植物乌药中分离得到的阿朴啡衍生物双苄基异喹啉的血流动力学效应,并在大鼠中与哌唑嗪进行了比较。2. 在麻醉的正常血压Wistar-Kyoto(WKY)大鼠中,静脉注射双苄基异喹啉(0.1、0.5、1.0mg/kg)和哌唑嗪(0.01、0.05、0.1mg/kg)可引起平均动脉压(MAP)的剂量相关性降低,注射后5-10分钟达到最大效应,并持续2小时。3. 在麻醉的WKY大鼠中,较高剂量的双苄基异喹啉(1.0mg/kg,静脉注射)对心率(HR)、心输出量(CO)和每搏输出量(SV)没有引起任何显著变化,但显著增加了尾血流量。相比之下,较高剂量的哌唑嗪(0.1mg/kg,静脉注射)使HR降低,这与降压反应的时间进程平行。4. 双苄基异喹啉的降压活性通过α-肾上腺素受体阻断完全消除。双苄基异喹啉和哌唑嗪均显著减弱对去甲肾上腺素的升压反应,但即使在最大降压剂量下,也未能损害血管紧张素II或血管加压素的升压作用。这些观察结果表明,双苄基异喹啉似乎通过α1-肾上腺素受体阻断发挥其降压作用。5. 在清醒的正常血压和自发性高血压(SH)大鼠中,双苄基异喹啉(0.5-2.0mg/kg,静脉注射)和哌唑嗪(0.05-0.2mg/kg,静脉注射)也引起MAP的剂量相关性降低,在SH大鼠中降低幅度更大。给清醒的SH大鼠口服双苄基异喹啉(5和8mg/kg)产生了持续超过15小时的降压作用。6. 这些结果表明,双苄基异喹啉作为一种通过α-肾上腺素受体阻断的口服抗高血压药物可能具有治疗潜力。

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