Nakagawa Y, Takeda K, Hashimoto T, Sakurai H, Mitomi A, Imai S, Hamamura M, Kumada M
Nihon Yakurigaku Zasshi. 1981 Mar;77(3):295-312.
Effects of an antihypertensive drug, guanfacine, on blood pressure and heart rate were studied in comparison with findings in a related drug, clonidine. Conscious rats (normotensive rat, SHR, DOCA-hypertensive rat and renal hypertensive rat), anesthetized rats and pithed rats were used. Effects of guanfacine resembled those of clonidine but were about 10 times less potent. Both drugs produced an initial transient increase in blood pressure and a prolonged decrease then followed. In the SHR, a decrease in blood pressure occurred. The vasopressor effect of guanfacine was inhibited by phentolamine (1 mg/kg i.v.) and potentiated after previous treatment of the rats with reserpine (5 mg/kg i.p. 24 hr prior to drug administration, indicating that the effect was produced through activation of peripheral alpha-adrenoceptors. The vasodepressor effect of guanfacine was clearly dose-dependent, and was more marked when the initial level of the blood pressure was high, while that of clonidine was dose-dependent, only within a limited dosage range. Vasodepressor effects of guanfacine were associated with a decrease in the efferent discharges of the renal sympathetic nerve. Guanfacine, when given intracisternally produced a greater fall of blood pressure and a greater inhibition of the renal nerve activity than when given intravenously. It is concluded that the antihypertensive effects of guanfacine are due to stimulation of alpha-adrenoceptors within the central nervous system.
研究了抗高血压药物胍法辛对血压和心率的影响,并与相关药物可乐定的研究结果进行了比较。使用了清醒大鼠(正常血压大鼠、自发性高血压大鼠、去氧皮质酮高血压大鼠和肾性高血压大鼠)、麻醉大鼠和脊髓横断大鼠。胍法辛的作用与可乐定相似,但效力约低10倍。两种药物均先引起血压短暂升高,随后出现持续降低。在自发性高血压大鼠中,出现了血压下降。胍法辛的升压作用可被酚妥拉明(1毫克/千克静脉注射)抑制,在用利血平(给药前24小时腹腔注射5毫克/千克)预处理大鼠后增强,表明该作用是通过激活外周α-肾上腺素能受体产生的。胍法辛的降压作用明显呈剂量依赖性,且在血压初始水平较高时更为显著,而可乐定的降压作用仅在有限的剂量范围内呈剂量依赖性。胍法辛的降压作用与肾交感神经传出放电减少有关。胍法辛脑池内给药比静脉给药引起的血压下降更大,对肾神经活动的抑制更强。得出的结论是,胍法辛的降压作用是由于刺激了中枢神经系统内的α-肾上腺素能受体。