Marwood J F, Stokes G S
Clin Exp Pharmacol Physiol. 1984 Mar-Apr;11(2):125-32. doi: 10.1111/j.1440-1681.1984.tb00249.x.
Ketanserin, 0.01-3.0 mg/kg i.v., was found to cause a dose-related fall in blood pressure in anaesthetized rats. However, these decreases were only significant after 1 and 3 mg/kg doses. Subsequent administration of prazosin, 0.2 mg/kg i.v., had no significant effect on blood pressure. In the presence of ketanserin 3 mg/kg, plus prazosin 0.2 mg/kg, adenosine caused a significant dose-dependent fall in blood pressure in anaesthetized rats. Methysergide, 1 mg/kg i.v., significantly attenuated the blood pressure responses to serotonin in anaesthetized rats whereas ketanserin (1 and 3 mg/kg) had no overall effect on serotonin responses. Ketanserin, 1 and 3 mg/kg i.v., was found to antagonize the pressor effects of phenylephrine and reverse the pressor effects of adrenaline in anaesthetized rats. Responses to angiotensin II were not significantly affected by ketanserin. These results suggest that ketanserin lowers blood pressure in anaesthetized rats by blockade of alpha-adrenoceptors.
在麻醉大鼠中,发现静脉注射0.01 - 3.0毫克/千克的酮色林会导致血压呈剂量依赖性下降。然而,只有在剂量为1毫克/千克和3毫克/千克时,这些血压下降才具有显著性。随后静脉注射0.2毫克/千克的哌唑嗪,对血压没有显著影响。在存在3毫克/千克酮色林和0.2毫克/千克哌唑嗪的情况下,腺苷在麻醉大鼠中引起显著的剂量依赖性血压下降。静脉注射1毫克/千克的甲基麦角新碱能显著减弱麻醉大鼠对血清素的血压反应,而酮色林(1毫克/千克和3毫克/千克)对血清素反应总体上没有影响。静脉注射1毫克/千克和3毫克/千克的酮色林能拮抗麻醉大鼠中去氧肾上腺素的升压作用,并逆转肾上腺素的升压作用。酮色林对血管紧张素II的反应没有显著影响。这些结果表明,酮色林通过阻断α-肾上腺素能受体降低麻醉大鼠的血压。