Morpurgo C, Faini D, Falcone A
Naunyn Schmiedebergs Arch Pharmacol. 1975;290(4):335-46. doi: 10.1007/BF00499947.
Phentolamine, dihydroergocristine and isoxsuprine were compared for their effects on the blood pressure in anaesthetized normotensive rats, in rats made hypotensive by ganglionic blockade or by pithing and in rats with noradrenaline-induced hypertension. Their ability to inhibit pressor responses elicited by electrical stimulation of the posterior hypothalamus and of the sympathetic outflow from the spinal cord was also investigated. All three drugs appeared very potent in inhibiting noradrenaline-induced hypertension and caused a dose-dependent fall in blood pressure in normotensive rats, which however was less pronounced with dihydroergocristine than with phentolamine and isoxsuprine. In hypotensive rats, dihydroergocristine caused a rise in blood pressure. At higher doses than those required to block noradrenaline-induced hypertension, the three drugs inhibited pressor responses elicited by electrical stimulation and were equally active on peripherally- and centrally-evoked responses. Simultaneous recording of heart rate and blood pressure, both in anaesthetized and in pithed rats, indicated a reflex origin for phentolamine-induced tachycardia and a direct cardiac stimulation for isoxsuprine. Reflex changes of heart rate were not observed with dihydroergocristine.
对酚妥拉明、双氢麦角汀和异克舒令在麻醉的正常血压大鼠、通过神经节阻断或脊髓破坏造成低血压的大鼠以及去甲肾上腺素诱导高血压的大鼠中对血压的影响进行了比较。还研究了它们抑制由下丘脑后部电刺激和脊髓交感神经传出引起的升压反应的能力。所有这三种药物在抑制去甲肾上腺素诱导的高血压方面似乎都非常有效,并且在正常血压大鼠中引起剂量依赖性的血压下降,然而双氢麦角汀引起的下降不如酚妥拉明和异克舒令明显。在低血压大鼠中,双氢麦角汀使血压升高。在高于阻断去甲肾上腺素诱导的高血压所需剂量时,这三种药物抑制电刺激引起的升压反应,并且对外周和中枢诱发的反应同样有效。在麻醉大鼠和脊髓破坏大鼠中同时记录心率和血压表明,酚妥拉明诱导的心动过速起源于反射,而异克舒令对心脏有直接刺激作用。双氢麦角汀未观察到心率的反射性变化。