Lee R J, Evans D B, Baky S H, Laffan R J
Eur J Pharmacol. 1975 Sep-Oct;33(2):371-82. doi: 10.1016/0014-2999(75)90182-x.
SQ 11725 was approximately 1/3 as potent as propranolol in blocking the stimulant effects of isoproterenol in vitro, but was 2-4 times more potent than propranolol in blocking the diastolic blood-pressure and heart-rate responses, respectively, to isoproterenol in vivo. SQ 11725 had no depressant effects on contractile force of isolated guinea pig atrial muscle at the largest bath concentration studied (1000 mug/ml), whereas propranolol caused significant depression at a concentration of 1-10 mug/ml. Propranolol was at least 20-30 times more depressant than SQ 11725 to canine myocardium in vivo. SQ 11725 was more effective then propranolol in inhibiting tachycardic responses to treadmill exercise in unanesthetized dogs. The duration of blockade of the heart-rate response to exercise or to isoproterenol administration in the unanesthetized dog was approximately 5 times greater with SQ 11725 than with propranolol.
SQ 11725在体外阻断异丙肾上腺素的兴奋作用时,其效力约为普萘洛尔的1/3,但在体内分别阻断异丙肾上腺素引起的舒张压和心率反应时,其效力比普萘洛尔强2至4倍。在所研究的最大浴槽浓度(1000微克/毫升)下,SQ 11725对离体豚鼠心房肌的收缩力没有抑制作用,而普萘洛尔在浓度为1至10微克/毫升时会引起显著抑制。在体内,普萘洛尔对犬心肌的抑制作用至少比SQ 11725强20至30倍。在未麻醉的犬中,SQ 11725在抑制对跑步机运动的心动过速反应方面比普萘洛尔更有效。在未麻醉的犬中,SQ 11725对运动或给予异丙肾上腺素引起的心率反应的阻断持续时间比普萘洛尔长约5倍。