Azuma M, Yamane M, Tachibana K, Morimoto Y, Kemmotsu O
Department of Anaesthesiology and Critical Care Medicine, Hokkaido University Graduate School of Medicine, N-15, W-7, Kita-ku, Sapporo 060-8638, Japan.
Br J Anaesth. 2003 Jan;90(1):66-71.
This study was designed to investigate the effects of epinephrine and the phosphodiesterase III inhibitors amrinone and milrinone on bupivacaine-induced myocardial depression in guinea-pig papillary muscles using an electrophysiological method.
Electrophysiological studies of the effects of bupivacaine, epinephrine, amrinone and milrinone in normal and high K(+) Tyrode's solution were measured with guinea-pig papillary muscles. Specifically, epinephrine, amrinone and milrinone reversal of bupivacaine-induced depression was measured.
Bupivacaine reduced the action potential duration (APD), the maximum rate of rise of the AP (V(max)) and contractile force. Although epinephrine increased the contractile force similarly to amrinone and milrinone, it shortened the APD at 50% repolarization (APD(50)) and 90% repolarization (APD(90)). A high concentration of amrinone shortened APD, while milrinone did not affect APD except for a prolongation of APD(20). In high K(+) Tyrode's solution (25 mM), epinephrine, amrinone and milrinone increased the APD and the contractile force. Epinephrine reversed bupivacaine depression of APD and contractile force to control levels. Amrinone and milrinone restored not only the contractile force but also APD. There was an incomplete recovery of APD(50) for amrinone and the prolongation of APD(20) for milrinone.
Our results suggest that bupivacaine decreases the Ca(+) current (I(Ca)) and Na(+) current (I(Na)). Epinephrine and amrinone may increase I(Ca) and the delayed outward current (I(k)), whereas milrinone may increase I(Ca). The profound cardiovascular depression caused by bupivacaine was effectively reversed by amrinone and milrinone in a manner similar to epinephrine.
本研究旨在采用电生理方法,研究肾上腺素以及磷酸二酯酶III抑制剂氨力农和米力农对布比卡因所致豚鼠乳头肌心肌抑制的影响。
使用豚鼠乳头肌,在正常和高钾(K⁺)台氏液中测量布比卡因、肾上腺素、氨力农和米力农作用的电生理研究。具体而言,测量肾上腺素、氨力农和米力农对布比卡因所致抑制的逆转作用。
布比卡因缩短动作电位时程(APD)、动作电位最大上升速率(Vmax)以及收缩力。尽管肾上腺素与氨力农和米力农类似地增加收缩力,但它缩短了复极化50%(APD50)和复极化90%(APD90)时的APD。高浓度氨力农缩短APD,而米力农除了延长APD20外对APD无影响。在高钾(25 mM)台氏液中,肾上腺素、氨力农和米力农增加APD和收缩力。肾上腺素将布比卡因对APD和收缩力的抑制作用逆转至对照水平。氨力农和米力农不仅恢复了收缩力,还恢复了APD。氨力农对APD50的恢复不完全,米力农则使APD20延长。
我们的结果提示,布比卡因降低钙电流(ICa)和钠电流(INa)。肾上腺素和氨力农可能增加ICa和延迟外向电流(Ik),而米力农可能增加ICa。氨力农和米力农以与肾上腺素类似的方式有效逆转了布比卡因所致的严重心血管抑制。