Bruguerolle B
Laboratoire de Pharmacologie Médicale, Faculté de Médecine de Marseille, France.
Life Sci. 1993;53(21):PL349-53. doi: 10.1016/0024-3205(93)90189-a.
The purpose of this study was to investigate the influence of calcium channel blockers on bupivacaine-induced acute toxicity. For each of the three tested calcium channel blockers (diltiazem, verapamil and bepridil) 6 groups of mice were treated by two different doses, i.e. 2 and 10 mg/kg/i.p., or an equal volume of saline for the control group (n = 20); 15 minutes later, all the animals were injected with a single 50 mg/kg/i.p. dose of bupivacaine. The convulsant activity, the time of latency to convulse and the mortality rate were assessed in each group. The local anesthetic-induced mortality was significantly increased by the three different calcium channel blockers. The convulsant activity of bupivacaine was not significantly modified but calcium channel blockers decreased the time of latency to obtain bupivacaine-induced convulsions; this effect was less pronounced with bepridil.
本研究的目的是探讨钙通道阻滞剂对布比卡因所致急性毒性的影响。对于三种受试钙通道阻滞剂(地尔硫䓬、维拉帕米和苄普地尔)中的每一种,6组小鼠分别接受两种不同剂量的处理,即2和10mg/kg腹腔注射,对照组给予等体积的生理盐水(n = 20);15分钟后,所有动物均腹腔注射单次剂量50mg/kg的布比卡因。评估每组的惊厥活性、惊厥潜伏期和死亡率。三种不同的钙通道阻滞剂均显著增加了局部麻醉药所致的死亡率。布比卡因的惊厥活性没有显著改变,但钙通道阻滞剂缩短了布比卡因诱发惊厥的潜伏期;苄普地尔的这种作用不太明显。