Lefer A M, Lefer D J, Levin R J
Adv Shock Res. 1980;3:167-74.
Two new beta-adrenergic blocking agents, timolol and MK-761, were found to effectively antagonize the positive inotropic effects of isoproterenol on isolated cat papillary muscles without depressing contractile force. However, appropriate doses of these beta-adrenergic blockers (ie, 12.5--25 microgram/kg) did not significantly prolong survival in hemorrhagic shock in anesthetized cats. MK-761 prevented some of the plasma accumulations of myocardial depressant factor (MDF) during shock. Nevertheless both beta-blockers failed to prevent the accumulation of the lysosomal protease cathepsin D or peptide fragments (ie, amino-nitrogen groups) in the blood during shock. We conclude that neither agent is of significant benefit in severe hemorrhagic shock, and probably beta-adrenergic blockade is not a productive approach to pursue in the therapeutics of hemorrhagic shock.
发现两种新型β-肾上腺素能阻滞剂——噻吗洛尔和MK-761,可有效拮抗异丙肾上腺素对离体猫乳头肌的正性肌力作用,而不降低收缩力。然而,这些β-肾上腺素能阻滞剂的适当剂量(即12.5 - 25微克/千克)并未显著延长麻醉猫失血性休克的存活时间。MK-761可防止休克期间心肌抑制因子(MDF)的一些血浆蓄积。尽管如此,两种β-阻滞剂均未能防止休克期间血液中溶酶体蛋白酶组织蛋白酶D或肽片段(即氨基氮基团)的蓄积。我们得出结论,这两种药物在严重失血性休克中均无显著益处,并且β-肾上腺素能阻断可能不是失血性休克治疗中值得追求的有效方法。