Laustiola K, Seppälä E, Nikkari T, Vapaatalo H
J Cardiovasc Pharmacol. 1984 May-Jun;6(3):449-54. doi: 10.1097/00005344-198405000-00012.
We examined the effects of beta-blockade with the nonselective antagonist propranolol, the cardioselective antagonist atenolol, and the cardioselective antagonist with partial agonist activity, practolol, on the levels of free arachidonic acid (AA), thromboxane B2 (TxB2), prostaglandin (PG) E2, and 6-keto-PGF1 alpha in plasma, and TxB2 production by platelets during clotting in six normal subjects during submaximal dynamic exercise. The drugs were given intravenously in equipotent increasing doses before the exercise test. Exercise induced a clear increase in AA, TxB2, and 6-keto-PGF1 alpha in plasma. During the first 60 min of exercise all three beta-blockers decreased the plasma levels of AA and TxB2. Propranolol (0.19 mg/kg) was slightly more effective than atenolol (0.19 mg/kg) or practolol (0.64 mg/kg); however, at exhaustion, propranolol was markedly more effective than the other two blockers. Plasma 6-keto-PGF1 alpha and PGE2 levels were less affected by beta-blockade during exercise, and no significant effect was seen on TxB2 formation by platelets. The plasma 6-keto-PGF1 alpha/TxB2 ratio was markedly higher after propranolol treatment than after treatment with the other two blockers during the exercise period. These results suggest that the capability of a nonselective blocker to inhibit both beta 1- and beta 2-adrenergic receptors may be of advantage because of the more effective inhibition of thromboxane formation than with a cardioselective blocker, especially when the sympathetic tone is markedly increased.
我们研究了非选择性拮抗剂普萘洛尔、心脏选择性拮抗剂阿替洛尔以及具有部分激动剂活性的心脏选择性拮抗剂普拉洛尔进行β受体阻滞,对6名正常受试者在次极量动态运动期间血浆中游离花生四烯酸(AA)、血栓素B2(TxB2)、前列腺素(PG)E2和6-酮-前列腺素F1α水平,以及血小板在凝血过程中TxB2生成的影响。在运动试验前,以等效递增剂量静脉注射这些药物。运动导致血浆中AA、TxB2和6-酮-前列腺素F1α明显升高。在运动的前60分钟内,所有三种β受体阻滞剂均降低了血浆中AA和TxB2的水平。普萘洛尔(0.19mg/kg)比阿替洛尔(0.19mg/kg)或普拉洛尔(0.64mg/kg)的效果略好;然而,在运动至疲惫时,普萘洛尔的效果明显优于其他两种阻滞剂。运动期间,血浆6-酮-前列腺素F1α和PGE2水平受β受体阻滞的影响较小,且对血小板TxB2的生成未见显著影响。在运动期间,普萘洛尔治疗后血浆6-酮-前列腺素F1α/TxB2比值明显高于其他两种阻滞剂治疗后。这些结果表明,非选择性阻滞剂抑制β1和β2肾上腺素能受体的能力可能具有优势,因为与心脏选择性阻滞剂相比,它对血栓素形成的抑制作用更有效,尤其是在交感神经张力明显增加时。