Hawksworth G, Betts T, Crowe A, Knight R, Nyemitei-Addo I, Parry K, Petrie J C, Raffle A, Parsons A
Br J Clin Pharmacol. 1984;17 Suppl 1(Suppl 1):69S-76S. doi: 10.1111/j.1365-2125.1984.tb02431.x.
The effects of diazepam on the pharmacokinetics and pharmacodynamics of two lipophilic beta-adrenoceptor antagonists (propranolol and metoprolol) and a hydrophilic beta-adrenoceptor antagonist (atenolol) were compared in 12 subjects. Administration of propranolol and metoprolol produced small increases in the AUC0-8h for diazepam compared with placebo (P less than 0.05 for metoprolol). Atenolol had no significant effect on the AUC0-8h for diazepam. The increase in the AUC0-8h was accompanied by increases in the plasma concentrations of N-desmethyldiazepam. Diazepam had no significant effect on the pharmacokinetics of either propranolol or atenolol. The pharmacokinetic interaction could be attributed to inhibition of diazepam metabolism by the lipophilic beta-adrenoceptor antagonists. The pharmacodynamic studies showed that when compared with placebo or atenolol there was a significant impairment of kinetic visual acuity (KVA) when diazepam was co-administered with metoprolol. Although there was a significant correlation (P less than 0.02) between plasma concentrations of diazepam and impairment of KVA, the pharmacodynamic interactions may not be due solely to the small pharmacokinetic interaction observed.
在12名受试者中比较了地西泮对两种亲脂性β-肾上腺素能拮抗剂(普萘洛尔和美托洛尔)以及一种亲水性β-肾上腺素能拮抗剂(阿替洛尔)的药代动力学和药效学的影响。与安慰剂相比,普萘洛尔和美托洛尔的给药使地西泮的AUC0-8h略有增加(美托洛尔P<0.05)。阿替洛尔对地西泮的AUC0-8h无显著影响。AUC0-8h的增加伴随着N-去甲基地西泮血浆浓度的升高。地西泮对普萘洛尔或阿替洛尔的药代动力学均无显著影响。药代动力学相互作用可归因于亲脂性β-肾上腺素能拮抗剂对地西泮代谢的抑制。药效学研究表明,与安慰剂或阿替洛尔相比,地西泮与美托洛尔合用时,动态视力(KVA)有显著损害。尽管地西泮血浆浓度与KVA损害之间存在显著相关性(P<0.02),但药效学相互作用可能并非仅由观察到的微小药代动力学相互作用所致。