Neil-Dwyer G, Bartlett J, McAinsh J, Cruickshank J M
Br J Clin Pharmacol. 1981 Jun;11(6):549-53. doi: 10.1111/j.1365-2125.1981.tb01169.x.
1 This study on 21 neurosurgical patients was set up to investigate the extent to which four chronically administered beta-adrenoceptor blockers, propranolol, oxprenolol, metoprolol and atenolol, cross and blood-brain barrier and enter the cerebrospinal fluid (CSF) and brain tissue. The concentration in the CSF of the three lipophilic beta-adrenoceptor blockers, propranolol, oxprenolol and metoprolol, approximated to the free drug concentration in the plasma, and was a poor predictor of brain concentration. These three lipophilic beta-adrenoceptor blockers appeared in brain tissue at concentrations 10-20 times greater than that of hydrophilic atenolol. The approximate brain/plasma ratio for propranolol was 26, for oxprenolol 50, for metoprolol 12 and for atenolol 0.2. 2 The low concentration of atenolol in brain tissue is possibly responsible for the low incidence of central nervous system-related side effects in patients on this agent compared to lipophilic beta-adrenoceptor blockers.
1 这项针对21名神经外科患者的研究旨在调查四种长期使用的β-肾上腺素受体阻滞剂(普萘洛尔、氧烯洛尔、美托洛尔和阿替洛尔)穿过血脑屏障并进入脑脊液(CSF)和脑组织的程度。三种亲脂性β-肾上腺素受体阻滞剂(普萘洛尔、氧烯洛尔和美托洛尔)在脑脊液中的浓度接近血浆中的游离药物浓度,且对脑内浓度的预测性较差。这三种亲脂性β-肾上腺素受体阻滞剂在脑组织中的浓度比亲水性阿替洛尔高10 - 20倍。普萘洛尔的脑/血浆比值约为26,氧烯洛尔为50,美托洛尔为12,阿替洛尔为0.2。2 与亲脂性β-肾上腺素受体阻滞剂相比,阿替洛尔在脑组织中的低浓度可能是使用该药物的患者中枢神经系统相关副作用发生率较低的原因。