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β-肾上腺素能受体阻滞剂与血脑屏障

beta-Adrenoreceptor-blocking agents and the blood-brain barrier.

作者信息

Cruickshank J M, Neil-Dwyer G, Cameron M M, McAinsh J

出版信息

Clin Sci (Lond). 1980 Dec;59 Suppl 6:453s-455s. doi: 10.1042/cs059453s.

Abstract
  1. Sixteen neurosurgical patients received (oral) beta-adrenoreceptor-blocking agents (beta-receptor blockers) for 3-22 days. 2. Lipophilic beta-receptor blockers (propranolol) and metoprolol appeared in cerebrospinal fluid at concentrations similar to the free drug plasma concentration. 3. Cerebrospinal fluid concentrations of beta-receptor blockers were poor predictors of brain concentrations. 4. Both lipophilic beta-receptor blockers appeared in high concentrations in the brain: the brain/plasma ratio was approximately 15:1. 5. Hydrophilic atenolol appeared at low concentrations in brain tissue (about 20 times lower than the lipophilic beta-receptor blockers): the brain/plasma ratio was approximately 0.1:1. 6. Central nervous system-related side effects associated mainly with lipophilic beta-receptor blockers possibly result from high brain tissue concentrations.
摘要
  1. 16名神经外科患者接受(口服)β-肾上腺素能受体阻滞剂(β受体阻滞剂)治疗3至22天。2. 亲脂性β受体阻滞剂(普萘洛尔)和美托洛尔在脑脊液中的浓度与游离药物血浆浓度相似。3. β受体阻滞剂的脑脊液浓度并不能很好地预测脑内浓度。4. 两种亲脂性β受体阻滞剂在脑内均以高浓度出现:脑/血浆比率约为15:1。5. 亲水性阿替洛尔在脑组织中的浓度较低(比亲脂性β受体阻滞剂低约20倍):脑/血浆比率约为0.1:1。6. 主要与亲脂性β受体阻滞剂相关的中枢神经系统副作用可能是由脑组织高浓度所致。

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