Abrahamsson T, Lignell E, Mikulski A, Olovson S G, Regårdh C G
Hässle Research Laboratories, Department of Pharmacology, Mölndal, Sweden.
Drug Metab Dispos. 1989 Jan-Feb;17(1):82-6.
Beagle dogs with catheters chronically implanted into the lateral cerebral ventricle were used to study the distribution of atenolol and metoprolol between the cerebrospinal fluid (CSF) and blood plasma over a 24-hr period during long term treatment. The concentration of atenolol declined more slowly in CSF than in blood plasma and the CSF/plasma ratio of atenolol (after iv administration for 7 days) increased from 0.08 +/- 0.02 (2 hr after dose) to 0.83 +/- 0.14 (24 hr after dose) (mean +/- SD). Furthermore, the CSF concentration of atenolol, relative to the plasma concentration, increased during repeated drug administration. The CSF/plasma ratio 24 hr after an iv dose was 0.48 +/- 0.12 on day 1 and 0.83 +/- 0.14 on day 7. The CSF concentration of the more lipophilic beta 1-adrenoceptor antagonist metoprolol was almost the same as the concentration of the drug in blood plasma. After 7 days of oral treatment, the CSF/plasma ratio of metoprolol 24 hr after dosing was 0.81 +/- 0.10. The regional CSF concentration of atenolol along the neuraxis was determined in anaesthetized dogs after acute iv administration of the drug. The atenolol concentration in CSF from the lateral cerebral ventricle was similar to that in the cisterna magna but lower than the concentration in CSF sampled from the lumbar region. It is concluded that the CSF concentration of the moderately lipophilic beta 1-adrenoceptor antagonist metoprolol equilibrates with the plasma concentration of the drug more rapidly compared with the hydrophilic drug atenolol.
将导管长期植入侧脑室的比格犬被用于研究在长期治疗的24小时期间,阿替洛尔和美托洛尔在脑脊液(CSF)和血浆之间的分布情况。阿替洛尔在脑脊液中的浓度下降速度比在血浆中慢,阿替洛尔的脑脊液/血浆比值(静脉给药7天后)从给药后2小时的0.08±0.02增加到给药后24小时的0.83±0.14(平均值±标准差)。此外,在重复给药期间,相对于血浆浓度,阿替洛尔的脑脊液浓度增加。静脉给药后24小时的脑脊液/血浆比值在第1天为0.48±0.12,在第7天为0.83±0.14。亲脂性更强的β1肾上腺素能受体拮抗剂美托洛尔的脑脊液浓度与血浆中药物浓度几乎相同。口服治疗7天后,给药后24小时美托洛尔的脑脊液/血浆比值为0.81±0.10。在急性静脉注射药物后,对麻醉犬沿神经轴的阿替洛尔脑脊液区域浓度进行了测定。侧脑室脑脊液中的阿替洛尔浓度与小脑延髓池中的相似,但低于从腰椎区域采集的脑脊液中的浓度。结论是,与亲水性药物阿替洛尔相比,亲脂性适中的β1肾上腺素能受体拮抗剂美托洛尔的脑脊液浓度与药物血浆浓度达到平衡的速度更快。