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腰椎脑脊液中的受体占有率作为阿替洛尔、美托洛尔和普萘洛尔在中枢神经系统中拮抗活性的一种衡量指标。

Receptor occupancy in lumbar CSF as a measure of the antagonist activity of atenolol, metoprolol and propranolol in the CNS.

作者信息

Kaila T, Marttila R

机构信息

Department of Clinical Pharmacology, University of Turku, Finland.

出版信息

Br J Clin Pharmacol. 1993 May;35(5):507-15. doi: 10.1111/j.1365-2125.1993.tb04177.x.

Abstract
  1. The antagonist activity of atenolol, metoprolol and propranolol in the CNS was estimated by determining the extent to which the drugs occupy animal beta 1- and beta 2-receptors in CSF ex vivo at the time of lumbar puncture. 2. Five CSF and plasma samples were obtained 4 h after drug intake from subjects treated for hypertension with atenolol, 100 mg once daily and five from subjects treated with metoprolol, 50 mg three times daily. Twenty-four samples were obtained 1, 2, 4 or 12 h after drug intake from subjects receiving a single 40 mg dose of propranolol. 3. The receptor occupancy in the samples was determined by adding beta 1-receptors of rabbit lung and beta 2-receptors of rat reticulocytes into the samples and labeling the receptors with a nonselective beta-adrenoceptor antagonist, (-)-[3H]-CGP-12177. 4. Atenolol and metoprolol occupied, as expected, larger fractions of beta 1- than beta 2-receptors in CSF and plasma samples. The receptor fraction occupied by atenolol in CSF was significantly (P < 0.05) lower than that occupied by metoprolol. The differences in occupancy between the drugs in plasma, however, were not statistically significant. 5. Propranolol occupied larger fractions of beta 2- than beta 1-receptors in the samples. Although propranolol concentrations in CSF were only 1/20-1/40 of those in plasma, the receptor occupancy of propranolol in CSF was similar to that in plasma.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 通过在腰椎穿刺时离体测定药物占据动物脑脊液中β1和β2受体的程度,评估阿替洛尔、美托洛尔和普萘洛尔在中枢神经系统中的拮抗活性。2. 从每日一次服用100mg阿替洛尔治疗高血压的受试者中,在服药4小时后采集5份脑脊液和血浆样本;从每日三次服用50mg美托洛尔治疗的受试者中,同样在服药4小时后采集5份样本。从单次服用40mg普萘洛尔的受试者中,在服药1、2、4或12小时后采集24份样本。3. 通过向样本中加入兔肺的β1受体和大鼠网织红细胞的β2受体,并用非选择性β肾上腺素能受体拮抗剂(-)-[3H]-CGP-12177标记受体,来测定样本中的受体占有率。4. 正如预期的那样,在脑脊液和血浆样本中,阿替洛尔和美托洛尔占据β1受体的比例大于β2受体。阿替洛尔在脑脊液中占据的受体比例显著低于美托洛尔(P<0.05)。然而,药物在血浆中占有率的差异无统计学意义。5. 在样本中,普萘洛尔占据β2受体的比例大于β1受体。尽管脑脊液中普萘洛尔的浓度仅为血浆中的1/20 - 1/40,但普萘洛尔在脑脊液中的受体占有率与血浆中的相似。(摘要截断于250字)

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