Rabey J M, Oberman Z, Scharf M, Isakov M, Bar M, Graff E
Department of Neurology and Chemical Pathology, Ichilov Hospital, Sackler School of Medicine, Tel-Aviv University, Israel.
Acta Neurol Scand. 1990 May;81(5):411-5. doi: 10.1111/j.1600-0404.1990.tb00986.x.
We recently demonstrated that when different drugs (mainly used for the treatment of Parkinson's disease) are administered in combination they interfere with the availability of bromocriptine in the brain of rats (striatum and hypothalamus). In the present study performed with parkinsonian patients, we measured plasma levels of bromocriptine (RIA) over 4 h after giving orally 5 mg bromocriptine alone; together with levodopa 250 mg plus 25 mg DCI (10 patients); with 100 mg amantadine HCl (5 patients) and with biperiden 5 mg (5 patients). Amantadine and biperiden did not interfere with the pharmacokinetics of bromocriptine. However, levodopa significantly diminished plasma levels (a mean increment of 1.78 mg +/- 0.30 vs 0.92 +/- 0.18 mg/ml). We postulate that levodopa may interfere with the metabolism of bromocriptine in the liver. Although we did not observe substantial clinical differences among the patients (Webster scale), this study supports our previous findings and suggests that one of the advantages of combined treatment may result from a modification of the plasma levels of bromocriptine by levodopa. A "smoothing" of the plasma bromocriptine curve possibly avoids sudden oscillations of the drug availability and enables a more "stable" penetrability of the medication into the central nervous system.
我们最近证明,当联合使用不同药物(主要用于治疗帕金森病)时,它们会干扰大鼠脑内(纹状体和下丘脑)溴隐亭的可利用性。在对帕金森病患者进行的本研究中,我们在单独口服5毫克溴隐亭后4小时内测量了血浆溴隐亭水平(放射免疫分析法);与左旋多巴250毫克加25毫克脱羧酶抑制剂(10例患者)联合使用;与100毫克盐酸金刚烷胺(5例患者)联合使用;与5毫克安坦(5例患者)联合使用。金刚烷胺和安坦不干扰溴隐亭的药代动力学。然而,左旋多巴显著降低了血浆水平(平均增量为1.78毫克±0.30对0.92±0.18毫克/毫升)。我们推测左旋多巴可能会干扰溴隐亭在肝脏中的代谢。虽然我们在患者中未观察到显著的临床差异(韦伯斯特量表),但本研究支持我们之前的发现,并表明联合治疗的优势之一可能源于左旋多巴对溴隐亭血浆水平的改变。血浆溴隐亭曲线的“平滑”可能避免了药物可利用性的突然波动,并使药物进入中枢神经系统的穿透性更“稳定”。