Department of Psychiatry, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Neurosci. 2010 Dec 1;30(48):16284-92. doi: 10.1523/JNEUROSCI.2590-10.2010.
Adenosine A(2a) receptor antagonists reduce symptom severity in Parkinson disease (PD) and animal models. Rodent studies support the hypothesis that A(2a) antagonists produce this benefit by reducing the inhibitory output of the basal ganglia indirect pathway. One way to test this hypothesis in humans is to quantify regional pharmacodynamic responses with cerebral blood flow (CBF) imaging. That approach has also been proposed as a tool to accelerate pharmaceutical dose finding, but has not yet been applied in humans to drugs in development. We successfully addressed both these aims with a perfusion magnetic resonance imaging (MRI) study of the novel adenosine A(2a) antagonist SYN115. During a randomized, double-blind, placebo-controlled, crossover study in 21 PD patients on levodopa but no agonists, we acquired pulsed arterial spin labeling MRI at the end of each treatment period. SYN115 produced a highly significant decrease in thalamic CBF, consistent with reduced pallidothalamic inhibition via the indirect pathway. Similar decreases occurred in cortical regions whose activity decreases with increased alertness and externally focused attention, consistent with decreased self-reported sleepiness on SYN115. Remarkably, we also derived quantitative pharmacodynamic parameters from the CBF responses to SYN115. These results suggested that the doses tested were on the low end of the effective dose range, consistent with clinical data reported separately. We conclude that (1) SYN115 enters the brain and exerts dose-dependent regional effects, (2) the most prominent of these effects is consistent with deactivation of the indirect pathway as predicted by preclinical studies; and (3) perfusion MRI can provide rapid, quantitative, clinically relevant dose-finding information for pharmaceutical development.
腺苷 A(2a)受体拮抗剂可减轻帕金森病 (PD) 患者的症状严重程度,也可改善动物模型的 PD 症状。啮齿类动物研究支持这样一种假说,即 A(2a)拮抗剂通过减少基底神经节间接通路的抑制性输出从而产生这种益处。在人类中检验这一假说的一种方法是使用脑血流 (CBF) 成像来量化区域性药效反应。这种方法也被提议作为一种工具来加速药物剂量发现,但尚未在开发中的药物的人类研究中应用。我们使用新型腺苷 A(2a)拮抗剂 SYN115 的灌注磁共振成像 (MRI) 研究成功地实现了这两个目标。在 21 名正在服用左旋多巴但未服用激动剂的 PD 患者的随机、双盲、安慰剂对照交叉研究中,我们在每个治疗期结束时采集脉冲动脉自旋标记 MRI。SYN115 可显著降低丘脑 CBF,这与间接通路中苍白球丘脑抑制作用的降低一致。皮质区域也出现了类似的降低,其活动随着警觉性和外部注意力的增加而降低,这与 SYN115 降低自我报告的嗜睡程度一致。值得注意的是,我们还从 SYN115 对 CBF 反应中得出了定量药效动力学参数。这些结果表明,所测试的剂量处于有效剂量范围的低端,与单独报告的临床数据一致。我们得出结论:(1)SYN115 进入大脑并产生剂量依赖性的区域性效应;(2)其中最显著的效应与临床前研究预测的间接通路失活一致;(3)灌注 MRI 可为药物开发提供快速、定量、与临床相关的剂量发现信息。