Turku PET Centre, University of Turku, Itäinen Pitkäkatu 4A, 6th floor, 6007, 20520, Turku, Finland.
Division of Clinical Neurosciences, Turku University Hospital and University of Turku, Turku, Finland.
J Neurol. 2023 Jan;270(1):300-310. doi: 10.1007/s00415-022-11342-1. Epub 2022 Sep 2.
Adenosine 2A (A) receptors co-localize with dopamine Dreceptors in striatopallidal medium spiny neurons of the indirect pathway. A receptor activation in the striatum or pallidum decreases Dsignaling. In contrast, A receptor antagonism may help potentiate it. Furthermore, previous PET studies have shown increased A receptor availability in striatum of late-stage PD patients with dyskinesia. However, human in vivo evidence for striatal A receptor availability in early-stage PD is limited. This study aimed to investigate possible differences in A receptor availability in the striatum and pallidum of early- and moderate-stage PD patients without dyskinesias.
Brain MRI and PET with [C]TMSX radioligand, targeting A receptors, was performed in 9 patients with early- and 9 with moderate-stage PD without dyskinesia and in 6 healthy controls. Distribution volume ratios (DVR) were calculated to assess specific [C]TMSX binding in caudate, putamen and pallidum.
A receptor availability (DVR) was decreased in the bilateral caudate of early-stage PD patients when compared with healthy controls (P = 0.02). Conversely, DVR was increased bilaterally in the pallidum of moderate-stage PD patients compared to healthy controls (P = 0.03). Increased mean striatal DVR correlated with higher motor symptom severity ([Formula: see text] = 0.47, P = 0.02).
Our results imply regional and disease stage-dependent changes in A receptor signaling in PD pathophysiology and in response to dopaminergic medication.
腺苷 2A(A)受体与多巴胺 D 受体在间接通路的纹状体苍白球中间神经元中共定位。纹状体或苍白球中的 A 受体激活可降低 D 信号。相反,A 受体拮抗可能有助于增强它。此外,以前的 PET 研究表明,运动障碍晚期 PD 患者纹状体中的 A 受体可用性增加。然而,早期 PD 患者纹状体 A 受体可用性的人体活体证据有限。本研究旨在研究无运动障碍的早期和中期 PD 患者纹状体和苍白球中 A 受体可用性的差异。
对 9 例早期和 9 例中期无运动障碍的 PD 患者和 6 名健康对照者进行 MRI 和脑 [C]TMSX 放射性配体 PET,以靶向 A 受体。计算分布容积比(DVR)以评估尾状核、壳核和苍白球中特定 [C]TMSX 结合的情况。
与健康对照组相比,早期 PD 患者双侧尾状核的 A 受体可用性(DVR)降低(P=0.02)。相反,与健康对照组相比,中度 PD 患者双侧苍白球的 DVR 增加(P=0.03)。增加的平均纹状体 DVR 与更高的运动症状严重程度相关([Formula: see text]=0.47,P=0.02)。
我们的研究结果表明,A 受体信号在 PD 病理生理学中存在区域和疾病阶段依赖性变化,并对多巴胺能药物有反应。