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早期和中期帕金森病患者的腺苷 A 受体可用性。

Adenosine A receptor availability in patients with early- and moderate-stage Parkinson's disease.

机构信息

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.

出版信息

J Neurol. 2023 Jan;270(1):300-310. doi: 10.1007/s00415-022-11342-1. Epub 2022 Sep 2.

Abstract

INTRODUCTION

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.

METHODS

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.

RESULTS

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).

CONCLUSION

Our results imply regional and disease stage-dependent changes in A receptor signaling in PD pathophysiology and in response to dopaminergic medication.

摘要

简介

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。

方法

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。

结果

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)。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad78/9813038/8f7ac942af3b/415_2022_11342_Fig1_HTML.jpg

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