Garbizu Maider, Mocha-Muñoz Naroa, Rubio-López Esther, Palacios Laura, Aguado Laura, Ardaya María, Joya Ana, Alduntzin Unai, Plaza-García Sandra, Padro Daniel, Gómez-Vallejo Vanessa, Cossío Unai, Higuchi Makoto, Ramos-Cabrer Pedro, Zugaza José Luis, Llop Jordi, Martín Abraham
Achucarro Basque Center for Neuroscience, Leioa, Spain.
CIC biomaGUNE, Basque Research and Technology Alliance, San Sebastian, Spain.
J Cereb Blood Flow Metab. 2025 Sep 8:271678X251370835. doi: 10.1177/0271678X251370835.
Adenosine A receptors (AARs) have shown promising therapeutic properties despite their controversial role in modulating stroke outcome. However, the temporal evolution of cerebral AARs density after cerebral ischemia and its subsequent neuroinflammatory response have been scarcely explored. In this study, the expression of AARs after transient middle cerebral artery occlusion (MCAO) was evaluated in rats by positron emission tomography (PET) with [C]SCH442416 and immunohistochemistry (IHC). In addition, the role of AARs in stroke inflammation with pharmacological modulation was assessed with magnetic resonance imaging (MRI), PET imaging with [F]DPA-714 (TSPO), IHC, western-blot, and autoradiography. After cerebral ischemia, [C]SCH442416 and IHC revealed neural expression of AARs in the striatum in healthy brains, followed by a binding decrease at day 1 and a subsequent significant increase at day 3 after ischemia in microglia and infiltrated leukocytes. Furthermore, activation of AARs with the agonist CGS-21680 resulted in a reduction in stroke volume, along with an increase in TSPO expression in immune cells in the striatum. Our results provide novel evidence on AARs density dynamics after cerebral ischemia that might guide the therapeutic management of stroke by modulating adenosine receptors.
尽管腺苷 A 受体(AARs)在调节中风预后中的作用存在争议,但已显示出有前景的治疗特性。然而,脑缺血后脑 AARs 密度的时间演变及其随后的神经炎症反应鲜有研究。在本研究中,通过用[C]SCH442416 进行正电子发射断层扫描(PET)和免疫组织化学(IHC),评估了大鼠短暂大脑中动脉闭塞(MCAO)后 AARs 的表达。此外,通过磁共振成像(MRI)、用[F]DPA - 714(TSPO)进行 PET 成像、IHC、蛋白质印迹和放射自显影,评估了 AARs 在中风炎症中的药理学调节作用。脑缺血后,[C]SCH442416 和 IHC 显示健康大脑纹状体中 AARs 的神经表达,随后在缺血后第 1 天结合减少,在小胶质细胞和浸润白细胞中于缺血后第 3 天随后显著增加。此外,用激动剂 CGS - 21680 激活 AARs 导致中风体积减小,同时纹状体免疫细胞中 TSPO 表达增加。我们的结果为脑缺血后 AARs 密度动态提供了新证据,这可能通过调节腺苷受体来指导中风的治疗管理。