Hines Rochelle M, Aquino Elaine A, Khumnark Matthew I, Dávila Maria P, Hines Dustin J
Department of Psychology, Psychological and Brain Sciences & Interdisciplinary Neuroscience Programs, University of Nevada, Las Vegas, Las Vegas, NV, United States.
Front Pharmacol. 2022 Apr 4;13:750554. doi: 10.3389/fphar.2022.750554. eCollection 2022.
Network communication in the CNS relies upon multiple neuronal and glial signaling pathways. In addition to synaptic transmission, other organelles such as mitochondria play roles in cellular signaling. One highly conserved mitochondrial signaling mechanism involves the 18 kDa translocator protein (TSPO) of the outer mitochondrial membrane. Originally, TSPO was identified as a binding site for benzodiazepines in the periphery. It was later discovered that TSPO is found in mitochondria, including in CNS cells. TSPO is implicated in multiple cellular processes, including the translocation of cholesterol and steroidogenesis, porphyrin transport, cellular responses to stress, inflammation, and tumor progression. Yet the impacts of modulating TSPO signaling on network activity and behavioral performance have not been characterized. In the present study, we assessed the effects of TSPO modulators PK11195, Ro5-4864, and XBD-173 via electroencephalography (EEG) and the open field test (OFT) at low to moderate doses. Cortical EEG recordings revealed increased power in the δ and θ frequency bands after administration of each of the three modulators, as well as compound- and dose-specific changes in α and γ. Behaviorally, these compounds reduced locomotor activity in the OFT in a dose-dependent manner, with XBD-173 having the subtlest behavioral effects while still strongly modulating the EEG. These findings indicate that TSPO modulators, despite their diversity, exert similar effects on the EEG while displaying a range of sedative/hypnotic effects at moderate to high doses. These findings bring us one step closer to understanding the functions of TSPO in the brain and as a target in CNS disease.
中枢神经系统中的网络通信依赖于多种神经元和神经胶质细胞信号通路。除了突触传递外,线粒体等其他细胞器也在细胞信号传导中发挥作用。一种高度保守的线粒体信号机制涉及线粒体外膜的18 kDa转位蛋白(TSPO)。最初,TSPO被确定为外周苯二氮䓬类药物的结合位点。后来发现TSPO存在于线粒体中,包括中枢神经系统细胞中。TSPO参与多种细胞过程,包括胆固醇转运和类固醇生成、卟啉运输、细胞对应激、炎症和肿瘤进展的反应。然而,调节TSPO信号对网络活动和行为表现的影响尚未得到明确。在本研究中,我们通过脑电图(EEG)和旷场试验(OFT)评估了低至中等剂量的TSPO调节剂PK11195、Ro5-4864和XBD-173的作用。皮层脑电图记录显示,给予这三种调节剂中的每一种后,δ和θ频段的功率增加,以及α和γ频段的复合物和剂量特异性变化。在行为上,这些化合物以剂量依赖的方式降低了旷场试验中的运动活动,XBD-173的行为影响最轻微,但仍能强烈调节脑电图。这些发现表明,TSPO调节剂尽管具有多样性,但对脑电图有相似的影响,同时在中高剂量时表现出一系列镇静/催眠作用。这些发现使我们更接近于了解TSPO在大脑中的功能以及作为中枢神经系统疾病的一个靶点。