Arumuham Atheeshaan, Shatalina Ekaterina, Nour Matthew M, Veronese Mattia, Onwordi Ellis Chika, Kaar Stephen J, Jauhar Sameer, Rabiner Eugenii A, Howes Oliver D
Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, Kings College London, De Crespigny Park, London, SE5 8AF, UK.
Institute of Clinical Sciences (ICS), Faculty of Medicine, Imperial College London, London, W12 0NN, UK.
Psychopharmacology (Berl). 2025 Jun;242(6):1321-1334. doi: 10.1007/s00213-024-06730-6. Epub 2024 Dec 22.
Working memory impairment is a prominent feature of schizophrenia which predicts clinical and functional outcomes. Preclinical data suggest histamine-3 receptor (H3R) expression in cortical pyramidal neurons may have a role in working memory, and post-mortem data has found disruptions of H3R expression in schizophrenia.
We examined the role of H3R in vivo to elucidate its role on working memory impairment in schizophrenia.
We used positron emission tomography (PET) with the selective H3R radioligand [C]MK-8278 to measure H3R availability, and employed a task during functional magnetic resonance imaging (fMRI) to assess working memory-evoked brain activation and cognitive task performance, in patients with schizophrenia (n = 12) and matched healthy volunteers (n = 12). We assessed the relationship between H3R availability and both task performance and working memory-evoked brain activation in regions of interest (ROIs), including the anterior cingulate cortex (ACC) and dorsolateral prefrontal cortex (DLPFC).
Patients with schizophrenia showed a strong positive correlation, after corrections for multiple comparisons, between ACC H3R availability and task performance (rho = 0.73, p = 0.007), which was absent in the control group (rho = 0.03, p = 0.94). Further ROI analysis did not find a significant relationship between H3R availability and working memory-evoked brain activation.
These results provide support for the role of H3R on working memory processes in patients with schizophrenia.
工作记忆损害是精神分裂症的一个突出特征,可预测临床和功能预后。临床前数据表明,皮质锥体神经元中的组胺3受体(H3R)表达可能在工作记忆中起作用,而尸检数据发现精神分裂症患者的H3R表达存在破坏。
我们在体内研究了H3R的作用,以阐明其在精神分裂症工作记忆损害中的作用。
我们使用正电子发射断层扫描(PET)和选择性H3R放射性配体[C]MK-8278来测量H3R可用性,并在功能磁共振成像(fMRI)期间采用一项任务来评估精神分裂症患者(n = 12)和匹配的健康志愿者(n = 12)的工作记忆诱发的大脑激活和认知任务表现。我们评估了H3R可用性与感兴趣区域(ROI)(包括前扣带回皮质(ACC)和背外侧前额叶皮质(DLPFC))的任务表现和工作记忆诱发的大脑激活之间的关系。
在进行多重比较校正后,精神分裂症患者的ACC中H3R可用性与任务表现之间存在强正相关(rho = 0.73,p = 0.007),而对照组中不存在这种相关性(rho = 0.03,p = 0.94)。进一步的ROI分析未发现H3R可用性与工作记忆诱发的大脑激活之间存在显著关系。
这些结果为H3R在精神分裂症患者工作记忆过程中的作用提供了支持。