Histamine H 2 receptor deficit in glutamatergic neurons contributes to the pathogenesis of schizophrenia

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 120; no. 9; p. e2207003120
• Main Authors: Ma, Qianyi, Jiang, Lei, Chen, Han, An, Dadao, Ping, Yiting, Wang, Yujia, Dai, Haibin, Zhang, Xiangnan, Wang, Yi, Chen, Zhong, Hu, Weiwei
• Format: Journal Article
• Language: English
• Published: United States 28.02.2023
• Subjects: Animals; Histamine - metabolism; Memory, Short-Term; Mice; Neurons - metabolism; Receptors, Histamine H2; Schizophrenia; HCN channel; medial prefrontal cortex; schizophrenia; glutamatergic neuron; histamine H2 receptor
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.2207003120

Schizophrenia is a serious mental disorder, and existing antipsychotic drugs show limited efficacy and cause unwanted side effects. The development of glutamatergic drugs for schizophrenia is currently challenging. Most functions of histamine in the brain are mediated by the histamine H receptor; however, the role of the H  receptor (H R) is not quite clear, especially in schizophrenia. Here, we found that expression of H R in glutamatergic neurons of the frontal cortex was decreased in schizophrenia patients. Selective knockout of the H R gene ( ) in glutamatergic neurons ( ) induced schizophrenia-like phenotypes including sensorimotor gating deficits, increased susceptibility to hyperactivity, social withdrawal, anhedonia, and impaired working memory, as well as decreased firing of glutamatergic neurons in the medial prefrontal cortex (mPFC) in in vivo electrophysiological tests. Selective knockdown of H R in glutamatergic neurons in the mPFC but not those in the hippocampus also mimicked these schizophrenia-like phenotypes. Furthermore, electrophysiology experiments established that H R deficiency decreased the firing of glutamatergic neurons by enhancing the current through hyperpolarization-activated cyclic nucleotide-gated channels. In addition, either H R overexpression in glutamatergic neurons or H R agonism in the mPFC counteracted schizophrenia-like phenotypes in an MK-801-induced mouse model of schizophrenia. Taken together, our results suggest that deficit of H R in mPFC glutamatergic neurons may be pivotal to the pathogenesis of schizophrenia and that H R agonists can be regarded as potentially efficacious medications for schizophrenia therapy. The findings also provide evidence for enriching the conventional glutamate hypothesis for the pathogenesis of schizophrenia and improve the understanding of the functional role of H R in the brain, especially in glutamatergic neurons.