Anxiety disorders and obsessive-compulsive disorder (OCD) are disabling psychiatric conditions and the major contributors to global burden of nonfatal illness. The lifetime prevalence of anxiety disorders in adults under 60 years ranged from approximately 30-35%, whereas the lifetime prevalence of in the general population is estimated at 2-3% for full OCD but over 25% for OCD symptoms. OCD is characterized by uncontrollable, reoccurring thoughts (called obsessions) and/or ritualized, repetitive behaviors (compulsions) that are aimed at getting rid of the obsessions and seeking relief from the anxiety caused by obsessions, indicating a close correlation between anxiety and OCD. Indeed, anxiety disorders have been reported epidemiologically as the most frequent comorbid conditions with OCD. Therefore, common pathologies may be present in anxiety disorders and OCD, and elucidation of the shared neural substrates will lead to greater insight into their pathophysiology and treatment.
In a study recently published in PNAS, Dr. Jing-Ning Zhu’s group in Nanjing University reports that a glutamatergic neuronal circuitry from the prelimbic prefrontal cortex (PrL) to the nucleus accumbens (NAc) core is responsible for co-occurrence of anxiety- and obsessive-compulsive-like behaviors. Notably, activation of the histamine presynaptic H3 heteroreceptor localized in the PrL-NAc glutamatergic terminals ameliorates stress-induced anxiety and obsessive-compulsive-like behaviors.
The nucleus accumbens (NAc) is a well-known brain structure in the basal ganglia limbic loop, which is critical for the emotional and motivational regulation. Deep brain stimulation (DBS) targeting the NAc core has been found to improve obsessive-compulsive symptoms and decrease ratings of anxiety in patients suffering from treatment-resistant OCD or depression. In previous studies, Jing-Ning Zhu’s group has reported that DBS can induce an increase in histamine release in the subthalamic nucleus to alleviate Parkinsonian motor deficits. Here, they create a new transgenic rat strain expressing Cre recombinase in the histamine-producing neurons, restrictedly localized in the tuberomammillary nucleus of the hypothalamus, and find that selective optogenetic activation of histaminergic afferent inputs in the NAc core remarkably improves anxiety as well as obsessive-compulsive-like behaviors induced by restraint stress. The amelioration effects of histamine on anxiety and obsessive-compulsive-like behaviors are mediated by the suppression of glutamatergic rather than GABAercigc transmission in the NAc core via presynaptic H3 heteroreceptors. Although the authors reveal that histamine H3 presynaptic receptor is expressed and localized in the glutamatergic terminals in NAc core from the PrL, basolateral amygdala, and ventral hippocampus, only the PrL-NAc pathway is the circuit mediating the co-occurrence of anxiety- and obsessive-compulsive-like behaviors. Chemogenetic inhibition of the PrL-NAc glutamatergic circuit significantly prevents the anxiogenic and obsessive-compulsive-like behaviors induced by acute restraint stress. Interestingly, microinjection of histamine or selective H3 receptor agonist RAMH locally into the NAc core alleviates both anxiety- and obsessive-compulsive-like phenotypes induced by optogenetic activation of PrL-NAc glutamatergic circuit.
Effective pharmacological interventions for the comorbidity of anxiety and OCD are still lacking. Presynaptic histamine H3 receptor, selectively acting on glutamatergic neurotransmission, may provide a potential target for the treatment of anxiety and OCD. Notably, several agonists for H3 receptor, including RAMH and its prodrugs, have entered clinical trials and been proved safe. Therefore, developing strategies, such as pharmacological and/or DBS therapy, for targeting H3 receptor/histaminergic afferents in the NAc core or PrL-NAc glutamatergic circuit may pave a new path for clinical treatment of anxiety disorders and OCD.
The researchers of this project include Xiao-Yang Zhang, Shi-Yu Peng, Li-Ping Shen, Qian-Xing Zhuang, Bin Li, Shu-Tao Xie, Qian-Xiao Li, Ming-Run Shi, Tian-Yu Ma, Qipeng Zhang, Jian-Jun Wang, and Jing-Ning Zhu of State Key Laboratory of Pharmaceutical Biotechnology and Department of Physiology, School of Life Sciences, and Institute for Brain Sciences, Nanjing University, 163 Xianlin Avenue, Nanjing 210023, China. The work was supported by the grants 32030044, 31961160724, 81671107, 81971263, 31600834 and 31500848 from the National Natural Science Foundation of China; and the grants BK20190008 and BK20180057 from the Natural Science Foundation of Jiangsu Province, China.
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