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New perspective on sustained antidepressant effect: focus on neurexins regulating synaptic plasticity

Yuan Ruan, Ruolan Yuan, Jiaqi He, Yutong Jiang, Shifeng Chu, Nai‐hong Chen

Cell Death Discovery May 1, 2024 DOI: 10.1038/s41420-024-01974-9 via OpenAlex

Summary

AI-generated from the abstract

Depression is common, but current medications often have low response rates and short-lasting effects, especially when depression co-occurs with other disorders and progresses to major depressive disorder. Recent research highlights ketamine and psilocybin as potential sustained antidepressants. A review of studies indicates that changes in synaptic plasticity are key to long-lasting antidepressant effects. Neurexins, molecules that regulate synaptic plasticity, are critical links between plasticity and sustained antidepressant effects, involving mechanisms such as protein level changes, selective splicing, epigenetics, astrocytes, positional redistribution, and protein structure. Drugs targeting neurexin-regulated plasticity show promise for sustained antidepressant development, representing a highly promising future direction.

Study at a glance

Characteristics Review Peer reviewed
Interventions Ketamine Psilocybin
Topics Neuroplasticity
Keywords Neuroscience Antidepressant Metaplasticity
Citations 11
Key finding Neurexins, through their regulation of synaptic plasticity, are critical links between synaptic plasticity and sustained antidepressant effects.

Abstract

Abstract Depression is highly prevalent globally, however, currently available medications face challenges such as low response rates and short duration of efficacy. Additionally, depression mostly accompany other psychiatric disorders, further progressing to major depressive disorder without long-term effective management. Thus, sustained antidepressant strategies are urgently needed. Recently, ketamine and psilocybin gained attention as potential sustained antidepressants. Review of recent studies highlights that synaptic plasticity changes as key events of downstream long-lasting changes in sustained antidepressant effect. This underscores the significance of synaptic plasticity in sustained antidepressant effect. Moreover, neurexins, key molecules involved in the regulation of synaptic plasticity, act as critical links between synaptic plasticity and sustained antidepressant effects, involving mechanisms including protein level, selective splicing, epigenetics, astrocytes, positional redistribution and protein structure. Based on the regulation of synaptic plasticity by neurexins, several drugs with potential for sustained antidepressant effect are also discussed. Focusing on neurexins in regulating synaptic plasticity promises much for further understanding underlying mechanisms of sustained antidepressant and the next step in new drug development. This research represents a highly promising future research direction.

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