5-羟色胺能                        
                
                                
                        
                            神经退行性变                        
                
                                
                        
                            疾病                        
                
                                
                        
                            神经科学                        
                
                                
                        
                            医学                        
                
                                
                        
                            痴呆                        
                
                                
                        
                            肌萎缩侧索硬化                        
                
                                
                        
                            失智症                        
                
                                
                        
                            生物信息学                        
                
                                
                        
                            生物                        
                
                                
                        
                            血清素                        
                
                                
                        
                            病理                        
                
                                
                        
                            受体                        
                
                                
                        
                            内科学                        
                
                        
                    
            作者
            
                Alina Brüge,Evgeni Ponimaskin,Josephine Labus            
         
                    
            出处
            
                                    期刊:Pharmacological Reviews
                                                         [American Society for Pharmacology and Experimental Therapeutics]
                                                        日期:2025-05-28
                                                        卷期号:77 (5): 100071-100071
                                                 
         
        
    
            
            标识
            
                                    DOI:10.1016/j.pharmr.2025.100071
                                    
                                
                                 
         
        
                
            摘要
            
            More than 65 million people worldwide experience neurodegenerative diseases, such as Alzheimer disease, frontotemporal dementia, Parkinson disease, and amyotrophic lateral sclerosis. As the risk of developing these diseases increases with age, increasing life expectancy will further accelerate their prevalence. Despite major advances in the understanding of the molecular mechanisms of neurodegeneration, no curative therapy is available to date. Neurodegenerative diseases are known to be associated with alterations in serotonergic neurotransmission, which might critically contribute to the pathogenesis of these diseases. Therefore, targeting the serotonergic system appears to be a promising therapeutic approach. In this review, we provide a comprehensive overview of pathological changes in serotonergic neurotransmission in different neurodegenerative diseases and discuss novel treatment strategies based on targeted modulation of the serotonergic system. We primarily focus on the therapeutic approaches modulating serotonin homeostasis, its biosynthesis, and the modulation of defined serotonin receptors. SIGNIFICANCE STATEMENT: A common feature of multiple neurodegenerative diseases is dysregulation of the serotonergic system at the cellular, molecular, and genetic levels that strongly contributes to specific pathological phenotypes. Targeting these alterations represents a suitable therapeutic strategy to combat disease-relevant pathomechanisms, slow down disease progression, and overcome pathological consequences.
         
            
 
                 
                
                    
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