PUBLICATION
            Plasticity of tyrosine hydroxylase and serotonergic systems in the regenerating spinal cord of adult zebrafish
- Authors
- Kuscha, V., Barreiro-Iglesias, A., Becker, C.G., and Becker, T.
- ID
- ZDB-PUB-110811-38
- Date
- 2012
- Source
- The Journal of comparative neurology 520(5): 933-951 (Journal)
- Registered Authors
- Barreiro-Iglesias, Antón, Becker, Catherina G., Becker, Thomas, Kuscha, Veronika
- Keywords
- regeneration, 5-HT, tyrosine hydroxylase, sonic hedgehog, neurogenesis
- MeSH Terms
- 
    
        
        
            
                - Age Factors
- Animals
- Neuronal Plasticity/physiology*
- Serotonergic Neurons/enzymology
- Serotonergic Neurons/metabolism*
- Serotonergic Neurons/pathology
- Tyrosine 3-Monooxygenase/genetics
- Tyrosine 3-Monooxygenase/metabolism*
- Animals, Genetically Modified
- Zebrafish
- Spinal Cord Regeneration*/genetics
- Swimming/physiology
- Spinal Cord Injuries/enzymology
- Spinal Cord Injuries/metabolism*
- Spinal Cord Injuries/pathology
 
- PubMed
- 21830219 Full text @ J. Comp. Neurol.
            Citation
        
        
            Kuscha, V., Barreiro-Iglesias, A., Becker, C.G., and Becker, T. (2012) Plasticity of tyrosine hydroxylase and serotonergic systems in the regenerating spinal cord of adult zebrafish. The Journal of comparative neurology. 520(5):933-951.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Monoaminergic innervation of the spinal cord has important modulatory functions for locomotion. Here we performed a quantitative study to determine the plastic changes of tyrosine hydroxylase positive (TH1+; mainly dopaminergic), and serotonergic (5-HT+) terminals and cells during successful spinal cord regeneration in adult zebrafish. TH1+ innervation in the spinal cord is derived from the brain. After spinal cord transection, TH1+ immunoreactivity is completely lost from the caudal spinal cord. Terminal varicosities increase in density rostral to the lesion site compared to unlesioned controls and are re-established in the caudal spinal cord at 6 weeks post-lesion. Interestingly, axons mostly fail to re-innervate to more caudal levels of the spinal cord even after prolonged survival times. However, densities of terminal varicosities correlate with recovery of swimming behavior, which is completely lost again after re-lesion of the spinal cord. Similar observations were made for terminals derived from descending 5-HT+ axons from the brain. In addition, spinal 5-HT+ neurons were newly-generated after a lesion and transiently increased in number up to 5-fold, which depended in part on hedgehog signaling. Overall, TH1+ and 5-HT+ innervation is massively altered in the successfully regenerated spinal cord of adult zebrafish. Despite these changes in TH and 5-HT systems, a remarkable recovery of swimming capability is achieved, suggesting significant plasticity of the adult spinal network during regeneration.
            
    
        
        
    
    
    
                
                    
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