möglich sobald  bei der ZB eingereicht worden ist.
		
    Human muscular mitochondrial fusion in athletes during exercise.
        
        FASEB J. 33, 12087-12098 (2019)
    
    
    
				The main objective of this work was to investigate whether mitochondrial fusion occurs in the skeletal muscle of well-trained athletes in response to high-intensity exercise. Well-trained swimmers (n = 9) performed a duration-matched sprint interval training (SIT) and high-intensity high-volume training (HIHVT) session on separate days. Muscle samples from triceps brachii were taken before, immediately after, and 3 h after the training sessions. Transmission electron microscopy (TEM) was applied to assess mitochondrial morphology. Moreover, expression of genes coding for regulators of mitochondrial fusion and fission were assessed by real-time quantitative PCR. In addition, mitofusin (MFN)2 and optic atrophy 1 (OPA1) were quantified by Western blot analysis. TEM analyses showed that mitochondrial morphology remained altered for 3 h after HIHVT, whereas SIT-induced changes were only evident immediately after exercise. Only SIT increased MFN1 and MFN2 mRNA expression, whereas SIT and HIHVT both increased MFN2 protein content 3 h after exercise. Notably, only HIHVT increased OPA1 protein content. Mitochondrial morphologic changes that suggest fusion occurs in well-adapted athletes during exercise. However, HIHVT appears as a more robust inducer of mitochondrial fusion events than SIT. Indeed, SIT induces a rapid and transient change in mitochondrial morphology.
			
			
		Impact Factor
					Scopus SNIP
					Web of Science
Times Cited
					Times Cited
Scopus
Cited By
					
					Cited By
Altmetric
					
				5.391
					1.102
					12
					15
					
					
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
     
    
    
        Schlagwörter
        Physical Activity ; Mitochondrial Fission ; Skeletal Muscle ; Mitofusin 2; Human Skeletal-muscle; Membrane Interactions; Fission; Protein; Reticulum; Adaptations; Activation; Fis1
    
 
     
    
    
        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2019
    
 
     
    
        HGF-Berichtsjahr
        2019
    
 
    
    
        ISSN (print) / ISBN
        0892-6638
    
 
    
        e-ISSN
        1530-6860
    
 
     
     
     
	     
	 
	 
    
        Zeitschrift
        FASEB Journal
    
 
		
    
        Quellenangaben
        
	    Band: 33,  
	    Heft: 11,  
	    Seiten: 12087-12098 
	    
	    
	
    
 
  
         
        
            Verlag
            Wiley
        
 
        
            Verlagsort
            Bethesda, Md.
        
 
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Begutachtungsstatus
        Peer reviewed
    
 
    
        Institut(e)
        Institute of Diabetes and Obesity (IDO)
    
 
    
        POF Topic(s)
        30502 - Diabetes: Pathophysiology, Prevention and Therapy
    
 
    
        Forschungsfeld(er)
        Helmholtz Diabetes Center
    
 
    
        PSP-Element(e)
        G-553400-001
    
 
     
     	
    
    
        WOS ID
        WOS:000507461600038
    
    
        Scopus ID
        85074379719
    
    
        PubMed ID
        31398297
    
    
        Erfassungsdatum
        2019-08-13