möglich sobald  bei der ZB eingereicht worden ist.
		
    Aqp5--/-- mice exhibit reduced maximal O2 consumption under cold exposure, normal pulmonary gas exchange, and impaired formation of brown adipose tissue.
        
        Am. J. Physiol.-Regul. Integr. Comp. Physiol. 324, R109-R119 (2022)
    
    
    
				The fundamental body functions that determine maximal O2 uptake (VO2,max) have not been studied in Aqp5 --/-- (aquaporin 5, AQP5) mice. We measured VO2,max to globally assess these functions and then investigated why it was found altered in Aqp5 --/-- mice. VO2,max was measured by the Helox technique, which elicits maximal metabolic rate by intense cold exposure of the animals. We found VO2,max reduced in Aqp5 --/-- mice by 20 - 30% compared to WT. Since AQP5 has been implicated to act as a membrane channel for respiratory gases, we studied whether this is due to the known lack of AQP5 in the alveolar epithelial membranes of Aqp5 --/-- mice. Lung function parameters as well as arterial O2 saturation were normal and identical between Aqp5 --/-- and WT mice, indicating that AQP5 does not contribute to pulmonary O2 exchange. The cause for the decreased VO2,max thus might be found in decreased O2 consumption of an intensely O2-consuming peripheral organ such as activated BAT. We found indeed that absence of AQP5 greatly reduces the amount of interscapular BAT formed in response to 4 weeks' cold exposure, from 63% in WT to 25% in Aqp5 --/-- animals. We conclude that lack of AQP5 does not affect pulmonary O2 exchange, but greatly inhibits transformation of white to brown adipose tissue. Since under cold exposure BAT is a major source of the animals' heat production, reduction of BAT likely causes the decrease in VO2,max under this condition.
			
			
		Impact Factor
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
     
    
    
        Schlagwörter
        Aquaporin 5 ; Alveolar-capillary Barrier ; Gas Channels ; Oxygen Transport Across Membranes ; Pulmonary Diffusion Capacity; Relative Co2/nh3 Selectivities; Oxygen-consumption; Co2 Permeability; Deer Mice; Exercise; Mouse; Aquaporin-1; Peromyscus; Mitochondria; Performance
    
 
     
    
    
        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2022
    
 
     
    
        HGF-Berichtsjahr
        2022
    
 
    
    
        ISSN (print) / ISBN
        0363-6119
    
 
    
        e-ISSN
        1522-1490
    
 
     
     
     
	     
	 
	 
     
		
    
        Quellenangaben
        
	    Band: 324,  
	    Heft: 1,  
	    Seiten: R109-R119 
	    
	    
	
    
 
  
         
        
            Verlag
            American Physiological Society
        
 
        
            Verlagsort
            6120 Executive Blvd, Suite 600, Rockville, Md, United States
        
 
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Begutachtungsstatus
        Peer reviewed
    
 
     
    
        POF Topic(s)
        30202 - Environmental Health
30201 - Metabolic Health
 
    30201 - Metabolic Health
        Forschungsfeld(er)
        Lung Research
Genetics and Epidemiology
 
    Genetics and Epidemiology
        PSP-Element(e)
        G-505000-007
G-500692-001
G-500600-001
 
    G-500692-001
G-500600-001
        Förderungen
        German Federal Ministry of Education and Research
Deutsche Forschungsgemeinschaft for financial
 
     	
    
    Deutsche Forschungsgemeinschaft for financial
        WOS ID
        000950636500010
    
    
        Scopus ID
        85145022368
    
    
        PubMed ID
        36409022
    
    
        Erfassungsdatum
        2022-12-05