Ghaffari, M.H.* ; Schuh, K.* ; Dusel, G.* ; Frieten, D.* ; Koch, C.* ; Prehn, C. ; Adamski, J. ; Sauerwein, H.* ; Sadri, H.*
     
 
    
        
Mammalian target of rapamycin signaling and ubiquitin-proteasome-related gene expression in skeletal muscle of dairy cows with high or normal body condition score around calving.
    
    
        
    
    
        
        J. Dairy Sci. 102, 11544-11560 (2019)
    
    
    
		
		
			
				The objective of the current study was to investigate the effects of overconditioning around calving on gene expression of key components of the mammalian target of rapamycin (mTOR) pathway and ubiquitin-proteasome system (UPS) in skeletal muscle as well as the AA profiles in both serum and muscle of periparturient cows. Fifteen weeks antepartum, 38 multiparous Holstein cows were allocated to either a high body condition group (HBCS; n = 19) or a normal body condition group (NBCS; n = 19) and were fed different diets until dry-off (d -49 relative to calving) to amplify the difference. The groups were also stratified for comparable milk yields (NBCS: 10,361 +/- 302 kg; HBCS: 10,315 +/- 437 kg). At dry-off, the NBCS cows (parity: 2.42 +/- 1.84; body weight: 665 +/- 64 kg) had a body condition score (BCS) <3.5 and backfat thickness (BFT) <1.2 cm, whereas the HBCS cows (parity: 3.37 +/- 1.67; body weight: 720 +/- 57 kg) had a BCS >3.75 and BFT >1.4 cm. During the dry period and the subsequent lactation, both groups were fed identical diets but maintained the BCS and BFT differences. Blood samples and skeletal muscle biopsies (semitendinosus) were repeatedly (d -49, +3, +21, and +84 relative to calving) collected for assessing the concentrations of free AA and the mRNA abundance of various components of mTOR and UPS. The differences in BCS and BFT were maintained throughout the study. The circulating concentrations of most AA with the exception of Gly, Gin, Met, and Phe increased in early lactation in both groups. The serum concentrations of Ala (d +21 and -184) and Orn (d +84) were lower in HBCS cows than in NBCS cows, but those of Gly, His, Leu, Val, Lys, Met, and Orn on d -49 and Ile on d +21 were greater in HBCS cows than in NBCS cows. The serum concentrations of 3-methylhistidine, creatinine, and 3-methylhistidine:creatinine ratio increased after calving (d +3) but did not differ between the groups. The muscle concentrations of all AA (except for Cys) remained unchanged over time and did not differ between groups. The muscle concentrations of Cys were greater on d -49 but tended to be lower on d +21 in HBCS cows than in NBCS cows. On d +21, TrITOR and eukaryotic translation initiation factor 4E binding protein 1 mRNA abundance was greater in HBCS cows than in NBCS cows, whereas ribosomal protein S6 kinase 1 was not different between the groups. The mRNA abundance of ubiquitin-activating enzyme 1 (d +21), ubiquitin-conjugating enzyme 1 (d +21), atrogin-1 (d +21), and ring finger protein-1 (d +3) enzymes was greater in HBCS cows than in NBCS cows, whereas ubiquitin-conjugating enzyme 2 was not different between the groups. The increased mRNA abundance of key components of mTOR signaling and of muscle-specific ligases of HBCS cows may indicate a simultaneous activation of anabolic and catabolic processes and thus increased muscle protein turnover, likely as a part of the adaptive response to prevent excessive loss of skeletal muscle mass during early lactation.
			
			
				
			
		 
		
			
				
					
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
    
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        Herausgeber
        
    
    
        Schlagwörter
        Mammalian Target Of Rapamycin ; Ubiquitin-proteasome System ; Body Condition Score ; Transition Cow; Free Amino-acids; Early Lactation; Energy-balance; Dry Period; Proteolytic Pathway; Tissue Mobilization; Fat Mobilization; Metabolic Status; Milk-production; Up-regulation
    
 
    
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        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2019
    
 
    
        Prepublished im Jahr 
        
    
 
    
        HGF-Berichtsjahr
        2019
    
 
    
    
        ISSN (print) / ISBN
        0022-0302
    
 
    
        e-ISSN
        1525-3198
    
 
    
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	    Band: 102,  
	    Heft: 12,  
	    Seiten: 11544-11560 
	    Artikelnummer: ,  
	    Supplement: ,  
	
    
 
  
        
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            Elsevier
        
 
        
            Verlagsort
            Ste 800, 230 Park Ave, New York, Ny 10169 Usa
        
 
	
        
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        Begutachtungsstatus
        Peer reviewed
    
 
     
    
        POF Topic(s)
        
30201 - Metabolic Health
    
 
    
        Forschungsfeld(er)
        
Genetics and Epidemiology
    
 
    
        PSP-Element(e)
        A-630440-001
G-500600-001
    
 
    
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        Erfassungsdatum
        2019-10-14