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ARS Home » Northeast Area » Beltsville, Maryland (BARC) » Beltsville Agricultural Research Center » Animal Genomics and Improvement Laboratory » Research » Publications at this Location » Publication #302999

Research Project: Understanding Genetic and Physiological Factors Affecting Nutrient Use Efficiency of Dairy Cattle

Location: Animal Genomics and Improvement Laboratory

Title: Comparative glycolysis and Krebs cycle metabolism of the bovine and murine mammary gland determined with [13C6] glucose and mass spectrometry

Author
item Juengst, Leslie - University Of Maryland
item Connor, Erin
item Baldwin, Ransom - Randy
item Bequette, Brian - University Of Maryland

Submitted to: Meeting Abstract
Publication Type: Abstract Only
Publication Acceptance Date: 2/20/2014
Publication Date: 7/20/2014
Citation: Juengst, L.J., Connor, E.E., Baldwin, R.L., Bequette, B.J. 2014. Comparative glycolysis and Krebs cycle metabolism of the bovine and murine mammary gland determined with [13C6] glucose and mass spectrometry. Journal of Dairy Science. 97(E-Suppl. 1):613. Abstract W146.

Interpretive Summary:

Technical Abstract: The compositions of bovine and murine milk differ significantly with respect to the proportions of lactose, protein, and fat. To better understand the metabolic origins of this difference, we interrogated the crossroads of glycolysis and the Krebs cycle in the mammary gland of cows and mice using a glucose stable isotope tracer approach in vitro. Mammary tissue was collected from mid-lactation dairy cows (n=4) and day 15 of lactation mice (n=6) then sliced to form explants (0.5 mm thick, 100-150 mg). Explants were incubated for 3 h (5% CO2) at 37°C in DMEM containing a 50:50 mix of unlabeled and [13C6] labeled glucose at 2.5, 5, 7.5 or 10 mM concentrations. Following incubation, tissue slices were rinsed in PBS and stored at -80°C. Intracellular metabolites were extracted and derivatized for determination of 13C-isotopomer enrichments employing gas chromatography-mass spectrometry. Alanine, glutamate, and aspartate 13C-isotopomer enrichments were monitored as representative surrogates of their Krebs cycle counterparts pyruvate, a-ketoglutarate, and oxaloacetate, respectively. These data provided the inputs to calculate glycolytic and Krebs cycle fluxes. In bovine explants, increasing media glucose concentration increased glycolytic flux as represented by an increasing contribution of glucose to pyruvate flux. However, the proportion of pyruvate derived from glucose catabolism reached a plateau (44-46%) at 7.5 mM glucose. Murine mammary tissue also increased glycolytic rate with increasing media glucose though no plateau was attained and glucose contributed to 43% of pyruvate flux at the highest glucose concentration. Krebs cycle flux was assessed by the relative activities of pyruvate dehydrogenase (PDH) vs. pyruvate carboxylase (PC) based on [13C] tracer kinetics. For bovine mammary explants, PDH flux activity increased with glucose to a maximum at 5.0 mM glucose whereas PDH vs PC activities of murine mammary explants was not responsive to glucose concentration. The current study suggests that the dairy cow mammary gland shifts from high anapleurotic flux rates into the Krebs cycle towards energy-producing (oxidative) fluxes with increasing glucose while the murine mammary gland maintains a more rigid metabolic balance, and thus is less adaptive to glucose availability.