Experimental Determination of Net Protein Charge and A tot and K a of Nonvolatile Buffers in Canine Plasma

Acid‐base abnormalities frequently are present in sick dogs. The mechanism for an acid‐base disturbance can be determined with the simplified strong ion approach, which requires accurate values for the total concentration of plasma nonvolatile buffers ( A tot ) and the effective dissociation constant for plasma weak acids ( K a ). The aims of this study were to experimentally determine A tot and K a values for canine plasma. Plasma was harvested from 10 healthy dogs; the concentrations of quantitatively important strong ions (Na+, K+, Ca 2+ , Mg 2+ , Cl ‐ , L‐lactate) and nonvolatile buffer ions (total protein, albumin, phosphate) were determined; and the plasma was tonometered with CO 2 at 37°C. Strong ion difference (SID) was calculated from the measured strong ion concentrations, and nonlinear regression was used to estimate values for A tot and K a , which were validated with data from an in vitro and in vivo study. Mean (±SD) values for canine plasma were A tot = (17.4 ± 8.6) mM (equivalent to 0.273 mmol/g of total protein or 0.469 mmol/g of albumin); K a = (0.17±0.11) × 10 ‐7 ; p K a = 7.77. The calculated SID for normal canine plasma (pH = 7.40; PCO 2 = 37 mm Hg; [total protein] = 64 g/L) was 27 mEq/L. The net protein charge for normal canine plasma was 0.25 mEq/g of total protein or 0.42 mEq/g of albumin. Application of the experimentally determined values for A tot , K a , and net protein charge should improve understanding of the mechanism for complex acid‐base disturbances in dogs.