Weak acid-concentration Atot and dissociation constant Ka of plasma proteins in racehorses.

H R Stampfli, S Misiaszek, J H Lumsden, G P Carlson, G J Heigenhauser
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Abstract

The plasma proteins are a significant contributor to the total weak acid concentration as a net anionic charge. Due to potential species difference, species-specific values must be confirmed for the weak acid anionic concentrations of proteins (Atot) and the effective dissociation constant for plasma weak acids (Ka). We studied the net anion load Atot of equine plasma protein in 10 clinically healthy mature Standardbred horses. A multi-step titration procedure, using a tonometer covering a titration range of PCO2 from 25 to 145 mmHg at 37 degrees C, was applied on the plasma of these 10 horses. Blood gases (pH, PCO2) and electrolytes required to calculate the strong ion difference ([SID] = [(Na(+) + K(+) + Ca(2+) + Mg(2+))-(Cl(-) + Lac(-) + PO4(2-))]) were simultaneously measured over a physiological pH range from 6.90-7.55. A nonlinear regression iteration to determine Atot and Ka was performed using polygonal regression curve fitting applied to the electrical neutrality equation of the physico-chemical system. The average anion-load Atot for plasma protein of 10 Standardbred horses was 14.89 +/- 0.8 mEq/l plasma and Ka was 2.11 +/- 0.50 x 10(-7) Eq/l (pKa = 6.67). The derived conversion factor (iterated Atot concentration/average plasma protein concentration) for calculation of Atot in plasma is 0.21 mEq/g protein (protein-unit: g/l). This value compares closely with the 0.24 mEq/g protein determined by titration of Van Slyke et al. (1928) and 0.22 mEq/g protein recently published by Constable (1997) for horse plasma. The Ka value compares closely with the value experimentally determined by Constable in 1997 (2.22 x 10(7) Eq/l). Linear regression of a set of experimental data from 5 Thoroughbred horses on a treadmill exercise test, showed excellent correlation with the regression lines not different from identity for the calculated and measured variables pH, HCO3 and SID. Knowledge of Atot and Ka for the horse is useful especially in exercise studies and in clinical conditions to quantify the mechanisms of the acid-base disturbances occurring.

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赛马血浆蛋白的弱酸浓度Atot和解离常数Ka。
血浆蛋白作为净阴离子电荷对总弱酸浓度有重要贡献。由于潜在的物种差异,必须确定蛋白质的弱酸阴离子浓度(Atot)和血浆弱酸的有效解离常数(Ka)的物种特异性值。我们研究了10匹临床健康成年标准种马血浆蛋白的净负离子负荷Atot。对这10匹马的血浆进行了多步滴定,使用眼压计在37摄氏度下覆盖25至145毫米汞柱的二氧化碳分压滴定范围。血气(pH、PCO2)和计算强离子差所需的电解质([SID] = [(Na(+) + K(+) + Ca(2+) + Mg(2+))-(Cl(-) + Lac(-) + PO4(2-)])在6.90-7.55的生理pH范围内同时测量。采用多边形回归曲线拟合物理-化学体系的电中性方程,进行非线性回归迭代求解Atot和Ka。10匹标准马血浆蛋白的平均阴离子负荷Atot为14.89 +/- 0.8 mEq/l血浆,Ka为2.11 +/- 0.50 × 10(-7) Eq/l (pKa = 6.67)。计算血浆中Atot的推导转换因子(迭代Atot浓度/平均血浆蛋白浓度)为0.21 mEq/g蛋白(蛋白单位:g/l)。该值与Van Slyke等人(1928)测定的0.24 mEq/g蛋白质和Constable(1997)最近公布的马血浆0.22 mEq/g蛋白质非常接近。Ka值与Constable在1997年的实验值(2.22 × 10(7) Eq/l)非常接近。对5匹纯种马在跑步机上运动试验的一组实验数据进行线性回归,结果表明,计算变量pH、HCO3、SID与实测变量的回归线具有良好的相关性。马的Atot和Ka的知识是有用的,特别是在运动研究和临床条件下量化酸碱干扰发生的机制。
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