His analysis gives new insights into what is really happening at the chemical level and this is different from the
conventional approach. The conventional understanding of acid-base balance is:
‘cluttered with jargon, chemically meaningless derived quantities, a misunderstanding of what is happening and an artificial use of the Henderson-Hasselbalch equation as the single equation determining acid-base balance in any body fluid’ (Stewart).
The Henderson-Hasselbalch equation is just one of the 6 equations which must always be simultaneously satisfied.
Changes in pCO2 can occur quickly as ventilation can be rapidly altered. Changes in SID are due to changes in the concentrations of strong ions. The basic system for strong ions is absorption from the gut and excretion via the kidneys. These are both much slower processes than pCO2 changes. The main contributor to [ATot] in body fluids are the proteins. For the ECF, this is essentially [albumin] as discussed previously. Most plasma proteins are produced by the liver. Changes in protein concentration occur even more slowly than strong ion changes so changes in SID account for most metabolic acid-base disturbances. If plasma protein levels are normal ([ATot] constant), then acid-base disturbances can be analysed in terms of changes in pCO2 and SID.
The Stewart approach seeks to determine the factors that determine the acid-base state in a given body fluid compartment. The fluid compartments in the body are separated by cell membranes or by epithelial layers. In each compartment, the [H+] is determined by the values of the independent variables. An acid-base disturbance in a compartment is due to a change in one or more of the independent variables occurring in that compartment.
Consider the following:
Carbon dioxide diffuses across membranes rapidly and easily. Changes in pCO2 can occur rapidly via ventilatory changes. This has 2 important consequences:
Proteins are present in significant concentrations in ICF and in plasma but the ISF level is low. Proteins such as albumin are large molecules which cannot cross membranes except in unusual circumstances. The effect of this is that [H+] changes across a membrane cannot be due to movement of protein between the fluids. The phosphate level in plasma is low and regulated by the calcium control system. Transfer of phosphates across membranes could produce acid-base changes but these movements do not contribute significantly to acid base interactions.
This leaves only SID to consider. Strong electrolytes can cross membranes but usually via specific mechanisms such as ion channels and transport pumps. Strong ions can move down or against a concentration gradient. The movement of strong ions can be varied (eg pumps can be activated, ion channels can be open or closed )
So of the 3 independent variables:
Important processes involved include Na+-H+ exchange and K+-H+ exchange across the cell membrane.
The kidney is usually said to excrete acid from the body (ie if urine has a lower pH than plasma, some net amount of H+ is being excreted). This is not correct. The kidney certainly has a role in decreasing the [H+] of plasma but the real mechanism is different from the conventional explanation. As proteins cannot cross membranes, this decrease in plasma [H+] must be due to the kidney causing changes in SID across the renal tubules. The change in [H+] is due to differential movement of strong electrolytes (eg Na+, Cl-, K+) across the tubules causing a change in the SID on each side of the membrane: it cannot be due directly to the secretion or absorption of H+ or HCO3- (or adjustment in any of the other dependent variables). For example in the distal tubule. it is not the secretion of H+ that causes the pH of the distal tubular fluid to fall but the movement of the strong ion (eg Na+) associated with the process.
A further example of acid-base interactions across a membrane is that occurring in the stomach. Gastric juice is acidic not because of the transport of H+ into the stomach but because of the movement of Cl- that occurs. Alternatively, if the H+ was exchanged for a positive ion like Na+ or K+ then the SID would be altered by the same amount and again gastric secretions would be acidic. The factor which determines the [H+] is the change in SID due to movement of Cl- into the gastric juice.
The intracellular pH is altered mostly by control of intracellular SID. The ion pumps regulate concentrations of the various ions and thereby indirectly control the intracellular SID and pH.
The control of [H+] in all body fluids is due to changes in the 3 independent variables.
Proteins don’t normally contribute much to acid-base interactions because they cannot cross membranes. Most plasma proteins are synthetised in the liver. If protein levels fall (eg due to hepatic dysfunction or excretion as in the nephrotic syndrome) this will have predictable effects on acid-base balance. Strong ions are normally absorbed in the gut and excreted by the kidney. What is important is not the absolute concentrations of the individual strong ions, but the total amount of charge which is present on them which is not balanced by other strong ions (ie SID). The pCO2 is under respiratory control. Changes in pCO2 can cause rapid changes in the [H+] of all body fluids.
Changes in SID are very important in controlling transmembrane exchanges which affect the acid-base situation in adjacent fluid compartments.
Respiratory acidosis and alkalosis are due to hypercapnia and hypocapnia respectively (ie the pCO2 is the important independent variable in these disorders).
Metabolic acidosis is mostly due to a decreased SID and metabolic alkalosis is mostly due to an increase in SID.
However changes in [ATot] can also cause metabolic acid-base disorders. Hypoalbuminaemia causes a metabolic alkalosis and hyperalbuminaemia causes a metabolic acidosis. An example is the contribution of low albumin levels to the alkalosis associated with cirrhosis or the nephrotic syndrome. An increase in phosphate in plasma occurs in renal failure and contributes to the metabolic acidosis of uraemia. The phosphate level is low in plasma so a drop in phosphate level in plasma cannot contribute to causing a detectable metabolic alkalosis.
The Stewart approach "shows the way to a complete quantitative treatment of body fluids as physico-chemical systems, through numerical solution of the sets of simultaneous equations that describe their acid-base behaviour." (Fencl & Leith, 1993).
This approach is slowly gaining acceptance in research papers and in modelling of the acid-base homeostasis of body fluids. It also provides an insight into the chemical processes that determine the pH of body fluids. The conclusions are often quite different to those of the traditional approach. For example, the traditional approach to metabolic acid-base disorders is concerned with bicarbonate but the Stewart approach emphasises that chloride is the most important anion when causative factors are considered.