The development of oral rehydration solutions (ORSs) has been one of t
he important therapeutic advances of this century. The optimal formula
tion, however, of ORSs for both cholera and other infective diarrhoeas
is still debated. Part of the problem in developing ORSs has been the
lack of adequate test systems for the assessment of new formulations
before clinical trial. We have developed a jejunal perfusion, cholera
toxin induced, secretory model in humans and have compared net water a
nd solute absorption from a hypotonic ORS (HYPO-ORS: sodium 60 mmol/l,
glucose 90 mmol/l, osmolality 240 mOsm/kg) and the British Pharmacopo
eia recommended ORS (UK-ORS: sodium 35 mmol/l, glucose 200 mmol/l, osm
olality 310 mOsm/kg) in six healthy volunteers. A plasma electrolyte s
olution (PES) was also perfused in all subjects to confirm a secretory
state, Only HYPO-ORS reversed sodium secretion to absorption (p<0.01)
. Both ORSs promoted net water absorption but this was greatest with H
YPO-ORS (p<0.01). Glucose and potassium absorption rates were similar
for both ORSs whereas chloride absorption mirrored sodium absorption a
nd was greatest from HYPO-ORS (p<0.05). These results, in a biological
ly relevant model of secretory diarrhoea, suggest it may be possible t
o achieve improved rates of rehydration by the use of hypotonic ORS wi
th mid range sodium concentrations.