EFFICACY OF A GLUTAMINE-BASED ORAL REHYDRATION SOLUTION ON THE ELECTROLYTE AND WATER-ABSORPTION IN A RABBIT MODEL OF SECRETORY DIARRHEA INDUCED BY CHOLERA-TOXIN
Ac. Silva et al., EFFICACY OF A GLUTAMINE-BASED ORAL REHYDRATION SOLUTION ON THE ELECTROLYTE AND WATER-ABSORPTION IN A RABBIT MODEL OF SECRETORY DIARRHEA INDUCED BY CHOLERA-TOXIN, Journal of pediatric gastroenterology and nutrition, 26(5), 1998, pp. 513-519
Background: Glutamine is absorbed in the intestinal tract coupled with
sodium and is the principal metabolic substrate for the enterocyte. T
herefore, an oral rehydration solution con taining this substance migh
t provide an effective oral means of restoring electrolyte losses as w
ell as speeding repair of mucosal damage. The objective of this work w
as to investigate the use of an oral rehydration solution based on glu
tamine in vivo in the perfused rabbit ileal loop model of secretory di
arrhea induced by choleratoxin. Methods: Phenolsulfonphthalein (PSP, 5
0 mg/l) was used as a nonabsorbable marker for calculations of net wat
er and electrolyte transport. Solutions tested included: (a) a glutami
ne-based oral rehydration solution with 111 mmol/l glutamine, (Gln-ORS
); (b) the oral rehydration solution recommended by the World Health O
rganization; (c) modified Ringer's solution. Choleratoxin (1 mu g/ml)
was injected into the lumen of the ileal rabbit segments for 30 minute
s prior to the initiation of the perfusion. Results: Choleratoxin indu
ced significant secretion of sodium in the control modified Ringer's s
olution (10.8 +/- 2.95 vs -14.05 +/- 5.95 mu Eq/g/min, n = 10; p < 0.0
1) and of water (0.06 +/- 0.03 vs -0.15 +/- 0.06 ml/g/min, n = 10; p <
0.01) with a maximum effect at 60 minutes after initiation of perfusi
on. World Health Organization oral rehydration solution was able to si
gnificantly reduce the intestinal secretion of sodium (control with ch
olera = -14.34 +/- 2.18 vs oral rehydration solution with cholera = -0
.50 +/- 0.48 mu Eq/g/min, n = 10;p < 0.01) and water (-0.15 +/- 0.02 v
s -0.012 +/- 0.005 ml/g/min, n = 10; p < 0.01). For comparison, glutam
ine-based oral rehydration solution had an even greater effect on sodi
um and water absorption (glutamine-based oral rehydration solution wit
h choleratoxin = 10.31 +/- 1.21 mu Eq/g/min, n = 5; p < 0.01 for sodiu
m and 0.08 +/- 0.008 ml water/g/min; n = 5; p < 0.01). Choleratoxin di
d not change the effect of glutamine-based oral rehydration solution o
n sodium and water absorption (12.90 +/- -1.09 mu Eq sodium/g/min, n =
5; and 0.11 +/- 0.01 ml water/g/min; n = 5). In addition glutamine-ba
sed oral rehydration solution also induced a greater absorption of pot
assium and chloride in the intestinal ileal segments treated with chol
era toxin compared with World Health Organization glutamin-based oral
rehydration solution. Conclusions: These results demonstrate the super
ior efficacy of glutamine-based oral rehydration solution in electroly
te and water absorption compared with modified Ringer's control soluti
on or even with World Health Organization-recommended oral rehydration
solution.