In vitro studies on the effects of Saccharomyces boulardii and Bacillus cereus var. toyoi on nutrient transport in pig jejunum

Citation
G. Breves et al., In vitro studies on the effects of Saccharomyces boulardii and Bacillus cereus var. toyoi on nutrient transport in pig jejunum, J ANIM PHYS, 84(1-2), 2000, pp. 9-20
Citations number
40
Categorie Soggetti
Veterinary Medicine/Animal Health
Journal title
JOURNAL OF ANIMAL PHYSIOLOGY AND ANIMAL NUTRITION-ZEITSCHRIFT FUR TIERPHYSIOLOGIE TIERERNAHRUNG UND FUTTERMITTELKUNDE
ISSN journal
09312439 → ACNP
Volume
84
Issue
1-2
Year of publication
2000
Pages
9 - 20
Database
ISI
SICI code
0931-2439(200009)84:1-2<9:IVSOTE>2.0.ZU;2-Q
Abstract
The probiotics Saccharomyces boulardii and Bacillus cereus var. toyoi are n onpathogenic microbes which have been shown to affect certain functions of the mucosal barrier in pig jejunum such as electrogenic ion transport capac ity and paracellular permeability. The present studies were performed to in vestigate potential effects of the probiotics on jejunal nutrient transport such as sodium-dependent glucose transport or proton-dependent dipeptide t ransport. For this purpose the in vitro Ussing-chamber technique was applie d in order to examine net electrogenic ion flux rates (short circuit curren ts, I-sc) across isolated intact jejunal epithelia in the absence and prese nce of either 10 mmol/l glucose (mucosal side) or two-fold application of 5 mmol/l glycyl-L-sarcosine or glycyl-L-glutamine to the mucosal bathing sol ution. Brush border membrane vesicles (BBMV) were prepared in order to char acterize kinetic parameters (V-max, K-m) of Na-dependent glucose transport. Intestinal tissues were obtained from growing pigs in a weight range betwe en 23 and 33 kg. All animals were fed twice daily and received 0.8-0.9 kg/d ay of a standard diet. After a 9- to 10-day adaptation period the diets for treated animals were either supplemented for 8 days with 1.7 x 10(7) colon y-forming units (CFU)/g feed of S. boulardii or for 3 weeks with 10(6) CFU/ g feed B. cereus var, toyoi. Under basal conditions I-sc values were not af fected by different treatment protocols (controls: 0.74+/-0.04 mu eq/cm(2) per h, n=9; S. boulardii: 0.74 +/- 0.12 mu eq/cm(2) per h, n = 7; B. cereus 0.68 +/- 0.09 mu eq/cm(2) per h, n= 5). Irrespective of dietary treatment, the addition of glucose resulted in significant increases of I-sc indicati ng substantial onset of electrogenic net Na/glucose cotransport. Maximal I- sc values occurred within 30 min and reached 2.79 +/- 0.41 mu eq/cm(2) per h in control epithelia. This was significantly lower than found in S. botil nrdii (4.47 +/- 0.43 mu eq/cm(2) per h, p < 0.05) and B. cereus var. toyoi tissues (4.45 +/- 0.31 mu eq/cm(2) per h, p < 0.05). G(t) values were 22.4 +/- 1.3 mS/cm(2) in control animals and were significantly lower as shown i n S. boulardii (p < 0.01) and B. cereus var. toyoi (p < 0.01)-treated anima ls (28.4 +/- 1.3 and 29.9 + 0 8 mS/cm(2), respectively). V-max values of Na -dependent glucose uptake into BBMV differed significantly between controls (0.64 +/- 0.08 nmol/mg protein per 10 s; n=5), S. boulardii (0.89 +/- 0.06 nmol/mg protein per 10 s; n = 5, p < 0.05) and B. cereus var. toyoi prepar ations (1.08 +/- 0.05 nmol/mg protein per 10s; n=3, p < 0.01). K-m values w ere not significantly affected (control: 0.31 +/- 0.04 mmol/l, S. boulardii : 0.29 +/- 0.05 mmol/l, B. cereus var, toyoi: 0.21 +/- 0.01 mmol/l). Irresp ective of dietary treatment, application of the dipeptide model substances glycyl-L-sarcosine or glycyl-L-glutamine resulted in significant increases of I-sc indicating marked stimulation of electrogenic net H+/dipeptide cotr ansport. Highest I-sc responses occurred in B. cereus var. toyoi preparatio ns and lowest were found in control tissues. However, these differences wer e not significant. G(t) values were not affected by different dietary treat ments. The results clearly demonstrate that oral administration of either S . boulardii or B. cereus var. toyoi stimulates Na-dependent glucose absorpt ion in pig jejunum.