Lactose flux occurs by differing mechanisms in the colon and jejunum of newborn piglets.

The unidirectional flux of 10- and 40-mM lactose was studied in newborn porcine jejunum and colon mounted in Ussing chambers. Polyethylene glycol 400 was used to measure passive paracellular permeability. The mucosal-to-serosal flux and the tissue accumulation of labeled lactose from the colon was similar to that of lactose-derived glucose from the jejunum. However, only jejunum showed a lactose-stimulated increase in short-circuit current. In jejunum, glucose was the sole sugar identified in the serosal bath, whereas in colon, only intact lactose was identified. Despite colonic lactose flux, polyethylene glycol oligomers were not found in the serosal bath, suggesting that they do not share the same route of absorption. Colonic lactose transport was nonsaturable between 1 and 40 mM. Under nongradient conditions, no net colonic lactose transport was observed. Cumulatively, these data suggest that the colon, unlike the jejunum, does not contain a glucose-galactose sodium cotransporter. The colon of the newborn piglet transports intact lactose at a flux equal to that of lactose-derived glucose by the small intestine, but by a different mechanism that is as yet undefined.