Transport Of L-alanyl-D-phenylalanyl-L-alanine was investigated with a
n in situ vascular perfusion preparation of rat lung and brush border
membrane vesicles prepared from type II pneumocytes. In the perfused l
ung 1 mM tripeptide was transported intact from the alveolar lumen to
the vascular perfusate at a mean rate of 25.1 +/- 1.29 (3) nmol/min pe
r g dry weight. D-Phenylalanine also appeared in the vascular perfusat
e at a rate of 21.9 +/- 1.74 (3) nmol/min per g dry weight indicating
that 47% of the absorbed tripeptide was split during passage across th
e epithelial layer. No dipeptide could be detected in the vascular eff
luent during perfusions with tripeptide. Rapid L-alanyl-D-phenylalanyl
-L-alanine uptake occurred with fresh apical membrane vesicles prepare
d from type II pneumocytes and this was abolished by treatment with 0.
1% triton. The related tripeptide, D-alanyl-L-phenylalanyl-D-alanine,
was taken up significantly more slowly by the vesicles. D-phenylalanyl
-L-alanine and D-phenylalanyl-D-alanine, were also studied with the va
scularly perfused preparation; the mixed dipeptide appeared in the vas
cular perfusate significantly faster than L-alanyl-D-phenylalanyl-L-al
anine whereas D-phenylalanyl-D-alanine appeared more slowly and was no
t hydrolysed.