Vol. 282, Issue 1, G41-G50, January 2002
Increased expression of ileal apical sodium-dependent bile
acid transporter in postpartum rats
Aldo D.
Mottino1,
Tim
Hoffman1,
Paul A.
Dawson2,
Marcelo G.
Luquita3,
Juan A.
Monti3,
Enrique J.
Sánchez Pozzi3,
Viviana A.
Catania3,
Jingsong
Cao1, and
Mary
Vore1
1 Graduate Center for Toxicology, University of Kentucky,
Lexington, Kentucky 40536-0305; 2 Departments of Internal
Medicine and Pathology, Wake Forest University, School of Medicine,
Winston-Salem, North Carolina 27157; and 3 Institute of
Experimental Physiology, School of Biochemical and Pharmaceutical
Sciences, National University of Rosario, 2000 Rosario, Argentina
The
expression and activity of the apical ileal sodium-dependent bile acid
transporter (asbt) was examined in the small intestine of control,
pregnant, and lactating postpartum rats 2, 12, and 21 days after
delivery. Western blot analysis of brush border membrane vesicles
(BBMV) prepared from different regions of the small intestine
demonstrated that expression of asbt was maximal in the most distal
segments for all experimental groups, was not substantially affected in
pregnant and 2-day postpartum rats, and was significantly increased in
12- and 21-day postpartum rats. Analysis of mRNA suggested that asbt
protein was regulated at the posttranscriptional level in postpartum
rats. Increased expression of asbt protein postpartum was maximal
(~2-fold) in the proximal region of the ileum, consistent with a 60%
increase in taurocholate (TC) transport in BBMV from the proximal ileum
in 14- to 21-day postpartum rats relative to control rats. Absorption
of TC, determined from the intact proximal ileum using an intestinal
loop model, demonstrated a 30% increase in TC uptake per unit weight
of tissue in 14- to 21-day postpartum rats relative to control rats.
Together with the marked increase in intestinal mass observed at peak
lactation, these data indicate a significant increase in asbt-mediated
reclamation of bile acids in the intestine of lactating rats.
dietary fat absorption; enterohepatic cycle; prolactin; enteroglucagon; lactation