Yk. Park et al., Intestinal protein and LPH synthesis in parenterally fed piglets receivingpartial enteral nutrition and enteral insulinlike growth factor 1, J PED GASTR, 33(2), 2001, pp. 189-195
Citations number
31
Categorie Soggetti
Pediatrics,"Medical Research General Topics
Journal title
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
Background: Providing partial enteral nutrition (PEN) supplemented with ins
ulinlike growth factor-1 (IGF-1) to parenterally fed piglets increases lact
ase-phlorizin hydrolase (LPH) activity, but not LPH mRNA. The current aim w
as to investigate potential mechanisms by which IGF-1 up-regulates LPH acti
vity.
Methods: Newborn piglets (n = 15) received 100% parenteral nutrition (TPN),
80% parenteral nutrition + 20% parenteral nutrition (PEN), or PEN + IGF-1
(1.0 mg . kg(-1) . d(-1)) for 7 days. On day 7, [H-2(3)]-leucine was intrav
enously administered to measure mucosal protein and brush border LPH (BB LP
H) synthesis.
Results: Weight gain, nutrient intake, and jejunal weight and length were s
imilar among the treatment groups. Partial enteral nutrition alone increase
d mucosal weight, villus width and cross-sectional area, LPH activity, mRNA
expression, and high mannose LPH precursor (proLPH(h)) abundance compared
with TPN (P<0.05). Insulinlike growth factor-1 further increased mucosal we
ight, LPH activity, and LPH activity per unit BB LPH approximately twofold
over PEN alone (P < 0.05) but did not affect LPH mRNA or the abundance of p
roLPH(h) (one of the LPH isoforms) or mature LPH. Isotopic enrichment of [H
-2(3)]-leucine in plasma, mucosal protein, and LPH precursors, and the frac
tional and absolute synthesis rates of mucosal protein and LPH were similar
among the treatment groups. Insulinlike growth factor-1 treatment increase
d total mucosal protein synthesis (60%, P < 0.05) but not LPH synthesis com
pared with the other two groups.
Conclusions: Because IGF-1 did not affect the fractional synthesis rate of
either mucosal protein or LPH, the authors suggest that enteral IGF-1 incre
ases mucosal protein mass and LPH activity by suppressing mucosal proteolyt
ic degradation.