Dietary cholesterol does not normalize low plasma cholesterol levels but induces hyperbilirubinemia and hypercholanemia in Mdr2 P-glycoprotein-deficient mice
Pj. Voshol et al., Dietary cholesterol does not normalize low plasma cholesterol levels but induces hyperbilirubinemia and hypercholanemia in Mdr2 P-glycoprotein-deficient mice, J HEPATOL, 34(2), 2001, pp. 202-209
Background/Aims: Mdr2 P-glycoprotein deficiency in mice (Mdr2((-/-))) leads
to formation of cholesterol/cholesterol-depleted bile and reduced plasma H
DL cholesterol. We addressed the questions: (1) does HDL in Mdr2((-/-)) mic
e normalize upon phospholipid and/or cholesterol feeding, and (2): is the M
dr2((-/-)) liver capable of handling excess dietary cholesterol.
Methods: Male and female Mdr2((-/-)) and Mdr2((+/+)) mice were fed diets wi
th or without additional phosphatidylcholine and/or cholesterol, Plasma, he
patic and biliary lipids as well as liver function parameters and expressio
n of transport proteins involved in bile formation were analyzed.
Results: Feeding excess phospholipids and/or cholesterol did not affect lip
oprotein levels in Mdr2((+/+)) or Mdr2((-/+)) mice. Dietary cholesterol cau
sed hyperbilirubinemia (male +100%; female +500%) and elevated plasma bile
salts (male +200 %; female +1250 %) in Mdr2((-/-)) mice only, independent o
f phospholipids. Bile flow nor biliary bile salt and bilirubin secretion we
re affected in cholesterol-fed Mdr2((-/-)) mice. Elevated plasma bile salts
may be related to cholesterol-induced reduction of hepatic Nac-taurocholat
e cotransporting protein expression in Mdr2((-/-)) mice.
Conclusion: Excess dietary phospholipids and cholesterol do not normalize l
ow HDL associated with Mdr2 P-glycoprotein-deficiency. Induction of hyperbi
lirubinemia and hypercholanemia by dietary cholesterol in Mdr2((-/-)) mice
delineates the important role of biliary lipid secretion in normal hepatic
functioning. (C) 2001 European Association for the Study of the Liver. Publ
ished by Elsevier Science B.V. All rights reserved.