Apo A-IV: an update on regulation and physiologic functions
S Stan, E Delvin, M Lambert, E Seidman… - Biochimica et Biophysica …, 2003 - Elsevier
Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids, 2003•Elsevier
Apolipoprotein (apo) A-IV, first identified 28 years ago as a plasma lipoprotein moiety, is now
known to participate in the regulation of various metabolic pathways. It is synthesized
primarily in the enterocytes of the small intestine during fat absorption. After entry into the
bloodstream, the 46-kDa glycoprotein apo A-IV appears associated with chylomicrons, high-
density lipoproteins, and in the lipoprotein-free fraction. It has a role in lipid absorption,
transport and metabolism, and may act as a post-prandial satiety signal, an anti-oxidant and …
known to participate in the regulation of various metabolic pathways. It is synthesized
primarily in the enterocytes of the small intestine during fat absorption. After entry into the
bloodstream, the 46-kDa glycoprotein apo A-IV appears associated with chylomicrons, high-
density lipoproteins, and in the lipoprotein-free fraction. It has a role in lipid absorption,
transport and metabolism, and may act as a post-prandial satiety signal, an anti-oxidant and …
Apolipoprotein (apo) A-IV, first identified 28 years ago as a plasma lipoprotein moiety, is now known to participate in the regulation of various metabolic pathways. It is synthesized primarily in the enterocytes of the small intestine during fat absorption. After entry into the bloodstream, the 46-kDa glycoprotein apo A-IV appears associated with chylomicrons, high-density lipoproteins, and in the lipoprotein-free fraction. It has a role in lipid absorption, transport and metabolism, and may act as a post-prandial satiety signal, an anti-oxidant and a major factor in the prevention of atherosclerosis. After summarizing and discussing these functions for reader's comprehension, the current review focuses on the regulation of apo A-IV by nutrients, biliary components, drugs, hormones and gastrointestinal peptides. The understanding of the involved mechanisms that underline apo A-IV regulation may in the long run allow us to switch on its gene, which may confer multiple beneficial effects, including the protection from atherosclerosis.
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