Affiliations: Department of Nutrition, Dietetics and Food Science, Curtin University of Technology, Perth, Australia
Correspondence:
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Corresponding author: Associate Professor John Mamo, Head, Department of Nutrition, Dietetics and Food Sciences, Curtin University of Technology, Hayman Road, Bentley, Western Australia 6102, OR, Box U1987, GPO Perth 6845, Australia. Tel.: +61 8 92667232; Fax: +61 8 92662958; E-mail: J.Mamo@curtin.edu.au.
Abstract: The aggregation and deposition of amyloid-β (Aβ) in the brain is thought to be an early event in the pathology of Alzheimer's disease (AD). Many studies have reported the association of Aβ with lipoproteins from plasma suggesting an involvement of lipoprotein particles in Aβ transport. Chylomicron-like lipid emulsions, resembling chylomicrons in composition, size and metabolism were prepared in the presence of [125I]Aβ1-40. Aβ was found to associate significantly with these lipid emulsions during their preparation. The chylomicron-like emulsions containing Aβ were then injected into a lateral ear vein of conscious rabbits and blood sampled at regular intervals up to 30 mins. It was observed that there was no difference in the plasma clearance of [125I]Aβ and that of the 3H-cholesteryl ester, a marker of the emulsion particles, demonstrating that Aβ remains associated with these particles throughout both their lipolysis and tissue uptake. Our results show that Aβ can be metabolised in association with triglyceride rich lipoproteins (TRLs). In addition we report the presence of specific markers of TRLs of hepatic and intestinal origin in human CSF thus suggesting a potential means of cerebral Aβ delivery.
