triolein and Lymphatic-Diseases

triolein has been researched along with Lymphatic-Diseases* in 1 studies

Other Studies

1 other study(ies) available for triolein and Lymphatic-Diseases

ArticleYear
Apolipoprotein A-V deficiency enhances chylomicron production in lymph fistula mice.
    American journal of physiology. Gastrointestinal and liver physiology, 2015, Apr-01, Volume: 308, Issue:7

    Apolipoprotein A-V (apoA-V), a liver-synthesized apolipoprotein discovered in 2001, strongly modulates fasting plasma triglycerides (TG). Little is reported on the effect of apoA-V on postprandial plasma TG, an independent predictor for atherosclerosis. Overexpressing apoA-V in mice suppresses postprandial TG, but mechanisms focus on increased lipolysis or clearance of remnant particles. Unknown is whether apoA-V suppresses the absorption of dietary lipids by the gut. This study examines how apoA-V deficiency affects the steady-state absorption and lymphatic transport of dietary lipids in chow-fed mice. Using apoA-V knockout (KO, n = 8) and wild-type (WT, n = 8) lymph fistula mice, we analyzed the uptake and lymphatic transport of lipids during a continuous infusion of an emulsion containing [(3)H]triolein and [(14)C]cholesterol. ApoA-V KO mice showed a twofold increase in (3)H (P < 0.001) and a threefold increase in (14)C (P < 0.001) transport into the lymph compared with WT. The increased lymphatic transport was accompanied by a twofold reduction (P < 0.05) in mucosal (3)H, suggesting that apoA-V KO mice more rapidly secreted [(3)H]TG out of the mucosa into the lymph. ApoA-V KO mice also produced chylomicrons more rapidly than WT (P < 0.05), as measured by the transit time of [(14)C]oleic acid from the intestinal lumen to lymph. Interestingly, apoA-V KO mice produced a steadily increasing number of chylomicron particles over time, as measured by lymphatic apoB output. The data suggest that apoA-V suppresses the production of chylomicrons, playing a previously unknown role in lipid metabolism that may contribute to the postprandial hypertriglyceridemia associated with apoA-V deficiency.

    Topics: Administration, Oral; Animals; Apolipoprotein A-V; Apolipoproteins; Cholesterol; Chylomicrons; Disease Models, Animal; Duodenum; Fistula; Intestinal Absorption; Lymph; Lymphatic Diseases; Lymphatic System; Male; Mice, Inbred C57BL; Mice, Knockout; Postprandial Period; Time Factors; Triolein; Up-Regulation

2015