Impact of Sequential Lipid Meals on Lymphatic Lipid Absorption and Transport in Rats

Qi Zhu, Qing Yang, Ling Shen, Jie Qu, Meifeng Xu, David Q.H. Wang, Patrick Tso, Min Liu

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

The sequential meal pattern has recently received more attention because it reflects a phycological diet style for human beings. The present study investigated the effects of the second lipid meal on lymphatic lipid absorption and transport in adult rats following a previous lipid meal. Using the well-established lymph fistula model, we found that the second lipid meal significantly increased the lymphatic output of triglycerides, cholesterol, phospholipids, and non-esterified fatty acids compared with a single lipid meal. Besides that, the time reaching the peak of each lipid output was significantly faster compared with the first lipid meal. Additionally, the second lipid meal significantly increased the lymphatic output of apolipoprotein A-IV (ApoA-IV), but not apolipoprotein B-48 (ApoB48) or apolipoprotein A-I (ApoA-I). Interestingly, the triglyceride/apoB-48 ratio was significantly increased after the second lipid meal, indicating the increased chylomicron size in the lymph. Finally, the second lipid meal increased the lymphatic output of rat mucosal mast cell protease II (RMCPII). No change was found in the expression of genes related to the permeability of lymphatic lacteals, including vascular endothelial growth factor-A (Vegfa), vascular endothelial growth factor receptor 1 (Flt1), and Neuropilin1 (Nrp1). Collectively, the second lipid meal led to the rapid appearance of bigger-sized chylomicrons in the lymph. It also increased the lymphatic output of various lipids and apoA-IV, and mucosal mast cell activity in the intestine.

Original languageEnglish (US)
Article number277
JournalGenes
Volume13
Issue number2
DOIs
StatePublished - Feb 2022

Keywords

  • Chylomicron
  • Lymph fistula model
  • Mucosal mast cells
  • Two-meal feeding

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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