Evidence map›Paper›PMID 26968208›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2016

Postprandial lymphatic pump function after a high-fat meal: a characterization of contractility, flow, and viscosity.

Timothy Kassis, Sri Charan Yarlagadda, Alison B Kohan, Patrick Tso, Victor Breedveld, J Brandon Dixon

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.5field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 48 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Understanding the Lymphatic System: Tissue-on-Chip Modeling.Annual review of biomedical engineering · 2025
    Review
  5. Article
  6. The impact of thoracic duct resection on the long-term body composition of patients who underwent esophagectomy for esophageal cancer and survived without recurrence.Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus · 2023
    Article
  7. Review
  8. Article
  9. Lymphoedema conditions disrupt endothelial barrier functionJournal of the Royal Society, Interface · 2022
    Article
  10. Adipose tissue microenvironments during aging: Effects on stimulated lipolysis.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2022
    Review
  11. Enterocyte-specific ATGL overexpression affects intestinal and systemic cholesterol homeostasis.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2022
    Article
  12. Passive and Active Microrheology for Biomedical Systems.Frontiers in bioengineering and biotechnology · 2022
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. The Intestinal Lymphatic System: Functions and Metabolic Implications.Cellular and molecular gastroenterology and hepatology · 2019
    Review
  19. Article
  20. Regulation of Chylomicron Secretion: Focus on Post-Assembly Mechanisms.Cellular and molecular gastroenterology and hepatology · 2019
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Timothy KassisParker H. Petit Institute for Bioengineering & Bioscience, Georgia Institute of Technology, Atlanta, Georgia; School of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, Georgia;
Sri Charan YarlagaddaSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia; and.
Alison B KohanDepartment of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, Ohio.
Patrick TsoDepartment of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, Ohio.
Victor BreedveldSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia; and.
J Brandon DixonParker H. Petit Institute for Bioengineering & Bioscience, Georgia Institute of Technology, Atlanta, Georgia; George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, Georgia; dixon@gatech.edu.
Georgia Institute of Technology · USUniversity of Cincinnati · US

Funding

LIPID, LIPOPROTEIN, AND GLUCOSE METABOLISM COREU24DK059630 · NIDDK · UNIVERSITY OF CINCINNATI · PI TSO, PATRICK · 2001 to 2015
$12.9M
Quantifying the role of load-induced remodeling in lymphedema progressionR01HL113061 · NHLBI · GEORGIA INSTITUTE OF TECHNOLOGY · PI DIXON, JAMES BRANDON · 2013 to 2017
$2.2M
Quantifying the role of lymphatics in lipid metabolism and transportR00HL091133 · NHLBI · GEORGIA INSTITUTE OF TECHNOLOGY · PI DIXON, JAMES BRANDON · 2009 to 2011
$716k
NHLBI NIH HHS R00 HL091133NHLBI NIH HHS R01 HL113061NIDDK NIH HHS U24 DK059630
6 · The paper itself

Abstract

Dietary lipids are transported from the intestine through contractile lymphatics. Chronic lipid loads can adversely affect lymphatic function. However, the acute lymphatic pump response in the mesentery to a postprandial lipid meal has gone unexplored. In this study, we used the rat mesenteric collecting vessel as an in vivo model to quantify the effect of lipoproteins on vessel function. Lipid load was continuously monitored by using the intensity of a fluorescent fatty-acid analog, which we infused along with a fat emulsion through a duodenal cannula. The vessel contractility was simultaneously quantified. We demonstrated for the first time that collecting lymphatic vessels respond to an acute lipid load by reducing pump function. High lipid levels decreased contraction frequency and amplitude. We also showed a strong tonic response through a reduction in the end-diastolic and systolic diameters. We further characterized the changes in flow rate and viscosity and showed that both increase postprandially. In addition, shear-mediated Ca(2+) signaling in lymphatic endothelial cells differed when cultured with lipoproteins. Together these results show that the in vivo response could be both shear and lipid mediated and provide the first evidence that high postprandial lipid has an immediate negative effect on lymphatic function even in the acute setting.

Indexed as

Muscle ContractionPostprandial PeriodAnimalsCalcium SignalingCells, CulturedDietary FatsEndothelial CellsHumansLymphLymphatic VesselsMaleMuscle, SmoothRatsRats, Sprague-DawleyViscosityDietary Fatschylomicronlipid absorptionlymphaticpump functionviscosity

Identifiers

PMID26968208
PMCPMC4888550
OpenAlexW2293666614

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.