Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

Bile but not chyle lipoprotein is an important source of arachidonic acid for the rat small intestine

Melin, T LU ; Qi, C and Nilsson, A LU (1996) In Prostaglandins, Leukotrienes and Essential Fatty Acids 55(5). p.43-337
Abstract

Arachidonic acid (AA) functions as a structural component, eicosanoid precursor and surface material for chylomicron production in the gastrointestinal tract. The origin of this AA is poorly characterized. [3H]AA labelled chylomicrons and [14C]AA albumin-FFA were injected intravenously into biliary diverted rats and controls. Radioactivity in tissue lipids was measured after different time intervals. Output of 3H and 14C in bile was 8% of the injected dose during 24 h. Radioactivity of the upper small intestine but not of colon and stomach increased with time. Bile drain reduced the recovered amounts of radioactivity in upper small intestine by 75% after 24 h. In stomach and colon 3H/g tissue was 16-20 fold lower than in liver after 24... (More)

Arachidonic acid (AA) functions as a structural component, eicosanoid precursor and surface material for chylomicron production in the gastrointestinal tract. The origin of this AA is poorly characterized. [3H]AA labelled chylomicrons and [14C]AA albumin-FFA were injected intravenously into biliary diverted rats and controls. Radioactivity in tissue lipids was measured after different time intervals. Output of 3H and 14C in bile was 8% of the injected dose during 24 h. Radioactivity of the upper small intestine but not of colon and stomach increased with time. Bile drain reduced the recovered amounts of radioactivity in upper small intestine by 75% after 24 h. In stomach and colon 3H/g tissue was 16-20 fold lower than in liver after 24 h. Recovery of 3H in liver was higher than of 14C. In liver 3H/g tissue was 15-40 fold higher than in stomach and colon after 10-60 min. Equilibration between AA pools of liver and other organs was not complete after 96 h. Biliary phospholipid is an important source of AA for the small intestine.

(Less)
Please use this url to cite or link to this publication:
author
; and
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Albumins/metabolism, Animals, Arachidonic Acid/metabolism, Bile/metabolism, Carbon Radioisotopes, Chyle/metabolism, Chylomicrons/metabolism, Drainage, Injections, Intravenous, Intestinal Mucosa/metabolism, Intestine, Small/metabolism, Lipoproteins/metabolism, Liver/metabolism, Male, Phospholipids/metabolism, Rats, Rats, Sprague-Dawley, Time Factors, Tissue Distribution, Tritium
in
Prostaglandins, Leukotrienes and Essential Fatty Acids
volume
55
issue
5
pages
7 pages
publisher
Elsevier
external identifiers
  • pmid:8981631
  • scopus:0029990859
ISSN
0952-3278
DOI
10.1016/s0952-3278(96)90040-x
language
English
LU publication?
no
id
e149da4e-8822-4703-8270-efb9bee90aa5
date added to LUP
2019-09-24 15:00:26
date last changed
2024-01-01 21:10:36
@article{e149da4e-8822-4703-8270-efb9bee90aa5,
  abstract     = {{<p>Arachidonic acid (AA) functions as a structural component, eicosanoid precursor and surface material for chylomicron production in the gastrointestinal tract. The origin of this AA is poorly characterized. [3H]AA labelled chylomicrons and [14C]AA albumin-FFA were injected intravenously into biliary diverted rats and controls. Radioactivity in tissue lipids was measured after different time intervals. Output of 3H and 14C in bile was 8% of the injected dose during 24 h. Radioactivity of the upper small intestine but not of colon and stomach increased with time. Bile drain reduced the recovered amounts of radioactivity in upper small intestine by 75% after 24 h. In stomach and colon 3H/g tissue was 16-20 fold lower than in liver after 24 h. Recovery of 3H in liver was higher than of 14C. In liver 3H/g tissue was 15-40 fold higher than in stomach and colon after 10-60 min. Equilibration between AA pools of liver and other organs was not complete after 96 h. Biliary phospholipid is an important source of AA for the small intestine.</p>}},
  author       = {{Melin, T and Qi, C and Nilsson, A}},
  issn         = {{0952-3278}},
  keywords     = {{Albumins/metabolism; Animals; Arachidonic Acid/metabolism; Bile/metabolism; Carbon Radioisotopes; Chyle/metabolism; Chylomicrons/metabolism; Drainage; Injections, Intravenous; Intestinal Mucosa/metabolism; Intestine, Small/metabolism; Lipoproteins/metabolism; Liver/metabolism; Male; Phospholipids/metabolism; Rats; Rats, Sprague-Dawley; Time Factors; Tissue Distribution; Tritium}},
  language     = {{eng}},
  number       = {{5}},
  pages        = {{43--337}},
  publisher    = {{Elsevier}},
  series       = {{Prostaglandins, Leukotrienes and Essential Fatty Acids}},
  title        = {{Bile but not chyle lipoprotein is an important source of arachidonic acid for the rat small intestine}},
  url          = {{http://dx.doi.org/10.1016/s0952-3278(96)90040-x}},
  doi          = {{10.1016/s0952-3278(96)90040-x}},
  volume       = {{55}},
  year         = {{1996}},
}