Evidence map›Paper›PMID 29206843›Full record

ArticlePloS one2017

Periparturient lipolysis and oxylipid biosynthesis in bovine adipose tissues.

G Andres Contreras, Clarissa Strieder-Barboza, Jonas de Souza, Jeff Gandy, Vengai Mavangira, Adam L Lock, Lorraine M Sordillo

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
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  5. Review
  6. Article
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  8. Article
  9. Review
  10. Article
  11. Article
  12. Redox Regulation of Lipid Mobilization in Adipose Tissues.Antioxidants (Basel, Switzerland) · 2021
    Review
  13. Review
  14. Molecular mechanisms of fat deposition:Archives animal breeding · 2021
    Article
  15. Article
  16. Article
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

7 authors at 1 institution in 1 country.

G Andres ContrerasDepartment of Large Animal Clinical Sciences, Michigan State University, East Lansing, MI, United States of America.ORCID http://orcid.org/0000-0003-4969-2178
Clarissa Strieder-BarbozaDepartment of Large Animal Clinical Sciences, Michigan State University, East Lansing, MI, United States of America.
Jonas de SouzaDepartment of Animal Science, Michigan State University, East Lansing, MI, United States of America.
Jeff GandyDepartment of Large Animal Clinical Sciences, Michigan State University, East Lansing, MI, United States of America.
Vengai MavangiraDepartment of Large Animal Clinical Sciences, Michigan State University, East Lansing, MI, United States of America.
Adam L LockDepartment of Animal Science, Michigan State University, East Lansing, MI, United States of America.
Lorraine M SordilloDepartment of Large Animal Clinical Sciences, Michigan State University, East Lansing, MI, United States of America.
Michigan State University · US

Funding

EPA EP-C-16-023
6 · The paper itself

Abstract

The periparturient period of dairy cows is characterized by intense lipolysis in adipose tissues (AT), which induces the release of free fatty acids (FFA) into circulation. Among FFA, polyunsaturated fatty acids are susceptible to oxidation and can modulate inflammatory responses during lipolysis within AT. Linoleic and arachidonic acid oxidized products (oxylipids) such as hydroxy-octadecadienoic acids (HODE) and hydroxy-eicosatetraenoic acids (HETE), were recently identified as products of lipolysis that could modulate AT inflammation during lipolysis. However, the effect of lipolysis intensity during the transition from gestation to lactation on fatty acid substrate availability and subsequent AT oxylipid biosynthesis is currently unknown. We hypothesized that in periparturient dairy cows, alterations in AT and plasma fatty acids and oxylipid profiles coincide with changes in lipolysis intensity and stage of lactation. Blood and subcutaneous AT samples were collected from periparturient cows at -27±7 (G1) and -10±5 (G2) d prepartum and at 8±3 d postpartum (PP). Targeted lipidomic analysis was performed on plasma and AT using HPLC-MS/MS. We report that FFA concentrations increased as parturition approached and were highest at PP. Cows exhibiting high lipolysis rate at PP (FFA>1.0 mEq/L) had higher body condition scores at G1 compared to cows with low lipolysis rate (FFA<1.0 mEq/L). Concentrations of plasma linoleic and arachidonic acids were increased at PP. In AT, 13-HODE, and 5-, 11- and 15-HETE were increased at PP compared to G1 and G2. Concentrations of beta hydroxybutyrate were positively correlated with those of 13-HODE and 15-HETE in AT. Plasma concentrations of 5- and 20-HETE were increased at PP. These data demonstrate that prepartum adiposity predisposes cows to intense lipolysis post-partum and may exacerbate AT inflammation because of increased production of pro-inflammatory oxylipids including 5- and 15-HETE and 13-HODE. These results support a role for certain linoleic and arachidonic acid-derived oxylipids as positive and negative modulators of AT inflammation during periparturient lipolysis.

Indexed as

LipolysisParturitionAdipose TissueAnimalsCattleChromatography, High Pressure LiquidDairyingFemaleHydroxyeicosatetraenoic AcidsPregnancyTandem Mass Spectrometry20-hydroxy-5,8,11,14-eicosatetraenoic acid5-hydroxy-6,8,11,14-eicosatetraenoic acidHydroxyeicosatetraenoic Acids

Identifiers

PMID29206843
PMCPMC5716552
OpenAlexW2775325223

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.