Evidence map›Paper›PMID 22370449›Full record

ArticleBiochimica et biophysica acta2012

Regulation of plasma cholesterol esterification by sphingomyelin: effect of physiological variations of plasma sphingomyelin on lecithin-cholesterol acyltransferase activity.

Papasani Venkata Subbaiah, Xian-Cheng Jiang, Natalia A Belikova, Buzulagu Aizezi, Zhi Hua Huang, Catherine A Reardon

Abstract read
In one paragraph

Article in Biochimica et biophysica acta, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Frontiers in endocrinology · 2023
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Unraveling the complexities of the HDL lipidome.Journal of lipid research · 2013
    Review
  20. 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.

Papasani Venkata SubbaiahDepartment of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA. psubbaia@uic.edu
Xian-Cheng Jiang
Natalia A Belikova
Buzulagu Aizezi
Zhi Hua Huang
Catherine A Reardon
University of Illinois Chicago · USUniversity of Chicago · US

Funding

ROLE OF SPHINGOMYELIN IN LIPOPROTEIN METABOLISMR01HL068585 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SUBBAIAH, PAPASANI V · 2002 to 2012
$3.3M
The effect of macrophage sphingomyelin synthase (SMS) on atherosclerosisR01HL093419 · NHLBI · SUNY DOWNSTATE MEDICAL CENTER · PI JIANG, XIAN-CHENG · 2009 to 2010
$853k
Physiological Significance of Conjugated Double Bonds in Membrane LipidsR21DK078165 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SUBBAIAH, PAPASANI V · 2008 to 2009
$432k
NHLBI NIH HHS R01 HL068585NHLBI NIH HHS R01 HL093419NHLBI NIH HHS R01 HL093419-01A1NIDDK NIH HHS R21 DK078165
6 · The paper itself

Abstract

Although sphingomyelin (SM) is the most abundant phospholipid in the plasma, next to phosphatidylcholine (PC), its physiological function in plasma is unclear. Here we employed plasma from various genetic models of mice which naturally differ in their plasma SM/PC ratios, to study the role of SM as a modulator of LCAT, the enzyme responsible for HDL maturation and the synthesis of cholesteryl esters (CE) in normal plasma. Serine palmitoyltransferase deficient mice, and SM synthase deficient mice, both of which have below normal SM/PC ratios, showed significantly elevated LCAT activities when assayed with the endogenous substrates. On the other hand, LDL receptor knockout mice, and apo E knockout mice, both of which have high SM/PC ratios, had markedly reduced (-80%) LCAT activities. The LCAT levels in plasma, as assayed with an exogenous substrate, were similar in all groups, except for a 45% decrease in apo E knockout mice. Plasma samples with high SM/PC ratios had lower percentage of 20:4, 22:5, and 22:6 CE all of which are formed by LCAT, and a higher percentage of the atherogenic 18:1 CE which is mainly derived from the action of liver ACAT, showing that in vivo, the contribution of LCAT to plasma CE is reduced while that of liver ACAT is increased. These results show that SM is a physiological modulator of LCAT activity as well as plasma CE composition, and this may contribute to the previously reported pro-atherogenic effect of high plasma SM levels.

Indexed as

AnimalsApolipoproteins ECholesterolCholesterol EstersEsterificationLipidsMass SpectrometryMiceMice, Inbred C57BLMice, KnockoutPhosphatidylcholinesPhosphatidylcholine-Sterol O-AcyltransferaseReceptors, LDLSerine C-PalmitoyltransferaseSphingomyelinsSubstrate SpecificityApolipoproteins ECholesterolCholesterol EstersLipidsPhosphatidylcholinesPhosphatidylcholine-Sterol O-AcyltransferaseReceptors, LDLSerine C-PalmitoyltransferaseSgms2 protein, mouseSphingomyelinsSptlc2 protein, mouseTransferases (Other Substituted Phosphate Groups)

Identifiers

PMID22370449
PMCPMC3340435
OpenAlexW2064352121

What OpenQuestion holds

Textmetadata
LicenceTDM
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.