Evidence map›Paper›PMID 20876113›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

Oleoyl serine, an endogenous N-acyl amide, modulates bone remodeling and mass.

Reem Smoum, Arik Bar, Bo Tan, Garry Milman, Malka Attar-Namdar, Orr Ofek, Jordyn M Stuart, Alon Bajayo, Joseph Tam, Vardit Kram and 5 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

44 citing papers in PubMed, 83 citations in OpenAlex.

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  7. TheApplied and environmental microbiology · 2024
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  16. Biomolecules · 2019
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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

15 authors at 2 institutions in 2 countries.

Reem SmoumBone Laboratory and Institute of Drug Research, Hebrew University of Jerusalem, Jerusalem 91120, Israel.
Arik Bar
Bo Tan
Garry Milman
Malka Attar-Namdar
Orr Ofek
Jordyn M Stuart
Alon Bajayo
Joseph Tam
Vardit Kram
David O'Dell
Michael J Walker
Heather B Bradshaw
Itai Bab
Raphael Mechoulam
Indiana University Bloomington · USHebrew University of Jerusalem · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone mass is determined by a continuous remodeling process, whereby the mineralized matrix is being removed by osteoclasts and subsequently replaced with newly formed bone tissue produced by osteoblasts. Here we report the presence of endogenous amides of long-chain fatty acids with amino acids or with ethanolamine (N-acyl amides) in mouse bone. Of these compounds, N-oleoyl-l-serine (OS) had the highest activity in an osteoblast proliferation assay. In these cells, OS triggers a Gi-protein-coupled receptor and Erk1/2. It also mitigates osteoclast number by promoting osteoclast apoptosis through the inhibition of Erk1/2 phosphorylation and receptor activator of nuclear-κB ligand (RANKL) expression in bone marrow stromal cells and osteoblasts. In intact mice, OS moderately increases bone volume density mainly by inhibiting bone resorption. However, in a mouse ovariectomy (OVX) model for osteoporosis, OS effectively rescues bone loss by increasing bone formation and markedly restraining bone resorption. The differential effect of exogenous OS in the OVX vs. intact animals is apparently a result of an OVX-induced decrease in skeletal OS levels. These data show that OS is a previously unexplored lipid regulator of bone remodeling. It represents a lead to antiosteoporotic drug discovery, advantageous to currently available therapies, which are essentially either proformative or antiresorptive.

Indexed as

AmidesAnalysis of VarianceAnimalsBlotting, WesternBone DensityBone RemodelingCell LineChromatography, High Pressure LiquidMass SpectrometryMiceMice, Inbred C57BLMitogen-Activated Protein Kinase 3Oleic AcidsOsteoblastsOsteoporosisReceptors, G-Protein-CoupledAmidesMitogen-Activated Protein Kinase 3Oleic AcidsReceptors, G-Protein-CoupledSerine

Identifiers

PMID20876113
PMCPMC2955099
OpenAlexW2097704313

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.