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a(MESH:"Thiobarbituric Acid Reactive Substances")

Equivalencies: 0 | Classes: 0 | Children: 0 | Explore

Entity

Name
Thiobarbituric Acid Reactive Substances
Namespace
MeSH
Namespace Version
20181007
Namespace URL
https://raw.githubusercontent.com/pharmacome/terminology/01c9daa61012b37dd0a1bc962521ba51a15b38f1/external/mesh-names.belns

Appears in Networks 1

Heme Curation v0.0.1-dev

Mechanistic knowledge surrounding heme

In-Edges 5

a(HM:"ruptured complicated lesions") positiveCorrelation a(MESH:"Thiobarbituric Acid Reactive Substances") View Subject | View Object

Concentrations of iron, conjugated dienes and lipid hydroperoxides were elevated by about 2- fold in ruptured complicated lesions, as compared to atheromatous lesions (0.433 ± 0.075 vs. 0.185 ± 0.096 nmol Fe/mg tissue; 0.047 ± 0.019 vs. 0.021 ± 0.003 A234 conjugated dienes/mg tissue and 0.465 ± 0.110 vs. 0.248 ± 0.106 nmol LOOH/mg tissue, respectively) and complicated lesions contained 5.6 times more TBARs than atheromatous lesions (0.028 ± 0.012 vs. 0.005 ± 0.001 nmol/mg tissue). PubMed:20378845

Appears in Networks:
Annotations
Cell Ontology (CL)
endothelial cell
MeSH
Plaque, Atherosclerotic
Text Location
Results

bp(HM:"Atheromatous lesions") positiveCorrelation a(MESH:"Thiobarbituric Acid Reactive Substances") View Subject | View Object

Levels of conjugated dienes, lipid hydroperoxides and TBARs were significantly higher in atheromatous lesions compared to controls (supplemental Table I). PubMed:20378845

Appears in Networks:
Annotations
Cell Ontology (CL)
endothelial cell
MeSH
Plaque, Atherosclerotic
Text Location
Results

complex(a(CHEBI:heme), a(HM:"Atheroma lipid")) increases a(MESH:"Thiobarbituric Acid Reactive Substances") View Subject | View Object

As is true of intact hemoglobin, lipid extracts from atheromatous lesions exposed to heme also underwent lipid peroxidation as reflected by the accumulation of thiobarbituric acid-reactive substances (TBARs) and lipid hydroperoxides (supplemental Fig I). PubMed:20378845

Appears in Networks:
Annotations
Cell Ontology (CL)
endothelial cell
MeSH
Plaque, Atherosclerotic
Text Location
Results

rxn(reactants(a(CHEBI:heme), a(HM:"Atheroma lipid")), products(a(MESH:"Thiobarbituric Acid Reactive Substances"))) hasProduct a(MESH:"Thiobarbituric Acid Reactive Substances") View Subject | View Object

Appears in Networks:

rxn(reactants(a(HM:"Atheroma lipid"), a(HM:ferrihemoglobin)), products(a(MESH:"Thiobarbituric Acid Reactive Substances"))) hasProduct a(MESH:"Thiobarbituric Acid Reactive Substances") View Subject | View Object

Appears in Networks:

Out-Edges 2

a(MESH:"Thiobarbituric Acid Reactive Substances") positiveCorrelation bp(HM:"Atheromatous lesions") View Subject | View Object

Levels of conjugated dienes, lipid hydroperoxides and TBARs were significantly higher in atheromatous lesions compared to controls (supplemental Table I). PubMed:20378845

Appears in Networks:
Annotations
Cell Ontology (CL)
endothelial cell
MeSH
Plaque, Atherosclerotic
Text Location
Results

a(MESH:"Thiobarbituric Acid Reactive Substances") positiveCorrelation a(HM:"ruptured complicated lesions") View Subject | View Object

Concentrations of iron, conjugated dienes and lipid hydroperoxides were elevated by about 2- fold in ruptured complicated lesions, as compared to atheromatous lesions (0.433 ± 0.075 vs. 0.185 ± 0.096 nmol Fe/mg tissue; 0.047 ± 0.019 vs. 0.021 ± 0.003 A234 conjugated dienes/mg tissue and 0.465 ± 0.110 vs. 0.248 ± 0.106 nmol LOOH/mg tissue, respectively) and complicated lesions contained 5.6 times more TBARs than atheromatous lesions (0.028 ± 0.012 vs. 0.005 ± 0.001 nmol/mg tissue). PubMed:20378845

Appears in Networks:
Annotations
Cell Ontology (CL)
endothelial cell
MeSH
Plaque, Atherosclerotic
Text Location
Results

About

BEL Commons is developed and maintained in an academic capacity by Charles Tapley Hoyt and Daniel Domingo-Fernández at the Fraunhofer SCAI Department of Bioinformatics with support from the IMI project, AETIONOMY. It is built on top of PyBEL, an open source project. Please feel free to contact us here to give us feedback or report any issues. Also, see our Publishing Notes and Data Protection information.

If you find BEL Commons useful in your work, please consider citing: Hoyt, C. T., Domingo-Fernández, D., & Hofmann-Apitius, M. (2018). BEL Commons: an environment for exploration and analysis of networks encoded in Biological Expression Language. Database, 2018(3), 1–11.