Matches in SemOpenAlex for { <https://semopenalex.org/work/W1974041941> ?p ?o ?g. }
- W1974041941 endingPage "2295" @default.
- W1974041941 startingPage "2287" @default.
- W1974041941 abstract "We sought to determine whether asymmetric dimethylarginine (ADMA) inhibits nitric oxide (NO) elaboration in cultured human endothelial cells and whether this is associated with the activation of oxidant-sensitive signaling mediating endothelial adhesiveness for monocytes.Endothelial NO elaboration is impaired in hypercholesterolemia and atherosclerosis, which may be due to elevated concentrations of ADMA, an endogenous inhibitor of NO synthase.Human umbilical vein endothelial cells (ECV 304) and human monocytoid cells (THP-1) were studied in a functional binding assay. Nitric oxide and superoxide anion (O2-) were measured by chemiluminescence; ADMA by high pressure liquid chromatography; monocyte chemotactic protein-1 (MCP-1) by ELISA and NF-KB by electromobility gel shift assay.Incubation of endothelial cells with ADMA (0.1 microM to 100 microM) inhibited NO formation, which was reversed by coincubation with L-arginine (1 mM). The biologically inactive stereoisomer symmetric dimethylarginine did not inhibit NO release. Asymmetric dimethylarginine (10 microM) or native low-density lipoprotein cholesterol (100 mg/dL) increased endothelial O2- to the same degree. Asymmetric dimethylarginine also stimulated MCP-1 formation by endothelial cells. This effect was paralleled by activation of the redox-sensitive transcription factor NF-KB. Preincubation of endothelial cells with ADMA increased the adhesiveness of endothelial cells for THP-1 cells in a concentration-dependent manner. Asymmetric dimethylarginine-induced monocyte binding was diminished by L-arginine or by a neutralizing anti-MCP-1 antibody.We concluded that the endogenous NO synthase inhibitor ADMA is synthesized in human endothelial cells. Asymmetric dimethylarginine increases endothelial oxidative stress and potentiates monocyte binding. Asymmetric dimethylarginine may be an endogenous proatherogenic molecule." @default.
- W1974041941 created "2016-06-24" @default.
- W1974041941 creator A5010081940 @default.
- W1974041941 creator A5022967341 @default.
- W1974041941 creator A5038106053 @default.
- W1974041941 creator A5039670487 @default.
- W1974041941 creator A5058198453 @default.
- W1974041941 creator A5061182191 @default.
- W1974041941 date "2000-12-01" @default.
- W1974041941 modified "2023-09-30" @default.
- W1974041941 title "An endogenous inhibitor of nitric oxide synthase regulates endothelial adhesiveness for monocytes" @default.
- W1974041941 cites W1769783081 @default.
- W1974041941 cites W1775749144 @default.
- W1974041941 cites W1963480212 @default.
- W1974041941 cites W1963781173 @default.
- W1974041941 cites W1966525844 @default.
- W1974041941 cites W1968141837 @default.
- W1974041941 cites W1969703987 @default.
- W1974041941 cites W1970161435 @default.
- W1974041941 cites W1970798352 @default.
- W1974041941 cites W1971061508 @default.
- W1974041941 cites W1977662482 @default.
- W1974041941 cites W1983392660 @default.
- W1974041941 cites W1984686431 @default.
- W1974041941 cites W1997640957 @default.
- W1974041941 cites W2000881220 @default.
- W1974041941 cites W2004381880 @default.
- W1974041941 cites W2007361075 @default.
- W1974041941 cites W2007375934 @default.
- W1974041941 cites W2010715396 @default.
- W1974041941 cites W2021873664 @default.
- W1974041941 cites W2028673656 @default.
- W1974041941 cites W2033974115 @default.
- W1974041941 cites W2036062936 @default.
- W1974041941 cites W2038505321 @default.
- W1974041941 cites W2042782418 @default.
- W1974041941 cites W2043595406 @default.
- W1974041941 cites W2044013576 @default.
- W1974041941 cites W2045600660 @default.
- W1974041941 cites W2048020333 @default.
- W1974041941 cites W2054949240 @default.
- W1974041941 cites W2071654814 @default.
- W1974041941 cites W2072265495 @default.
- W1974041941 cites W2076995420 @default.
- W1974041941 cites W2082233445 @default.
- W1974041941 cites W2083217753 @default.
- W1974041941 cites W2083285004 @default.
- W1974041941 cites W2087576623 @default.
- W1974041941 cites W2094470225 @default.
- W1974041941 cites W2103079216 @default.
- W1974041941 cites W2106478344 @default.
- W1974041941 cites W2126795982 @default.
- W1974041941 cites W2139319526 @default.
- W1974041941 cites W2141537184 @default.
- W1974041941 cites W2151554519 @default.
- W1974041941 cites W2157961837 @default.
- W1974041941 cites W2161887334 @default.
- W1974041941 cites W2162010936 @default.
- W1974041941 cites W2170748270 @default.
- W1974041941 cites W2172296189 @default.
- W1974041941 cites W2328664855 @default.
- W1974041941 cites W2338686524 @default.
- W1974041941 cites W2415194500 @default.
- W1974041941 doi "https://doi.org/10.1016/s0735-1097(00)01013-5" @default.
- W1974041941 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/11127475" @default.
- W1974041941 hasPublicationYear "2000" @default.
- W1974041941 type Work @default.
- W1974041941 sameAs 1974041941 @default.
- W1974041941 citedByCount "222" @default.
- W1974041941 countsByYear W19740419412012 @default.
- W1974041941 countsByYear W19740419412013 @default.
- W1974041941 countsByYear W19740419412014 @default.
- W1974041941 countsByYear W19740419412015 @default.
- W1974041941 countsByYear W19740419412016 @default.
- W1974041941 countsByYear W19740419412017 @default.
- W1974041941 countsByYear W19740419412018 @default.
- W1974041941 countsByYear W19740419412019 @default.
- W1974041941 countsByYear W19740419412020 @default.
- W1974041941 countsByYear W19740419412021 @default.
- W1974041941 countsByYear W19740419412022 @default.
- W1974041941 countsByYear W19740419412023 @default.
- W1974041941 crossrefType "journal-article" @default.
- W1974041941 hasAuthorship W1974041941A5010081940 @default.
- W1974041941 hasAuthorship W1974041941A5022967341 @default.
- W1974041941 hasAuthorship W1974041941A5038106053 @default.
- W1974041941 hasAuthorship W1974041941A5039670487 @default.
- W1974041941 hasAuthorship W1974041941A5058198453 @default.
- W1974041941 hasAuthorship W1974041941A5061182191 @default.
- W1974041941 hasBestOaLocation W19740419412 @default.
- W1974041941 hasConcept C123012128 @default.
- W1974041941 hasConcept C126322002 @default.
- W1974041941 hasConcept C134018914 @default.
- W1974041941 hasConcept C16613235 @default.
- W1974041941 hasConcept C181199279 @default.
- W1974041941 hasConcept C185592680 @default.
- W1974041941 hasConcept C202751555 @default.
- W1974041941 hasConcept C2776992346 @default.
- W1974041941 hasConcept C2777411675 @default.