Matches in SemOpenAlex for { <https://semopenalex.org/work/W1903522567> ?p ?o ?g. }
- W1903522567 endingPage "959" @default.
- W1903522567 startingPage "954" @default.
- W1903522567 abstract "Susceptibility to atherosclerosis is determined by a combination of genetic and environmental factors, including diet. Consumption of diets rich in soy protein has been claimed to protect against the development of atherosclerosis. Potential mechanisms include cholesterol lowering, inhibition of lipoprotein oxidation and inhibition of cell proliferation by soy proteins or isoflavones, such as genistein, that are present in soy. This study was designed to determine whether soy isoflavones confer protection against atherosclerosis in mice and whether they reduce serum cholesterol levels and lipoprotein oxidation. C57BL/6 and LDL receptor-deficient (LDLr-null) mice were fed soy protein-based, high fat diets with isoflavones present (IF+, 20.85 g/100 g protein, 0.027 g/100 g genistein, 0.009 g/100 g daidzein) or diets from which isoflavones, and possibly other components, had been extracted (IF-, 20.0 g/100 g protein, 0.002 g/100 g genistein, 0.001 g/100 g daidzein). Because LDLr-null mice develop extensive atherosclerosis and hypercholesterolemia after minimal time on a high fat diet, they were fed the diets for 6 wk, whereas C57BL/6 mice were fed the diets for 10 wk. Plasma cholesterol levels did not differ between LDLr-null mice fed IF- and those fed IF+, but were 30% lower in C57BL/6 mice fed the IF+ diet than in those fed the IF- diet. Susceptibility of LDL to oxidative modification, measured as the lag phase of conjugated diene formation in LDLr-null mice, was not altered by isoflavone consumption. All LDLr-null mice developed atherosclerosis, and the presence or deficiency of dietary isoflavones did not influence atherosclerotic lesion area. In contrast, atherosclerotic lesion area was significantly reduced in C57BL/6 mice fed IF+ compared with those fed IF-. Thus, this study demonstrates that although the isoflavone-containing diet resulted in a reduction in cholesterol levels in C57BL/6 mice, it had no effect on cholesterol levels or on susceptibility of LDL to oxidative modification in LDLr-null mice. Further, dietary isoflavones did not protect against the development of atherosclerosis in LDLr-null mice but did decrease atherosclerosis in C57BL/6 mice. These findings suggest that soy isoflavones might lower cholesterol levels by increasing LDL receptor activity, and the reduction in cholesterol may offer some protection against atherosclerosis." @default.
- W1903522567 created "2016-06-24" @default.
- W1903522567 creator A5022745436 @default.
- W1903522567 creator A5026450314 @default.
- W1903522567 creator A5026874116 @default.
- W1903522567 creator A5055183455 @default.
- W1903522567 creator A5073356240 @default.
- W1903522567 date "1998-06-01" @default.
- W1903522567 modified "2023-10-10" @default.
- W1903522567 title "Dietary Isoflavones Reduce Plasma Cholesterol and Atherosclerosis in C57BL/6 Mice but not LDL Receptor–Deficient Mice ," @default.
- W1903522567 cites W1529541870 @default.
- W1903522567 cites W1537961425 @default.
- W1903522567 cites W1554134239 @default.
- W1903522567 cites W1595516692 @default.
- W1903522567 cites W1596602458 @default.
- W1903522567 cites W1656644300 @default.
- W1903522567 cites W1982775851 @default.
- W1903522567 cites W1992085688 @default.
- W1903522567 cites W2000027451 @default.
- W1903522567 cites W2008176752 @default.
- W1903522567 cites W2009856458 @default.
- W1903522567 cites W2031595603 @default.
- W1903522567 cites W2032303692 @default.
- W1903522567 cites W2038846370 @default.
- W1903522567 cites W2046547573 @default.
- W1903522567 cites W2047631084 @default.
- W1903522567 cites W2056245899 @default.
- W1903522567 cites W2062019500 @default.
- W1903522567 cites W2082668049 @default.
- W1903522567 cites W2086718179 @default.
- W1903522567 cites W2095314310 @default.
- W1903522567 cites W2099450181 @default.
- W1903522567 cites W2116371832 @default.
- W1903522567 cites W2124237530 @default.
- W1903522567 cites W2128570255 @default.
- W1903522567 cites W2137570167 @default.
- W1903522567 cites W2138091254 @default.
- W1903522567 cites W2172031005 @default.
- W1903522567 cites W2172216800 @default.
- W1903522567 cites W2172243901 @default.
- W1903522567 cites W2212323528 @default.
- W1903522567 cites W2333028705 @default.
- W1903522567 cites W3022864527 @default.
- W1903522567 cites W572771 @default.
- W1903522567 doi "https://doi.org/10.1093/jn/128.6.954" @default.
- W1903522567 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9614153" @default.
- W1903522567 hasPublicationYear "1998" @default.
- W1903522567 type Work @default.
- W1903522567 sameAs 1903522567 @default.
- W1903522567 citedByCount "227" @default.
- W1903522567 countsByYear W19035225672012 @default.
- W1903522567 countsByYear W19035225672013 @default.
- W1903522567 countsByYear W19035225672014 @default.
- W1903522567 countsByYear W19035225672015 @default.
- W1903522567 countsByYear W19035225672016 @default.
- W1903522567 countsByYear W19035225672017 @default.
- W1903522567 countsByYear W19035225672018 @default.
- W1903522567 countsByYear W19035225672019 @default.
- W1903522567 countsByYear W19035225672020 @default.
- W1903522567 countsByYear W19035225672021 @default.
- W1903522567 countsByYear W19035225672022 @default.
- W1903522567 crossrefType "journal-article" @default.
- W1903522567 hasAuthorship W1903522567A5022745436 @default.
- W1903522567 hasAuthorship W1903522567A5026450314 @default.
- W1903522567 hasAuthorship W1903522567A5026874116 @default.
- W1903522567 hasAuthorship W1903522567A5055183455 @default.
- W1903522567 hasAuthorship W1903522567A5073356240 @default.
- W1903522567 hasBestOaLocation W19035225671 @default.
- W1903522567 hasConcept C126322002 @default.
- W1903522567 hasConcept C134018914 @default.
- W1903522567 hasConcept C185592680 @default.
- W1903522567 hasConcept C2777014122 @default.
- W1903522567 hasConcept C2778163477 @default.
- W1903522567 hasConcept C2778298627 @default.
- W1903522567 hasConcept C2779620165 @default.
- W1903522567 hasConcept C2779705811 @default.
- W1903522567 hasConcept C2780072125 @default.
- W1903522567 hasConcept C2780955279 @default.
- W1903522567 hasConcept C43554185 @default.
- W1903522567 hasConcept C55493867 @default.
- W1903522567 hasConcept C71924100 @default.
- W1903522567 hasConcept C86803240 @default.
- W1903522567 hasConceptScore W1903522567C126322002 @default.
- W1903522567 hasConceptScore W1903522567C134018914 @default.
- W1903522567 hasConceptScore W1903522567C185592680 @default.
- W1903522567 hasConceptScore W1903522567C2777014122 @default.
- W1903522567 hasConceptScore W1903522567C2778163477 @default.
- W1903522567 hasConceptScore W1903522567C2778298627 @default.
- W1903522567 hasConceptScore W1903522567C2779620165 @default.
- W1903522567 hasConceptScore W1903522567C2779705811 @default.
- W1903522567 hasConceptScore W1903522567C2780072125 @default.
- W1903522567 hasConceptScore W1903522567C2780955279 @default.
- W1903522567 hasConceptScore W1903522567C43554185 @default.
- W1903522567 hasConceptScore W1903522567C55493867 @default.
- W1903522567 hasConceptScore W1903522567C71924100 @default.
- W1903522567 hasConceptScore W1903522567C86803240 @default.
- W1903522567 hasIssue "6" @default.
- W1903522567 hasLocation W19035225671 @default.