Please use this identifier to cite or link to this item: https://doi.org/10.3390/nu9070722
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dc.titleMetabolic and blood pressure effects of walnut supplementation in a mouse model of the metabolic syndrome
dc.contributor.authorScott, N.J.A
dc.contributor.authorEllmers, L.J
dc.contributor.authorPilbrow, A.P
dc.contributor.authorThomsen, L
dc.contributor.authorRichards, A.M
dc.contributor.authorFrampton, C.M
dc.contributor.authorCameron, V.A
dc.date.accessioned2020-10-21T07:49:39Z
dc.date.available2020-10-21T07:49:39Z
dc.date.issued2017
dc.identifier.citationScott, N.J.A, Ellmers, L.J, Pilbrow, A.P, Thomsen, L, Richards, A.M, Frampton, C.M, Cameron, V.A (2017). Metabolic and blood pressure effects of walnut supplementation in a mouse model of the metabolic syndrome. Nutrients 9 (7) : 722. ScholarBank@NUS Repository. https://doi.org/10.3390/nu9070722
dc.identifier.issn20726643
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178666
dc.description.abstractThere is extensive evidence that walnut consumption is protective against cardiovascular disease and diabetes in the healthy population, but the beneficial effects of walnut consumption in individuals with the metabolic syndrome (MetS) remain uncertain. We compared a range of cardiometabolic traits and related tissue gene expression associated with 21 weeks of dietary walnut supplementation in a mouse model of MetS (MetS-Tg) and wild-type (WT) mice (n = 10 per genotype per diet, equal males and females). Compared to standard diet, walnuts did not significantly alter food consumption or body weight trajectory of either MetS-Tg or WT mice. In MetS-Tg mice, walnuts were associated with reductions in oral glucose area under the curve (gAUC, standard diet 1455 ± 54, walnut 1146 ± 91, p = 0.006) and mean arterial blood pressure (MAP, standard diet 100.6 ± 1.9, walnut 73.2 ± 1.8 mmHg, p < 0.001), with neutral effects on gAUC and MAP in WT mice. However, in MetS-Tg mice, walnuts were also associated with trends for higher plasma cholesterol (standard diet 4.73 ± 0.18, walnut 7.03 ± 1.99 mmol/L, p = 0.140) and triglyceride levels (standard diet 2.4 ± 0.5, walnut 5.4 ± 1.6 mmol/L, p = 0.061), despite lowering cholesterol and having no effect on triglycerides in WT mice. Moreover, in both MetS-Tg and WT mice, walnuts were associated with significantly increased liver expression of genes associated with metabolism (Fabp1, Insr), cell stress (Atf6, Ddit3, Eif2ak3), fibrosis (Hgf, Sp1, Timp1) and inflammation (Tnf, Ptpn22, Pparg). In conclusion, dietary walnuts were associated with modest favourable effects in WT mice, but a combination of beneficial and adverse effects in MetS-Tg mice, and up-regulation of hepatic pro-fibrotic and pro-inflammatory genes in both mouse strains. © 2017 by the authors. Licensee MDPI, Basel, Switzerland.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectactivating transcription factor 6
dc.subjectcholesterol
dc.subjectcreatinine
dc.subjectgrowth arrest and DNA damage inducible protein 153
dc.subjectinitiation factor 2
dc.subjectnon receptor protein tyrosine phosphatase 22
dc.subjectperoxisome proliferator activated receptor gamma
dc.subjecttissue inhibitor of metalloproteinase 1
dc.subjecttranscription factor Sp1
dc.subjecttriacylglycerol
dc.subjecttumor necrosis factor
dc.subjectapolipoprotein E
dc.subjectaromatase
dc.subjectlipid
dc.subjectplant extract
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectarea under the curve
dc.subjectArticle
dc.subjectblood pressure
dc.subjectblood pressure measurement
dc.subjectbody weight
dc.subjectcell stress
dc.subjectcontrolled study
dc.subjectdiet supplementation
dc.subjectfemale
dc.subjectfood intake
dc.subjectgene expression
dc.subjectgenotype
dc.subjectglucose blood level
dc.subjectinflammation
dc.subjectinsulin sensitivity
dc.subjectkidney fibrosis
dc.subjectliver metabolism
dc.subjectmale
dc.subjectmean arterial pressure
dc.subjectmetabolic rate
dc.subjectmetabolic syndrome X
dc.subjectmouse
dc.subjectnonhuman
dc.subjectoral glucose tolerance test
dc.subjectquantitative analysis
dc.subjectreal time polymerase chain reaction
dc.subjectwalnut
dc.subjectanimal
dc.subjectblood
dc.subjectblood pressure
dc.subjectC57BL mouse
dc.subjectchemistry
dc.subjectcross breeding
dc.subjectdeficiency
dc.subjectdietary supplement
dc.subjectdisease model
dc.subjectdrug effects
dc.subjectgenetics
dc.subjectknockout mouse
dc.subjectliver
dc.subjectmetabolic syndrome X
dc.subjectmetabolism
dc.subjectnut
dc.subjectpathophysiology
dc.subjecttransgenic mouse
dc.subjectwalnut
dc.subjectAnimals
dc.subjectApolipoproteins E
dc.subjectAromatase
dc.subjectBlood Pressure
dc.subjectCrosses, Genetic
dc.subjectDietary Supplements
dc.subjectDisease Models, Animal
dc.subjectFemale
dc.subjectGene Expression
dc.subjectJuglans
dc.subjectLipids
dc.subjectLiver
dc.subjectMale
dc.subjectMetabolic Syndrome
dc.subjectMice
dc.subjectMice, Inbred C57BL
dc.subjectMice, Knockout
dc.subjectMice, Transgenic
dc.subjectNuts
dc.subjectPlant Extracts
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.description.doi10.3390/nu9070722
dc.description.sourcetitleNutrients
dc.description.volume9
dc.description.issue7
dc.description.page722
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