Please use this identifier to cite or link to this item:
https://doi.org/10.3390/nu9070722
DC Field | Value | |
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dc.title | Metabolic and blood pressure effects of walnut supplementation in a mouse model of the metabolic syndrome | |
dc.contributor.author | Scott, N.J.A | |
dc.contributor.author | Ellmers, L.J | |
dc.contributor.author | Pilbrow, A.P | |
dc.contributor.author | Thomsen, L | |
dc.contributor.author | Richards, A.M | |
dc.contributor.author | Frampton, C.M | |
dc.contributor.author | Cameron, V.A | |
dc.date.accessioned | 2020-10-21T07:49:39Z | |
dc.date.available | 2020-10-21T07:49:39Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Scott, 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.issn | 20726643 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/178666 | |
dc.description.abstract | There 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.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | activating transcription factor 6 | |
dc.subject | cholesterol | |
dc.subject | creatinine | |
dc.subject | growth arrest and DNA damage inducible protein 153 | |
dc.subject | initiation factor 2 | |
dc.subject | non receptor protein tyrosine phosphatase 22 | |
dc.subject | peroxisome proliferator activated receptor gamma | |
dc.subject | tissue inhibitor of metalloproteinase 1 | |
dc.subject | transcription factor Sp1 | |
dc.subject | triacylglycerol | |
dc.subject | tumor necrosis factor | |
dc.subject | apolipoprotein E | |
dc.subject | aromatase | |
dc.subject | lipid | |
dc.subject | plant extract | |
dc.subject | animal model | |
dc.subject | animal tissue | |
dc.subject | area under the curve | |
dc.subject | Article | |
dc.subject | blood pressure | |
dc.subject | blood pressure measurement | |
dc.subject | body weight | |
dc.subject | cell stress | |
dc.subject | controlled study | |
dc.subject | diet supplementation | |
dc.subject | female | |
dc.subject | food intake | |
dc.subject | gene expression | |
dc.subject | genotype | |
dc.subject | glucose blood level | |
dc.subject | inflammation | |
dc.subject | insulin sensitivity | |
dc.subject | kidney fibrosis | |
dc.subject | liver metabolism | |
dc.subject | male | |
dc.subject | mean arterial pressure | |
dc.subject | metabolic rate | |
dc.subject | metabolic syndrome X | |
dc.subject | mouse | |
dc.subject | nonhuman | |
dc.subject | oral glucose tolerance test | |
dc.subject | quantitative analysis | |
dc.subject | real time polymerase chain reaction | |
dc.subject | walnut | |
dc.subject | animal | |
dc.subject | blood | |
dc.subject | blood pressure | |
dc.subject | C57BL mouse | |
dc.subject | chemistry | |
dc.subject | cross breeding | |
dc.subject | deficiency | |
dc.subject | dietary supplement | |
dc.subject | disease model | |
dc.subject | drug effects | |
dc.subject | genetics | |
dc.subject | knockout mouse | |
dc.subject | liver | |
dc.subject | metabolic syndrome X | |
dc.subject | metabolism | |
dc.subject | nut | |
dc.subject | pathophysiology | |
dc.subject | transgenic mouse | |
dc.subject | walnut | |
dc.subject | Animals | |
dc.subject | Apolipoproteins E | |
dc.subject | Aromatase | |
dc.subject | Blood Pressure | |
dc.subject | Crosses, Genetic | |
dc.subject | Dietary Supplements | |
dc.subject | Disease Models, Animal | |
dc.subject | Female | |
dc.subject | Gene Expression | |
dc.subject | Juglans | |
dc.subject | Lipids | |
dc.subject | Liver | |
dc.subject | Male | |
dc.subject | Metabolic Syndrome | |
dc.subject | Mice | |
dc.subject | Mice, Inbred C57BL | |
dc.subject | Mice, Knockout | |
dc.subject | Mice, Transgenic | |
dc.subject | Nuts | |
dc.subject | Plant Extracts | |
dc.type | Article | |
dc.contributor.department | MEDICINE | |
dc.description.doi | 10.3390/nu9070722 | |
dc.description.sourcetitle | Nutrients | |
dc.description.volume | 9 | |
dc.description.issue | 7 | |
dc.description.page | 722 | |
Appears in Collections: | Elements Staff Publications |
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