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  • 1
    In: Circulation, Ovid Technologies (Wolters Kluwer Health), Vol. 144, No. Suppl_1 ( 2021-11-16)
    Abstract: Background: A healthy diet is a cornerstone of CVD prevention and management. The vascular impact of very-low-carbohydrate (CHO), high-fat diets, or ketogenic diets (KD), remains unclear. Hypothesis: A KD will be protective against atherogenesis compared to a moderate-CHO, high-fat diet (HFD). Methods: Seven-week-old male apoE -/- mice, a model for human atherosclerosis, were fed two casein-based diets ad libitum for 12 weeks (Kcal%, CHO/fat/protein): KD (1/81/18) or HFD (42/40/18). Animals (6-8/group) were weighed weekly, and plasma was collected for quantification of beta-hydroxybutyrate (BHB) by a colorimetric assay, the inflammatory cytokines MCP1 and TNFα by immunoassays, and targeted metabolites by LC-MS/MS. Aortic atherosclerotic lesions were quantified ex-vivo by MRI on a 14-tesla-system. Results: KD mice weighed significantly less than HFD mice, reflecting the anti-obesogenic effect of the KD diet. Relative to HFD mice, the BHB level was markedly higher, and cytokines were significantly lower in the KD group, confirming the presence of ketosis in KD mice that alleviated the well-established fat-induced systemic inflammation. Several changes in the plasma metabolome driven by KD included a significant decrease in lipophilic metabolites, with increases in hydrophilic ones. Despite the higher fat content of KD versus HFD, KD mice presented significantly lower levels of several lipid metabolites including phosphatidylcholines, cholesterol esters, sphingomyelins, and ceramides. Consistent with the shift in energy metabolism toward fatty acid oxidation caused by the KD, the ratio of acyl-carnitines to free carnitine was significantly higher in KD than in HFD mice. Mice under nutritional ketosis displayed a distinct plasma amino acid profile evidencing a KD-induced alteration in protein metabolism. These included increased levels of the constituents of the major antioxidant glutathione, suggesting a more favorable redox status in the animals under nutritional ketosis. Lastly, the aortic plaque burden was significantly lower in the KD (4.8t±2.4 vol%) versus the HFD (12.8±6.72 vol%) group. Conclusion: Nutritional ketosis induced by the KD was associated with specific metabolic changes and an atheroprotective phenotype versus HFD.
    Type of Medium: Online Resource
    ISSN: 0009-7322 , 1524-4539
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2021
    detail.hit.zdb_id: 1466401-X
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  • 2
    Online Resource
    Online Resource
    Elsevier BV ; 2022
    In:  Current Developments in Nutrition Vol. 6 ( 2022-06), p. 438-
    In: Current Developments in Nutrition, Elsevier BV, Vol. 6 ( 2022-06), p. 438-
    Type of Medium: Online Resource
    ISSN: 2475-2991
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2022
    detail.hit.zdb_id: 2908329-1
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  • 3
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2023
    In:  Magnetic Resonance Materials in Physics, Biology and Medicine
    In: Magnetic Resonance Materials in Physics, Biology and Medicine, Springer Science and Business Media LLC
    Abstract: Pre-clinical models of human atherosclerosis are extensively used; however, traditional histological methods do not allow for a holistic view of vascular lesions. We describe an ex-vivo, high-resolution MRI method that allows the 3 dimensional imaging of the vessel for aortic plaque visualization and quantification. Materials and methods Aortas from apolipoprotein-E-deficient ( apoE −/− ) mice fed an atherogenic diet (group 1) or a control diet (group 2) were subjected to 14 T MR imaging using a 3D gradient echo sequence. The obtained data sets were reconstructed (Matlab), segmented, and analyzed (Avizo). The aortas were further sectioned and subjected to traditional histological analysis (Oil-Red O and hematoxylin staining) for comparison. Results A resolution up to 15 × 10x10 μm 3 revealed that plaque burden (mm 3 ) was significantly ( p   〈  0.05) higher in group 1 (0.41 ± 0.25, n  = 4) than in group 2 (0.01 ± 0.01, n  = 3). The achieved resolution provided similar detail on the plaque and the vessel wall morphology compared with histology. Digital image segmentation of the aorta's lumen, plaque, and wall offered three-dimensional visualizations of the entire, intact aortas. Discussion 14 T MR microscopy provided histology-like details of pathologically relevant vascular lesions. This work may provide the path research needs to take to enable plaque characterization in clinical applications.
    Type of Medium: Online Resource
    ISSN: 1352-8661
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2023
    detail.hit.zdb_id: 1502491-X
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  • 4
    In: Biomedicines, MDPI AG, Vol. 10, No. 5 ( 2022-05-18), p. 1159-
    Abstract: Ketogenic diets (KDs) are very low-carbohydrate, very high-fat diets which promote nutritional ketosis and impact energetic metabolism. Aquaporins (AQPs) are transmembrane channels that facilitate water and glycerol transport across cell membranes and are critical players in energy homeostasis. Altered AQP expression or function impacts fat accumulation and related comorbidities, such as the metabolic syndrome. Here, we sought to determine whether nutritional ketosis impacts AQPs expression in the context of an atherogenic model. To do this, we fed ApoE−/− (apolipoprotein E-deficient) mice, a model of human atherosclerosis, a KD (Kcal%: 1/81/18, carbohydrate/fat/protein) or a control diet (Kcal%: 70/11/18, carbohydrate/fat/protein) for 12 weeks. Plasma was collected for biochemical analysis. Upon euthanasia, livers, white adipose tissue (WAT), and brown adipose tissue (BAT) were used for gene expression studies. Mice fed the KD and control diets exhibited similar body weights, despite the profoundly different fat contents in the two diets. Moreover, KD-fed mice developed nutritional ketosis and showed increased expression of thermogenic genes in BAT. Additionally, these mice presented an increase in Aqp9 transcripts in BAT, but not in WAT, which suggests the participation of Aqp9 in the influx of excess plasma glycerol to fuel thermogenesis, while the up-regulation of Aqp7 in the liver suggests the involvement of this aquaporin in glycerol influx into hepatocytes. The relationship between nutritional ketosis, energy homeostasis, and the AQP network demands further investigation.
    Type of Medium: Online Resource
    ISSN: 2227-9059
    Language: English
    Publisher: MDPI AG
    Publication Date: 2022
    detail.hit.zdb_id: 2720867-9
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  • 5
    In: Current Developments in Nutrition, Elsevier BV, Vol. 5 ( 2021-06), p. 953-
    Type of Medium: Online Resource
    ISSN: 2475-2991
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2021
    detail.hit.zdb_id: 2908329-1
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  • 6
    In: Nutrients, MDPI AG, Vol. 13, No. 10 ( 2021-10-13), p. 3576-
    Abstract: Hyperhomocysteneinemia (HHcy) is common in the general population and is a risk factor for atherosclerosis by mechanisms that are still elusive. A hypomethylated status of epigenetically relevant targets may contribute to the vascular toxicity associated with HHcy. Ketogenic diets (KD) are diets with a severely restricted amount of carbohydrates that are being widely used, mainly for weight-loss purposes. However, studies associating nutritional ketosis and HHcy are lacking. This pilot study investigates the effects of mild HHcy induced by nutritional manipulation of the methionine metabolism in the absence of dietary carbohydrates on disease progression and specific epigenetic changes in the apolipoprotein-E deficient (apoE–/–) mouse model. ApoE–/– mice were either fed a KD, a diet with the same macronutrient composition but low in methyl donors (low methyl KD, LMKD), or control diet. After 4, 8 or 12 weeks plasma was collected for the quantification of: (1) nutritional ketosis, (i.e., the ketone body beta-hydroxybutyrate using a colorimetric assay); (2) homocysteine by HPLC; (3) the methylating potential S-adenosylmethionine to S-adenosylhomocysteine ratio (AdoHcy/AdoMet) by LC-MS/MS; and (4) the inflammatory cytokine monocyte chemoattractant protein 1 (MCP1) by ELISA. After 12 weeks, aortas were collected to assess: (1) the vascular AdoHcy/AdoMet ratio; (2) the volume of atherosclerotic lesions by high-field magnetic resonance imaging (14T-MRI); and (3) the content of specific epigenetic tags (H3K27me3 and H3K27ac) by immunofluorescence. The results confirmed the presence of nutritional ketosis in KD and LMKD mice but not in the control mice. As expected, mild HHcy was only detected in the LMKD-fed mice. Significantly decreased MCP1 plasma levels and plaque burden were observed in control mice versus the other two groups, together with an increased content of one of the investigated epigenetic tags (H3K27me3) but not of the other (H3K27ac). Moreover, we are unable to detect any significant differences at the p 〈 0.05 level for MCP1 plasma levels, vascular AdoMet:AdoHcy ratio levels, plaque burden, and specific epigenetic content between the latter two groups. Nevertheless, the systemic methylating index was significantly decreased in LMKD mice versus the other two groups, reinforcing the possibility that the levels of accumulated homocysteine were insufficient to affect vascular transmethylation reactions. Further studies addressing nutritional ketosis in the presence of mild HHcy should use a higher number of animals and are warranted to confirm these preliminary observations.
    Type of Medium: Online Resource
    ISSN: 2072-6643
    Language: English
    Publisher: MDPI AG
    Publication Date: 2021
    detail.hit.zdb_id: 2518386-2
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