Diet-induced dyslipidemia leads to nonalcoholic fatty liver disease and oxidative stress in guinea pigs

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Diet-induced dyslipidemia leads to nonalcoholic fatty liver disease and oxidative stress in guinea pigs. / Tveden-Nyborg, Pernille; Birck, Malene Muusfeldt; Ipsen, David Højland; Thiessen, Tina Salløe; Feldmann, Linda de Bie; Lindblad, Maiken Marie; Jensen, Henrik Elvang; Lykkesfeldt, Jens.

In: Translational Research, Vol. 168, 01.02.2016, p. 146-160.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Tveden-Nyborg, P, Birck, MM, Ipsen, DH, Thiessen, TS, Feldmann, LDB, Lindblad, MM, Jensen, HE & Lykkesfeldt, J 2016, 'Diet-induced dyslipidemia leads to nonalcoholic fatty liver disease and oxidative stress in guinea pigs', Translational Research, vol. 168, pp. 146-160. https://doi.org/10.1016/j.trsl.2015.10.001

APA

Tveden-Nyborg, P., Birck, M. M., Ipsen, D. H., Thiessen, T. S., Feldmann, L. D. B., Lindblad, M. M., Jensen, H. E., & Lykkesfeldt, J. (2016). Diet-induced dyslipidemia leads to nonalcoholic fatty liver disease and oxidative stress in guinea pigs. Translational Research, 168, 146-160. https://doi.org/10.1016/j.trsl.2015.10.001

Vancouver

Tveden-Nyborg P, Birck MM, Ipsen DH, Thiessen TS, Feldmann LDB, Lindblad MM et al. Diet-induced dyslipidemia leads to nonalcoholic fatty liver disease and oxidative stress in guinea pigs. Translational Research. 2016 Feb 1;168:146-160. https://doi.org/10.1016/j.trsl.2015.10.001

Author

Tveden-Nyborg, Pernille ; Birck, Malene Muusfeldt ; Ipsen, David Højland ; Thiessen, Tina Salløe ; Feldmann, Linda de Bie ; Lindblad, Maiken Marie ; Jensen, Henrik Elvang ; Lykkesfeldt, Jens. / Diet-induced dyslipidemia leads to nonalcoholic fatty liver disease and oxidative stress in guinea pigs. In: Translational Research. 2016 ; Vol. 168. pp. 146-160.

Bibtex

@article{2f5333bbb7374c40a466f4a63f611521,
title = "Diet-induced dyslipidemia leads to nonalcoholic fatty liver disease and oxidative stress in guinea pigs",
abstract = "Chronic dyslipidemia imposed by a high-fat and high-caloric dietary regime leads to debilitating disorders such as obesity, nonalcoholic fatty liver disease (NAFLD), and insulin resistance. As disease rates surge, so does the need for high validity animal models to effectively study the causal relationship between diet and disease progression. The dyslipidemic guinea pig displays a high similarity with the human lipoprotein profile and may in this aspect be superior to other rodent models. This study investigated the effects of 2 long-term Westernized diets (0.35% cholesterol, 18.5% vegetable oil and either 15% or 20% sucrose) compared with isocaloric standard chow in adult guinea pigs. Biochemical markers confirmed dyslipidemia in agreement with dietary regimens; however, both high-fat groups displayed a decreased tissue fat percentage compared with controls. Macroscopic appearance, histopathologic evaluation, and plasma markers of liver function confirmed NAFLD in high-fat groups, supported by liver redox imbalance and markers suggesting hepatic endothelial dysfunction. Plasma markers indicated endothelial dysfunction in response to a high-fat diet, although atherosclerotic lesions were not evident. Evaluation of glucose tolerance showed no indication of insulin resistance. The 5% increase in sucrose between the 2 high-fat diets did not lead to significant differences between groups. In conclusion, we find the dyslipidemic guinea pig to be a valid model of diet imposed dyslipidemia, particularly with regards to hepatic steatosis and endothelial dysfunction. Furthermore, the absence of obesity supports the present study setup as targeting NAFLD in nonobese individuals.Keywords",
author = "Pernille Tveden-Nyborg and Birck, {Malene Muusfeldt} and Ipsen, {David H{\o}jland} and Thiessen, {Tina Sall{\o}e} and Feldmann, {Linda de Bie} and Lindblad, {Maiken Marie} and Jensen, {Henrik Elvang} and Jens Lykkesfeldt",
year = "2016",
month = feb,
day = "1",
doi = "10.1016/j.trsl.2015.10.001",
language = "English",
volume = "168",
pages = "146--160",
journal = "Translational Research",
issn = "1931-5244",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Diet-induced dyslipidemia leads to nonalcoholic fatty liver disease and oxidative stress in guinea pigs

AU - Tveden-Nyborg, Pernille

AU - Birck, Malene Muusfeldt

AU - Ipsen, David Højland

AU - Thiessen, Tina Salløe

AU - Feldmann, Linda de Bie

AU - Lindblad, Maiken Marie

AU - Jensen, Henrik Elvang

AU - Lykkesfeldt, Jens

PY - 2016/2/1

Y1 - 2016/2/1

N2 - Chronic dyslipidemia imposed by a high-fat and high-caloric dietary regime leads to debilitating disorders such as obesity, nonalcoholic fatty liver disease (NAFLD), and insulin resistance. As disease rates surge, so does the need for high validity animal models to effectively study the causal relationship between diet and disease progression. The dyslipidemic guinea pig displays a high similarity with the human lipoprotein profile and may in this aspect be superior to other rodent models. This study investigated the effects of 2 long-term Westernized diets (0.35% cholesterol, 18.5% vegetable oil and either 15% or 20% sucrose) compared with isocaloric standard chow in adult guinea pigs. Biochemical markers confirmed dyslipidemia in agreement with dietary regimens; however, both high-fat groups displayed a decreased tissue fat percentage compared with controls. Macroscopic appearance, histopathologic evaluation, and plasma markers of liver function confirmed NAFLD in high-fat groups, supported by liver redox imbalance and markers suggesting hepatic endothelial dysfunction. Plasma markers indicated endothelial dysfunction in response to a high-fat diet, although atherosclerotic lesions were not evident. Evaluation of glucose tolerance showed no indication of insulin resistance. The 5% increase in sucrose between the 2 high-fat diets did not lead to significant differences between groups. In conclusion, we find the dyslipidemic guinea pig to be a valid model of diet imposed dyslipidemia, particularly with regards to hepatic steatosis and endothelial dysfunction. Furthermore, the absence of obesity supports the present study setup as targeting NAFLD in nonobese individuals.Keywords

AB - Chronic dyslipidemia imposed by a high-fat and high-caloric dietary regime leads to debilitating disorders such as obesity, nonalcoholic fatty liver disease (NAFLD), and insulin resistance. As disease rates surge, so does the need for high validity animal models to effectively study the causal relationship between diet and disease progression. The dyslipidemic guinea pig displays a high similarity with the human lipoprotein profile and may in this aspect be superior to other rodent models. This study investigated the effects of 2 long-term Westernized diets (0.35% cholesterol, 18.5% vegetable oil and either 15% or 20% sucrose) compared with isocaloric standard chow in adult guinea pigs. Biochemical markers confirmed dyslipidemia in agreement with dietary regimens; however, both high-fat groups displayed a decreased tissue fat percentage compared with controls. Macroscopic appearance, histopathologic evaluation, and plasma markers of liver function confirmed NAFLD in high-fat groups, supported by liver redox imbalance and markers suggesting hepatic endothelial dysfunction. Plasma markers indicated endothelial dysfunction in response to a high-fat diet, although atherosclerotic lesions were not evident. Evaluation of glucose tolerance showed no indication of insulin resistance. The 5% increase in sucrose between the 2 high-fat diets did not lead to significant differences between groups. In conclusion, we find the dyslipidemic guinea pig to be a valid model of diet imposed dyslipidemia, particularly with regards to hepatic steatosis and endothelial dysfunction. Furthermore, the absence of obesity supports the present study setup as targeting NAFLD in nonobese individuals.Keywords

U2 - 10.1016/j.trsl.2015.10.001

DO - 10.1016/j.trsl.2015.10.001

M3 - Journal article

C2 - 26518991

VL - 168

SP - 146

EP - 160

JO - Translational Research

JF - Translational Research

SN - 1931-5244

ER -

ID: 145719214