High fat diet is associated with gut microbiota dysbiosis and decreased gut microbial derived metabolites related to metabolic health in young Göttingen Minipigs

Research output: Contribution to journalJournal articleResearchpeer-review

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High fat diet is associated with gut microbiota dysbiosis and decreased gut microbial derived metabolites related to metabolic health in young Göttingen Minipigs. / Lützhøft, Ditte Olsen; Bækgård, Cecilie; Wimborne, Elizabeth; Straarup, Ellen Marie; Pedersen, Karen Margrethe; Swann, Jonathan R.; Pedersen, Henrik Duelund; Kristensen, Kim; Morgills, Line; Nielsen, Dennis Sandris; Hansen, Axel Kornerup; Bracken, Marianne Kronborg; Cirera, Susanna; Christoffersen, Berit Østergaard.

In: PLoS ONE, Vol. 19, No. 3, e0298602, 2024.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Lützhøft, DO, Bækgård, C, Wimborne, E, Straarup, EM, Pedersen, KM, Swann, JR, Pedersen, HD, Kristensen, K, Morgills, L, Nielsen, DS, Hansen, AK, Bracken, MK, Cirera, S & Christoffersen, BØ 2024, 'High fat diet is associated with gut microbiota dysbiosis and decreased gut microbial derived metabolites related to metabolic health in young Göttingen Minipigs', PLoS ONE, vol. 19, no. 3, e0298602. https://doi.org/10.1371/journal.pone.0298602

APA

Lützhøft, D. O., Bækgård, C., Wimborne, E., Straarup, E. M., Pedersen, K. M., Swann, J. R., Pedersen, H. D., Kristensen, K., Morgills, L., Nielsen, D. S., Hansen, A. K., Bracken, M. K., Cirera, S., & Christoffersen, B. Ø. (2024). High fat diet is associated with gut microbiota dysbiosis and decreased gut microbial derived metabolites related to metabolic health in young Göttingen Minipigs. PLoS ONE, 19(3), [e0298602]. https://doi.org/10.1371/journal.pone.0298602

Vancouver

Lützhøft DO, Bækgård C, Wimborne E, Straarup EM, Pedersen KM, Swann JR et al. High fat diet is associated with gut microbiota dysbiosis and decreased gut microbial derived metabolites related to metabolic health in young Göttingen Minipigs. PLoS ONE. 2024;19(3). e0298602. https://doi.org/10.1371/journal.pone.0298602

Author

Lützhøft, Ditte Olsen ; Bækgård, Cecilie ; Wimborne, Elizabeth ; Straarup, Ellen Marie ; Pedersen, Karen Margrethe ; Swann, Jonathan R. ; Pedersen, Henrik Duelund ; Kristensen, Kim ; Morgills, Line ; Nielsen, Dennis Sandris ; Hansen, Axel Kornerup ; Bracken, Marianne Kronborg ; Cirera, Susanna ; Christoffersen, Berit Østergaard. / High fat diet is associated with gut microbiota dysbiosis and decreased gut microbial derived metabolites related to metabolic health in young Göttingen Minipigs. In: PLoS ONE. 2024 ; Vol. 19, No. 3.

Bibtex

@article{a4f5748a0f6e481ba3a231c64eb14cb0,
title = "High fat diet is associated with gut microbiota dysbiosis and decreased gut microbial derived metabolites related to metabolic health in young G{\"o}ttingen Minipigs",
abstract = "The objectives were 1) to characterize a G{\"o}ttingen Minipig model of metabolic syndrome regarding its colon microbiota and circulating microbial products, and 2) to assess whether ovariectomized female and castrated male minipigs show similar phenotypes. Twenty-four nine-week-old G{\"o}ttingen Minipigs were allocated to four groups based on sex and diet: ovariectomized females and castrated males fed either chow or high-fat diet (HFD) for 12 weeks. At study end, body composition and plasma biomarkers were measured, and a mixed meal tolerance test (MMT) and an intravenous glucose tolerance test (IVGTT) were performed. The HFD groups had significantly higher weight gain, fat percentage, fasting plasma insulin and glucagon compared to the chow groups. Homeostatic model assessment of insulin resistance index (HOMA-IR) was increased and glucose effectiveness derived from the IVGTT and Matsuda´s insulin sensitivity index from the MMT were decreased in the HFD groups. The HFD groups displayed dyslipidemia, with significantly increased total-, LDL- and HDL-cholesterol, and decreased HDL/non-HDL cholesterol ratio. The colon microbiota of HFD minipigs clearly differed from the lean controls (GuniFrac distance matrix). The main bacteria families driving this separation were Clostridiaceae, Fibrobacteraceae, Flavobacteriaceae and Porphyromonadaceae. Moreover, the species richness was significantly decreased by HFD. In addition, HFD decreased the circulating level of short chain fatty acids and beneficial microbial metabolites hippuric acid, xanthine and trigonelline, while increasing the level of branched chain amino acids. Six and nine metabolically relevant genes were differentially expressed between chow-fed and HFD-fed animals in liver and omental adipose tissue, respectively. The HFD-fed pigs presented with metabolic syndrome, gut microbial dysbiosis and a marked decrease in healthy gut microbial products and thus displayed marked parallels to human obesity and insulin resistance.",
author = "L{\"u}tzh{\o}ft, {Ditte Olsen} and Cecilie B{\ae}kg{\aa}rd and Elizabeth Wimborne and Straarup, {Ellen Marie} and Pedersen, {Karen Margrethe} and Swann, {Jonathan R.} and Pedersen, {Henrik Duelund} and Kim Kristensen and Line Morgills and Nielsen, {Dennis Sandris} and Hansen, {Axel Kornerup} and Bracken, {Marianne Kronborg} and Susanna Cirera and Christoffersen, {Berit {\O}stergaard}",
note = "Publisher Copyright: {\textcopyright} 2024 L{\"u}tzh{\o}ft et al. This is an open access article distributed under the terms of the Creative Commons Attribution License,",
year = "2024",
doi = "10.1371/journal.pone.0298602",
language = "English",
volume = "19",
journal = "PLoS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "3",

}

RIS

TY - JOUR

T1 - High fat diet is associated with gut microbiota dysbiosis and decreased gut microbial derived metabolites related to metabolic health in young Göttingen Minipigs

AU - Lützhøft, Ditte Olsen

AU - Bækgård, Cecilie

AU - Wimborne, Elizabeth

AU - Straarup, Ellen Marie

AU - Pedersen, Karen Margrethe

AU - Swann, Jonathan R.

AU - Pedersen, Henrik Duelund

AU - Kristensen, Kim

AU - Morgills, Line

AU - Nielsen, Dennis Sandris

AU - Hansen, Axel Kornerup

AU - Bracken, Marianne Kronborg

AU - Cirera, Susanna

AU - Christoffersen, Berit Østergaard

N1 - Publisher Copyright: © 2024 Lützhøft et al. This is an open access article distributed under the terms of the Creative Commons Attribution License,

PY - 2024

Y1 - 2024

N2 - The objectives were 1) to characterize a Göttingen Minipig model of metabolic syndrome regarding its colon microbiota and circulating microbial products, and 2) to assess whether ovariectomized female and castrated male minipigs show similar phenotypes. Twenty-four nine-week-old Göttingen Minipigs were allocated to four groups based on sex and diet: ovariectomized females and castrated males fed either chow or high-fat diet (HFD) for 12 weeks. At study end, body composition and plasma biomarkers were measured, and a mixed meal tolerance test (MMT) and an intravenous glucose tolerance test (IVGTT) were performed. The HFD groups had significantly higher weight gain, fat percentage, fasting plasma insulin and glucagon compared to the chow groups. Homeostatic model assessment of insulin resistance index (HOMA-IR) was increased and glucose effectiveness derived from the IVGTT and Matsuda´s insulin sensitivity index from the MMT were decreased in the HFD groups. The HFD groups displayed dyslipidemia, with significantly increased total-, LDL- and HDL-cholesterol, and decreased HDL/non-HDL cholesterol ratio. The colon microbiota of HFD minipigs clearly differed from the lean controls (GuniFrac distance matrix). The main bacteria families driving this separation were Clostridiaceae, Fibrobacteraceae, Flavobacteriaceae and Porphyromonadaceae. Moreover, the species richness was significantly decreased by HFD. In addition, HFD decreased the circulating level of short chain fatty acids and beneficial microbial metabolites hippuric acid, xanthine and trigonelline, while increasing the level of branched chain amino acids. Six and nine metabolically relevant genes were differentially expressed between chow-fed and HFD-fed animals in liver and omental adipose tissue, respectively. The HFD-fed pigs presented with metabolic syndrome, gut microbial dysbiosis and a marked decrease in healthy gut microbial products and thus displayed marked parallels to human obesity and insulin resistance.

AB - The objectives were 1) to characterize a Göttingen Minipig model of metabolic syndrome regarding its colon microbiota and circulating microbial products, and 2) to assess whether ovariectomized female and castrated male minipigs show similar phenotypes. Twenty-four nine-week-old Göttingen Minipigs were allocated to four groups based on sex and diet: ovariectomized females and castrated males fed either chow or high-fat diet (HFD) for 12 weeks. At study end, body composition and plasma biomarkers were measured, and a mixed meal tolerance test (MMT) and an intravenous glucose tolerance test (IVGTT) were performed. The HFD groups had significantly higher weight gain, fat percentage, fasting plasma insulin and glucagon compared to the chow groups. Homeostatic model assessment of insulin resistance index (HOMA-IR) was increased and glucose effectiveness derived from the IVGTT and Matsuda´s insulin sensitivity index from the MMT were decreased in the HFD groups. The HFD groups displayed dyslipidemia, with significantly increased total-, LDL- and HDL-cholesterol, and decreased HDL/non-HDL cholesterol ratio. The colon microbiota of HFD minipigs clearly differed from the lean controls (GuniFrac distance matrix). The main bacteria families driving this separation were Clostridiaceae, Fibrobacteraceae, Flavobacteriaceae and Porphyromonadaceae. Moreover, the species richness was significantly decreased by HFD. In addition, HFD decreased the circulating level of short chain fatty acids and beneficial microbial metabolites hippuric acid, xanthine and trigonelline, while increasing the level of branched chain amino acids. Six and nine metabolically relevant genes were differentially expressed between chow-fed and HFD-fed animals in liver and omental adipose tissue, respectively. The HFD-fed pigs presented with metabolic syndrome, gut microbial dysbiosis and a marked decrease in healthy gut microbial products and thus displayed marked parallels to human obesity and insulin resistance.

U2 - 10.1371/journal.pone.0298602

DO - 10.1371/journal.pone.0298602

M3 - Journal article

C2 - 38427692

AN - SCOPUS:85186322330

VL - 19

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 3

M1 - e0298602

ER -

ID: 385697013