High-fat diet consumption alters energy metabolism in the mouse hypothalamus
Background/Objectives High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of pro-inflammatory genes followed by hypothalamic astrocytosis, microgliosis, and the appearance of neuronal injury markers. The sp...
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Published in | International Journal of Obesity Vol. 43; no. 6; pp. 1295 - 1304 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.06.2019
Nature Publishing Group |
Subjects | |
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Abstract | Background/Objectives
High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of pro-inflammatory genes followed by hypothalamic astrocytosis, microgliosis, and the appearance of neuronal injury markers. The specific effects of high-fat diet on hypothalamic energy metabolism and neurotransmission are however not yet known and have not been investigated before.
Subjects/Methods
We used
1
H and
13
C magnetic resonance spectroscopy (MRS) and immunofluorescence techniques to evaluate in vivo the consequences of high-saturated fat diet administration to mice, and explored the effects on hypothalamic metabolism in three mouse cohorts at different time points for up to 4 months.
Results
We found that high-fat diet increases significantly the hypothalamic levels of glucose (
P
< 0.001), osmolytes (
P
< 0.001), and neurotransmitters (
P
< 0.05) from 2 months of diet, and alters the rates of metabolic (
P
< 0.05) and neurotransmission fluxes (
P
< 0.001), and the contribution of non-glycolytic substrates to hypothalamic metabolism (
P
< 0.05) after 10 weeks of high-fat feeding.
Conclusions/interpretation
We report changes that reveal a high-fat diet-induced alteration of hypothalamic metabolism and neurotransmission that is quantifiable by
1
H and
13
C MRS in vivo, and present the first evidence of the extension of the inflammation pathology to a localized metabolic imbalance. |
---|---|
AbstractList | Background/Objectives
High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of pro-inflammatory genes followed by hypothalamic astrocytosis, microgliosis, and the appearance of neuronal injury markers. The specific effects of high-fat diet on hypothalamic energy metabolism and neurotransmission are however not yet known and have not been investigated before.
Subjects/Methods
We used
1
H and
13
C magnetic resonance spectroscopy (MRS) and immunofluorescence techniques to evaluate in vivo the consequences of high-saturated fat diet administration to mice, and explored the effects on hypothalamic metabolism in three mouse cohorts at different time points for up to 4 months.
Results
We found that high-fat diet increases significantly the hypothalamic levels of glucose (
P
< 0.001), osmolytes (
P
< 0.001), and neurotransmitters (
P
< 0.05) from 2 months of diet, and alters the rates of metabolic (
P
< 0.05) and neurotransmission fluxes (
P
< 0.001), and the contribution of non-glycolytic substrates to hypothalamic metabolism (
P
< 0.05) after 10 weeks of high-fat feeding.
Conclusions/interpretation
We report changes that reveal a high-fat diet-induced alteration of hypothalamic metabolism and neurotransmission that is quantifiable by
1
H and
13
C MRS in vivo, and present the first evidence of the extension of the inflammation pathology to a localized metabolic imbalance. High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of pro-inflammatory genes followed by hypothalamic astrocytosis, microgliosis, and the appearance of neuronal injury markers. The specific effects of high-fat diet on hypothalamic energy metabolism and neurotransmission are however not yet known and have not been investigated before. We used H and C magnetic resonance spectroscopy (MRS) and immunofluorescence techniques to evaluate in vivo the consequences of high-saturated fat diet administration to mice, and explored the effects on hypothalamic metabolism in three mouse cohorts at different time points for up to 4 months. We found that high-fat diet increases significantly the hypothalamic levels of glucose (P < 0.001), osmolytes (P < 0.001), and neurotransmitters (P < 0.05) from 2 months of diet, and alters the rates of metabolic (P < 0.05) and neurotransmission fluxes (P < 0.001), and the contribution of non-glycolytic substrates to hypothalamic metabolism (P < 0.05) after 10 weeks of high-fat feeding. We report changes that reveal a high-fat diet-induced alteration of hypothalamic metabolism and neurotransmission that is quantifiable by H and C MRS in vivo, and present the first evidence of the extension of the inflammation pathology to a localized metabolic imbalance. High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of pro-inflammatory genes followed by hypothalamic astrocytosis, microgliosis, and the appearance of neuronal injury markers. The specific effects of high-fat diet on hypothalamic energy metabolism and neurotransmission are however not yet known and have not been investigated before. We found that high-fat diet increases significantly the hypothalamic levels of glucose (P < 0.001), osmolytes (P < 0.001), and neurotransmitters (P < 0.05) from 2 months of diet, and alters the rates of metabolic (P < 0.05) and neurotransmission fluxes (P < 0.001), and the contribution of non-glycolytic substrates to hypothalamic metabolism (P < 0.05) after 10 weeks of high-fat feeding. We report changes that reveal a high-fat diet-induced alteration of hypothalamic metabolism and neurotransmission that is quantifiable by .sup.1H and .sup.13C MRS in vivo, and present the first evidence of the extension of the inflammation pathology to a localized metabolic imbalance. High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of pro-inflammatory genes followed by hypothalamic astrocytosis, microgliosis, and the appearance of neuronal injury markers. The specific effects of high-fat diet on hypothalamic energy metabolism and neurotransmission are however not yet known and have not been investigated before.BACKGROUND/OBJECTIVESHigh-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of pro-inflammatory genes followed by hypothalamic astrocytosis, microgliosis, and the appearance of neuronal injury markers. The specific effects of high-fat diet on hypothalamic energy metabolism and neurotransmission are however not yet known and have not been investigated before.We used 1H and 13C magnetic resonance spectroscopy (MRS) and immunofluorescence techniques to evaluate in vivo the consequences of high-saturated fat diet administration to mice, and explored the effects on hypothalamic metabolism in three mouse cohorts at different time points for up to 4 months.SUBJECTS/METHODSWe used 1H and 13C magnetic resonance spectroscopy (MRS) and immunofluorescence techniques to evaluate in vivo the consequences of high-saturated fat diet administration to mice, and explored the effects on hypothalamic metabolism in three mouse cohorts at different time points for up to 4 months.We found that high-fat diet increases significantly the hypothalamic levels of glucose (P < 0.001), osmolytes (P < 0.001), and neurotransmitters (P < 0.05) from 2 months of diet, and alters the rates of metabolic (P < 0.05) and neurotransmission fluxes (P < 0.001), and the contribution of non-glycolytic substrates to hypothalamic metabolism (P < 0.05) after 10 weeks of high-fat feeding.RESULTSWe found that high-fat diet increases significantly the hypothalamic levels of glucose (P < 0.001), osmolytes (P < 0.001), and neurotransmitters (P < 0.05) from 2 months of diet, and alters the rates of metabolic (P < 0.05) and neurotransmission fluxes (P < 0.001), and the contribution of non-glycolytic substrates to hypothalamic metabolism (P < 0.05) after 10 weeks of high-fat feeding.We report changes that reveal a high-fat diet-induced alteration of hypothalamic metabolism and neurotransmission that is quantifiable by 1H and 13C MRS in vivo, and present the first evidence of the extension of the inflammation pathology to a localized metabolic imbalance.CONCLUSIONS/INTERPRETATIONWe report changes that reveal a high-fat diet-induced alteration of hypothalamic metabolism and neurotransmission that is quantifiable by 1H and 13C MRS in vivo, and present the first evidence of the extension of the inflammation pathology to a localized metabolic imbalance. Background/Objectives High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of pro-inflammatory genes followed by hypothalamic astrocytosis, microgliosis, and the appearance of neuronal injury markers. The specific effects of high-fat diet on hypothalamic energy metabolism and neurotransmission are however not yet known and have not been investigated before. Subjects/Methods We used .sup.1H and .sup.13C magnetic resonance spectroscopy (MRS) and immunofluorescence techniques to evaluate in vivo the consequences of high-saturated fat diet administration to mice, and explored the effects on hypothalamic metabolism in three mouse cohorts at different time points for up to 4 months. Results We found that high-fat diet increases significantly the hypothalamic levels of glucose (P < 0.001), osmolytes (P < 0.001), and neurotransmitters (P < 0.05) from 2 months of diet, and alters the rates of metabolic (P < 0.05) and neurotransmission fluxes (P < 0.001), and the contribution of non-glycolytic substrates to hypothalamic metabolism (P < 0.05) after 10 weeks of high-fat feeding. Conclusions/interpretation We report changes that reveal a high-fat diet-induced alteration of hypothalamic metabolism and neurotransmission that is quantifiable by .sup.1H and .sup.13C MRS in vivo, and present the first evidence of the extension of the inflammation pathology to a localized metabolic imbalance. Background/Objectives: High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of pro-inflammatory genes followed by hypothalamic astrocytosis, microgliosis, and the appearance of neuronal injury markers. The specific effects of high-fat diet on hypothalamic energy metabolism and neurotransmission are however not yet known and have not been investigated before. Subjects/Methods: We used 1H and 13C magnetic resonance spectroscopy (MRS) and immunofluorescence techniques to evaluate in vivo the consequences of high-saturated fat diet administration to mice, and explored the effects on hypothalamic metabolism in three mouse cohorts at different time points for up to 4 months. Results: We found that high-fat diet increases significantly the hypothalamic levels of glucose (P < 0.001), osmolytes (P < 0.001), and neurotransmitters (P < 0.05) from 2 months of diet, and alters the rates of metabolic (P < 0.05) and neurotransmission fluxes (P < 0.001), and the contribution of non-glycolytic substrates to hypothalamic metabolism (P < 0.05) after 10 weeks of high-fat feeding. Conclusions/interpretation: We report changes that reveal a high-fat diet-induced alteration of hypothalamic metabolism and neurotransmission that is quantifiable by 1H and 13C MRS in vivo, and present the first evidence of the extension of the inflammation pathology to a localized metabolic imbalance. Background/ObjectivesHigh-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of pro-inflammatory genes followed by hypothalamic astrocytosis, microgliosis, and the appearance of neuronal injury markers. The specific effects of high-fat diet on hypothalamic energy metabolism and neurotransmission are however not yet known and have not been investigated before.Subjects/MethodsWe used 1H and 13C magnetic resonance spectroscopy (MRS) and immunofluorescence techniques to evaluate in vivo the consequences of high-saturated fat diet administration to mice, and explored the effects on hypothalamic metabolism in three mouse cohorts at different time points for up to 4 months.ResultsWe found that high-fat diet increases significantly the hypothalamic levels of glucose (P < 0.001), osmolytes (P < 0.001), and neurotransmitters (P < 0.05) from 2 months of diet, and alters the rates of metabolic (P < 0.05) and neurotransmission fluxes (P < 0.001), and the contribution of non-glycolytic substrates to hypothalamic metabolism (P < 0.05) after 10 weeks of high-fat feeding.Conclusions/interpretationWe report changes that reveal a high-fat diet-induced alteration of hypothalamic metabolism and neurotransmission that is quantifiable by 1H and 13C MRS in vivo, and present the first evidence of the extension of the inflammation pathology to a localized metabolic imbalance. |
Audience | Academic |
Author | Duarte, João M. N. Lizarbe, Blanca Cherix, Antoine Cardinaux, Jean-René Gruetter, Rolf |
Author_xml | – sequence: 1 givenname: Blanca orcidid: 0000-0002-5531-4088 surname: Lizarbe fullname: Lizarbe, Blanca email: blanca.lizarbeserra@epfl.ch organization: Laboratory of Functional and Metabolic Imaging (LIFMET), Ecole Polytechnique Fédérale de Lausanne – sequence: 2 givenname: Antoine surname: Cherix fullname: Cherix, Antoine organization: Laboratory of Functional and Metabolic Imaging (LIFMET), Ecole Polytechnique Fédérale de Lausanne – sequence: 3 givenname: João M. N. surname: Duarte fullname: Duarte, João M. N. organization: Laboratory of Functional and Metabolic Imaging (LIFMET), Ecole Polytechnique Fédérale de Lausanne, Department of Experimental Medical Science, Faculty of Medicine, Lund University, Wallenberg Centre for Molecular Medicine, Lund University – sequence: 4 givenname: Jean-René surname: Cardinaux fullname: Cardinaux, Jean-René organization: Center for Psychiatric Neuroscience (CNP), Centre Hospitalier Universitaire Vaudois (CHUV) – sequence: 5 givenname: Rolf surname: Gruetter fullname: Gruetter, Rolf organization: Laboratory of Functional and Metabolic Imaging (LIFMET), Ecole Polytechnique Fédérale de Lausanne, Department of Radiology, University of Geneva, Department of Radiology, University of Lausanne |
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ContentType | Journal Article |
Copyright | Springer Nature Limited 2018 COPYRIGHT 2019 Nature Publishing Group Copyright Nature Publishing Group Jun 2019 |
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CorporateAuthor | Diabetes and Brain Function Lunds universitet Institutionen för experimentell medicinsk vetenskap Profile areas and other strong research environments WCMM-Wallenberg Centre for Molecular Medicine Lund University WCMM- Wallenberg center för molekylär medicinsk forskning Strategiska forskningsområden (SFO) Department of Experimental Medical Science Diabetes och hjärnans funktion EXODIAB: Excellence of Diabetes Research in Sweden Faculty of Medicine Strategic research areas (SRA) Medicinska fakulteten Profilområden och andra starka forskningsmiljöer |
CorporateAuthor_xml | – name: Faculty of Medicine – name: Medicinska fakulteten – name: Diabetes and Brain Function – name: Strategiska forskningsområden (SFO) – name: Department of Experimental Medical Science – name: WCMM-Wallenberg Centre for Molecular Medicine – name: Strategic research areas (SRA) – name: Lunds universitet – name: Profilområden och andra starka forskningsmiljöer – name: Lund University – name: EXODIAB: Excellence of Diabetes Research in Sweden – name: Institutionen för experimentell medicinsk vetenskap – name: Profile areas and other strong research environments – name: WCMM- Wallenberg center för molekylär medicinsk forskning – name: Diabetes och hjärnans funktion |
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PublicationSubtitle | Official journal of the International Association for the Study of Obesity |
PublicationTitle | International Journal of Obesity |
PublicationTitleAbbrev | Int J Obes |
PublicationTitleAlternate | Int J Obes (Lond) |
PublicationYear | 2019 |
Publisher | Nature Publishing Group UK Nature Publishing Group |
Publisher_xml | – name: Nature Publishing Group UK – name: Nature Publishing Group |
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High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial... High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial expression of... Background/Objectives High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial... Background/ObjectivesHigh-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial... Background/Objectives: High-fat diet consumption is known to trigger an inflammatory response in the hypothalamus, which has been characterized by an initial... |
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Title | High-fat diet consumption alters energy metabolism in the mouse hypothalamus |
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