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Middle-Aged Lpaatδ-Deficient Mice Have Altered Metabolic Measures

Lysophosphatidic acid acyltransferases/acylglycerophosphate acyltransferases (LPAATs/AGPATs) are a group of homologous enzymes that catalyze the formation of phosphatidic acid (PA) from lysophosphatidic acid. We have previously reported that LPAATδ/AGPAT4 localizes to mitochondria, suggesting a pote...

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Autores principales: Tomczewski, Michelle Victoria, Fernandes, Maria Fernanda, Grewal, Rajan Singh, Duncan, Robin Elaine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696958/
https://www.ncbi.nlm.nih.gov/pubmed/36362872
http://dx.doi.org/10.3390/life12111717
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author Tomczewski, Michelle Victoria
Fernandes, Maria Fernanda
Grewal, Rajan Singh
Duncan, Robin Elaine
author_facet Tomczewski, Michelle Victoria
Fernandes, Maria Fernanda
Grewal, Rajan Singh
Duncan, Robin Elaine
author_sort Tomczewski, Michelle Victoria
collection PubMed
description Lysophosphatidic acid acyltransferases/acylglycerophosphate acyltransferases (LPAATs/AGPATs) are a group of homologous enzymes that catalyze the formation of phosphatidic acid (PA) from lysophosphatidic acid. We have previously reported that LPAATδ/AGPAT4 localizes to mitochondria, suggesting a potential role in energy metabolism. However, in prior studies of young Lpaatδ-deficient mice (age 9–12 weeks old), we found no differences in body weights, food intakes, activity levels, respiratory gas exchange, or energy expenditure compared to their wildtype (Wt) littermates. To test whether Lpaatδ(−/−) mice may develop differences in metabolic measures with advancing age, we recorded body weights and food intakes, and used metabolic chambers to assess ambulatory and locomotor activity levels, oxygen consumption (VO(2)), carbon dioxide production (VCO(2)), respiratory exchange ratio (RER), and total energy expenditure (heat). Fourteen-month-old Lpaatδ(−/−) mice had significantly lower mean body weights compared to Wt littermate controls (44.6 ± 1.08 g vs. 53.5 ± 0.42 g, respectively), but no significant differences in food intake or activity levels. This phenotypic difference was accompanied by significantly elevated 24 h daily, and 12 h light and dark photoperiod average VO(2) (~20% higher) and VCO(2) (~30% higher) measures, as well as higher RER and total energy expenditure (heat) values compared to Wt control littermates. Thus, an age-related metabolic phenotype is evident in Lpaatδ(−/−) mice. Future studies should examine the role of the lipid-modifying enzyme LPAATδ across the lifespan for greater insight into its role in normal and pathophysiology.
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spelling pubmed-96969582022-11-26 Middle-Aged Lpaatδ-Deficient Mice Have Altered Metabolic Measures Tomczewski, Michelle Victoria Fernandes, Maria Fernanda Grewal, Rajan Singh Duncan, Robin Elaine Life (Basel) Article Lysophosphatidic acid acyltransferases/acylglycerophosphate acyltransferases (LPAATs/AGPATs) are a group of homologous enzymes that catalyze the formation of phosphatidic acid (PA) from lysophosphatidic acid. We have previously reported that LPAATδ/AGPAT4 localizes to mitochondria, suggesting a potential role in energy metabolism. However, in prior studies of young Lpaatδ-deficient mice (age 9–12 weeks old), we found no differences in body weights, food intakes, activity levels, respiratory gas exchange, or energy expenditure compared to their wildtype (Wt) littermates. To test whether Lpaatδ(−/−) mice may develop differences in metabolic measures with advancing age, we recorded body weights and food intakes, and used metabolic chambers to assess ambulatory and locomotor activity levels, oxygen consumption (VO(2)), carbon dioxide production (VCO(2)), respiratory exchange ratio (RER), and total energy expenditure (heat). Fourteen-month-old Lpaatδ(−/−) mice had significantly lower mean body weights compared to Wt littermate controls (44.6 ± 1.08 g vs. 53.5 ± 0.42 g, respectively), but no significant differences in food intake or activity levels. This phenotypic difference was accompanied by significantly elevated 24 h daily, and 12 h light and dark photoperiod average VO(2) (~20% higher) and VCO(2) (~30% higher) measures, as well as higher RER and total energy expenditure (heat) values compared to Wt control littermates. Thus, an age-related metabolic phenotype is evident in Lpaatδ(−/−) mice. Future studies should examine the role of the lipid-modifying enzyme LPAATδ across the lifespan for greater insight into its role in normal and pathophysiology. MDPI 2022-10-27 /pmc/articles/PMC9696958/ /pubmed/36362872 http://dx.doi.org/10.3390/life12111717 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tomczewski, Michelle Victoria
Fernandes, Maria Fernanda
Grewal, Rajan Singh
Duncan, Robin Elaine
Middle-Aged Lpaatδ-Deficient Mice Have Altered Metabolic Measures
title Middle-Aged Lpaatδ-Deficient Mice Have Altered Metabolic Measures
title_full Middle-Aged Lpaatδ-Deficient Mice Have Altered Metabolic Measures
title_fullStr Middle-Aged Lpaatδ-Deficient Mice Have Altered Metabolic Measures
title_full_unstemmed Middle-Aged Lpaatδ-Deficient Mice Have Altered Metabolic Measures
title_short Middle-Aged Lpaatδ-Deficient Mice Have Altered Metabolic Measures
title_sort middle-aged lpaatδ-deficient mice have altered metabolic measures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696958/
https://www.ncbi.nlm.nih.gov/pubmed/36362872
http://dx.doi.org/10.3390/life12111717
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