Cited by 102Fatty Acid Research and HealthAdipokines, Inflammation, and Metabolic DiseasesDiet, Metabolism, and Disease

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Diets Containing α-Linolenic (ω3) or Oleic (ω9) Fatty Acids Rescues Obese Mice From Insulin Resistance

Oliveira, V., Marinho, R., Vitorino, D., Santos, G. A., Moraes, J. C., Dragano, N., Sartori-Cintra, A., Pereira, L., Catharino, R. R., da Silva, A. S. R., Ropelle, E. R., Pauli, J. R., De Souza, C. T., Velloso, L. A., Cintra, D. E.·2015·Endocrinology

DOI 10.1210/en.2014-1880

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Abstract

Subclinical systemic inflammation is a hallmark of obesity and insulin resistance. The results obtained from a number of experimental studies suggest that targeting different components of the inflammatory machinery may result in the improvement of the metabolic phenotype. Unsaturated fatty acids exert antiinflammatory activity through several distinct mechanisms. Here, we tested the capacity of ω3 and ω9 fatty acids, directly from their food matrix, to exert antiinflammatory activity through the G protein-coupled receptor (GPR)120 and GPR40 pathways. GPR120 was activated in liver, skeletal muscle, and adipose tissues, reverting inflammation and insulin resistance in obese mice. Part of this action was also mediated by GPR40 on muscle, as a novel mechanism described. Pair-feeding and immunoneutralization experiments reinforced the pivotal role of GPR120 as a mediator in the response to the nutrients. The improvement in insulin sensitivity in the high-fat substituted diets was associated with a marked reduction in tissue inflammation, decreased macrophage infiltration, and increased IL-10 levels. Furthermore, improved glucose homeostasis was accompanied by the reduced expression of hepatic gluconeogenic enzymes and reduced body mass. Thus, our data indicate that GPR120 and GPR40 play a critical role as mediators of the beneficial effects of dietary unsaturated fatty acids in the context of obesity-induced insulin resistance.

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Short-Term Strength Exercise Reduces Hepatic Insulin Resistance in Obese Mice by Reducing PTP1B Content, Regardless of Changes in Body Weight
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Short-Term Combined Exercise Improves Inflammatory Profile in the Retina of Obese Mice
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Short-term combined training reduces hepatic steatosis and improves hepatic insulin signaling
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BackgroundResult
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Additional file 1 of PA and OA induce abnormal glucose metabolism by inhibiting KLF15 in adipocytes
Wang, C., Chu, X., Deng, Y., Wang, J., Qiu, T., Zhu, J., Yang, X., Pan, C., Xiong, J., Xie, J., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17058701
Additional file 1 of Omega-3 mechanism of action in inflammation and endoplasmic reticulum stress in mononuclear cells from overweight non-alcoholic fatty liver disease participants: study protocol for the “Brazilian Omega Study” (BROS)—a randomized controlled trial
Batista, E. S., da Silva Rios, T., Muñoz, V. R., Jesus, J. S., Vasconcelos, M. M., da Cunha, D. T., Marques-Rocha, J. L., Nakandakari, S. C. B. R., Lara, R., da Silva, A. S. R., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17284452
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Etude de l'effet protecteur chez la descendance de la supplémentation maternelle en acide docosahexaénoïque (DHA) pendant la gestation et la lactation contre les altérations métaboliques et cognitives induites par une alimentation hypercalorique
Abdi, A. D. (2021) · theses.fr (ABES) · doi:10.70675/3aa29f25za3d3z4850zb0a0z56967344e58f

Authors: Oliveira, V., Marinho, R., Vitorino, D., Santos, G. A., Moraes, J. C., Dragano, N., Sartori-Cintra, A., Pereira, L., Catharino, R. R., da Silva, A. S. R., Ropelle, E. R., Pauli, J. R., De Souza, C. T., Velloso, L. A., & Cintra, D. E.
Affiliations: Universidade Estadual de Campinas (UNICAMP) (BR)
Molecular Biology of Exercise (R.M., L.P., A.S.R.d.S., E.R.R., J.R.P.), School of Applied Sciences, State University of Campinas, Campinas, Brazil 13083-887
Laboratory of Exercise Biochemistry and Physiology (C.T.D.S.), Health Sciences Unit, Universidade do Extremo Sul Catarinense Criciúma, Brazil 88806-000
Corresponding author: Cintra, D. E.
ORCID: Marinho, R.
Santos, G. A.
Moraes, J. C.
Dragano, N.
Pereira, L.
Catharino, R. R.
Ropelle, E. R.
Pauli, J. R.
Velloso, L. A.
Cintra, D. E.
Venue: Endocrinology
Publisher: The Endocrine Society
Published: 2015-08-17
Volume: 156
Issue: 11
Pages: 4033-4046
ISSN: 0013-7227 (ISSN-L)
1945-7170
DOI: 10.1210/en.2014-1880
OpenAlex: W2131862502
Cited by: 102
References: 32
Citations by year: 2026: 3 · 2025: 9 · 2023: 7 · 2022: 11 · 2021: 23 · 2020: 15 · 2019: 10 · 2018: 5 · 2017: 13 · 2016: 6
FWCI: 7.70
Type: journal article
Language: en
Open access: closed
Locations: Endocrinology (publishedVersion)
PubMed (publishedVersion)
Funders: Fundação de Amparo à Pesquisa do Estado de São Paulo (12/07129-6)
Universidade Estadual de Campinas
Topics: Health Sciences › Nursing › Nutrition and Dietetics › Fatty Acid Research and Health
Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diet, Metabolism, and Disease
Keywords: alpha-linolenic acid, oleic acid, omega-3 fatty acids, omega-9 fatty acids, obesity, insulin resistance, GPR120, GPR40, G protein-coupled receptors, anti-inflammatory activity, systemic inflammation, macrophage infiltration, IL-10, hepatic gluconeogenesis, glucose homeostasis, skeletal muscle, adipose tissue, high-fat diet, pair feeding, immunoneutralization
MeSH terms: Adipose Tissue, Animals, Dietary Fats, Glucose, Homeostasis, Hypoglycemic Agents, Inflammation, Insulin, Insulin Resistance, Liver, Male, Mice, Obese, Obesity, Immunoblotting, Signal Transduction, Weight Gain, alpha-Linolenic Acid, Muscle, Skeletal, Oleic Acid, RNA Interference, Receptors, G-Protein-Coupled

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Diets Containing α-Linolenic (ω3) or Oleic (ω9) Fatty Acids Rescues Obese Mice From Insulin Resistance

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