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1.
Int J Mol Sci ; 25(8)2024 Apr 13.
Artigo em Inglês | MEDLINE | ID: mdl-38673906

RESUMO

Air pollution poses a significant global health risk, with fine particulate matter (PM2.5) such as diesel exhaust particles (DEPs) being of particular concern due to their potential to drive systemic toxicities through bloodstream infiltration. The association between PM2.5 exposure and an increased prevalence of metabolic disorders, including obesity, metabolic syndrome, and type 2 diabetes mellitus (T2DM), is evident against a backdrop of rising global obesity and poor metabolic health. This paper examines the role of adipose tissue in mediating the effects of PM2.5 on metabolic health. Adipose tissue, beyond its energy storage function, is responsive to inhaled noxious stimuli, thus disrupting metabolic homeostasis and responding to particulate exposure with pro-inflammatory cytokine release, contributing to systemic inflammation. The purpose of this study was to characterize the metabolic response of adipose tissue in mice exposed to either DEPs or room air (RA), exploring both the adipokine profile and mitochondrial bioenergetics. In addition to a slight change in fat mass and a robust shift in adipocyte hypertrophy in the DEP-exposed animals, we found significant changes in adipose mitochondrial bioenergetics. Furthermore, the DEP-exposed animals had a significantly higher expression of adipose inflammatory markers compared with the adipose from RA-exposed mice. Despite the nearly exclusive focus on dietary factors in an effort to better understand metabolic health, these results highlight the novel role of environmental factors that may contribute to the growing global burden of poor metabolic health.


Assuntos
Tecido Adiposo , Inflamação , Mitocôndrias , Material Particulado , Emissões de Veículos , Animais , Emissões de Veículos/toxicidade , Mitocôndrias/metabolismo , Mitocôndrias/efeitos dos fármacos , Camundongos , Material Particulado/efeitos adversos , Material Particulado/toxicidade , Tecido Adiposo/metabolismo , Tecido Adiposo/efeitos dos fármacos , Inflamação/metabolismo , Inflamação/induzido quimicamente , Inflamação/patologia , Masculino , Camundongos Endogâmicos C57BL , Metabolismo Energético/efeitos dos fármacos , Adipocinas/metabolismo , Poluentes Atmosféricos/efeitos adversos , Poluentes Atmosféricos/toxicidade , Adipócitos/metabolismo , Adipócitos/efeitos dos fármacos
2.
Nutrients ; 16(12)2024 Jun 10.
Artigo em Inglês | MEDLINE | ID: mdl-38931176

RESUMO

The global rise in type 2 diabetes (T2D) and obesity necessitates innovative dietary interventions. This study investigates the effects of allulose, a rare sugar shown to reduce blood glucose, in a rat model of diet-induced obesity and T2D. Over 12 weeks, we hypothesized that allulose supplementation would improve body weight, insulin sensitivity, and glycemic control. Our results showed that allulose mitigated the adverse effects of high-fat, high-sugar diets, including reduced body weight gain and improved insulin resistance. The allulose group exhibited lower food consumption and increased levels of glucagon-like peptide-1 (GLP-1), enhancing glucose regulation and appetite control. Additionally, allulose prevented liver triglyceride accumulation and promoted mitochondrial uncoupling in adipose tissue. These findings suggest that allulose supplementation can improve metabolic health markers, making it a promising dietary component for managing obesity and T2D. Further research is needed to explore the long-term benefits and mechanisms of allulose in metabolic disease prevention and management. This study supports the potential of allulose as a safe and effective intervention for improving metabolic health in the context of dietary excess.


Assuntos
Glicemia , Diabetes Mellitus Tipo 2 , Dieta Hiperlipídica , Frutose , Resistência à Insulina , Obesidade , Animais , Frutose/administração & dosagem , Masculino , Obesidade/metabolismo , Diabetes Mellitus Tipo 2/prevenção & controle , Diabetes Mellitus Tipo 2/metabolismo , Glicemia/metabolismo , Ratos , Dieta Hiperlipídica/efeitos adversos , Fígado/metabolismo , Peptídeo 1 Semelhante ao Glucagon/metabolismo , Peptídeo 1 Semelhante ao Glucagon/sangue , Triglicerídeos/sangue , Ratos Sprague-Dawley , Tecido Adiposo/metabolismo , Aumento de Peso , Modelos Animais de Doenças
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