Literature DB >> 30517031

Sex differences in subcutaneous adipose tissue redox homeostasis and inflammation markers in control and high-fat diet fed rats.

Renata Prado Vasconcelos1, Milena Simões Peixoto2, Keciany Alves de Oliveira1, Andrea Claudia Freitas Ferreira3,4, Andrelina Noronha Coelho-de-Souza1, Denise P Carvalho3, Ariclécio Cunha de Oliveira1,3, Rodrigo S Fortunato2.   

Abstract

The development of obesity-related metabolic disorders is more evident in male in comparison with female subjects, but the mechanisms are unknown. Several studies have shown that oxidative stress is involved in the pathophysiology of obesity, but the majority of these studies were performed with male animals. The aim of this study was to evaluate the sex-related differences in subcutaneous adipose tissue redox homeostasis and inflammation of rats chronically fed a high-fat diet. NADPH oxidase (NOX), glutathione peroxidase (GPx), superoxide dismutase (SOD), and catalase activities were evaluated in the subcutaneous adipose tissue (SC) of adult male and female rats fed either a standard chow (SCD) or a high-fat diet (HFD) for 11 weeks. NOX2 and NOX4 messenger RNA (mRNA) levels, total reduced thiols, interleukin (IL)-1β, tumor necrosis factor α (TNF-α), and IL-6 were also determined. Higher antioxidant enzyme activities and total reduced thiol levels were detected in SC of control male compared with female rats. Chronic HFD administration increased NOX activity and NOX2 and NOX4 mRNA levels and decreased SOD and GPx activities only in male animals. IL-1β, TNF-α, and IL-6 levels, as well as Adgre1, CD11b, and CD68 mRNA levels, were also higher in SC of males after HFD feeding. In SC of females, catalase activity was higher after HFD feeding. Taken together, our results show that redox homeostasis and inflammation of SC is sexually dimorphic. Furthermore, males show higher oxidative stress in SC after 11 weeks of HFD feeding owing to both increased reactive oxygen species (ROS) production through NOX2 and NOX4 and decreased ROS detoxification.

Entities:  

Keywords:  adipose tissue; antioxidant; antioxydant; dimorphisme sexuel; espèces réactives de l’oxygène; inflammation; obesity; obésité; reactive oxygen species; sexual dimorphism; tissu adipeux

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Year:  2018        PMID: 30517031     DOI: 10.1139/apnm-2018-0611

Source DB:  PubMed          Journal:  Appl Physiol Nutr Metab        ISSN: 1715-5312            Impact factor:   2.665


  3 in total

Review 1.  Sexual dimorphism in cardiometabolic health: the role of adipose tissue, muscle and liver.

Authors:  Gijs H Goossens; Johan W E Jocken; Ellen E Blaak
Journal:  Nat Rev Endocrinol       Date:  2020-11-10       Impact factor: 43.330

Review 2.  High Fat Rodent Models of Type 2 Diabetes: From Rodent to Human.

Authors:  Nicole L Stott; Joseph S Marino
Journal:  Nutrients       Date:  2020-11-27       Impact factor: 5.717

3.  Sex-Dependent Role of Adipose Tissue HDAC9 in Diet-Induced Obesity and Metabolic Dysfunction.

Authors:  Brandee Goo; Samah Ahmadieh; Abdalrahman Zarzour; Nicole K H Yiew; David Kim; Hong Shi; Jacob Greenway; Stephen Cave; Jenny Nguyen; Swetha Aribindi; Mark Wendolowski; Praneet Veerapaneni; Mourad Ogbi; Weiqin Chen; Yun Lei; Xin-Yun Lu; Ha Won Kim; Neal L Weintraub
Journal:  Cells       Date:  2022-08-30       Impact factor: 7.666

  3 in total

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