scholarly journals Gonadal Steroids Negatively Modulate Oxidative Stress in CBA/Ca Female Mice Infected withP. bergheiANKA

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Néstor Aarón Mosqueda-Romo ◽  
Ana Laura Rodríguez-Morales ◽  
Fidel Orlando Buendía-González ◽  
Margarita Aguilar-Sánchez ◽  
Jorge Morales-Montor ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Nitric Oxide ◽  
Superoxide Dismutase ◽  
Sexual Dimorphism ◽  
Stress Response ◽  
Glutathione Peroxidase ◽  
Oxidative Stress Response ◽  
Gonadal Steroids ◽  
Male Mice ◽  
Female Mice

We decreased the level of gonadal steroids in female and male mice by gonadectomy. We infected these mice withP. bergheiANKA and observed the subsequent impact on the oxidative stress response. Intact females developed lower levels of parasitaemia and lost weight faster than intact males. Gonadectomised female mice displayed increased levels of parasitaemia, increased body mass, and increased anaemia compared with their male counterparts. In addition, gonadectomised females exhibited lower specific catalase, superoxide dismutase, and glutathione peroxidase activities in their blood and spleen tissues compared with gonadectomised males. To further study the oxidative stress response inP. bergheiANKA-infected gonadectomised mice, nitric oxide levels were assessed in the blood and spleen, and MDA levels were assessed in the spleen. Intact, sham-operated, and gonadectomised female mice exhibited higher levels of nitric oxide in the blood and spleen compared with male mice. MDA levels were higher in all of the female groups. Finally, gonadectomy significantly increased the oxidative stress levels in females but not in males. These data suggest that differential oxidative stress is influenced by oestrogens that may contribute to sexual dimorphism in malaria.

Oxidative stress response in eukaryotes: effect of glutathione, superoxide dismutase and catalase on adaptation to peroxide and menadione stresses inSaccharomyces cerevisiae

Redox Report ◽  
2007 ◽  
Vol 12 (5) ◽  
pp. 236-244 ◽  
Author(s):  
Patricia N. Fernandes ◽  
Sergio C. Mannarino ◽  
Carmelita G. Silva ◽  
Marcos D. Pereira ◽  
Anita D. Panek ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Superoxide Dismutase ◽  
Stress Response ◽  
Oxidative Stress Response

scholarly journals Nitric oxide, lipid peroxidation products, and antioxidants in primary fibromyalgia and correlation with disease severity

2019 ◽  
Vol 0 (0) ◽  
Author(s):  
Varsha Shukla ◽  
Siddharth Kumar Das ◽  
Abbas Ali Mahdi ◽  
Shweta Agarwal ◽  
Sukhanshi Khandpur
Keyword(s):  
Oxidative Stress ◽  
Nitric Oxide ◽  
Lipid Peroxidation ◽  
Superoxide Dismutase ◽  
Glutathione Peroxidase ◽  
Glutathione Reductase ◽  
Disease Severity ◽  
Pain Perception ◽  
High Plasma ◽  
Primary Fibromyalgia

Summary Background Fibromyalgia syndrome (FMS) is characterized by altered pain perception with chronic, widespread musculoskeletal pain. The relationship between nitric oxide, oxidative stress and the severity of FMS has not been studied. This study evaluated NO levels in plasma, LPO products and antioxidants in Red Cell lysate in patients of FMS and correlated it with disease severity. Methods 105 FMS patients who fulfilled 1990 ACR Criteria and 105 age- and sex-matched healthy controls were recruited over two years from 2013 to 2015. Antioxidative enzyme activity was assessed by the estimation of catalase, glutathione peroxidase (GPx) and glutathione reductase (GR) and superoxide dismutase (SOD). Nitric oxide in plasma, MDA marker of lipid peroxidation (LPO) in the lysate was donen for estimating oxidative stress. FIQR was used to assess the severity of fibromyalgia. Results The catalase, superoxide dismutase, glutathione reductase and glutathione peroxidase levels were significantly low in patients than controls (p<0.001). Plasma NO levels and LPO were also significantly high (p<0.05). NO and LPO levels showed a significant positive correlation with FIQR (r: 0.57, 0.8 and p: <0.001) whereas a negative correlation was observed between antioxidants (Cat, GR and GPx, but not SOD) and FIQR. Conclusions Low antioxidants and raised LPO in RBC lysate in patients with FM together with high plasma NO correlated with the severity of FMS.

scholarly journals Genetic Analysis of Glutathione Peroxidase in Oxidative Stress Response ofSaccharomyces cerevisiae

1999 ◽  
Vol 274 (38) ◽  
pp. 27002-27009 ◽  
Author(s):  
Yoshiharu Inoue ◽  
Toshifumi Matsuda ◽  
Kei-ichi Sugiyama ◽  
Shingo Izawa ◽  
Akira Kimura
Keyword(s):  
Oxidative Stress ◽  
Stress Response ◽  
Genetic Analysis ◽  
Glutathione Peroxidase ◽  
Oxidative Stress Response

scholarly journals Correlation between 3-MCPD-induced organ toxicity and oxidative stress response in male mice

2020 ◽  
Vol 136 ◽  
pp. 110957 ◽  
Author(s):  
Katharina Schultrich ◽  
Colin J. Henderson ◽  
Albert Braeuning ◽  
Thorsten Buhrke
Keyword(s):  
Oxidative Stress ◽  
Stress Response ◽  
Oxidative Stress Response ◽  
Male Mice ◽  
Organ Toxicity ◽  
And Oxidative Stress

scholarly journals Antioxidants-Related Superoxide Dismutase (SOD), Catalase (CAT), Glutathione Peroxidase (GPX), Glutathione-S-Transferase (GST), and Nitric Oxide Synthase (NOS) Gene Variants Analysis in an Obese Population: A Preliminary Case-Control Study

Antioxidants ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 595
Author(s):  
Amani M. T. Gusti ◽  
Safaa Y. Qusti ◽  
Eida M. Alshammari ◽  
Eman A. Toraih ◽  
Manal S. Fawzy
Keyword(s):  
Oxidative Stress ◽  
Nitric Oxide ◽  
Superoxide Dismutase ◽  
Nitric Oxide Synthase ◽  
Glutathione Peroxidase ◽  
Disease Risk ◽  
Nucleotide Polymorphisms ◽  
Obesity Risk ◽  
Glutathione S Transferase ◽  
Oxide Synthase

Oxidative stress and antioxidants play an important role in obesity etiopathology. Genetic variants, including single nucleotide polymorphisms (SNPs) of the antioxidant-related genes, may impact disease risk in several populations. This preliminary study aimed to explore the association of 12 SNPs related to superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX), glutathione-S-transferase (GST), and nitric oxide synthase (NOS) genes with obesity susceptibility in a Saudi population. A total of 384 unrelated participants, including 154 (40.1%) obese individuals, were enrolled. TaqMan OpenArray Genotyping assays were used. Six SNPs were significantly more prevalent in obese cohorts: (1) GSTM1 rs1056806*C/T; (2) SOD1 rs2234694*A; (3) SOD2 rs4880*G; (4) SOD3 rs2536512*A; (5) GPX1 rs1800668*A; (6) NOS3 rs1799983*G. Four SNPs were associated with higher obesity risk under heterozygote and dominant models for GSTM1 rs1056806 (C/T), homozygote model for SOD2 rs4880 (A/G), and homozygote and recessive models for GPX1 rs1800668 (A/G). In contrast, SOD3 rs2536512 (A/G) were less likely to be obese under heterozygote and dominant models. The CGAG, CAAA, TGGG, and CGAG combined genotypes showed a higher risk of obesity. In conclusion, the present results suggest that oxidative-stress-related genetic determinants could significantly associate with obesity risk in the study population.

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