Gamma Oryzanol Treats Obesity-Induced Kidney Injuries by Modulating the Adiponectin Receptor 2/PPAR-α Axis

• Published in: Oxidative medicine and cellular longevity 2018-01, Vol.2018 (2018), p.1-9
• Main Authors: Minatel, Igor O., Correa, C. R., Ferreira, Ana Lúcia A., Moreto, Fernando, dos Santos, Klinsmann Carolo, Garcia, Jéssica L., Alves, Pedro Henrique Rizzi, Hasimoto, Fabiana Kurokawa, Ferron, Artur J. T., Francisqueti, Fabiane Valentini, Silva, Vanessa dos Santos
• Format: Article
• Language: English
• Subjects: Animals; Antioxidants - pharmacology; Blood pressure; Diet; Dietary minerals; Endocrinology; Hormones; Hypertension; Inflammation; Injuries; Insulin resistance; Kidney diseases; Kidney Diseases - etiology; Kidney Diseases - metabolism; Kidney Diseases - pathology; Laboratory animals; Male; Medical research; Metabolism; Metabolites; Nutrition research; Obesity; Obesity - complications; Oxidative stress; Oxidative Stress - drug effects; Phenylpropionates - pharmacology; PPAR alpha - drug effects; PPAR alpha - metabolism; Proteins; Rats; Rats, Wistar; Receptors, Adiponectin - drug effects; Receptors, Adiponectin - metabolism; Signal Transduction - drug effects; Sorghum; Soybeans; Studies; Sucrose
• ISSN: 1942-0900; 1942-0994
• DOI: 10.1155/2018/1278392

The kidney is an important organ in the maintenance of body homeostasis. Dietary compounds, reactive metabolites, obesity, and metabolic syndrome (MetS) can affect renal filtration and whole body homeostasis, increasing the risk of chronic kidney disease (CKD) development. Gamma oryzanol (γOz) is a compound with antioxidant and anti-inflammatory activity that has shown a positive action in the treatment of obesity and metabolic diseases. Aim. To evaluate the effect of γOz to recover renal function in obese animals by high sugar-fat diet by modulation of adiponectin receptor 2/PPAR-α axis Methods. Male Wistar rats were initially randomly divided into 2 experimental groups: control and high sugar-fat diet (HSF) for 20 weeks. When proteinuria was detected, HSF animals were allocated to receive γOz or maintain HSF for more than 10 weeks. The following were analyzed: nutritional and biochemical parameters, systolic blood pressure, and renal function. In the kidney, the following were evaluated: inflammation, oxidative stress, and protein expression by Western blot. Results. After 10 weeks of γOz treatment, γOz was effective to improve inflammation, increase antioxidant enzyme activities, increase the protein expression of adiponectin receptor 2 and PPAR-α, and recover renal function. Conclusion. These results permit us to confirm that γOz is able to modulate PPAR-α expression, inflammation, and oxidative stress pathways improving obesity-induced renal disease.