Key result
SHROB rats develop marked cardiometabolic dysfunction, hypertension, and oxidative stress compared to controls.
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SHROB rats have been suggested as a model for metabolic syndrome (MetS) as a situation prior to the onset of CVD or type-2 diabetes, but information on descriptive biochemical parameters for this model is limited. Here, we extensively evaluate parameters related to CVD and oxidative stress (OS) in SHROB rats. SHROB rats were monitored for 15 weeks and compared to a control group of Wistar rats. Body weight was recorded weekly. At the end of the study, parameters related to CVD and OS were evaluated in plasma, urine and different organs. SHROB rats presented statistically significant differences from Wistar rats in CVD risk factors: total cholesterol, LDL-cholesterol, triglycerides, apoA1, apoB100, abdominal fat, insulin, blood pressure, C-reactive protein, ICAM-1 and PAI-1. In adipose tissue, liver and brain, the endogenous antioxidant systems were activated, yet there was no significant oxidative damage to lipids (MDA) or proteins (carbonylation). We conclude that SHROB rats present significant alterations in parameters related to inflammation, endothelial dysfunction, thrombotic activity, insulin resistance and OS measured in plasma as well as enhanced redox defence systems in vital organs that will be useful as markers of MetS and CVD for nutrition interventions.
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Molinar‐Toribio et al. (2014) studied Metabolic syndrome and cardiovascular disease risk. SHROB rat phenotype (metabolic syndrome model) vs. Wistar rats (control group) was evaluated on Cardiovascular disease-related biochemical parameters and oxidative stress markers in plasma, urine, and organs. SHROB rats monitored for 15 weeks showed significant alterations in lipids, insulin, blood pressure, inflammation, and plasma oxidative stress compared to control Wistar rats.
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