TY - JOUR T1 - Rosuvastatin Attenuates Progression of Atherosclerosis and Reduces Serum IL6 and CCL2 Levels in Apolipoprotein-E-deficient Mice JF - In Vivo JO - In Vivo SP - 994 LP - 1002 DO - 10.21873/invivo.13173 VL - 37 IS - 3 AU - DIAMANTIS I. TSILIMIGRAS AU - KALLIOPI THANOPOULOU AU - MARIA SALAGIANNI AU - GERASIMOS SIASOS AU - EVANGELOS OIKONOMOU AU - DESPINA D. PERREA AU - NIKOLAOS NIRAKIS AU - KONSTANTINOS FILIS AU - KONSTANTINOS TSIOUFIS AU - DIMITRIOS TOUSOULIS AU - FRAGISKA SIGALA Y1 - 2023/05/01 UR - http://iv.iiarjournals.org/content/37/3/994.abstract N2 - Background/Aim: Apolipoprotein E-deficient (Apoe−/−) mice develop atherosclerotic lesions that closely resemble metabolic syndrome in humans. We sought to investigate how rosuvastatin mitigates the atherosclerotic profile of Apoe−/− mice over time and its effects on certain inflammatory chemokines. Materials and Methods: Eighteen Apoe−/− mice were allocated into three groups of six mice each receiving: standard chow diet (SCD; control group); high-fat diet (HFD); and HFD and rosuvastatin at 5 mg/kg/d orally via gavage for 20 weeks. Analysis of aortic plaques and lipid deposition was conducted by means of en face Sudan IV staining and Oil Red O staining. Serum cholesterol, low-density lipoprotein, high-density lipoprotein, plasma glucose and triglyceride levels were determined at baseline and after 20 weeks of treatment. Serum interleukin 6 (IL6), C-C motif chemokine ligand 2 (CCL2) and tumor necrosis factor-α (TNFα) levels were measured by enzyme-linked immunosorbent assay at the time of euthanasia. Results: The lipidemic profile of Apoe−/− mice on HFD deteriorated over time. Apoe−/− mice on HFD developed atherosclerotic lesions over time. Sudan IV and Oil Red O-stained sections of the aorta revealed increased plaque formation and plaque lipid deposition in HFD-fed mice compared with SCD-fed mice and reduced plaque development in HFD-fed mice treated with rosuvastatin compared with mice not receiving statin treatment. Serum analysis revealed reduced metabolic parameters in HFD-fed mice on rosuvastatin compared with non-statin, HFD-fed mice. At the time of euthanasia, HFD-fed mice treated with rosuvastatin had significantly lower IL6 as well as CCL2 levels when compared with HFD-fed mice not receiving rosuvastatin. TNFα levels were comparable among all groups of mice, irrespective of treatment. IL6 and CCL2 positively correlated with the extent of atherosclerotic lesions and lipid deposition in atherosclerotic plaques. Conclusion: Serum IL6 and CCL2 levels might potentially be used as clinical markers of progression of atherosclerosis during statin treatment for hypercholesterolemia. ER -