Host: The Japanese Pharmacological Society, The Japanese Society of Clinical Pharmacology
Name : WCP2018 (18th World Congress of Basic and Clinical Pharmacology)
Location : Kyoto
Date : July 01, 2018 - July 06, 2018
Background
Cardiovascular disease is the major cause of morbidity and mortality in chronic kidney disease (CKD). Interstitial and perivascular fibrosis as a constant finding in heart biopsies in patients with CKD. The therapeutic strategies aimed to reduce cardiac fibrosis may provide a particular cardioprotective benefit in patients. The aim of this study was to determine whether treatment with simvastatin for 2 weeks would lead to change in collagen deposition on the heart in a mice model with CKD.
Methods
A total of 15 male swiss were used in this study. Chronic kidney disease was induced in the mice by 5/6 subtotal nephrectomy. The animals were randomized into three groups: sham-operated (SO, n=5), 5/6 subtotal nephrectomy (SN, n=5) and 5/6 subtotal nephrectomy followed by 20 mg/kgBW simvastatin (SIMV, n=5). After 2 weeks, blood and heart were harvested for histologic analysis.
Results
Administration of simvastatin significantly improved creatinine serum on SIMV group (0.49±0.09 mg/dl) compared to SN group (1.92±0.34 mg/dl). The collagen deposition was also more significant on SIMV group (8.95±0.65 mg/dl) compared to SN group (16.64±2.7 mg/dl). The collagen deposition was more prominent on coronary perivascular than that on interstitial myocardial.
Conclusions
Administration of 20 mg/kgBW simvastatin significantly improved coronary perivascular fibrosis.
Keywords: simvastatin, coronary fibrosis, chronic kidney disease