Folia Biologica
Journal of Cellular and Molecular Biology, Charles University 

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Fol. Biol. 2006, 52, 181-183

https://doi.org/10.14712/fb2006052060181

Simvastatin Could Prevent Increase of the Serum MMP-9/TIMP-1 Ratio in Acute Ischaemic Stroke

Jacek Kurzepa1, A. Szczepanska-Szerej2, M. Stryjecka-Zimmer1, T. Malecka-Massalska3, Z. Stelmasiak2

1Department of Biochemistry and Molecular Biology, Medical University of Lublin, Poland
2Department of Neurology, Medical University of Lublin, Poland
3Department of Nephrology, Medical University of Lublin, Poland

Received August 2006
Accepted November 2006

MMP-9 plays an important role in the pathogenesis of AIS and predicts haemorrhagic transformation of the ischaemic focus. The aim of our study was to analyse both serum MMP-9 and its most specific endogenous inhibitor (TIMP-1) levels in AIS and to check whether HMG-CoA reductase inhibitor (simvastatin) affects the MMP-9/TIMP-1 ratio value. Fifty patients with AIS were randomly divided into two groups: Group I (N = 25) treated with 40 mg/day with simvastatin within 24 hours after the onset of stroke and Group II (N = 25) non-treated with statin. To evaluate MMP-9 and TIMP-1 serum levels, the ELISA method was used. The serum MMP-9 level was significantly elevated on the 7th day of stroke in both groups (from 668 to 862 ng/ml and 670 to 855 ng/ml, respectively, in Group I and II). The serum TIMP-1 level was also elevated on the 7th day of stroke in both groups but the results were not significant. The MMP-9/TIMP-1 ratio was elevated on the 7th day of stroke in both groups, but the result was significant only in the Group II (P < 0.01). These findings indicate that simvastatin given during 24 hours after the onset of stroke could have an influence on the MMP-9/TIMP-1 ratio during AIS.

Funding

This study was supported by allowance of the Department of Biochemistry and Molecular Biology, Medical University of Lublin.

References

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