Antioxidant effect of bisphosphonates and simvastatin on chondrocyte lipid peroxidation

被引:22
|
作者
Dombrecht, E. J.
De Tollenaere, C. B.
Aerts, K.
Cos, P.
Schuerwegh, A. J.
Bridts, C. H.
Van Offel, J. F.
Ebo, D. G.
Stevens, W. J.
De Clerck, L. S.
机构
[1] Univ Antwerp VIB, Fac Med, B-2610 Antwerp, Belgium
[2] Univ Antwerp VIB, Dept Pharmaceut Sci, Lab Microbiol Parasitol & Hyg, B-2610 Antwerp, Belgium
关键词
bisphosphonates; simvastatin; chondrocytes; lipid peroxidation; rheumatoid arthritis; RHEUMATOID-ARTHRITIS; SYNOVIAL-FLUID; OCULAR TOXICITY; DEGRADATION; LIPOPROTEIN; PREVENTION; DECREASES; DENSITY; STATINS; PLASMA;
D O I
10.1016/j.bbrc.2006.07.075
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The objective of this study was to evaluate the effect of bisphosphonates (BPs) and simvastatin on chondrocyte lipid peroxidation. For this purpose, a flow cytometrical method using C11-BODIPY581/591 was developed to detect hydroperoxide-induced lipid peroxidation in chondrocytes. Tertiary butylhydroperoxide (t-BHP) induced a time and concentration dependent increase in chondrocyte lipid peroxidation. Addition of a Fe2+/EDTA complex to t-BHP or hydrogen peroxide (H2O2) clearly enhanced lipid peroxidation. The lipophilic simvastatin demonstrated a small inhibition in the chondrocyte lipid peroxidation. None of three tested BPs (clodronate, pamidronate, and risedronate) had an effect on chondrocyte lipid peroxidation induced by t-BHP. However, when Fe2+/EDTA complex was added to t-BHP or H2O2, BPs inhibited the lipid peroxidation process varying from 25% to 58%. This study demonstrates that BPs have antioxidant properties as iron chelators, thereby inhibiting the chondrocyte lipid peroxidation. These findings add evidence to the therapeutic potential of bisphosphonates and statins in rheumatoid arthritis. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:459 / 464
页数:6
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