Curcumin protects cardiac cells against ischemia-reperfusion injury:: effects on oxidative stress, NF-κB, and JNK pathways

被引:95
作者
Fiorillo, Claudia [1 ]
Becatti, Matteo [1 ]
Pensalfini, Anna [1 ]
Cecchi, Cristina [1 ]
Lanzilao, Luisa [1 ]
Donzelli, Gianpaolo [2 ]
Nassi, Niccolo [2 ]
Giannini, Lara [1 ]
Borchi, Elisabetta [1 ]
Nassi, Paolo [1 ]
机构
[1] Univ Florence, Dept Biochem Sci, I-50134 Florence, Italy
[2] Univ Florence, Dept Pediat, I-50134 Florence, Italy
关键词
oxidative stress; ischemia-reperfusion; curcumin; JNK; NF-kappa B; free radicals;
D O I
10.1016/j.freeradbiomed.2008.06.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
In this study we explored the effects of curcumin in cardiac cells subjected to a protocol simulating ischemia-reperfusion (IR). Curcumin (10 mu M) was administered before ischemia (pretreatment) or at the moment of repefusion (posttreatment) and its effects were compared to those produced by a reference antioxidant (Trolox) with an equal antioxidant capacity. IR cardiac cells showed clear signs of oxidative Stress, impaired mitochondrial activity, and a marked development of both necrotic and apoptotic processes; at the same time, increases in NF-kappa B nuclear translocation and JNK phosphorylation were observed. Curcumin pretreatment was revealed to be the most effective in attenuating all these modifications and, in particular, in reducing the death of IR cells. This confirms that the protective effect of curcumin is not related simply to its antioxidant properties but involves other mechanisms, notably interactions in the NF-kappa B and JNK pathways. These findings suggest that curcumin administration, in particular before the hypoxic challenge, represents a promising approach to protecting cardiac cells against IR injury. In this scenario our results point out the importance of the chronology for the outcome of the treatment and provide a differential valuation of the degree of protection that curcumin can exert by its antioxidant activity or by other mechanisms. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:839 / 846
页数:8
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