Enhanced Glutathione Efflux from Astrocytes in Culture by Low Extracellular Ca2+ and Curcumin

被引:49
作者
Stridh, Malin H. [1 ,2 ]
Correa, Fernando [3 ]
Nodin, Christina [2 ]
Weber, Stephen G. [4 ]
Blomstrand, Fredrik [2 ]
Nilsson, Michael [2 ]
Sandberg, Mats [2 ,3 ]
机构
[1] Tech Univ Kaiserslautern, Fachbereich Biol, Abt Allgemeine Zool, D-67663 Kaiserslautern, Germany
[2] Univ Gothenburg, Inst Neurosci & Physiol, Gothenburg, Sweden
[3] Univ Gothenburg, Inst Biomed, Gothenburg, Sweden
[4] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
基金
瑞典研究理事会; 美国国家卫生研究院;
关键词
Astrocyte; Glutathione; Connexin; 43; Nrf2; Curcumin; CONNEXIN HEMICHANNELS; ATP RELEASE; NEURONAL GLUTATHIONE; HIPPOCAMPAL SLICES; OXIDATIVE STRESS; RAT HIPPOCAMPUS; AMINO-ACIDS; IN-VITRO; CELLS; PROTEIN-1;
D O I
10.1007/s11064-010-0179-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Efflux of glutathione (GSH) from astrocytes has been suggested as a key factor for neuroprotection by astrocytes. Here we evaluated if the Nrf2 activator curcumin affects basal and stimulated (Ca2+ omission) GSH efflux from cultures of astroglial cells. Stimulated efflux of GSH was observed at medium concentration of 0, 0.1 mM Ca2+, but not at 0.2 or 0.3 mM Ca2+. Astroglia treated with 30 mu M curcumin increased the cellular content of GSH in parallel with elevated basal and stimulated efflux. Conversely treatment with buthionine sulfoximine lowered efflux of GSH. The efflux stimulated by Ca2+- omission was not affected by the P2X7-receptor antagonist Blue Brilliant G (100 nM) or the pannexin mimetic/blocking peptide (10)Panx1 but inhibited by the gap junction blocker carbenoxolone (100 mu M) and a hemichannel blocker Gap26 (300 mu M). RNAi directed against Nrf2 partly inhibited the effect of curcumin. The results show that elevated cellular GSH by curcumin treatment enhance efflux from astroglial cells, a process which appear to be a prerequisite for astroglial mediated neuroprotection.
引用
收藏
页码:1231 / 1238
页数:8
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