期刊
NEUROSCIENCE LETTERS
卷 536, 期 -, 页码 41-46出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2013.01.007
关键词
Apoptosis; Curcumin; Necroptosis; Primary cortical neuron; Receptor interacting protein 1
资金
- Shanghai Committee of Science and Technology [10JC1410700, 10411954200]
- SJTU Medical-Engineering Cross Research fund [YG2012MS06]
Necroptosis was reported as one backup way of programmed cell death when apoptosis was blocked, and the receptor interacting protein 1 was considered as the key necroptosis regulator protein. Here, we report the neuroprotective effects of curcumin which attenuates necroptosis. Primary cortical neurons were cultured and were injured by ferrous chloride, z.vad.fmk was applied to block apoptosis, curcumin was administrated to protect neurons, necrostatin-1 was applied to inhibit necroptosis if needed. Cell viability was measured by detecting lactate dehydrogenase activity in lysates of surviving cells, and assessed by cell counting kit-8. The expression of receptor interacting protein 1 was detected by immunoblot and immunofluorescence. Results showed that necroptosis mainly occurred in the concentrations of ferrous chloride ranging from 100 to 200 mu M, curcumin attenuated necroptosis in a dose-dependent manner. Furthermore, curcumin decreased expression of receptor interacting protein 1 in a dose- and time-dependent manner. Taken together, these findings suggest that curcumin protects against iron induced neurotoxicity in primary cortical neurons by attenuating necroptosis. Crown Copyright (C) 2013 Published by Elsevier Ireland Ltd. All rights reserved.
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