Curcumin Protects against NMDA-Induced Toxicity: A Possible Role for NR2A Subunit

被引:57
作者
Matteucci, Andrea [1 ]
Cammarota, Roberta [3 ]
Paradisi, Silvia [1 ]
Varano, Monica [4 ]
Balduzzi, Maria [5 ,6 ]
Leo, Lanfranco [1 ]
Bellenchi, Gian C. [1 ]
De Nuccio, Chiara [1 ]
Carnovale-Scalzo, Giovanna [7 ]
Scorcia, Giovanni [7 ]
Frank, Claudio [2 ]
Mallozzi, Cinzia [1 ]
Di Stasi, Annamaria M. [1 ]
Visentin, Sergio [1 ]
Malchiodi-Albedi, Fiorella [1 ]
机构
[1] Ist Super Sanita, Dept Cell Biol & Neurosci, I-00161 Rome, Italy
[2] Ist Super Sanita, Natl Ctr Rare Dis, I-00161 Rome, Italy
[3] Univ Roma Tor Vergata, Dept Expt Med & Biochem Sci, Rome, Italy
[4] GB Bietti Fdn Study & Res Ophthalmol IRCCS, Rome, Italy
[5] ENEA CR Casaccia, Biotechnol, Agroind, Rome, Italy
[6] ENEA CR Casaccia, Hlth Protect Dept, Rome, Italy
[7] Magna Graecia Univ Catanzaro, Eye Clin, Catanzaro, Italy
关键词
FOCAL CEREBRAL-ISCHEMIA; RECEPTOR SUBUNIT; IN-VIVO; MESSENGER-RNAS; RAT RETINA; NEURONS; NEUROPROTECTION; EXCITOTOXICITY; LOCALIZATION; MECHANISMS;
D O I
10.1167/iovs.10-5966
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. Curcumin, a phenolic compound extracted from the rhizome of Curcuma longa, was found to attenuate NMDA-induced excitotoxicity in primary retinal cultures. This study was conducted to further characterize curcumin neuroprotective ability and analyze its effects on NMDA receptor (NMDAr). METHODS. NMDAr modifications were analyzed in primary retinal cell cultures using immunocytochemistry, whole-cell patch-clamp recording and western blot analysis. Cell death was evaluated with the TUNEL assay in primary retinal and hippocampal cultures. Optical fluorometric recordings with Fura 2-AM were used to monitor [Ca(2+)](t). RESULTS. Curcumin dose-and time-dependently protected both retinal and hippocampal neurons against NMDA-induced cell death, confirming its anti-excitotoxic property. In primary retinal cultures, in line with the observed reduction of NMDA-induced [Ca(2+)] i rise, whole-cell patch-clamp experiments showed that a higher percentage of retinal neurons responded to NMDA with low amplitude current after curcumin treatment. In parallel, curcumin induced an increase in NMDAr subunit type 2A (NR2A) level, with kinetics closely correlated to time-course of neuroprotection and decrease in [Ca(2+)](t). The relation between neuroprotection and NR2A level increase was also in line with the observation that curcumin neuroprotection required protein synthesis. Electrophysiology confirmed an increased activity of NR2A-containing NMDAr at the plasma membrane level. CONCLUSIONS. These results confirm the neuroprotective activity of curcumin against NMDA toxicity, possibly related to an increased level of NR2A, and encourage further studies for a possible therapeutic use of curcumin based on neuromodula-tion of NMDArs. (Invest Ophthalmol Vis Sci. 2011; 52:1070-1077) DOI:10.1167/iovs.10-5966
引用
收藏
页码:1070 / 1077
页数:8
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