Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5814592 | Neuropharmacology | 2014 | 15 Pages |
Abstract
5-FU (in saline)-treated aged and also young mice exhibited specific altered cognitive flexibility and behavioral hyper-reactivity to novelty, whereas the combination 5-FU (in saline)/oxaliplatin (in glucose) did not provoke any cognitive dysfunction. We thus observed that glucose counteracted 5-FU-induced altered executive functions and hippocampal cell proliferation in vivo, and protected neural stem cells in vitro from toxicity of 5-FU or oxaliplatin. In conclusion, these data suggest that the lasting chemotherapy-induced selective impairment of executive functions, whatever the age, and associated with a reduced number of hippocampal proliferating cells, can be counteracted by co-administration with glucose.
Keywords
5-FUsouth-westWFIMTXfield CA1 of the hippocampusSVZSGZPRLfield CA3 of the hippocampusCA35-bromo-2-deoxyuridineGCLFSTaCSFi.p.SfMEPCINSBLALSDNSCCA1water for injectionforced swim testFRAinsulinBrdUPirleast significant differenceintraperitonealdentate gyrus of the hippocampusAgingserum free mediumNeural stem cellcytochrome oxidaseNorth-WestChemotherapy5-fluorouracilFrontal association cortexMotor cortexRetrosplenial cortexpiriform cortexdorsal peduncular cortexprelimbic cortexgranule cell layermolecular layerartificial cerebral spinal fluidMethotrexatedorsal subiculumsubgranular zonesubventricular zoneMousebasolateral amygdaloid nucleuslaterodorsal thalamic nucleusMediodorsal thalamic nucleusreuniens thalamic nucleusLateral amygdaloid nucleusExecutive functionsGluGlucose
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Authors
M. Dubois, N. Lapinte, V. Villier, C. Lecointre, V. Roy, M.-C. Tonon, P. Gandolfo, F. Joly, P. Hilber, H. Castel,