دورية أكاديمية

Differential mechanisms of tolerance induced by NMDA and 3,5-dihydroxyphenylglycine (DHPG) preconditioning

التفاصيل البيبلوغرافية
العنوان: Differential mechanisms of tolerance induced by NMDA and 3,5-dihydroxyphenylglycine (DHPG) preconditioning
المؤلفون: Gerace E., Zianni E., Landucci E., Scartabelli T., Berlinguer Palmini R., Iezzi D., Moroni F., Di Luca M., Mannaioni G., Gardoni F., Pellegrini-Giampietro D. E.
المساهمون: E. Gerace, E. Zianni, E. Landucci, T. Scartabelli, R. Berlinguer Palmini, D. Iezzi, F. Moroni, M. Di Luca, G. Mannaioni, F. Gardoni, D.E. Pellegrini-Giampietro
بيانات النشر: Wiley Blackwell Publishing
سنة النشر: 2020
المجموعة: The University of Milan: Archivio Istituzionale della Ricerca (AIR)
مصطلحات موضوعية: endocannabinoid, glutamate receptor, neuroprotection, organotypic hippocampal slice, post-synaptic densitie, preconditioning, sEPSCs, Settore BIO/14 - Farmacologia
الوصف: We investigated the molecular events triggered by NMDA and 3,5-dihydroxyphenylglycine (DHPG) preconditioning, that lead to neuroprotection against excitotoxic insults (AMPA or oxygen and glucose deprivation) in rat organotypic hippocampal slices, with particular attention on glutamate receptors and on cannabinoid system. We firstly evaluated the protein expression of NMDA and AMPA receptor subunits after preconditioning using western blot analysis performed in post-synaptic densities. We observed that following NMDA, but not DHPG preconditioning, the expression of GluA1 was significantly reduced and this reduction appeared to be associated with the internalization of AMPA receptors. Whole-cell voltage clamp recordings on CA1 pyramidal neurons of organotypic slices show that 24hr after exposure to NMDA and DHPG preconditioning, AMPA-induced currents were significantly reduced. To clarify the mechanisms induced by DHPG preconditioning, we then investigated the involvement of the endocannabinoid system. Exposure of slices to the CB1 antagonist AM251 prevented the development of tolerance to AMPA toxicity induced by DHPG but not NMDA. Accordingly, the MAG-lipase inhibitor URB602, that increases arachidonoylglycerol (2-AG) content, but not the FAAH inhibitor URB597, that limits the degradation of anandamide, was also able to induce tolerance versus AMPA and OGD toxicity, suggesting that 2-AG is responsible for the DHPG-induced tolerance. In conclusion, preconditioning with NMDA or DHPG promotes differential neuroprotective mechanisms: NMDA by internalization of GluA1-AMPA receptors, DHPG by producing the endocannabinoid 2-AG. (Figure presented.).
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32343420; info:eu-repo/semantics/altIdentifier/wos/WOS:000533445100001; volume:155; issue:6; firstpage:638; lastpage:649; numberofpages:12; journal:JOURNAL OF NEUROCHEMISTRY; http://hdl.handle.net/2434/783320Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85084844272
DOI: 10.1111/jnc.15033
الإتاحة: https://doi.org/10.1111/jnc.15033Test
http://hdl.handle.net/2434/783320Test
حقوق: info:eu-repo/semantics/closedAccess
رقم الانضمام: edsbas.1A02AD30
قاعدة البيانات: BASE