4-Oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione derivatives as NMDA receptor- and VGCC blockers with neuroprotective potential

dc.contributor.authorEgunlusi, Ayodeji O
dc.contributor.authorOmoruyi, Sylvester I
dc.contributor.authorMalan, Sarel F
dc.date.accessioned2020-12-01T13:21:13Z
dc.date.available2020-12-01T13:21:13Z
dc.date.issued2020
dc.description.abstractThe impact of excitotoxicity mediated by N-methyl-D-aspartate (NMDA) receptor overactivation and voltage gated calcium channel (VGCC) depolarization is prominent among the postulated processes involved in the development of neurodegenerative disorders. NGP1-01, a polycyclic amine, has been shown to be neuroprotective through modulation of the NMDA receptor and VGCC, and attenuation of MPP+-induced neurotoxicity. Recently, we reported on the calcium modulating effects of tricycloundecene derivatives, structurally similar to NGP1-01, on the NMDA receptor and VGCC of synaptoneurosomes. In the present study, we investigated novel 4-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione derivatives for their cytotoxicity, neuroprotective effects via attenuation of MPP+-induced neurotoxicity and calcium influx inhibition abilities through the NMDA receptor and VGCC using neuroblastoma SH-SY5Y cells. All compounds, in general, showed low or no toxicity against neuroblastoma cells at 10–50 µM concentrations. At 10 µM, all compounds significantly attenuated MPP+-induced neurotoxicity as evident by the enhancement in cell viability between 23.05 ± 3.45% to 53.56 ± 9.29%. In comparison to known active compounds, the derivatives demonstrated mono or dual calcium modulating effect on the NMDA receptor and/or VGCC. Molecular docking studies using the NMDA receptor protein structure indicated that the compounds are able to bind in a comparable manner to the crystallographic pose of MK-801 inside the NMDA ion channel. The biological characteristics, together with results from in silico studies, suggest that these compounds could act as neuroprotective agents for the purpose of halting or slowing down the degenerative processes in neuronal cells.en_US
dc.identifier.citationEgunlusi. A.O. et al. (2020). 4-Oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione derivatives as NMDA receptor- and VGCC blockers with neuroprotective potential. Molecule, 25(19),4552en_US
dc.identifier.issn14203049
dc.identifier.uri10.3390/molecules25194552
dc.identifier.urihttp://hdl.handle.net/10566/5474
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.subjectNeurodegenerative disordersen_US
dc.subjectNMDA receptoren_US
dc.subjectVoltage gated calcium channelsen_US
dc.subjectPolycyclic cagesen_US
dc.title4-Oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione derivatives as NMDA receptor- and VGCC blockers with neuroprotective potentialen_US
dc.typeArticleen_US

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