Synthesis, Neuroprotection, and Antioxidant Activity of 1,1′-Biphenylnitrones as α-Phenyl-N-tert-butylnitrone Analogues in In Vitro Ischemia Models

Herein, we report the neuroprotective and antioxidant activity of 1,1 '-biphenyl nitrones (BPNs) 1-5 as alpha-phenyl-N-tert-butylnitrone analogues prepared from commercially available [1,1 '-biphenyl]-4-carbaldehyde and [1,1 '-biphenyl]-4,4 '-dicarbaldehyde. The neuroprotection of BPNs 1-5 has been measured against oligomycin A/rotenone and in an oxygen-glucose deprivation in vitro ischemia model in human neuroblastoma SH-SY5Y cells. Our results indicate that BPNs 1-5 have better neuroprotective and antioxidant properties than alpha-phenyl-N-tert-butylnitrone (PBN), and they are quite similar to N-acetyl-L-cysteine (NAC), which is a well-known antioxidant agent. Among the nitrones studied, homo-bis-nitrone BPHBN5, bearing two N-tert-Bu radicals at the nitrone motif, has the best neuroprotective capacity (EC50 = 13.16 +/- 1.65 and 25.5 +/- 3.93 mu M, against the reduction in metabolic activity induced by respiratory chain blockers and oxygen-glucose deprivation in an in vitro ischemia model, respectively) as well as anti-necrotic, anti-apoptotic, and antioxidant activities (EC50 = 11.2 +/- 3.94 mu M), which were measured by its capacity to reduce superoxide production in human neuroblastoma SH-SY5Y cell cultures, followed by mononitrone BPMN3, with one N-Bn radical, and BPMN2, with only one N-tert-Bu substituent. The antioxidant activity of BPNs 1-5 has also been analyzed for their capacity to scavenge hydroxyl free radicals (82% at 100 mu M), lipoxygenase inhibition, and the inhibition of lipid peroxidation (68% at 100 mu M). Results showed that although the number of nitrone groups improves the neuroprotection profile of these BPNs, the final effect is also dependent on the substitutent that is being incorporated. Thus, BPNs bearing N-tert-Bu and N-Bn groups show better neuroprotective and antioxidant properties than those substituted with Me. All these results led us to propose homo-bis-nitrone BPHBN5 as the most balanced and interesting nitrone based on its neuroprotective capacity in different neuronal models of oxidative stress and in vitro ischemia as well as its antioxidant activity.

Automated summary

The neuroprotective and antioxidant activities of 1,1'-biphenyl nitrones (BPNs) 1-5 were investigated and compared to alpha-phenyl-N-tert-butylnitrone and N-acetyl-L-cysteine. Results showed that BPNs 1-5, particularly homo-bis-nitrone BPHBN5, exhibited superior neuroprotective and antioxidant properties, making it a promising compound for potential therapeutic applications in oxidative stress and ischemia models.