S-2474, a novel nonsteroidal anti-inflammatory drug, rescues cortical neurons from human group IIA secretory phospholipase A 2-induced apoptosis

Abstract

The elevated level of group IIA secretory phospholipase A 2 (sPLA 2-IIA) activity contributes to neurodegeneration in the cerebral cortex after ischemia. The up-regulation of cyclooxygenase-2 (COX-2) is also relevant to cerebral ischemia in humans. Studies of ischemia with COX-2 inhibitors suggest a clinical benefit. In the present study, we investigated effects of S-2474 on sPLA 2-IIA-induced cell death in primary cultures of rat cortical neurons, which was established as an in vitro model of brain ischemia. S-2474 is a novel nonsteroidal anti-inflammatory drug (NSAID), which inhibits COX-2 and contains the di- tert-butylphenol antioxidant moiety. S-2474 significantly prevented neurons from undergoing sPLA 2-IIA-induced cell death. S-2474 completely ameliorated sPLA 2-IIA-induced apoptotic features such as the condensation of chromatin and the fragmentation of DNA. sPLA 2 also generated neurotoxic prostaglandin D 2 (PGD 2) and free radicals from neurons before cell death. S-2474 significantly inhibited the sPLA 2-IIA-induced generation of PGD 2. The present cortical cultures contained few non-neuronal cells, indicating that S-2474 affected neuronal survival directly, but not indirectly via non-neuronal cells. The inhibitory effect of S-2474 on COX-2 might contribute to its neuroprotective effect. In conclusion, S-2474 exhibits neuroprotective effects against sPLA 2-IIA. Furthermore, the present study suggests that S-2474 may possess therapeutic potential for stroke via ameliorating neurodegeneration.