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Updated: Apr 17, 2026

Modeling Neuronal Death and Degeneration in Mouse Primary Cerebellar Granule Neurons
Published on: November 6, 2017
Tat-NR2B9c prevents excitotoxic neuronal superoxide production
Yanting Chen1, Angela M Brennan-Minnella2, Sunil Sheth2
11] Department of Neurology, Drum Tower Hospital, Medical School of Nanjing University, Nanjing, Jiangsu, PR China [2] Department of Neurology, San Francisco Veterans Affairs Medical Center, University of California, San Francisco, California, USA.
Abstract:
The Tat-NR2B9c peptide has shown clinical efficacy as a neuroprotective agent in acute stroke. Tat-NR2B9c is designed to prevent nitric oxide (NO) production by preventing postsynaptic density protein 95 (PSD-95) binding to N-methyl-D-aspartate (NMDA) receptors and neuronal nitric oxide synthase; however, PSD-95 is a scaffolding protein that also couples NMDA receptors to other downstream effects. Here, using neuronal cultures, we show that Tat-NR2B9c also prevents NMDA-induced activation of neuronal NADPH oxidase, thereby blocking superoxide production. Given that both superoxide and NO are required for excitotoxic injury, the neuroprotective effect of Tat-NR2B9c may alternatively be attributable to uncoupling neuronal NADPH oxidase from NMDA receptor activation.
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