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Updated: Mar 18, 2026

Quantification of Neurovascular Protection Following Repetitive Hypoxic Preconditioning and Transient Middle Cerebral Artery Occlusion in Mice
Published on: May 4, 2015
NOS knockout or inhibition but not disrupting PSD-95-NOS interaction protect against ischemic brain damage
Christoph Kleinschnitz1, Stine Mencl2, Pamela W M Kleikers3
1Department of Neurology, University Hospital Würzburg, Würzburg, Germany Department of Neurology, University Hospital Essen, Essen, Germany christoph.kleinschnitz@uk-essen.de.
Abstract:
Promising results have been reported in preclinical stroke target validation for pharmacological principles that disrupt the N-methyl-D-aspartate receptor-post-synaptic density protein-95-neuronal nitric oxide synthase complex. However, post-synaptic density protein-95 is also coupled to potentially neuroprotective mechanisms. As post-synaptic density protein-95 inhibitors may interfere with potentially neuroprotective mechanisms and sufficient validation has often been an issue in translating basic stroke research, we wanted to close that gap by comparing post-synaptic density protein-95 inhibitors with NOS1(-/-) mice and a NOS inhibitor. We confirm the deleterious role of NOS1 in stroke both in vivo and in vitro, but find three pharmacological post-synaptic density protein-95 inhibitors to be therapeutically ineffective.
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