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Harmon, P.

Publications and source records attributed to Harmon, P..

2 recordsLinked to original sources

A fiducial-based framework for precise MRI-guided stereotaxic targeting in nonhuman primates

Background Accurate MRI-guided stereotaxic targeting in nonhuman primates requires reliable registration between MRI coordinates and stereotaxic space. We evaluated skull-fixed MR-compatible screw fiducials as a practical reference for this registration. Results Using a 3D-printed skull model with 28 fiducials and three internal targets, we compared offset translation, rigid registration, and affine registration under aligned and misaligned conditions. Offset translation was most sensitive to misalignment. Affine registration fit skull-surface fiducials closely, but rigid registration produced lower overall target errors. In vivo validation showed that implanted fiducials could be identified on MRI and re-measured during a later surgery. Comparison with existing methods This approach builds on previous fiducial-based stereotaxic methods by systematically comparing registration transforms, testing misalignment, evaluating fiducial number, and measuring accuracy at independent internal targets. Conclusions Skull-fixed fiducials provide a practical framework for MRI-to-stereotaxic registration. Rigid registration may offer the safest balance between correcting positioning differences and preserving accuracy at internal targets.

neuroscience↗

Discrete interneuron subsets participate in GluN1/GluN3A excitatory glycine receptor (eGlyR)-mediated regulation of hippocampal network activity throughout development and evolution.

Decades of studies implicating GluN3A N-methyl-D-aspartate receptor (NMDAR) subunits in physiological and pathological function have largely been interpreted through direct regulation of conventional glutamatergic NMDARs. However, emerging evidence indicates that GluN3A frequently assembles with GluN1 forming unconventional glutamate-insensitive NMDARs that operate as native excitatory glycine receptors (eGlyRs). Here we demonstrate that hippocampal somatostatin and neurogliaform interneurons (Sst-INs and NGFCs) express functional eGlyRs from early postnatal through adult ages. In the developing hippocampus eGlyR-mediated excitation of NGFCs with ambient glycine dramatically increases GABAergic tone, with consequences for the generation of giant depolarizing potentials (GDPs). In the mature hippocampus, eGlyR- mediated excitation of Sst-INs regulates sharp wave ripples (SWRs). Finally, we reveal evolutionary conservation of hippocampal Sst-IN eGlyRs and eGlyR- mediated SWR regulation in non-human primates confirming functional eGlyR availability for therapeutic potential in higher species. Our findings underscore that eGlyR mediated regulation of cell and circuit excitability through both cell autonomous and cell non-autonomous mechanisms must be considered to understand GluN3A roles in brain development, plasticity, and disease.

neuroscience↗