{"paper_id":"138f1fe9-3682-40a2-a7d5-e66a7ae24a88","body_text":"ABSTRACT\nEpilepsy often becomes treatment-resistant, partly due to impaired inhibitory neurotransmission and reduced γ-aminobutyric acid (GABA) function. Enhancing inhibitory neuron activity via gene therapy may restore excitation–inhibition (E/I) balance. We developed a compact 410-bp glutamic acid decarboxylase 67 promoter (cmGAD67) that enables strong, selective transgene expression in inhibitory neurons while preserving AAV packaging capacity. When delivered systemically, AAV vectors carrying cmGAD67 preferentially targeted parvalbumin interneurons and supported effective circuit manipulation.\nTo evaluate therapeutic potential, we expressed glutamic acid decarboxylase 65 (GAD65) under cmGAD67 (AAV-GAD65) in pentylenetetrazole (PTZ) epilepsy models. Systemic AAV-GAD65 suppressed abnormal delta oscillations, reduced seizure-like events, normalized anxiety-like behavior, and improved survival in a severe PTZ paradigm. Biochemical analyses confirmed increased cortical and hippocampal GABA levels, linking behavioral and electrophysiological improvements to enhanced inhibitory neurotransmitter synthesis.\nPrior clinical evidence indicates that AAV-GAD65 delivery to the subthalamic nucleus is safe and effective in Parkinson’s disease. Building on this foundation, our findings establish the cmGAD67 promoter as a powerful platform for inhibitory neuron-targeted AAV gene therapy and highlight AAV-cmGAD67-GAD65 as a promising approach for treatment-resistant epilepsy and other disorders involving disrupted E/I balance.\nCompeting Interest Statement\nGunma University, with H.H., A.K., and Y.F. listed as inventors, has filed patent applications in the EU (23803614.9), China (202380040106.1), the US (18/865107), and Japan (2024-520489) for the inhibitory neuron-specific promoter described in this study.\nFootnotes\n↵4 Lead contact","source_license":"CC-BY-4.0","license_restricted":false}