Geometric principles of dendritic integration of excitation and inhibition in cortical neurons

preprint OA: closed
📄 Open PDF Full text JSON View at publisher

Abstract

We use two-color uncaging of glutamate and gamma -aminobutyric acid (GABA) on layer-5 (L5) pyramidal neurons of the cingulate cortex to define how inhibitory control of excitation is controlled by dendritic geometry. Traditionally, GABAergic input was considered as the gatekeeper, thus, receptors closest to the soma were ideally placed to veto excitation. However, recently modeling has advanced several counter-intuitive hypotheses. Since laser uncaging can be directed at will to any position, we used photostimulation to show that inhibition near the sealed end of dendrites distal to excitation is more effective than inhibition near the soma in modulating excitation. Further, dendritic inhibition was found to be branch specific. Finally, we demonstrate that inhibitory input from multiple thin basal dendrites can centripetally elevate to effectively tune distant excitation at the soma. These findings provide direct experimental evidence supporting theoretical predictions based on dendritic cable properties, revealing the critical role of dendritic geometry in shaping the interaction between excitatory and inhibitory neurotransmission. Teaser By activating excitatory (E) and inhibitory (I) synapses selectively with light we explored the geometric based interaction of E/I transmission in dendrites of pyramidal neurons.
Full text 1,422 characters · extracted from oa-doi-fallback · click to expand
Abstract We use two-color uncaging of glutamate and gamma-aminobutyric acid (GABA) on layer-5 (L5) pyramidal neurons of the cingulate cortex to define how inhibitory control of excitation is controlled by dendritic geometry. Traditionally, GABAergic input was considered as the gatekeeper, thus, receptors closest to the soma were ideally placed to veto excitation. However, recently modeling has advanced several counter-intuitive hypotheses. Since laser uncaging can be directed at will to any position, we used photostimulation to show that inhibition near the sealed end of dendrites distal to excitation is more effective than inhibition near the soma in modulating excitation. Further, dendritic inhibition was found to be branch specific. Finally, we demonstrate that inhibitory input from multiple thin basal dendrites can centripetally elevate to effectively tune distant excitation at the soma. These findings provide direct experimental evidence supporting theoretical predictions based on dendritic cable properties, revealing the critical role of dendritic geometry in shaping the interaction between excitatory and inhibitory neurotransmission. Teaser By activating excitatory (E) and inhibitory (I) synapses selectively with light we explored the geometric based interaction of E/I transmission in dendrites of pyramidal neurons. Competing Interest Statement The authors have declared no competing interest.

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2025) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

Source provenance

europepmc
last seen: 2026-05-20T01:45:00.602351+00:00