# The Synaptic and Intrinsic Cellular Mechanisms of Persistent Firing in Neurogliaform Cells

**Authors:** Shiyuan Chen, Xiaoshan Chen, Jianwen Zhou, Jinzhao Wang, Kaiyuan Li, Wenyuan Xie, Cheng Long, Gangyi Wu

PMC · DOI: 10.3390/biom15111603 · 2025-11-15

## TL;DR

This study identifies the mechanisms behind persistent firing in neurogliaform cells, a type of brain cell involved in memory processes.

## Contribution

The study reveals a dual-mechanism framework involving T-type calcium channels and 5-HT receptors for persistent firing in GABAergic interneurons.

## Key findings

- Persistent firing in NGFCs is driven by a long-lasting delayed afterdepolarization (L-ADP) mediated by T-type calcium channels.
- 5-HT receptors modulate persistent firing, and blocking them with olanzapine abolishes the phenomenon.
- 62.96% of SLM neurons exhibited persistent firing, which was eliminated by T-type calcium channel blockers.

## Abstract

While persistent firing in glutamatergic neurons has been well-characterized, the intrinsic and synaptic mechanisms driving this phenomenon in neurogliaform cells (NGFCs), a subtype of GABAergic interneurons, remain unclear. This study investigates the mechanisms underlying persistent firing in hippocampal NGFCs. Whole-cell current-clamp recordings were performed on acute brain slices from C57BL/6J mice to examine the electrophysiological properties of NGFCs in the hippocampal stratum lacunosum-moleculare (SLM). Pharmacological interventions, including T-type calcium channel blocker ML218 and 5-hydroxytryptamine (5-HT) receptor antagonist olanzapine, were used to dissect the mechanisms of persistent firing. Biocytin labeling and confocal microscopy were employed to confirm neuronal morphology and location. The study revealed that persistent firing in NGFCs is induced by a long-lasting delayed afterdepolarization (L-ADP), which depends on T-type calcium channels (intrinsic mechanism) and is modulated by 5-HT receptors (synaptic mechanism). Persistent firing was observed in 62.96% of SLM neurons and was abolished by ML218 or olanzapine. The findings bridge a gap in understanding how inhibitory interneurons contribute to memory processes. The dual-mechanism framework (T-type channels and 5-HT receptors) aligns with prior work on glutamatergic systems but highlights unique features of GABAergic persistent firing. These insights advance the understanding of inhibitory circuit dynamics and their potential role in cognitive functions, paving the way for further research into interneuron-specific memory encoding.

## Linked entities

- **Chemicals:** ML218 (PubChem CID 45115620), olanzapine (PubChem CID 135398745), 5-hydroxytryptamine (PubChem CID 5202)

## Full-text entities

- **Chemicals:** calcium (MESH:D002118), ML218 (-), Biocytin (MESH:C013411), olanzapine (MESH:D000077152)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** /6J — Homo sapiens (Human), Cutaneous melanoma, Cancer cell line (CVCL_W797)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12650491/full.md

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Source: https://tomesphere.com/paper/PMC12650491