ArticleeNeuro2025
Dentate Granule Cell Capacitance Is Stable across the Light/Dark Cycle.
Article in eNeuro, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Scaling of Neuronal Growth and Excitability Through Separable mTORC1 and mTORC2 Pathways.bioRxiv : the preprint server for biology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
The plasma membrane acts as a capacitor that plays a critical role in neuronal excitability and signal propagation. Neuronal capacitance is proportional to the area of the cell membrane; thus it is often used as a measure of the cell size that is assumed to be relatively stable. Recent work proposes that the capacitance of dentate granule cells (dGCs) and cortical pyramidal cells changes across the light/dark (LD) cycle in a manner that alters synaptic integration. We addressed this potential change in capacitance using a large dataset of dGC recordings from adult male and female mice across the light cycle. Our data show that daily changes in the membrane time constant result from fluctuation in membrane resistance rather than capacitance. We also confirm the ability to resolve changes in neuronal capacitance induced by altering dGC membrane area via acute axotomy or genetically induced overgrowth using either voltage-clamp or current-clamp approaches. Our results demonstrate that the capacitance of dGCs remains stable over the LD cycle and that daily changes in the membrane time constant and excitability are mediated by fluctuations in membrane resistance.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.