Evidence map›Paper›PMID 41527707›Full record

ArticleNeuroreport2026

Deep patch-clamp recordings in awake mice from medial septal neurons during hippocampal sharp-wave ripples.

Hana Samejima, Yu Sato, Yuji Ikegaya, Tetsuhiko Kashima

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In one paragraph

Article in Neuroreport, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hana SamejimaGraduate School of Pharmaceutical Sciences, The University of Tokyo.
Yu SatoGraduate School of Pharmaceutical Sciences, The University of Tokyo.
Yuji IkegayaGraduate School of Pharmaceutical Sciences, The University of Tokyo.
Tetsuhiko KashimaGraduate School of Pharmaceutical Sciences, The University of Tokyo.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe medial septum modulates hippocampal oscillations, including ripples, which are critical for memory consolidation. While the role of the medial septum in theta rhythms is well-established, its specific contribution to hippocampal ripple activity remains poorly understood. This study sought to investigate the relationship between medial septal activity and hippocampal ripples in vivo .

methodsThis study aimed to characterize the in-vivo membrane potential dynamics of putative medial septal neuron subtypes and their contribution to hippocampal ripples in awake mice. We performed in-vivo whole-cell patch-clamp recordings from medial septal neurons in head-fixed, awake mice, while simultaneously acquiring hippocampal local field potentials.

resultsMedial septal neurons were classified into glutamatergic, cholinergic, and GABAergic subtypes using hierarchical clustering based on their intrinsic electrophysiological properties. We analyzed the firing rates and subthreshold membrane potential dynamics of these neurons during hippocampal ripple events and examined their correlations with ripple parameters (duration, frequency, and power). Our results revealed subtype-specific responses. Notably, putative glutamatergic neurons exhibited a slight decrease in firing rate, yet displayed a pronounced depolarization of their membrane potential approximately 100 ms before ripple onset, peaking at the initiation of ripples. This depolarization was inversely correlated with subsequent ripple amplitude and power. In addition, membrane hyperpolarization was positively correlated with ripple duration.

conclusionThese findings elucidate the contribution of glutamatergic medial septal neurons to hippocampal ripple dynamics and suggest a tightly regulated interaction between the medial septum and hippocampus in shaping ripple activity.

Indexed as

HippocampusNeuronsSeptal NucleiAction PotentialsAnimalsLocal Field Potential MeasurementMaleMembrane PotentialsMiceMice, Inbred C57BLPatch-Clamp TechniquesWakefulnessmedial septumpatch-clampsharp-wave ripples

Identifiers

PMID41527707
PMCPMC12955948

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