ArticleScientific reports2026
Median Raphe projection into the dorsal dentate gyrus modulates anxiety behavior and coping with learning under stress.
Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
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 Median Raphe (MR) provides a major, mainly serotonergic, input to the hippocampus, particularly influencing the dentate gyrus (DG), but its specific role remains unclear. Here, focusing on the dorsal DG, we investigated its contribution to anxiety-like behavior and learning under stress, using a pathway-specific chemogenetic approach in male Sprague-Dawley rats. Retrograde Cre-expressing AAV was injected into the dorsal DG, and Cre-dependent excitatory (hM3Dq) or inhibitory (hM4Di) DREADDs were expressed in MR neurons. Behavioral assessments included the Open Field (OF), Elevated Plus Maze (EPM), and an extended Two-Way Shuttle Avoidance task (eTWSA). MR-dorsal DG pathway activation had no significant impact, but its inhibition decreased anxiety-like behavior in the EPM and improved eTWSA performance, particularly in behaviorally “diverged” animals. Knocked down in the dorsal DG EphA7, a molecule involved in basket cell synapse stabilization on DG granule cells, prevented the anxiolytic effects and behavioral divergence induced by MR-dorsal DG inhibition, but did not prevent improved eTWSA performance. These findings suggest a dissociation between mechanisms of emotional regulation and stress-related learning mechanisms within the dorsal DG, with the MR input to DG basket interneurons modulating anxiety but not learning flexibility. The results highlight a subregion- and pathway-specific role of the MR-hippocampal input in modulating behavior.
Indexed as
Identifiers
What Socratic holds
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.