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Rat

PL (Prelimbic area) functionally connects to DR (Dorsal nucleus raphe)

2 claims from 1 source: 2 found, 0 tested and absent, 0 ambiguous. Evidence: optogenetic circuit mapping.

The claims behind it

clm-h7ehw3ksx4presentoptogenetic circuit mappingproposed

With ChR2 expressed in mPFC and DRN neurons retrogradely labelled from mPFC, light stimulation of mPFC axons within DRN evoked excitatory postsynaptic currents in mPFC-projecting 5-HT neurons (recorded with picrotoxin present); these currents were abolished by TTX and restored by 4-AP, indicating a direct monosynaptic glutamatergic input. Amplitudes averaged about 47 pA in controls and were larger in prenatally ethanol-exposed rats, which also showed a reduced paired-pulse ratio; the NO donor SNAP potentiated these currents in controls.

DOI 10.1038/s41598-025-99181-8 · PubMed 40275074 · PMC12022358, Fig. 2A–D; Fig. 3D–E

Made by an AI model reading the paper (claude-opus-5, extract@0.3.0); a second AI model (claude-opus-5) agrees.

clm-r1j4f0s8dzpresentoptogenetic circuit mappingproposed

In slices with ChR2 in mPFC and DRN neurons retrogradely labelled from the central amygdala, photostimulation of mPFC fibres evoked monosynaptic excitatory currents (TTX-sensitive, rescued by 4-AP) in CeA-projecting 5-HT neurons, with mean amplitude near 49 pA in both control and prenatal-ethanol rats; paired-pulse ratio was lower after prenatal ethanol and SNAP enhanced the currents in controls.

DOI 10.1038/s41598-025-99181-8 · PubMed 40275074 · PMC12022358, Fig. 5A–D; Fig. 6D–E

Made by an AI model reading the paper (claude-opus-5, extract@0.3.0); a second AI model (claude-opus-5) agrees.