Journal article
Disrupted basolateral amygdala circuits supports negative valence bias in depressive states
Translational Psychiatry, 2024
DOI 10.1038/s41398-024-03085-6 · PubMed 39300117 · PMC11412998Licence: CC-BY-NC-ND-4.0
9 claims from this source
LA (Lateral amygdalar nucleus) MBA:131 synapses onto BLA (Basolateral amygdalar nucleus) MBA:295 · Mouse
The percentage of rabies-labelled inputs to BLA-to-CeA neurons was quantified separately for the lateral amygdala and the BLA, showing that LA neurons provide inputs to this population.
Fig. 3I
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LA (Lateral amygdalar nucleus) MBA:131 projects to CEA (Central amygdalar nucleus) MBA:536 · Mouse
CTB injected into the CeA labelled lateral amygdala neurons, including cells double-labelled from the NAc injection.
Fig. S5; Table S3
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PVT (Paraventricular nucleus of the thalamus) MBA:149 synapses onto BLA (Basolateral amygdalar nucleus) MBA:295 · Mouse
Projection-specific monosynaptic rabies tracing from BLA neurons projecting to NAc labelled input cells in anterior and posterior PVT. The PVT supplied about 67% of thalamic inputs, and about a third of these inputs were CaMKIIα-positive. Chronic CORT reduced anterior PVT inputs.
Results, presynaptic connectivity section; Fig. 3H
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PVT (Paraventricular nucleus of the thalamus) MBA:149 synapses onto BLA (Basolateral amygdalar nucleus) MBA:295 · Mouse
Rabies tracing from BLA neurons projecting to CeA labelled PVT input neurons, which made up about 64% of thalamic inputs. Many were CaMKIIα-positive, and their number did not change with CORT.
Results, presynaptic connectivity section
Made by an AI model reading the paper (claude-opus-5-5, extract@0.3.0); a second AI model (claude-opus-5-5) agrees.
PAL (Pallidum) MBA:803 synapses onto BLA (Basolateral amygdalar nucleus) MBA:295 · Mouse
Rabies-labelled input neurons to BLA-to-CeA cells were found in the pallidum, and their number was reduced after CORT.
Fig. 3G; Fig. S6I
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BLA (Basolateral amygdalar nucleus) MBA:295 projects to CEA (Central amygdalar nucleus) MBA:536 · Mouse
CTB555 injected into the central amygdala, aimed at its centromedial part, retrogradely labelled BLA neurons. Some BLA cells were double-labelled from both NAc and CeA injections.
Fig. 2A-C; Fig. S4D
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LA (Lateral amygdalar nucleus) MBA:131 projects to ACB (Nucleus accumbens) MBA:56 · Mouse
CTB injected into the NAc also labelled lateral amygdala neurons. Activity of this LA-to-NAc population was analysed separately from basal BLA.
Fig. S5; Table S3
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MO (Somatomotor areas) MBA:500 synapses onto BLA (Basolateral amygdalar nucleus) MBA:295 · Mouse
Somatomotor areas contained rabies-labelled input neurons to BLA-to-NAc cells, and these were fewer in CORT-treated mice.
Fig. 3F; Fig. S6H
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BLA (Basolateral amygdalar nucleus) MBA:295 projects to ACB (Nucleus accumbens) MBA:56 · Mouse
CTB647 injected into the nucleus accumbens retrogradely labelled neurons in the basal BLA, defining a BLA-to-NAc population whose c-Fos recruitment was then quantified.
Fig. 2A-C; Fig. S4D
Made by an AI model reading the paper (claude-opus-5-5, extract@0.3.0); a second AI model (claude-opus-5-5) agrees.