- claim_text
Nicotinic agonists selectively depolarize VIP/CCK cortical interneurons but not pyramidal cells, PV-fast spiking, or SST interneurons; the response persists in TTX/low-Ca2+ (postsynaptic), is blocked by DHβE/mecamylamine but not the α7-antagonist MLA, and the responsive cells co-express α4/α5/β2 nAChR subunits.
- raw_fields
{
"n": null,
"doi": "10.1523/jneurosci.19-13-05228.1999",
"claim": "Nicotinic agonists selectively depolarize VIP/CCK cortical interneurons but not pyramidal cells, PV-fast spiking, or SST interneurons; the response persists in TTX/low-Ca2+ (postsynaptic), is blocked by DHβE/mecamylamine but not the α7-antagonist MLA, and the responsive cells co-express α4/α5/β2 nAChR subunits.",
"title": null,
"cite_key": "Porter1999",
"evidence": "Whole-cell recordings + single-cell RT-PCR in rat neocortical slices.",
"effect_size": "qualitative cell-type-specific selectivity; pharmacological identity α4β2-like (lacking α7) nAChR.",
"text_access": "abstract_only",
"study_system": "rat neocortex slice",
"_source_cluster": "cluster_05_synaptic_connectivity",
"replication_status": "independently_replicated",
"_source_cluster_index": 4,
"claim_source_sentence": "Nicotinic receptor agonists had no effect on pyramidal neurons and on most types of interneurons, including parvalbumin-expressing fast spiking interneurons and somatostatin-expressing interneurons, but selectively excited a subpopulation of interneurons coexpressing the neuropeptides vasoactive intestinal peptide (VIP) and cholecystokinin.",
"replication_evidence_dois": [
"10.1038/nn.4002",
"10.1523/jneurosci.22-17-07389.2002"
],
"effect_size_source_sentence": "The responses were blocked by the nicotinic receptor antagonists dihydro-beta-erythroidine and mecamylamine and persisted in the presence of the alpha7 selective nicotinic receptor antagonist methyllycaconitine, suggesting that the involved nicotinic receptors lacked the alpha7 subunit."
}- source_refs
[
"paper:paper-5f194b747ea7"
]
- source_span
Nicotinic receptor agonists had no effect on pyramidal neurons and on most types of interneurons, including parvalbumin-expressing fast spiking interneurons and somatostatin-expressing interneurons, but selectively excited a subpopulation of interneurons coexpressing the neuropeptides vasoactive intestinal peptide (VIP) and cholecystokinin.
- evidence_refs
[
{
"ref": "paper:paper-5f194b747ea7"
}
]- source_policy
{
"mode": "public_source_pointer_with_short_context",
"notes": [
"Local review repositories are read-only inputs.",
"SciDEX stores paper metadata, structured evidence, file pointers, and short citation contexts; it does not copy full review prose."
],
"source_commit_sha": "95e761177f7d2ec565983d3307c14ec238f9677c",
"source_repository_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewVIP"
}