{
"title": "Nicotinic vs Muscarinic Contributions to Cortical Desynchronization",
"papers": [
{
"n": null,
"doi": "10.1152/jn.00244.2013",
"value": "both nicotinic and muscarinic",
"method": "LFP recording + pharmacology",
"metric": "LFP desynchronization receptor component",
"n_analyzed": null,
"CI_or_error": null,
"text_access": "fulltext",
"n_definition": "mice under urethane anesthesia",
"scope_region": "primary somatosensory cortex",
"study_system": "mouse somatosensory cortex, urethane-anesthetized",
"taxonomic_level": "species (mouse)",
"scope_population": "cortical neurons",
"value_source_sentence": "Desynchronization (1-6 Hz) was localized, extending ≤ 1 mm from the edge of stimulation, and consisted of both nicotinic and muscarinic receptor-mediated components that were inhibited by mecamylamine and atropine, respectively.",
"experimental_conditions": "ChR2 stimulation of BF cholinergic axons"
},
{
"n": null,
"doi": "10.1101/2025.06.09.658740",
"value": "L1 inhibitory neurons (nAChR) and L6 pyramidal neurons (nAChR + mAChR)",
"method": "in vivo electrophysiology + slice patch-clamp + in situ hybridization",
"metric": "cholinergic receptor hub location",
"n_analyzed": null,
"CI_or_error": null,
"text_access": "fulltext",
"n_definition": "mice, acute slices and in vivo",
"scope_region": "auditory cortex",
"study_system": "mouse auditory cortex",
"taxonomic_level": "species (mouse)",
"scope_population": "L1-L6 neurons",
"value_source_sentence": "In vivo optogenetic activation of BFCN axons revealed persistent modulation of regular spiking (RS) units in L2-6 but a rapid phasic activation only in L6.",
"experimental_conditions": "optogenetic activation of BF cholinergic axons"
},
{
"n": null,
"doi": "10.1101/2023.11.14.567116",
"value": "high correlation between axon activity and GRAB-ACh fluorescence",
"method": "simultaneous GCaMP + GRAB-ACh imaging",
"metric": "ACh dynamics prediction accuracy",
"n_analyzed": null,
"CI_or_error": null,
"text_access": "fulltext",
"n_definition": "awake behaving mice",
"scope_region": "cortex (sensory)",
"study_system": "mouse cortex, in vivo two-photon",
"taxonomic_level": "species (mouse)",
"scope_population": "BF cholinergic axons and local ACh levels",
"value_source_sentence": "GRAB-ACh fluorescence could be accurately predicted from axonal activity alone, providing the first validation that neuromodulator axon activity is a reliable proxy for nearby neuromodulator levels.",
"experimental_conditions": "spontaneous behavior + locomotion"
}
],
"comparison_id": "fig_sec4_ach_desync_mechanism",
"comparison_type": "cross-study mechanism comparison",
"homogeneity_check": {
"caveats": [
"Different cortical regions: somatosensory vs auditory vs general sensory cortex",
"Different experimental states: urethane anesthesia vs awake behaving",
"Different metrics: LFP power changes vs EPSP latency vs correlation coefficient",
"These studies are complementary rather than directly quantitatively comparable"
],
"comparable": false
},
"suggested_plot_type": "grouped_bar"
}