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{ "kind": "infographic", "prompt": "Interneuron proportions across mammalian species", "provider": "other", "raw_fields": { "title": "Interneuron proportions across mammalian species", "papers": [ { "doi": "10.1186/s13287-025-04603-z", "unit": "percentage of total neurons", "metric": "interneuron proportion", "cite_key": "Du2025", "comparison_value": "50%", "value_source_sentence": "Calretinin-expressing interneurons, the most prominent type, constitute approximately 50% of human cortical GABAergic neurons and are closely linked to cognition." }, { "doi": "10.3389/fnsyn.2026.1766413", "unit": "percentage of total neurons", "metric": "interneuron proportion", "cite_key": null, "comparison_value": "54%", "value_source_sentence": "Specifically, we observed acute enhancement of excitatory postsynaptic current (EPSC) amplitudes in 54% of fast-spiking interneurons and in 15% of non-fast-spiking interneuron types." }, { "doi": "10.3389/fncir.2025.1644572", "unit": "percentage of total neurons", "metric": "interneuron proportion", "cite_key": null, "comparison_value": "85.3%", "value_source_sentence": "Based on our serial-section electron microscopy (ssEM) reconstructions and corresponding light microscopy (LM) databases of CBP dendrites, it was calculated that on average a single CB+, CR+, and PV+ interneuron receives 2,136, 2,148, and 2,589 synapses, respectively, of which 74.6, 81.5, and 85.3% are excitatory, that is, asymmetric, and the remaining inhibitory, that is, symmetric." }, { "doi": "10.1016/j.neuroimage.2022.119813", "unit": "percentage of total neurons", "metric": "interneuron proportion", "cite_key": null, "comparison_value": "10%", "value_source_sentence": "However, the physiological basis of the large changes in GABA and glutamate observed by fMRS (>10%) over short time scales of less than a minute remain unclear as such changes cannot be accounted for by known synthesis or degradation metabolic pathways." }, { "doi": "10.3389/fnana.2014.00103", "unit": "percentage of total neurons", "metric": "interneuron proportion", "cite_key": null, "comparison_value": "50%", "value_source_sentence": "Equally important to the changes in glutamatergic population, we found that literature data suggest a 50% increase in the proportion of neocortical GABAergic neurons between primates and rodents." }, { "doi": "10.3389/fnana.2014.00050", "unit": "percentage of total neurons", "metric": "interneuron proportion", "cite_key": null, "comparison_value": "7%", "value_source_sentence": "In most mammalians, parvalbumin and somatostatin interneurons have constant proportions, each representing 5-7% of the total neuron number." }, { "doi": "10.1038/s41586-019-1506-7", "unit": "percentage of total interneurons", "metric": "MGE vs CGE interneuron proportions", "cite_key": "Hodge2019", "comparison_value": "Human: 50.2% MGE, 44.2% CGE; Mouse: 67.8% MGE, 30.8% CGE", "value_source_sentence": "Again, we found similar proportions of MGE (50.2 ± 2.3%) and CGE (44.2 ± 2.4%) interneurons in human, and >2 times as many MGE (67.8 ± 0.9%) than CGE (30.8 ± 1.2%) interneurons in mouse." }, { "doi": "10.1038/s41586-019-1506-7", "unit": "cortical layers", "metric": "rosehip cell laminar distribution", "cite_key": "Hodge2019", "comparison_value": "Rosehip cells (Inh L1-4 LAMP5 LCP2) present in all cortical layers, not just L1", "value_source_sentence": "Inh L1-4 LAMP5 LCP2 matched rosehip cells, discovered in L1 but present in all cortical layers." } ], "figure_id": "fig_sec11_interneuron_proportions_species", "n_analyzed": null, "description": "Percentage of GABAergic neurons among total cortical neurons across species", "n_definition": "varies - stereological counts, single-cell studies, or immunohistochemistry", "scope_region": "neocortex (various areas)", "comparison_type": "cross-species comparison", "taxonomic_level": "class level (GABAergic vs glutamatergic)", "scope_population": "GABAergic neurons as fraction of total neurons", "homogeneity_check": "Different methodologies across studies (stereology vs scRNA-seq vs immunohistochemistry). Cortical region varies. Direct numerical comparison requires caution." }, "section_id": "section_10_evidence", "source_url": "https://github.com/AllenNeuralDynamics/ComputationReviewInhibitory/blob/934e0675cc6d5ffd9978a4a9883b31166ce000e2/evidence/section_10_evidence.json", "target_ref": "wiki_page:computationreviewinhibitory-10", "review_repo": "ComputationReviewInhibitory", "section_ref": "wiki_page:computationreviewinhibitory-10", "source_path": "evidence/section_10_evidence.json", "source_refs": [ "paper:paper-183ef13f84fd", "paper:paper-1c04e7d4ce5c", "paper:paper-pm-31435019", "paper:paper-8fbcb0e752b7", "paper:paper-9af6e0492426", "paper:paper-a428435bf623", "paper:paper-a448c24e8347" ], "section_title": "Plasticity and Development of Inhibitory Circuits", "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": "934e0675cc6d5ffd9978a4a9883b31166ce000e2", "source_repository_url": "https://github.com/AllenNeuralDynamics/ComputationReviewInhibitory" }, "generation_status": "complete", "review_bundle_ref": "analysis_bundle:ab-5fc3c0c0505b", "origin_url": "https://github.com/AllenNeuralDynamics/ComputationReviewInhibitory/blob/934e0675cc6d5ffd9978a4a9883b31166ce000e2/evidence/section_10_evidence.json", "commit_sha": "934e0675cc6d5ffd9978a4a9883b31166ce000e2", "created_by": "persona-jerome-lecoq-gbo-neuroscience", "repository_url": "https://github.com/AllenNeuralDynamics/ComputationReviewInhibitory" }