Version history

1 version on record. Newest first; the live version sits at the top with a live indicator.

  1. Live 6ceb1156ad31
    5/17/2026, 4:45:12 PM
    Content snapshot
    {
      "kind": "infographic",
      "prompt": "AQP4 deletion (~70% clearance loss; Iliff 2012), TBI (~60% reduction; Iliff 2014 JNeurosci), aging (~40% Aβ clearance loss; Kress 2014), and sleep state (~60% ECS volume swing; Xie 2013) each independently converge on glymphatic flow being a major, quantitatively dominant clearance route — while also revealing substantial residual clearance in AQP4-null conditions, setting the stage for later replication challenges.",
      "provider": "other",
      "raw_fields": {
        "papers": [
          {
            "n": null,
            "doi": "10.1126/scitranslmed.3003748",
            "value": "~70%",
            "method": "intracortical tracer injection + two-photon imaging",
            "metric": "Reduction in interstitial solute clearance in AQP4-knockout mice",
            "n_analyzed": null,
            "ci_or_error": null,
            "text_access": "abstract_only",
            "n_definition": "mice genotype groups",
            "scope_region": "mouse cortex and brain parenchyma",
            "study_system": "mouse Aqp4-/- vs wild-type",
            "taxonomic_level": "whole-brain clearance",
            "scope_population": "interstitial-fluid solute tracers",
            "value_source_sentence": "Animals lacking the water channel aquaporin-4 (AQP4) in astrocytes exhibit slowed CSF influx through this system and a ~70% reduction in interstitial solute clearance, suggesting that the bulk fluid flow between these anatomical influx and efflux routes is supported by astrocytic water transport.",
            "experimental_conditions": "in vivo 2-photon imaging of CSF tracers"
          },
          {
            "n": 6,
            "doi": "10.1126/science.1241224",
            "value": "+67% (13.6% awake → 22.7% anesthesia)",
            "method": "real-time TMA+ iontophoresis, two-photon imaging",
            "metric": "Increase in interstitial volume fraction (awake vs anesthetized/sleep)",
            "n_analyzed": null,
            "ci_or_error": "±1.6% awake; ±1.3% anesth",
            "text_access": "fulltext",
            "n_definition": "mice measured with real-time iontophoresis",
            "scope_region": "mouse cortex (in vivo)",
            "study_system": "adult mouse cortex (in vivo)",
            "taxonomic_level": "regional tissue measurement",
            "scope_population": "ECS volume fraction",
            "value_source_sentence": "This approach, which eliminated interanimal variability in electrode placement and TMA calibration, showed that anesthesia consistently increased the interstitial space volume fraction by >60%, from 13.6 ± 1.6% for awake mice to 22.7 ± 1.3% in the same mice after anesthesia.",
            "experimental_conditions": "awake vs natural-sleep vs anesthetized"
          },
          {
            "n": null,
            "doi": "10.1002/ana.24271",
            "value": "40% decrease",
            "method": "radiotracer clearance assay + in vivo fluorescence microscopy",
            "metric": "Reduction in amyloid-β clearance (old vs young mice)",
            "n_analyzed": null,
            "ci_or_error": null,
            "text_access": "abstract_only",
            "n_definition": "mice per age group",
            "scope_region": "mouse cortex (in vivo)",
            "study_system": "young (2-3 mo), middle-aged (10-12 mo), old (18-20 mo) C57BL/6 mice",
            "taxonomic_level": "whole-brain clearance",
            "scope_population": "interstitial amyloid-β",
            "value_source_sentence": "Relative to the young, clearance of intraparenchymally injected amyloid-β was impaired by 40% in the old mice.",
            "experimental_conditions": "intraparenchymal radiotracer clearance"
          },
          {
            "n": null,
            "doi": "10.1523/jneurosci.3020-14.2014",
            "value": "~60% reduction",
            "method": "in vivo tracer imaging of CSF-ISF exchange",
            "metric": "Reduction in glymphatic pathway function after traumatic brain injury",
            "n_analyzed": null,
            "ci_or_error": null,
            "text_access": "abstract_only",
            "n_definition": "mice per condition",
            "scope_region": "mouse cortex",
            "study_system": "mouse, controlled cortical impact TBI",
            "taxonomic_level": "whole-brain clearance",
            "scope_population": "CSF-ISF tracer clearance",
            "value_source_sentence": "After TBI, glymphatic pathway function was reduced by ∼60%, with this impairment persisting for at least 1 month post injury.",
            "experimental_conditions": "TBI vs sham"
          }
        ],
        "comparison_id": "glymphatic-aqp4-clearance-magnitude",
        "comparison_name": "Magnitude of AQP4/glymphatic dependence of interstitial solute clearance across perturbations",
        "comparison_type": "convergent evidence",
        "what_it_reveals": "AQP4 deletion (~70% clearance loss; Iliff 2012), TBI (~60% reduction; Iliff 2014 JNeurosci), aging (~40% Aβ clearance loss; Kress 2014), and sleep state (~60% ECS volume swing; Xie 2013) each independently converge on glymphatic flow being a major, quantitatively dominant clearance route — while also revealing substantial residual clearance in AQP4-null conditions, setting the stage for later replication challenges.",
        "homogeneity_check": {
          "caveats": [
            "Metrics differ: Iliff 2012 and Iliff 2014 TBI report tracer clearance reduction; Kress 2014 reports Aβ-specific clearance; Xie 2013 reports ECS volume fraction",
            "Different tracers (fluorescent dextrans, radiolabeled Aβ) and different imaging modalities (in vivo 2P, radiotracer, real-time iontophoresis)",
            "All measurements are on mouse cortex but perturbations span genetic, traumatic, aging, and state-dependent axes"
          ],
          "n_definition_uniform": "false",
          "scope_region_uniform": "true",
          "taxonomic_level_uniform": "false",
          "scope_population_uniform": "false"
        },
        "suggested_plot_type": "grouped bar"
      },
      "section_id": "section_05_evidence_package",
      "source_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewAstrocytes/blob/1a55da0634a3bc04e5688792ed12141ce271d28e/evidence/section_05_evidence_package.json",
      "target_ref": "wiki_page:computationalreviewastrocytes-05",
      "review_repo": "ComputationalReviewAstrocytes",
      "section_ref": "wiki_page:computationalreviewastrocytes-05",
      "source_path": "evidence/section_05_evidence_package.json",
      "source_refs": [
        "paper:efa35561-2c36-4936-9d8f-f9be6b4d1355",
        "paper:paper-9863a7faec5d",
        "paper:paper-61ea5edf3da7",
        "paper:4c39161e-1d2a-424b-bb0b-0d9e894d349b"
      ],
      "section_title": "Astrocytic Modulation of Synaptic Transmission",
      "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": "1a55da0634a3bc04e5688792ed12141ce271d28e",
        "source_repository_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewAstrocytes"
      },
      "generation_status": "complete",
      "review_bundle_ref": "analysis_bundle:ab-029ee9411fe2",
      "origin_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewAstrocytes/blob/1a55da0634a3bc04e5688792ed12141ce271d28e/evidence/section_05_evidence_package.json",
      "commit_sha": "1a55da0634a3bc04e5688792ed12141ce271d28e",
      "created_by": "persona-jerome-lecoq-gbo-neuroscience",
      "repository_url": "https://github.com/AllenNeuralDynamics/ComputationalReviewAstrocytes"
    }