Component

SH-SY5Y cell viability by MTT

SH-SY5Y cell viability by MTT

2 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What acts on it

  1. Pyridoxine reduced MTT-measured viability of differentiated SH-SY5Y cells after 24 hours in a concentration-dependent manner.

    Pyridoxine → SH-SY5Y cell viability by MTT source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    Differentiated human SH-SY5Y and CaCo-2 cells; isolated enzyme assays
    exposure
    Pyridoxine 0-5 micromolar for 24 hours.
    exposure-class
    Experimental excess pyridoxine; not dietary B6 deficiency · Pyridoxine
    limitations
    Tumor-derived cells and MTT endpoint; no oral-dose conversion or human toxicity threshold.
    nutrient_topic
    Vitamin B6 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin B6
    organism
    Homo sapiens
    plain_language
    Added pyridoxine harmed this experimental neuronal cell model.
    primary_references
    [vrolijk-2017-pn] The vitamin B6 paradox: Supplementation with high concentrations of pyridoxine leads to decreased vitamin B6 function (2017). https://doi.org/10.1016/j.tiv.2017.07.009 DOI: 10.1016/j.tiv.2017.07.009
    tissue_or_cell_type
    Differentiated SH-SY5Y neuroblastoma cells

    Vitamin B6: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 1232–1243

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Differentiated human SH-SY5Y and CaCo-2 cells; isolated enzyme assays · source_derived_draft · unverified_draft

    ### b6-neuro-pn-cell-viability Pyridoxine reduced MTT-measured viability of differentiated SH-SY5Y cells after 24 hours in a concentration-dependent manner. Condition category: normal nutrient_topic: Vitamin B6 research collection; topical membership is not evidence of a direct dietary effect. plain_language: Added pyridoxine harmed this experimental neuronal cell model. organism: Homo sapiens tissue_or_cell_type: Differentiated SH-SY5Y neuroblastoma cells experimental_model: Differentiated human SH-SY5Y and CaCo-2 cells; isolated enzyme assays limitations: Tumor-derived cells and MTT endpoint; no oral-dose conversion or human toxicity threshold. exposure: Pyridoxine 0-5 micromolar for 24 hours. exposure-class: Experimental excess pyridoxine; not dietary B6 deficiency [vrolijk-2017-pn] The vitamin B6 paradox: Supplementation with high concentrations of pyridoxine leads to decreased vitamin B6 function (2017). https://doi.org/10.1016/j.tiv.2017.07.009 DOI: 10.1016/j.tiv.2017.07.009
    Complete structured claim and evidence
  2. Pyridoxal, pyridoxamine, PLP and PMP did not reduce viability in the tested 24-hour cell assay.

    PLP → SH-SY5Y cell viability by MTT source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    Differentiated human SH-SY5Y and CaCo-2 cells; isolated enzyme assays
    exposure
    Comparators 0-500 micromolar for 24 hours.
    exposure-class
    Experimental excess pyridoxine; not dietary B6 deficiency · Pyridoxine
    limitations
    A negative short-term cell assay proves neither universal safety nor equivalent toxicity.
    nutrient_topic
    Vitamin B6 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin B6
    organism
    Homo sapiens
    plain_language
    The tested B6 forms behaved differently in this assay.
    primary_references
    [vrolijk-2017-pn] The vitamin B6 paradox: Supplementation with high concentrations of pyridoxine leads to decreased vitamin B6 function (2017). https://doi.org/10.1016/j.tiv.2017.07.009 DOI: 10.1016/j.tiv.2017.07.009
    tissue_or_cell_type
    SH-SY5Y and CaCo-2 cells

    Vitamin B6: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 1245–1256

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Differentiated human SH-SY5Y and CaCo-2 cells; isolated enzyme assays · source_derived_draft · unverified_draft

    ### b6-neuro-pn-vitamer-specificity Pyridoxal, pyridoxamine, PLP and PMP did not reduce viability in the tested 24-hour cell assay. Condition category: normal nutrient_topic: Vitamin B6 research collection; topical membership is not evidence of a direct dietary effect. plain_language: The tested B6 forms behaved differently in this assay. organism: Homo sapiens tissue_or_cell_type: SH-SY5Y and CaCo-2 cells experimental_model: Differentiated human SH-SY5Y and CaCo-2 cells; isolated enzyme assays limitations: A negative short-term cell assay proves neither universal safety nor equivalent toxicity. exposure: Comparators 0-500 micromolar for 24 hours. exposure-class: Experimental excess pyridoxine; not dietary B6 deficiency [vrolijk-2017-pn] The vitamin B6 paradox: Supplementation with high concentrations of pyridoxine leads to decreased vitamin B6 function (2017). https://doi.org/10.1016/j.tiv.2017.07.009 DOI: 10.1016/j.tiv.2017.07.009
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards