Component

meso-Zeaxanthin / (3R,3-prime-S)-zeaxanthin

meso-Zeaxanthin / (3R,3-prime-S)-zeaxanthin. Species, exposure and limitations are retained in each linked claim.

14 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. Expression temperature and detergent choice affected recombinant BCO2 binding and xanthophyll turnover, including meso-zeaxanthin.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/lutein-research/26307071.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "6b225e90d2edb66a12583bcdaefb8247cf57c26dffd4f02a1a189907c6f97916", "start_char": 0, "end_char": 1495, "text_sha256": "6b225e90d2edb66a12583bcdaefb8247cf57c26dffd4f02a1a189907c6f97916"}
    experimental_model
    Comparative recombinant enzyme and cell experiments
    exposure
    Low-temperature expression and detergent variation
    limitations
    Conserved activity does not demonstrate identical rates across species or diets.
    nutrient_topic
    Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
    organism
    Primate and murine BCO2
    plain_language
    How the protein was prepared changed the measured activity.
    primary_references
    [lutein-p26307071] Characterization of the Role of β-Carotene 9,10-Dioxygenase in Macular Pigment Metabolism. (2015). https://pubmed.ncbi.nlm.nih.gov/26307071/ DOI: 10.1074/jbc.m115.668822
    tissue_or_cell_type
    Protein preparations and human hepatic cell line

    Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 320–331

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Comparative recombinant enzyme and cell experiments · source_derived_draft · unverified_draft

    ### lutein-bco2-method-dependence Expression temperature and detergent choice affected recombinant BCO2 binding and xanthophyll turnover, including meso-zeaxanthin. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: How the protein was prepared changed the measured activity. organism: Primate and murine BCO2 tissue_or_cell_type: Protein preparations and human hepatic cell line experimental_model: Comparative recombinant enzyme and cell experiments limitations: Conserved activity does not demonstrate identical rates across species or diets. exposure: Low-temperature expression and detergent variation evidence_span: {"source_cache": "artifacts/lutein-research/26307071.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "6b225e90d2edb66a12583bcdaefb8247cf57c26dffd4f02a1a189907c6f97916", "start_char": 0, "end_char": 1495, "text_sha256": "6b225e90d2edb66a12583bcdaefb8247cf57c26dffd4f02a1a189907c6f97916"} [lutein-p26307071] Characterization of the Role of β-Carotene 9,10-Dioxygenase in Macular Pigment Metabolism. (2015). https://pubmed.ncbi.nlm.nih.gov/26307071/ DOI: 10.1074/jbc.m115.668822
    Complete structured claim and evidence
  2. Chicken RPE65 overexpression supported meso-zeaxanthin production from lutein.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/lutein-research/28874556.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "240bde60bb175fdfd5f556b9f2f7aab97f5d5b03e9640160418c34c74194d8c9", "start_char": 0, "end_char": 1679, "text_sha256": "240bde60bb175fdfd5f556b9f2f7aab97f5d5b03e9640160418c34c74194d8c9"}
    experimental_model
    Overexpression, developmental expression and pharmacological inhibition
    exposure
    RPE65 expression with lutein; inhibitor experiments in developing chicken eye
    limitations
    Cell and animal evidence; docking near iron is not a human iron-supplementation experiment.
    nutrient_topic
    Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
    organism
    Human/chicken proteins in cells and chicken embryos
    plain_language
    The conversion was also observed with the chicken enzyme.
    primary_references
    [lutein-p28874556] RPE65 has an additional function as the lutein to meso-zeaxanthin isomerase in the vertebrate eye. (2017). https://pubmed.ncbi.nlm.nih.gov/28874556/ DOI: 10.1073/pnas.1706332114
    tissue_or_cell_type
    Cultured cells and embryonic RPE/choroid

    Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 164–175

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Overexpression, developmental expression and pharmacological inhibition · source_derived_draft · unverified_draft

    ### lutein-chicken-rpe65-isomerase Chicken RPE65 overexpression supported meso-zeaxanthin production from lutein. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: The conversion was also observed with the chicken enzyme. organism: Human/chicken proteins in cells and chicken embryos tissue_or_cell_type: Cultured cells and embryonic RPE/choroid experimental_model: Overexpression, developmental expression and pharmacological inhibition limitations: Cell and animal evidence; docking near iron is not a human iron-supplementation experiment. exposure: RPE65 expression with lutein; inhibitor experiments in developing chicken eye evidence_span: {"source_cache": "artifacts/lutein-research/28874556.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "240bde60bb175fdfd5f556b9f2f7aab97f5d5b03e9640160418c34c74194d8c9", "start_char": 0, "end_char": 1679, "text_sha256": "240bde60bb175fdfd5f556b9f2f7aab97f5d5b03e9640160418c34c74194d8c9"} [lutein-p28874556] RPE65 has an additional function as the lutein to meso-zeaxanthin isomerase in the vertebrate eye. (2017). https://pubmed.ncbi.nlm.nih.gov/28874556/ DOI: 10.1073/pnas.1706332114
    Complete structured claim and evidence
  3. Overexpressed human RPE65 supported conversion of lutein into meso-zeaxanthin in cultured cells.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/lutein-research/28874556.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "240bde60bb175fdfd5f556b9f2f7aab97f5d5b03e9640160418c34c74194d8c9", "start_char": 0, "end_char": 1679, "text_sha256": "240bde60bb175fdfd5f556b9f2f7aab97f5d5b03e9640160418c34c74194d8c9"}
    experimental_model
    Overexpression, developmental expression and pharmacological inhibition
    exposure
    RPE65 expression with lutein; inhibitor experiments in developing chicken eye
    limitations
    Cell and animal evidence; docking near iron is not a human iron-supplementation experiment.
    nutrient_topic
    Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
    organism
    Human/chicken proteins in cells and chicken embryos
    plain_language
    The visual-cycle enzyme can also rearrange lutein.
    primary_references
    [lutein-p28874556] RPE65 has an additional function as the lutein to meso-zeaxanthin isomerase in the vertebrate eye. (2017). https://pubmed.ncbi.nlm.nih.gov/28874556/ DOI: 10.1073/pnas.1706332114
    tissue_or_cell_type
    Cultured cells and embryonic RPE/choroid

    Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 151–162

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Overexpression, developmental expression and pharmacological inhibition · source_derived_draft · unverified_draft

    ### lutein-human-rpe65-isomerase Overexpressed human RPE65 supported conversion of lutein into meso-zeaxanthin in cultured cells. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: The visual-cycle enzyme can also rearrange lutein. organism: Human/chicken proteins in cells and chicken embryos tissue_or_cell_type: Cultured cells and embryonic RPE/choroid experimental_model: Overexpression, developmental expression and pharmacological inhibition limitations: Cell and animal evidence; docking near iron is not a human iron-supplementation experiment. exposure: RPE65 expression with lutein; inhibitor experiments in developing chicken eye evidence_span: {"source_cache": "artifacts/lutein-research/28874556.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "240bde60bb175fdfd5f556b9f2f7aab97f5d5b03e9640160418c34c74194d8c9", "start_char": 0, "end_char": 1679, "text_sha256": "240bde60bb175fdfd5f556b9f2f7aab97f5d5b03e9640160418c34c74194d8c9"} [lutein-p28874556] RPE65 has an additional function as the lutein to meso-zeaxanthin isomerase in the vertebrate eye. (2017). https://pubmed.ncbi.nlm.nih.gov/28874556/ DOI: 10.1073/pnas.1706332114
    Complete structured claim and evidence
  4. Mouse RPE65 supported lutein isomerization in cultured cells despite mice not normally concentrating meso-zeaxanthin in the eye.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/lutein-research/41415389.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "b4eb5b9290310947be962df7dae42190e5afa6ffd726e869cb842d7f7ed15a41", "start_char": 0, "end_char": 1304, "text_sha256": "b4eb5b9290310947be962df7dae42190e5afa6ffd726e869cb842d7f7ed15a41"}
    experimental_model
    Cultured-cell enzyme expression, mutagenesis and structural modeling
    exposure
    Lutein substrate; E148Q substitution; binding-protein coexpression
    limitations
    Proposed radical transition state remains a mechanistic interpretation, not directly observed chemistry.
    nutrient_topic
    Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
    organism
    Human, chicken and mouse RPE65
    plain_language
    Enzyme capacity and whole-tissue pigment accumulation are different.
    primary_references
    [lutein-p41415389] Mechanism of Lutein to meso-Zeaxanthin Isomerization by RPE65 Catalysis. (2025). https://pubmed.ncbi.nlm.nih.gov/41415389/ DOI: 10.64898/2025.12.10.693550
    tissue_or_cell_type
    Cultured cells and molecular models

    Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 190–201

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Cultured-cell enzyme expression, mutagenesis and structural modeling · source_derived_draft · unverified_draft

    ### lutein-mouse-rpe65-isomerase Mouse RPE65 supported lutein isomerization in cultured cells despite mice not normally concentrating meso-zeaxanthin in the eye. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: Enzyme capacity and whole-tissue pigment accumulation are different. organism: Human, chicken and mouse RPE65 tissue_or_cell_type: Cultured cells and molecular models experimental_model: Cultured-cell enzyme expression, mutagenesis and structural modeling limitations: Proposed radical transition state remains a mechanistic interpretation, not directly observed chemistry. exposure: Lutein substrate; E148Q substitution; binding-protein coexpression evidence_span: {"source_cache": "artifacts/lutein-research/41415389.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "b4eb5b9290310947be962df7dae42190e5afa6ffd726e869cb842d7f7ed15a41", "start_char": 0, "end_char": 1304, "text_sha256": "b4eb5b9290310947be962df7dae42190e5afa6ffd726e869cb842d7f7ed15a41"} [lutein-p41415389] Mechanism of Lutein to meso-Zeaxanthin Isomerization by RPE65 Catalysis. (2025). https://pubmed.ncbi.nlm.nih.gov/41415389/ DOI: 10.64898/2025.12.10.693550
    Complete structured claim and evidence
  5. This ARPE-19 delivery experiment detected no lutein conversion to meso-zeaxanthin.

    Lutein → meso-Zeaxanthin / (3R,3-prime-S)-zeaxanthin source_derived_draftungraded
    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/lutein-research/27538825.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "1db014221931676349f15dc3c5138fba122417fb49fec5de481594c72b0596f3", "start_char": 0, "end_char": 1346, "text_sha256": "1db014221931676349f15dc3c5138fba122417fb49fec5de481594c72b0596f3"}
    experimental_model
    Carotenoid delivery using isolated human lipoproteins
    exposure
    Carotenoid-loaded LDL versus HDL
    limitations
    Cell delivery ranking is not identical to circulating carriage fractions or the WHAM-chicken phenotype.
    nutrient_topic
    Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
    organism
    Human ARPE-19 cells
    plain_language
    Uptake alone did not reproduce the separate RPE65 overexpression result.
    primary_references
    [lutein-p27538825] Mechanisms of selective delivery of xanthophylls to retinal pigment epithelial cells by human lipoproteins. (2016). https://pubmed.ncbi.nlm.nih.gov/27538825/ DOI: 10.1194/jlr.m070193
    tissue_or_cell_type
    Retinal pigment epithelial model

    Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 658–669

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Carotenoid delivery using isolated human lipoproteins · source_derived_draft · unverified_draft

    ### lutein-rpe-isomerization-null This ARPE-19 delivery experiment detected no lutein conversion to meso-zeaxanthin. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: Uptake alone did not reproduce the separate RPE65 overexpression result. organism: Human ARPE-19 cells tissue_or_cell_type: Retinal pigment epithelial model experimental_model: Carotenoid delivery using isolated human lipoproteins limitations: Cell delivery ranking is not identical to circulating carriage fractions or the WHAM-chicken phenotype. exposure: Carotenoid-loaded LDL versus HDL evidence_span: {"source_cache": "artifacts/lutein-research/27538825.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "1db014221931676349f15dc3c5138fba122417fb49fec5de481594c72b0596f3", "start_char": 0, "end_char": 1346, "text_sha256": "1db014221931676349f15dc3c5138fba122417fb49fec5de481594c72b0596f3"} [lutein-p27538825] Mechanisms of selective delivery of xanthophylls to retinal pigment epithelial cells by human lipoproteins. (2016). https://pubmed.ncbi.nlm.nih.gov/27538825/ DOI: 10.1194/jlr.m070193
    Complete structured claim and evidence
  6. GSTP1 bound meso-zeaxanthin with apparent Kd 0.52 micromolar.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/zeaxanthin-research/15355982.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "6365b1d54aafda71be4dbf6c8e5252fa6ce0af3b808d9af6fe07c37ae188ea92", "start_char": 0, "end_char": 1907, "text_sha256": "6365b1d54aafda71be4dbf6c8e5252fa6ce0af3b808d9af6fe07c37ae188ea92"}
    experimental_model
    Human macular protein purification and recombinant binding
    exposure
    Equilibrium binding and immunocytochemistry
    limitations
    Binding affinity is assay-specific and does not quantify uptake or clinical benefit.
    nutrient_topic
    Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. · Dietary (3R,3-prime-R)-zeaxanthin
    organism
    Human tissue/proteins
    plain_language
    The stereoisomer also has a binding site.
    primary_references
    [zeaxanthin-p15355982] Identification and characterization of a Pi isoform of glutathione S-transferase (GSTP1) as a zeaxanthin-binding protein in the macula of the human eye. (2004). https://pubmed.ncbi.nlm.nih.gov/15355982/ DOI: 10.1074/jbc.m405334200
    tissue_or_cell_type
    Macula and purified proteins

    Zeaxanthin: metabolism, signaling and nutrient connections (2026-09-17) · lines 223–234

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Human macular protein purification and recombinant binding · source_derived_draft · unverified_draft

    ### zeaxanthin-gstp1-meso GSTP1 bound meso-zeaxanthin with apparent Kd 0.52 micromolar. Condition category: normal nutrient_topic: Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. plain_language: The stereoisomer also has a binding site. organism: Human tissue/proteins tissue_or_cell_type: Macula and purified proteins experimental_model: Human macular protein purification and recombinant binding limitations: Binding affinity is assay-specific and does not quantify uptake or clinical benefit. exposure: Equilibrium binding and immunocytochemistry evidence_span: {"source_cache": "artifacts/zeaxanthin-research/15355982.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "6365b1d54aafda71be4dbf6c8e5252fa6ce0af3b808d9af6fe07c37ae188ea92", "start_char": 0, "end_char": 1907, "text_sha256": "6365b1d54aafda71be4dbf6c8e5252fa6ce0af3b808d9af6fe07c37ae188ea92"} [zeaxanthin-p15355982] Identification and characterization of a Pi isoform of glutathione S-transferase (GSTP1) as a zeaxanthin-binding protein in the macula of the human eye. (2004). https://pubmed.ncbi.nlm.nih.gov/15355982/ DOI: 10.1074/jbc.m405334200
    Complete structured claim and evidence
  7. No meso-zeaxanthin formation was detected over the trial sampling period.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/zeaxanthin-research/15137922.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "6410a0f5d52cf32390f90f59a7b17d2340a889f888836129f8a93482ca055be0", "start_char": 0, "end_char": 1847, "text_sha256": "6410a0f5d52cf32390f90f59a7b17d2340a889f888836129f8a93482ca055be0"}
    experimental_model
    Randomized single-blind crossover meal trial
    exposure
    5 mg free zeaxanthin equivalents as free pigment or dipalmitate in yoghurt/breakfast; 24 h sampling
    limitations
    Meal- and formulation-specific response; no proof of disease prevention or an optimal universal formulation.
    nutrient_topic
    Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. · Dietary (3R,3-prime-R)-zeaxanthin
    organism
    12 volunteers
    plain_language
    The study did not show rapid conversion of dietary zeaxanthin into meso-zeaxanthin.
    primary_references
    [zeaxanthin-p15137922] Comparison of plasma responses in human subjects after the ingestion of 3R,3R'-zeaxanthin dipalmitate from wolfberry (Lycium barbarum) and non-esterified 3R,3R'-zeaxanthin using chiral high-performance liquid chromatography. (2004). https://pubmed.ncbi.nlm.nih.gov/15137922/ DOI: 10.1079/bjn20041105
    tissue_or_cell_type
    Plasma response

    Zeaxanthin: metabolism, signaling and nutrient connections (2026-09-17) · lines 808–819

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized single-blind crossover meal trial · source_derived_draft · unverified_draft

    ### zeaxanthin-human-meso-null No meso-zeaxanthin formation was detected over the trial sampling period. Condition category: normal nutrient_topic: Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. plain_language: The study did not show rapid conversion of dietary zeaxanthin into meso-zeaxanthin. organism: 12 volunteers tissue_or_cell_type: Plasma response experimental_model: Randomized single-blind crossover meal trial limitations: Meal- and formulation-specific response; no proof of disease prevention or an optimal universal formulation. exposure: 5 mg free zeaxanthin equivalents as free pigment or dipalmitate in yoghurt/breakfast; 24 h sampling evidence_span: {"source_cache": "artifacts/zeaxanthin-research/15137922.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "6410a0f5d52cf32390f90f59a7b17d2340a889f888836129f8a93482ca055be0", "start_char": 0, "end_char": 1847, "text_sha256": "6410a0f5d52cf32390f90f59a7b17d2340a889f888836129f8a93482ca055be0"} [zeaxanthin-p15137922] Comparison of plasma responses in human subjects after the ingestion of 3R,3R'-zeaxanthin dipalmitate from wolfberry (Lycium barbarum) and non-esterified 3R,3R'-zeaxanthin using chiral high-performance liquid chromatography. (2004). https://pubmed.ncbi.nlm.nih.gov/15137922/ DOI: 10.1079/bjn20041105
    Complete structured claim and evidence

Where it participates (unsigned role)

  1. The equal-ratio meso-zeaxanthin, zeaxanthin and lutein mixture quenched more singlet oxygen than each individual pigment at the same total concentration.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/lutein-research/20678467.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "aaf88f567941ed16adb101981a218960bbd8ae3cfe0919868de63462e7c7be01", "start_char": 0, "end_char": 989, "text_sha256": "aaf88f567941ed16adb101981a218960bbd8ae3cfe0919868de63462e7c7be01"}
    experimental_model
    EPR of donor eye tissue and solution quenching assays
    exposure
    White-light challenge and equal-total-concentration carotenoid comparisons
    limitations
    Solution mixture effects do not establish an optimal oral ratio or clinical benefit; exogenous pigment addition differs from delivery in a living eye.
    nutrient_topic
    Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
    organism
    Postmortem human tissue and cell-free systems
    plain_language
    The three pigments worked better together in this solution experiment.
    primary_references
    [lutein-p20678467] Studies on the singlet oxygen scavenging mechanism of human macular pigment. (2010). https://pubmed.ncbi.nlm.nih.gov/20678467/ DOI: 10.1016/j.abb.2010.07.024
    tissue_or_cell_type
    Macula, RPE/choroid and carotenoid solutions

    Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 229–240

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · EPR of donor eye tissue and solution quenching assays · source_derived_draft · unverified_draft

    ### lutein-mixture-quenching The equal-ratio meso-zeaxanthin, zeaxanthin and lutein mixture quenched more singlet oxygen than each individual pigment at the same total concentration. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: The three pigments worked better together in this solution experiment. organism: Postmortem human tissue and cell-free systems tissue_or_cell_type: Macula, RPE/choroid and carotenoid solutions experimental_model: EPR of donor eye tissue and solution quenching assays limitations: Solution mixture effects do not establish an optimal oral ratio or clinical benefit; exogenous pigment addition differs from delivery in a living eye. exposure: White-light challenge and equal-total-concentration carotenoid comparisons evidence_span: {"source_cache": "artifacts/lutein-research/20678467.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "aaf88f567941ed16adb101981a218960bbd8ae3cfe0919868de63462e7c7be01", "start_char": 0, "end_char": 989, "text_sha256": "aaf88f567941ed16adb101981a218960bbd8ae3cfe0919868de63462e7c7be01"} [lutein-p20678467] Studies on the singlet oxygen scavenging mechanism of human macular pigment. (2010). https://pubmed.ncbi.nlm.nih.gov/20678467/ DOI: 10.1016/j.abb.2010.07.024
    Complete structured claim and evidence
  2. RPE65 inhibition reduced meso-zeaxanthin biosynthesis during chicken eye development.

    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    evidence_span
    {"source_cache": "artifacts/lutein-research/28874556.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "240bde60bb175fdfd5f556b9f2f7aab97f5d5b03e9640160418c34c74194d8c9", "start_char": 0, "end_char": 1679, "text_sha256": "240bde60bb175fdfd5f556b9f2f7aab97f5d5b03e9640160418c34c74194d8c9"}
    experimental_model
    Overexpression, developmental expression and pharmacological inhibition
    exposure
    RPE65 expression with lutein; inhibitor experiments in developing chicken eye
    limitations
    Cell and animal evidence; docking near iron is not a human iron-supplementation experiment.
    nutrient_topic
    Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
    organism
    Human/chicken proteins in cells and chicken embryos
    plain_language
    An enzyme block reduced pigment production despite the distinct dietary precursor.
    primary_references
    [lutein-p28874556] RPE65 has an additional function as the lutein to meso-zeaxanthin isomerase in the vertebrate eye. (2017). https://pubmed.ncbi.nlm.nih.gov/28874556/ DOI: 10.1073/pnas.1706332114
    tissue_or_cell_type
    Cultured cells and embryonic RPE/choroid
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 177–188

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Overexpression, developmental expression and pharmacological inhibition · source_derived_draft · unverified_draft

    ### lutein-rpe65-inhibition RPE65 inhibition reduced meso-zeaxanthin biosynthesis during chicken eye development. Condition category: machinery_impairment nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: An enzyme block reduced pigment production despite the distinct dietary precursor. organism: Human/chicken proteins in cells and chicken embryos tissue_or_cell_type: Cultured cells and embryonic RPE/choroid experimental_model: Overexpression, developmental expression and pharmacological inhibition limitations: Cell and animal evidence; docking near iron is not a human iron-supplementation experiment. exposure: RPE65 expression with lutein; inhibitor experiments in developing chicken eye evidence_span: {"source_cache": "artifacts/lutein-research/28874556.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "240bde60bb175fdfd5f556b9f2f7aab97f5d5b03e9640160418c34c74194d8c9", "start_char": 0, "end_char": 1679, "text_sha256": "240bde60bb175fdfd5f556b9f2f7aab97f5d5b03e9640160418c34c74194d8c9"} [lutein-p28874556] RPE65 has an additional function as the lutein to meso-zeaxanthin isomerase in the vertebrate eye. (2017). https://pubmed.ncbi.nlm.nih.gov/28874556/ DOI: 10.1073/pnas.1706332114
    Complete structured claim and evidence
  3. The GSTP1–zeaxanthin protective effect did not require glutathione in this liposome experiment.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/zeaxanthin-research/15949677.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194", "start_char": 0, "end_char": 1404, "text_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194"}
    experimental_model
    Lipid-peroxyl radical challenge in liposomes
    exposure
    AAPH or AMVN challenge; dietary and meso zeaxanthin
    limitations
    Protein-associated antioxidant synergy is demonstrated in this assay, not a clinical supplement combination.
    nutrient_topic
    Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. · Dietary (3R,3-prime-R)-zeaxanthin
    organism
    Cell-free system with human GSTP1
    plain_language
    This binding-related effect persisted without glutathione.
    primary_references
    [zeaxanthin-p15949677] Synergistic effects of zeaxanthin and its binding protein in the prevention of lipid membrane oxidation. (2005). https://pubmed.ncbi.nlm.nih.gov/15949677/ DOI: 10.1016/j.bbadis.2005.02.002
    tissue_or_cell_type
    Egg-yolk phosphatidylcholine liposomes

    Zeaxanthin: metabolism, signaling and nutrient connections (2026-09-17) · lines 288–299

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Lipid-peroxyl radical challenge in liposomes · source_derived_draft · unverified_draft

    ### zeaxanthin-gsh-independent The GSTP1–zeaxanthin protective effect did not require glutathione in this liposome experiment. Condition category: normal nutrient_topic: Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. plain_language: This binding-related effect persisted without glutathione. organism: Cell-free system with human GSTP1 tissue_or_cell_type: Egg-yolk phosphatidylcholine liposomes experimental_model: Lipid-peroxyl radical challenge in liposomes limitations: Protein-associated antioxidant synergy is demonstrated in this assay, not a clinical supplement combination. exposure: AAPH or AMVN challenge; dietary and meso zeaxanthin evidence_span: {"source_cache": "artifacts/zeaxanthin-research/15949677.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194", "start_char": 0, "end_char": 1404, "text_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194"} [zeaxanthin-p15949677] Synergistic effects of zeaxanthin and its binding protein in the prevention of lipid membrane oxidation. (2005). https://pubmed.ncbi.nlm.nih.gov/15949677/ DOI: 10.1016/j.bbadis.2005.02.002
    Complete structured claim and evidence
  4. GSTP1 association increased resistance of zeaxanthin diastereomers to chemical degradation.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/zeaxanthin-research/15949677.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194", "start_char": 0, "end_char": 1404, "text_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194"}
    experimental_model
    Lipid-peroxyl radical challenge in liposomes
    exposure
    AAPH or AMVN challenge; dietary and meso zeaxanthin
    limitations
    Protein-associated antioxidant synergy is demonstrated in this assay, not a clinical supplement combination.
    nutrient_topic
    Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. · Dietary (3R,3-prime-R)-zeaxanthin
    organism
    Cell-free system with human GSTP1
    plain_language
    The protein helped preserve the pigments during oxidation.
    primary_references
    [zeaxanthin-p15949677] Synergistic effects of zeaxanthin and its binding protein in the prevention of lipid membrane oxidation. (2005). https://pubmed.ncbi.nlm.nih.gov/15949677/ DOI: 10.1016/j.bbadis.2005.02.002
    tissue_or_cell_type
    Egg-yolk phosphatidylcholine liposomes

    Zeaxanthin: metabolism, signaling and nutrient connections (2026-09-17) · lines 275–286

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Lipid-peroxyl radical challenge in liposomes · source_derived_draft · unverified_draft

    ### zeaxanthin-gstp1-stability GSTP1 association increased resistance of zeaxanthin diastereomers to chemical degradation. Condition category: normal nutrient_topic: Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. plain_language: The protein helped preserve the pigments during oxidation. organism: Cell-free system with human GSTP1 tissue_or_cell_type: Egg-yolk phosphatidylcholine liposomes experimental_model: Lipid-peroxyl radical challenge in liposomes limitations: Protein-associated antioxidant synergy is demonstrated in this assay, not a clinical supplement combination. exposure: AAPH or AMVN challenge; dietary and meso zeaxanthin evidence_span: {"source_cache": "artifacts/zeaxanthin-research/15949677.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194", "start_char": 0, "end_char": 1404, "text_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194"} [zeaxanthin-p15949677] Synergistic effects of zeaxanthin and its binding protein in the prevention of lipid membrane oxidation. (2005). https://pubmed.ncbi.nlm.nih.gov/15949677/ DOI: 10.1016/j.bbadis.2005.02.002
    Complete structured claim and evidence
  5. GSTP1-bound dietary zeaxanthin synergistically inhibited peroxidation induced by either radical generator.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/zeaxanthin-research/15949677.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194", "start_char": 0, "end_char": 1404, "text_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194"}
    experimental_model
    Lipid-peroxyl radical challenge in liposomes
    exposure
    AAPH or AMVN challenge; dietary and meso zeaxanthin
    limitations
    Protein-associated antioxidant synergy is demonstrated in this assay, not a clinical supplement combination.
    nutrient_topic
    Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. · Dietary (3R,3-prime-R)-zeaxanthin
    organism
    Cell-free system with human GSTP1
    plain_language
    Binding enhanced protection of the test membrane.
    primary_references
    [zeaxanthin-p15949677] Synergistic effects of zeaxanthin and its binding protein in the prevention of lipid membrane oxidation. (2005). https://pubmed.ncbi.nlm.nih.gov/15949677/ DOI: 10.1016/j.bbadis.2005.02.002
    tissue_or_cell_type
    Egg-yolk phosphatidylcholine liposomes

    Zeaxanthin: metabolism, signaling and nutrient connections (2026-09-17) · lines 262–273

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Lipid-peroxyl radical challenge in liposomes · source_derived_draft · unverified_draft

    ### zeaxanthin-gstp1-synergy GSTP1-bound dietary zeaxanthin synergistically inhibited peroxidation induced by either radical generator. Condition category: normal nutrient_topic: Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. plain_language: Binding enhanced protection of the test membrane. organism: Cell-free system with human GSTP1 tissue_or_cell_type: Egg-yolk phosphatidylcholine liposomes experimental_model: Lipid-peroxyl radical challenge in liposomes limitations: Protein-associated antioxidant synergy is demonstrated in this assay, not a clinical supplement combination. exposure: AAPH or AMVN challenge; dietary and meso zeaxanthin evidence_span: {"source_cache": "artifacts/zeaxanthin-research/15949677.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194", "start_char": 0, "end_char": 1404, "text_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194"} [zeaxanthin-p15949677] Synergistic effects of zeaxanthin and its binding protein in the prevention of lipid membrane oxidation. (2005). https://pubmed.ncbi.nlm.nih.gov/15949677/ DOI: 10.1016/j.bbadis.2005.02.002
    Complete structured claim and evidence
  6. GSTP1-bound meso-zeaxanthin was more protective than bound dietary zeaxanthin in this assay.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/zeaxanthin-research/15949677.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194", "start_char": 0, "end_char": 1404, "text_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194"}
    experimental_model
    Lipid-peroxyl radical challenge in liposomes
    exposure
    AAPH or AMVN challenge; dietary and meso zeaxanthin
    limitations
    Protein-associated antioxidant synergy is demonstrated in this assay, not a clinical supplement combination.
    nutrient_topic
    Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. · Dietary (3R,3-prime-R)-zeaxanthin
    organism
    Cell-free system with human GSTP1
    plain_language
    The two stereoisomers were not identical in this comparison.
    primary_references
    [zeaxanthin-p15949677] Synergistic effects of zeaxanthin and its binding protein in the prevention of lipid membrane oxidation. (2005). https://pubmed.ncbi.nlm.nih.gov/15949677/ DOI: 10.1016/j.bbadis.2005.02.002
    tissue_or_cell_type
    Egg-yolk phosphatidylcholine liposomes

    Zeaxanthin: metabolism, signaling and nutrient connections (2026-09-17) · lines 301–312

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Lipid-peroxyl radical challenge in liposomes · source_derived_draft · unverified_draft

    ### zeaxanthin-meso-bound-protection GSTP1-bound meso-zeaxanthin was more protective than bound dietary zeaxanthin in this assay. Condition category: normal nutrient_topic: Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. plain_language: The two stereoisomers were not identical in this comparison. organism: Cell-free system with human GSTP1 tissue_or_cell_type: Egg-yolk phosphatidylcholine liposomes experimental_model: Lipid-peroxyl radical challenge in liposomes limitations: Protein-associated antioxidant synergy is demonstrated in this assay, not a clinical supplement combination. exposure: AAPH or AMVN challenge; dietary and meso zeaxanthin evidence_span: {"source_cache": "artifacts/zeaxanthin-research/15949677.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194", "start_char": 0, "end_char": 1404, "text_sha256": "4ed175c0b5cf937df5a37c94739b40d713261c3a99e2bebc02b3b6a37ea3f194"} [zeaxanthin-p15949677] Synergistic effects of zeaxanthin and its binding protein in the prevention of lipid membrane oxidation. (2005). https://pubmed.ncbi.nlm.nih.gov/15949677/ DOI: 10.1016/j.bbadis.2005.02.002
    Complete structured claim and evidence
  7. The diacetate micromicelle formulation raised serum zeaxanthin more than the other active formulations.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/zeaxanthin-research/32824736.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "c5e70eca7c596aeb48b7f1cfccb9af65134926ab26737bc67e3594e4453d09f4", "start_char": 0, "end_char": 1173, "text_sha256": "c5e70eca7c596aeb48b7f1cfccb9af65134926ab26737bc67e3594e4453d09f4"}
    experimental_model
    Randomized double-blind placebo-controlled formulation trial
    exposure
    Six months; free pigments in sunflower/omega-3 oil versus mixed diacetate micromicelles
    limitations
    Combined delivery and ester changes prevent attribution to esterification alone; serum response is not a retinal outcome.
    nutrient_topic
    Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. · Dietary (3R,3-prime-R)-zeaxanthin
    organism
    81 healthy volunteers
    plain_language
    How the pigments were packaged changed their blood response.
    primary_references
    [zeaxanthin-p32824736] The Impact of Formulation on Lutein, Zeaxanthin, and meso-Zeaxanthin Bioavailability: A Randomised Double-Blind Placebo-Controlled Study. (2020). https://pubmed.ncbi.nlm.nih.gov/32824736/ DOI: 10.3390/antiox9080767
    tissue_or_cell_type
    Fasting serum carotenoids

    Zeaxanthin: metabolism, signaling and nutrient connections (2026-09-17) · lines 834–845

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized double-blind placebo-controlled formulation trial · source_derived_draft · unverified_draft

    ### zeaxanthin-micromicelles The diacetate micromicelle formulation raised serum zeaxanthin more than the other active formulations. Condition category: normal nutrient_topic: Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. plain_language: How the pigments were packaged changed their blood response. organism: 81 healthy volunteers tissue_or_cell_type: Fasting serum carotenoids experimental_model: Randomized double-blind placebo-controlled formulation trial limitations: Combined delivery and ester changes prevent attribution to esterification alone; serum response is not a retinal outcome. exposure: Six months; free pigments in sunflower/omega-3 oil versus mixed diacetate micromicelles evidence_span: {"source_cache": "artifacts/zeaxanthin-research/32824736.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "c5e70eca7c596aeb48b7f1cfccb9af65134926ab26737bc67e3594e4453d09f4", "start_char": 0, "end_char": 1173, "text_sha256": "c5e70eca7c596aeb48b7f1cfccb9af65134926ab26737bc67e3594e4453d09f4"} [zeaxanthin-p32824736] The Impact of Formulation on Lutein, Zeaxanthin, and meso-Zeaxanthin Bioavailability: A Randomised Double-Blind Placebo-Controlled Study. (2020). https://pubmed.ncbi.nlm.nih.gov/32824736/ DOI: 10.3390/antiox9080767
    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