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.
Other things that act on it
Enzymes, hormones, genes, and other components with a recorded effect. These are not nutrients, so they do not count toward the arrows above. Each finding names the chapter that recorded it.
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.
What acts on it
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 evidenceChicken 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 evidenceOverexpressed 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 evidenceMouse 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 evidenceThis ARPE-19 delivery experiment detected no lutein conversion to meso-zeaxanthin.
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 evidenceGSTP1 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 evidenceNo 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)
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 evidenceRPE65 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 evidenceThe 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 evidenceGSTP1 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 evidenceGSTP1-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 evidenceGSTP1-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 evidenceThe 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
The events it takes part in
A mechanism often involves more than two components. These are the full events, with every participant and its role.
Situations it appears in
Low-supply and faulty-machinery situations recorded in the chapters where this component plays a part.
In the sources
Preserved passages that mention this component, quoted exactly. Open one to read it in context.
Open hypotheses
Proposed ideas that involve this component. They are labeled as hypotheses and do not change any recorded statement.
This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.