Lutein (BioDeep_00000000574)

 

Secondary id: BioDeep_00000018740, BioDeep_00000227840, BioDeep_00000402745

human metabolite PANOMIX_OTCML-2023 blood metabolite Antitumor activity natural product


代谢物信息卡片


(1R,4R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]-3,5,5-trimethylcyclohex-2-en-1-ol

化学式: C40H56O2 (568.428)
中文名称: 叶黄素
谱图信息: 最多检出来源 Homo sapiens(blood) 36.02%

Reviewed

Last reviewed on 2024-07-12.

Cite this Page

Lutein. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/lutein (retrieved 2024-12-26) (BioDeep RN: BioDeep_00000000574). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: C/C(=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)C[C@H](CC1(C)C)O)/C=C/C=C(\C)/C=C/[C@H]1C(=C[C@@H](CC1(C)C)O)C
InChI: InChI=1S/C40H56O2/c1-29(17-13-19-31(3)21-23-37-33(5)25-35(41)27-39(37,7)8)15-11-12-16-30(2)18-14-20-32(4)22-24-38-34(6)26-36(42)28-40(38,9)10/h11-25,35-37,41-42H,26-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+/t35-,36+,37-/m0/s1

描述信息

Lutein is a common carotenoid xanthophyll found in nature. Carotenoids are among the most common pigments in nature and are natural lipid-soluble antioxidants. Lutein is one of the two carotenoids (the other is zeaxanthin) that accumulate in the eye lens and macular region of the retina with concentrations in the macula greater than those found in plasma and other tissues. Lutein and zeaxanthin have identical chemical formulas and are isomers, but they are not stereoisomers. The main difference between them is in the location of a double bond in one of the end rings. This difference gives lutein three chiral centers whereas zeaxanthin has two. A relationship between macular pigment optical density, a marker of lutein and zeaxanthin concentration in the macula, and lens optical density, an antecedent of cataractous changes, has been suggested. The xanthophylls may act to protect the eye from ultraviolet phototoxicity via quenching reactive oxygen species and/or other mechanisms. Some observational studies have shown that generous intakes of lutein and zeaxanthin, particularly from certain xanthophyll-rich foods like spinach, broccoli, and eggs, are associated with a significant reduction in the risk for cataracts (up to 20\\\\\%) and age-related macular degeneration (up to 40\\\\\%). While the pathophysiology of cataract and age-related macular degeneration is complex and contains both environmental and genetic components, research studies suggest dietary factors including antioxidant vitamins and xanthophylls may contribute to a reduction in the risk of these degenerative eye diseases. Further research is necessary to confirm these observations (PMID: 11023002).
Lutein is a carotenol. It has a role as a food colouring and a plant metabolite. It derives from a hydride of a (6R)-beta,epsilon-carotene.
Lutein is an xanthophyll and one of 600 known naturally occurring carotenoids. Lutein is synthesized only by plants and like other xanthophylls is found in high quantities in green leafy vegetables such as spinach, kale and yellow carrots. In green plants, xanthophylls act to modulate light energy and serve as non-photochemical quenching agents to deal with triplet chlorophyll (an excited form of chlorophyll), which is overproduced at very high light levels, during photosynthesis.
Lutein is a natural product found in Eupatorium cannabinum, Hibiscus syriacus, and other organisms with data available.
Lutein is lutein (LOO-teen) is a oxygenated carotenoid found in vegetables and fruits. lutein is found in the macula of the eye, where it is believed to act as a yellow filter. Lutein acts as an antioxidant, protecting cells against the damaging effects of free radicals.
A xanthophyll found in the major LIGHT-HARVESTING PROTEIN COMPLEXES of plants. Dietary lutein accumulates in the MACULA LUTEA.
See also: Calendula Officinalis Flower (part of); Corn (part of); Chicken; lutein (component of) ... View More ...
Pigment from egg yolk and leaves. Found in all higher plants. Nutriceutical with anticancer and antioxidation props. Potentially useful for the treatment of age-related macular degeneration (AMD) of the eye

Lutein A. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=127-40-2 (retrieved 2024-07-12) (CAS RN: 127-40-2). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Lutein (Xanthophyll) is a carotenoid with reported anti-inflammatory properties. A large body of evidence shows that lutein has several beneficial effects, especially on eye health[1]. Lutein exerts its biological activities, including anti-inflammation, anti-oxidase and anti-apoptosis, through effects on reactive oxygen species (ROS)[2][3]. Lutein is able to arrive in the brain and shows antidepressant-like and neuroprotective effects. Lutein is orally active[4].
Lutein (Xanthophyll) is a carotenoid with reported anti-inflammatory properties. A large body of evidence shows that lutein has several beneficial effects, especially on eye health[1]. Lutein exerts its biological activities, including anti-inflammation, anti-oxidase and anti-apoptosis, through effects on reactive oxygen species (ROS)[2][3]. Lutein is able to arrive in the brain and shows antidepressant-like and neuroprotective effects. Lutein is orally active[4].

同义名列表

96 个代谢物同义名

(1R,4R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]-3,5,5-trimethylcyclohex-2-en-1-ol; (1R,4R)-4-((1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-((4R)-4-HYDROXY-2,6,6-TRIMETHYL-1-CYCLOHEXEN-1-YL)-3,7,12,16-TETRAMETHYL-1,3,5,7,9,11,13,15,17-OCTADECANONAEN-1-YL)-3,5,5-TRIMETHYL-2-CYCLOHEXEN-1-OL; (1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1R,4R)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol; (1R,4R)-4-((1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-((R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl)-3,5,5-trimethylcyclohex-2-enol; 4-(18-(4-hydroxy-2,6,6-trimethyl-1-cyclohex-2-enyl)-3,7,12,16-tetramethyl-octadeca-1,3,5,7,9,11,13,15,17-nonaenyl)-3,5,5-trimethyl-cyclohex-3-en-1-ol; .BETA.,.BETA.-CAROTENE-3,3-DIOL, 4,5-DIDEHYDRO-5,6-DIHYDRO-, (3R,3R,6R)-; Lutein, Pharmaceutical Secondary Standard; Certified Reference Material; (3R,3R,6R)-4,5-DIDEHYDRO-5,6-DIHYDRO-.BETA.,.BETA.-CAROTENE-3,3-DIOL; beta,beta-CAROTENE-3,3-DIOL, 4,5-DIDEHYDRO-5,6-DIHYDRO-, (3R,3R,6R)-; (3R,3R,6R)-4,5-DIDEHYDRO-5,6-DIHYDRO-.BETA.,.BETA.-CAROTIN-3,3-DIOL; (3R,3R,6S)-4,5-DIDEHYDRO-5,6-DIHYDRO-BETA,BETA-CAROTENE-3,3-DIOL; (3R,3R,6R)-4,5-didehydro-5,6-dihydro-beta,beta-carotene-3,3-diol; (3R,3R,6R)-4,5-DIDEHYDRO-5,6-DIHYDRO-beta,beta-CAROTIN-3,3-DIOL; (3R,3r,6S)-4,5-DIDEHYDRO-5,6-dihydro-b,b-carotene-3,3-diol; (3R,3r,6S)-4,5-DIDEHYDRO-5,6-dihydro-β,β-carotene-3,3-diol; 4,5-Didehydro-6-hydro-.beta.-carotene-3,3-diol #; .beta.,.epsilon.-Carotene-3,3-diol, (3R,3R,6R)-; beta,epsilon-Carotene-3, 3-Diol, (3R,3R,6S)-; 6’-Hydro-4’,5’-dehydro-β-carotene-3,3’-diol; beta,epsilon-Carotene-3,3-diol, (3R,3R,6R)-; beta,epsilon-Carotene-3,3-diol, (3S,3R,6S)-; 6-Hydro-4,5-dehydro-beta-carotene-3,3-diol; (3R,3R,6R)-beta,epsilon-carotene-3,3-diol; 6-Hydro-4,5-dehydro-β-carotene-3,3-diol; ( inverted exclamation markA)-Lutein; (3R,3’R,6’R)-β,ε-Carotene-3,3’-diol; .beta.,.epsilon.-Carotene-3,3-diol; (invertedexclamationmarkA)-Lutein; (3R,3R,6R)-β,ε-Carotene-3,3-diol; (3R,3R)-dihydroxy-alpha-carotene; beta,epsilon-Carotene-3,3-diol; 3,3-Dihydroxy-alpha-carotene; Lutein, analytical standard; Xanthophyll, all-trans-(+)-; Lutein from tagetes erecta; Xanthophyll, from marigold; all-trans-(+)-Xanthophyll; xanthophyll from alfalfa; |A,|A-carotene-3,3-diol; Xanthophyll, tech grade; all-trans-Xanthophyll; Lutein (Xanthophyll); Xanthophyll (~80\\%); e-carotene-3,3-diol; (3R,3’R,6’R)-Lutein; Lutein, all-trans-; XANTOFYL [WHO-DD]; (3R,3R,6R)-Lutein; XANTHOPHYLL [MI]; Vegetable luteol; all-trans-Lutein; BCBcMAP01_000190; Vegetable lutein; FloraGLO Lutein; UNII-X72A60C9MT; LUTEIN (USP-RS); LEUTEIN [VANDF]; LUTEIN [USP-RS]; LUTEIN [MART.]; (all-E)-Lutein; LUTEIN [VANDF]; LUTEIN (MART.); Lutein - 20\\%; Lutein, gamma; Lutein - 10\\%; Noon for Kids; LUTEIN [FCC]; gamma Lutein; trans-Lutein; Tox21_112594; LUTEIN [DSC]; Lutein ester; Lutein - 5\\%; XANTHOPHYLL; SMP1_000317; X72A60C9MT; carotenoid; Oro Glo 7; ()-Lutein; Lutein G; Lutein F; Xantofyl; Lutein A; FloraGLO; Lutamax; Leutein; Luteine; e 161b; Lutein; Bo-Xan; Leutin; OS 24; β, ε-carotene-3,3-diol; β, ε-carotene; α-Carotene-3,3-diol; Lutein



数据库引用编号

26 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(2)

PlantCyc(2)

代谢反应

466 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(3)

WikiPathways(0)

Plant Reactome(216)

INOH(0)

PlantCyc(247)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

693 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 9 ANG, APOE, CAT, GPX1, GSTP1, NOS2, PIK3CA, PTGS2, TP53
Peripheral membrane protein 2 CYP1B1, PTGS2
Endoplasmic reticulum membrane 2 CYP1B1, PTGS2
Nucleus 6 ANG, APOE, GSTP1, MPO, NOS2, TP53
cytosol 10 ANG, BCO1, CAT, GPX1, GSR, GSTP1, LIPE, NOS2, PIK3CA, TP53
dendrite 1 APOE
centrosome 1 TP53
nucleoplasm 3 MPO, NOS2, TP53
Cell membrane 1 LIPE
lamellipodium 1 PIK3CA
glutamatergic synapse 1 APOE
Golgi apparatus 1 APOE
Golgi membrane 1 INS
growth cone 1 ANG
lysosomal membrane 1 EGF
mitochondrial inner membrane 1 CYP24A1
neuronal cell body 2 ANG, APOE
Cytoplasm, cytosol 3 BCO1, LIPE, NOS2
Lysosome 1 MPO
plasma membrane 4 APOE, EGF, NOS2, PIK3CA
Membrane 6 APOE, CAT, CYP1B1, EGF, LIPE, TP53
caveola 2 LIPE, PTGS2
extracellular exosome 6 APOE, CAT, EGF, GSR, GSTP1, MPO
endoplasmic reticulum 3 APOE, PTGS2, TP53
extracellular space 8 ANG, APOE, CGA, CRP, EGF, GSTP1, INS, MPO
perinuclear region of cytoplasm 2 NOS2, PIK3CA
intercalated disc 1 PIK3CA
mitochondrion 8 BCO2, CAT, CYP1B1, CYP24A1, GPX1, GSR, GSTP1, TP53
protein-containing complex 3 CAT, PTGS2, TP53
intracellular membrane-bounded organelle 3 CAT, CYP1B1, MPO
Microsome membrane 2 CYP1B1, PTGS2
Secreted 5 ANG, APOE, CGA, CRP, INS
extracellular region 9 ANG, APOE, CAT, CGA, CRP, EGF, GSTP1, INS, MPO
Mitochondrion matrix 1 TP53
mitochondrial matrix 5 BCO2, CAT, GPX1, GSR, TP53
transcription regulator complex 1 TP53
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 TP53
external side of plasma membrane 1 GSR
Endosome, multivesicular body 1 APOE
Extracellular vesicle 1 APOE
Secreted, extracellular space, extracellular matrix 1 APOE
chylomicron 1 APOE
high-density lipoprotein particle 1 APOE
low-density lipoprotein particle 1 APOE
multivesicular body 1 APOE
very-low-density lipoprotein particle 1 APOE
actin cytoskeleton 1 ANG
nucleolus 2 ANG, TP53
Cytoplasm, P-body 1 NOS2
P-body 1 NOS2
Early endosome 1 APOE
vesicle 1 GSTP1
Cytoplasm, perinuclear region 1 NOS2
Cytoplasm, cytoskeleton 1 TP53
focal adhesion 1 CAT
extracellular matrix 1 APOE
Peroxisome 2 CAT, NOS2
basement membrane 1 ANG
Peroxisome matrix 1 CAT
peroxisomal matrix 2 CAT, NOS2
peroxisomal membrane 1 CAT
Nucleus, PML body 1 TP53
PML body 1 TP53
collagen-containing extracellular matrix 1 APOE
secretory granule 1 MPO
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
neuron projection 1 PTGS2
chromatin 1 TP53
Chromosome 1 ANG
Secreted, extracellular space 1 APOE
Nucleus, nucleolus 1 ANG
blood microparticle 1 APOE
site of double-strand break 1 TP53
endosome lumen 1 INS
Lipid droplet 1 LIPE
Membrane, caveola 1 LIPE
Melanosome 1 APOE
Cytoplasm, Stress granule 1 ANG
cytoplasmic stress granule 1 ANG
germ cell nucleus 1 TP53
replication fork 1 TP53
azurophil granule 1 MPO
ficolin-1-rich granule lumen 2 CAT, GSTP1
secretory granule lumen 3 CAT, GSTP1, INS
Golgi lumen 2 CGA, INS
endoplasmic reticulum lumen 3 APOE, INS, PTGS2
nuclear matrix 1 TP53
transcription repressor complex 1 TP53
platelet alpha granule lumen 1 EGF
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
endocytic vesicle 1 ANG
transport vesicle 1 INS
azurophil granule lumen 1 MPO
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
clathrin-coated endocytic vesicle membrane 2 APOE, EGF
phagocytic vesicle lumen 1 MPO
[Isoform 1]: Nucleus 1 TP53
synaptic cleft 1 APOE
discoidal high-density lipoprotein particle 1 APOE
endocytic vesicle lumen 1 APOE
follicle-stimulating hormone complex 1 CGA
pituitary gonadotropin complex 1 CGA
chylomicron remnant 1 APOE
intermediate-density lipoprotein particle 1 APOE
lipoprotein particle 1 APOE
multivesicular body, internal vesicle 1 APOE
cortical cytoskeleton 1 NOS2
angiogenin-PRI complex 1 ANG
catalase complex 1 CAT
TRAF2-GSTP1 complex 1 GSTP1
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA


文献列表

  • Zhilei Qin, Mengsu Liu, Xuefeng Ren, Weizhu Zeng, Zhengshan Luo, Jingwen Zhou. De Novo Biosynthesis of Lutein in Yarrowia lipolytica. Journal of agricultural and food chemistry. 2024 Mar; 72(10):5348-5357. doi: 10.1021/acs.jafc.3c09080. [PMID: 38412053]
  • Jolanta Flieger, Natalia Żuk, Sylwia Pasieczna-Patkowska, Marcin Kuśmierz, Rafał Panek, Wojciech Franus, Jacek Baj, Grzegorz Buszewicz, Grzegorz Teresiński, Wojciech Płaziński. Selective Removal of Chlorophyll and Isolation of Lutein from Plant Extracts Using Magnetic Solid Phase Extraction with Iron Oxide Nanoparticles. International journal of molecular sciences. 2024 Mar; 25(6):. doi: 10.3390/ijms25063152. [PMID: 38542125]
  • María Dolores Requena-Ramírez, Cristina Rodríguez-Suárez, Dámaso Hornero-Méndez, Sergio G Atienza. Lutein esterification increases carotenoid retention in durum wheat grain. A step further in breeding and improving the commercial and nutritional quality during grain storage. Food chemistry. 2024 Mar; 435(?):137660. doi: 10.1016/j.foodchem.2023.137660. [PMID: 37832338]
  • Veronika Gunjević, Mirta Majerić Musa, Dora Zurak, Zlatko Svečnjak, Marija Duvnjak, Darko Grbeša, Kristina Kljak. Carotenoid degradation rate in milled grain of dent maize hybrids and its relationship with the grain physicochemical properties. Food research international (Ottawa, Ont.). 2024 Feb; 177(?):113909. doi: 10.1016/j.foodres.2023.113909. [PMID: 38225147]
  • Jiawen Yan, Zhihui Liu, Tongtong Wang, Ruoman Wang, Shuya Wang, Weijie Chen, Jinwei Suo, Jingwei Yan, Jiasheng Wu. TgLUT1 regulated by TgWRKY10 enhances the tolerance of Torreya grandis to drought stress. Plant physiology and biochemistry : PPB. 2024 Feb; 207(?):108436. doi: 10.1016/j.plaphy.2024.108436. [PMID: 38367388]
  • Weidong Chen, Yuanqing Li, Min Li, Hai Li, Caifang Chen, Yanzhao Lin. Association between dietary carotenoid intakes and abdominal aortic calcification in adults: National Health and Nutrition Examination Survey 2013-2014. Journal of health, population, and nutrition. 2024 Feb; 43(1):20. doi: 10.1186/s41043-024-00511-9. [PMID: 38303096]
  • Grzegorz Dąbrowski, Sylwester Czaplicki, Marcin Szustak, Eliza Korkus, Edyta Gendaszewska-Darmach, Iwona Konopka. The impact of selected xanthophylls on oil hydrolysis by pancreatic lipase: in silico and in vitro studies. Scientific reports. 2024 02; 14(1):2731. doi: 10.1038/s41598-024-53312-9. [PMID: 38302772]
  • Emilia Reszczyńska, Anna Wiśniewska-Becker, Mariusz Duda, Alicja Sęk, Wiesław I Gruszecki, Agnieszka Hanaka. The presence of free palmitic acid modulates the effects of lutein on structural and dynamic properties of lipid membranes. Archives of biochemistry and biophysics. 2024 Feb; 752(?):109883. doi: 10.1016/j.abb.2024.109883. [PMID: 38211638]
  • Sharayah Carter, Alison M Hill, Catherine Yandell, Jonathan D Buckley, Alison M Coates. Study protocol for a 15-week randomised controlled trial assessing the independent effects of high-cholesterol and high-saturated fat diets on LDL cholesterol. BMJ open. 2024 01; 14(1):e081664. doi: 10.1136/bmjopen-2023-081664. [PMID: 38272555]
  • Hideo Takekoshi, Masaki Fujishima, Taiki Miyazawa, Ohki Higuchi, Takahiko Fujikawa, Teruo Miyazawa. Simultaneous Intake of Chlorella and Ascidian Ethanolamine Plasmalogen Accelerates Activation of BDNF-TrkB-CREB Signaling in Rats. Molecules (Basel, Switzerland). 2024 Jan; 29(2):. doi: 10.3390/molecules29020357. [PMID: 38257270]
  • Qing Liu, Chenyun Miao, Fangxuan Lin, Han Zhang, Qin Zhang. A case-control retrospective study for the effect of Shoutai Wan on IVF-ET pregnancy outcome. Medicine. 2024 Jan; 103(1):e36846. doi: 10.1097/md.0000000000036846. [PMID: 38181258]
  • Yang Meng, Yuanhui Wang, Weimin Guo, Ke Lei, Zuxiao Chen, Hang Xu, Aiguo Wang, Qiang Xu, Jianjun Liu, Qiang Zeng. Analysis of the relationship between color and natural pigments of tobacco leaves during curing. Scientific reports. 2024 01; 14(1):166. doi: 10.1038/s41598-023-50801-1. [PMID: 38167588]
  • Zhenhua Xu, Haiying Liu, Yanmin Yu, Dawei Gao, Chunxu Leng, Shuli Zhang, Ping Yan. MWCNTs Alleviated saline-alkali stress by optimizing photosynthesis and sucrose metabolism in rice seedling. Plant signaling & behavior. 2023 Dec; 18(1):2283357. doi: 10.1080/15592324.2023.2283357. [PMID: 38053501]
  • Serafino Suriano, Pasquale Codianni, Anna Iannucci. Carotenoids and tocols comparison in different Subspecies of Triticum turgidum and aestivum. Food research international (Ottawa, Ont.). 2023 Dec; 174(Pt 1):113620. doi: 10.1016/j.foodres.2023.113620. [PMID: 37986473]
  • Shaohua Yan, Siyu Chen, Yumiao Liu, Hongbin Liang, Xinlu Zhang, Qiuxia Zhang, Jiancheng Xiu. Associations of serum carotenoids with visceral adiposity index and lipid accumulation product: a cross-sectional study based on NHANES 2001-2006. Lipids in health and disease. 2023 Nov; 22(1):209. doi: 10.1186/s12944-023-01945-6. [PMID: 38037060]
  • Jadwiga Hamulka, Agnieszka Sulich, Magdalena Górnicka, Marta Jeruszka-Bielak. Changes in Plasma Carotenoid Concentrations during the AntioxObesity Weight Reduction Program among Adults with Excessive Body Weight. Nutrients. 2023 Nov; 15(23):. doi: 10.3390/nu15234890. [PMID: 38068747]
  • Dieudonné M Dansou, Han Chen, Yanan Yu, Youyou Yang, Isabelle N Tchana, Liyuan Zhao, Chaohua Tang, Qingyu Zhao, Yuchang Qin, Junmin Zhang. Enrichment efficiency of lutein in eggs and its function in improving fatty liver hemorrhagic syndrome in aged laying hens. Poultry science. 2023 Nov; 103(2):103286. doi: 10.1016/j.psj.2023.103286. [PMID: 38100949]
  • Yang Liu, Guanlin Yang, Shiqiao Huo, Jiabi Wu, Ping Ren, Yonggang Cao, Jingquan Gao, Liquan Tong, Dongyu Min. Lutein suppresses ferroptosis of cardiac microvascular endothelial cells via positive regulation of IRF in cardiac hypertrophy. European journal of pharmacology. 2023 Nov; 959(?):176081. doi: 10.1016/j.ejphar.2023.176081. [PMID: 37797674]
  • Altevir Rossato Viana, Isadora Nicola, Camila Franco, Patrícia Acosta Caetano, Eduardo Jacob-Lopes, Leila Queiroz Zepka, Daniel Santos, Erico Marlon Moraes Flores, Bruno Stefanello Vizzotto, Katianne Wolf, Aline Ferreira Ourique, Sergio Roberto Mortari, Cristiano Rodrigo Bohn Rhoden, Luciana Maria Fontanari Krause. Phytochemical characterization and toxicological activity attributed to the acetonic extract of South American Vassobia breviflora. Journal of toxicology and environmental health. Part A. 2023 Nov; 86(21):816-832. doi: 10.1080/15287394.2023.2254316. [PMID: 37667472]
  • Kodai Ueno, Tetsuya Matsushita, Monami Sugihara, Kohei Yamada, Hideyuki Sato, Satomi Onoue. Solid lipid nanoparticles of lutein with improved dissolution behavior and oral absorption. Pharmaceutical development and technology. 2023 Nov; 28(9):877-883. doi: 10.1080/10837450.2023.2270032. [PMID: 37828716]
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