15-HETE (BioDeep_00000003302)
Secondary id: BioDeep_00001868162
human metabolite Endogenous blood metabolite
代谢物信息卡片
化学式: C20H32O3 (320.2351)
中文名称: 15-羟基二十碳四烯酸
谱图信息:
最多检出来源 Homo sapiens(blood) 15.75%
Last reviewed on 2024-09-14.
Cite this Page
15-HETE. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/15-hete (retrieved
2024-12-18) (BioDeep RN: BioDeep_00000003302). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: C(CC/C=C\C/C=C\C/C=C\C=C\[C@H](CCCCC)O)C(=O)O
InChI: InChI=1S/C20H32O3/c1-2-3-13-16-19(21)17-14-11-9-7-5-4-6-8-10-12-15-18-20(22)23/h4-5,8-11,14,17,19,21H,2-3,6-7,12-13,15-16,18H2,1H3,(H,22,23)/t19-/m0/s1
描述信息
15-HETE is a hydroxyeicosatetraenoic acid. Hydroxyeicosatetraenoic acids (HETEs) are formed by the 5-, 12-, and 15-lipoxygenase (LO) pathways. The 5- and 12-LO products are mainly proinflammatory in the skin whereas the main 15-LO product 15-HETE has antiinflammatory capacities. In vitro, 15-HETE has been shown to inhibit LTB4 formation, 12-HETE formation, and specifically inhibits the neutrophil chemotactic effect of LTB4. The inhibition of LTB4 formation is probably due to modulation of the 5-LO because no changes in PGE2 formation have been determined. In vivo, 15-HETE inhibits LTB4-induced erythema and edema, and reduces LTB4 in the synovial fluid of carragheenan-induced experimental arthritis in dogs. 15-HETE also has some immunomodulatory effects. It inhibits the mixed lymphocyte reaction, induces generation of murine cytotoxic suppressor T cells, and it decreases interferon production by murine lymphoma cells. Furthermore, IL-4 and IL-13 have recently been shown to be potent activators of the 15-LO in mononuclear cells (PMID: 11104340). 15(S)-HETE is found to be associated with Zellweger syndrome, which is an inborn error of metabolism.
15(S)-HETE is a hydroxyeicosatetraenoic acid. Hydroxyeicosatetraenoic acids (HETEs) are formed by the 5-, 12- and 15-lipoxygenase (LO) pathways. 5- and 12-LO products are mainly proinflammatory in the skin whereas the main 15-LO product 15-HETE has antiinflammatory capacities. In vitro 15-HETE has been shown to inhibit LTB4 formation, 12-HETE formation and specifically inhibits the neutrophil chemotactic effect of LTB4. The inhibition of LTB4 formation is probably due to modulation of the 5-LO because no changes in PGE2 formation have been determined. In vivo, 15-HETE inhibits LTB4-induced erythema and edema, and reduces LTB4 in the synovial fluid of carragheenan-induced experimental arthritis in dogs. 15-HETE has also some immunomodulatory effects. It inhibits the mixed lymphocyte reaction, induces generation of murine cytotoxic suppressor T cells, and it decreases interferon production by murine lymphoma cells. Furthermore, IL-4 and IL-13 have recently been shown to be potent activators of the 15-LO in mononuclear cells. (PMID: 11104340) [HMDB]
15(S)-HETE. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=54845-95-3 (retrieved 2024-07-10) (CAS RN: 54845-95-3). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
同义名列表
42 个代谢物同义名
15-Hydroxy-5,8,11,13-eicosatetraenoic acid, (S-(e,Z,Z,Z))-isomer; (5Z,8Z,11Z,13E)-(15S)-15-Hydroxyicosa-5,8,11,13-tetraenoic acid; (5Z,8Z,11Z,13E,15S)-15-Hydroxyeicosa-5,8,11,13-tetraenoic acid; (5Z,8Z,11Z,13E,15S)-15-Hydroxy-5,8,11,13-eicosatetraenoic acid; (5Z,8Z,11Z,13E,15S)-15-hydroxyicosa-5,8,11,13-tetraenoic acid; (5Z,8Z,11Z,13E)-(15S)-15-Hydroxyicosa-5,8,11,13-tetraenoate; (15S)-15-Hydroxy-5,8,11-cis-13-trans-eicosatetraenoic acid; (5Z,8Z,11Z,13E,15S)-15-Hydroxyeicosa-5,8,11,13-tetraenoate; (5Z,8Z,11Z,13E,15S)-15-Hydroxy-5,8,11,13-eicosatetraenoate; (15S)-15-Hydroxy-5,8,11-cis-13-trans-icosatetraenoic acid; 15(S)-Hydroxy-5,8,11-cis-13-trans-eicosatetraenoic acid; (15S)-15-Hydroxy-5,8,11-cis-13-trans-eicosatetraenoate; 15S-Hydroxy-5,8,11,13-(Z,Z,Z,e)-eicosatetraenoic acid; (15S)-15-Hydroxy-5,8,11-cis-13-trans-icosatetraenoate; (5Z,8Z,11Z,13E,15S)-15-Hydroxyeicosatetraenoic acid; 15(S)-Hydroxy-(5Z,8Z,11Z,13E)-eicosatetraenoic acid; (15S,5Z,8Z,11Z,13E)-15-Hydroxyeicosatetraenoic acid; (15S)-Hydroxyeicosa-(5Z,8Z,11Z,13E)-tetraenoic acid; (15S)-Hydroxy-(5Z,8Z,11Z,13E)-eicosatetraenoic acid; 15(S)-Hydroxy-5Z,8Z,11Z,13E-eicosatetraenoic acid; (15S)-15-Hydroxy-5,8,11-cis-13-trans-eicosic acid; (15S,5Z,8Z,11Z,13E)-15-Hydroxyeicosatetraenoate; (15S)-Hydroxy-(5Z,8Z,11Z,13E)-eicosatetraenoate; 15S-hydroxy-5Z,8Z,11Z,13E-eicosatetraenoic acid; 15(S)-Hydroxy-(5Z,8Z,11Z,13E)-eicosatetraenoate; (15S)-Hydroxyeicosa-(5Z,8Z,11Z,13E)-tetraenoate; 15S-Hydroxy-5Z,8Z,11Z,13E-eicosatetraenoate; 15-Hydroxy-5,8,11,13-eicosatetraenoic acid; 15(S)-Hydroxyeicosatetraenoic acid; 15-Hydroxyeicosatetraenoic acid; 15(S)-Hydroxyeicosatetraenoate; FA(20:4(5Z,8Z,11Z,13E,15S-OH)); FA(20:4(5Z,8Z,11Z,13E,15-OH)); 15-Hydroxyarachidonic acid; (S)-15-HETE; 15(S)-HETE; 15(R)-HETE; Icomucret; 15S-HETE; 15 Hete; 15-HETE; (15S)-15-Hydroxy-5,8,11-cis-13-trans-eicosatetraenoate
数据库引用编号
28 个数据库交叉引用编号
- ChEBI: CHEBI:15558
- KEGG: C04742
- KEGGdrug: D08931
- PubChem: 5280724
- PubChem: 1436
- HMDB: HMDB0003876
- Metlin: METLIN45055
- ChEMBL: CHEMBL594621
- KNApSAcK: C00000427
- foodb: FDB023242
- chemspider: 4444307
- CAS: 54845-95-3
- MoNA: UT000113
- MoNA: UT000117
- MoNA: UT000109
- MoNA: UT000116
- MoNA: UT000110
- MoNA: UT000111
- MoNA: UT000114
- MoNA: UT000112
- MoNA: UT000115
- PMhub: MS000008755
- LipidMAPS: LMFA03060001
- 3DMET: B01783
- NIKKAJI: J303.917J
- RefMet: 15-HETE
- PubChem: 7313
- KNApSAcK: 15558
分类词条
相关代谢途径
BioCyc(0)
PlantCyc(0)
代谢反应
79 个相关的代谢反应过程信息。
Reactome(29)
- Metabolism:
3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-one-CoA + CoA-SH ⟶ choloyl-CoA + propionyl CoA
- Metabolism of lipids:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Fatty acid metabolism:
ATP + PROP-CoA + carbon dioxide ⟶ ADP + MEMA-CoA + Pi
- Arachidonic acid metabolism:
H+ + e- + prostaglandin G2 ⟶ H2O + prostaglandin H2
- Synthesis of 15-eicosatetraenoic acid derivatives:
15S-HpETE + GSH ⟶ 15S-HETE + GSSG + H2O
- Synthesis of 15-eicosatetraenoic acid derivatives:
15S-HpETE + GSH ⟶ 15S-HETE + GSSG + H2O
- Metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA
- Fatty acid metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Synthesis of 15-eicosatetraenoic acid derivatives:
15S-HpETE + GSH ⟶ 15S-HETE + GSSG + H2O
- Synthesis of 15-eicosatetraenoic acid derivatives:
15S-HpETE + GSH ⟶ 15S-HETE + GSSG + H2O
- Synthesis of 15-eicosatetraenoic acid derivatives:
15S-HpETE + GSH ⟶ 15S-HETE + GSSG + H2O
- Arachidonic acid metabolism:
H+ + e- + prostaglandin G2 ⟶ H2O + prostaglandin H2
- Synthesis of 15-eicosatetraenoic acid derivatives:
15S-HpETE + GSH ⟶ 15S-HETE + GSSG + H2O
- Metabolism:
ATP + PROP-CoA + carbon dioxide ⟶ ADP + MEMA-CoA + Pi
- Metabolism of lipids:
ATP + PROP-CoA + carbon dioxide ⟶ ADP + MEMA-CoA + Pi
- Fatty acid metabolism:
ATP + PROP-CoA + carbon dioxide ⟶ ADP + MEMA-CoA + Pi
- Arachidonic acid metabolism:
H+ + e- + prostaglandin G2 ⟶ H2O + prostaglandin H2
- Synthesis of 15-eicosatetraenoic acid derivatives:
15S-HpETE + GSH ⟶ 15S-HETE + GSSG + H2O
- Metabolism of lipids:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Synthesis of 15-eicosatetraenoic acid derivatives:
15S-HpETE + GSH ⟶ 15S-HETE + GSSG + H2O
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Metabolism of lipids:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Fatty acid metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Arachidonic acid metabolism:
H+ + e- + prostaglandin G2 ⟶ H2O + prostaglandin H2
- Synthesis of 15-eicosatetraenoic acid derivatives:
AA + Oxygen ⟶ 15S-HpETE
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Metabolism of lipids:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Fatty acid metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Arachidonic acid metabolism:
H+ + e- + prostaglandin G2 ⟶ H2O + prostaglandin H2
BioCyc(0)
WikiPathways(4)
- Eicosanoid metabolism via lipoxygenases (LOX):
Arachidonic acid ⟶ 12-HETE
- Eicosanoid metabolism via cyclooxygenases (COX):
Arachidonic acid ⟶ 15(S)-HETE
- Eicosanoid metabolism via cyclooxygenases (COX):
Arachidonic acid ⟶ 15(S)-HETE
- Eicosanoid synthesis:
PGD2 ⟶ PGJ2
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(46)
- Leukotriene C4 Synthesis Deficiency:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Piroxicam Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Acetylsalicylic Acid Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Etodolac Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Ketoprofen Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Ibuprofen Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Rofecoxib Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Diclofenac Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Sulindac Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Celecoxib Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Ketorolac Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Suprofen Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Bromfenac Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Indomethacin Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Mefenamic Acid Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Oxaprozin Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Nabumetone Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Naproxen Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Diflunisal Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Meloxicam Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Valdecoxib Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Antipyrine Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Antrafenine Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Carprofen Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Etoricoxib Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Fenoprofen Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Flurbiprofen Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Nepafenac Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Trisalicylate-Choline Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Tolmetin Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Tiaprofenic Acid Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Tenoxicam Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Salsalate Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Arachidonic Acid Metabolism:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Salicylic Acid Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Acetaminophen Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Magnesium Salicylate Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Arachidonic Acid Metabolism:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Leukotriene C4 Synthesis Deficiency:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Salicylate-Sodium Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Arachidonic Acid Metabolism:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Leukotriene C4 Synthesis Deficiency:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Lumiracoxib Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Lornoxicam Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Phenylbutazone Action Pathway:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
- Arachidonic Acid Metabolism:
Glutathione + Leukotriene A4 ⟶ Leukotriene C4
PharmGKB(0)
1 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。
文献列表
- Jana H Badrani, Kellen Cavagnero, Jacqueline J Eastman, Alex S Kim, Allyssa Strohm, Carol Yan, Adam Deconde, Bruce L Zuraw, Andrew A White, Sandra C Christiansen, Taylor A Doherty. Lower serum 15-HETE predicts nasal ILC2 accumulation during COX-1 inhibition in AERD.
The Journal of allergy and clinical immunology.
2023 Aug; ?(?):. doi:
10.1016/j.jaci.2023.06.028
. [PMID: 37543185] - Kristen J Polinski, Elizabeth A Bemis, Fan Yang, Tessa Crume, M Kristen Demoruelle, Marie Feser, Jennifer Seifert, James R O'Dell, Ted R Mikuls, Michael H Weisman, Peter K Gregersen, Richard M Keating, Jane Buckner, Nichole Reisdorph, Kevin D Deane, Michael Clare-Salzler, V Michael Holers, Jill M Norris. Association of Lipid Mediators With Development of Future Incident Inflammatory Arthritis in an Anti-Citrullinated Protein Antibody-Positive Population.
Arthritis & rheumatology (Hoboken, N.J.).
2021 06; 73(6):955-962. doi:
10.1002/art.41631
. [PMID: 33381911] - Anna-Karin Johnsson, Elin Rönnberg, David Fuchs, Johan Kolmert, Jesper Säfholm, Hans-Erik Claesson, Mats Hamberg, Craig E Wheelock, Gunnar Nilsson, Sven-Erik Dahlén. COX-1 dependent biosynthesis of 15-hydroxyeicosatetraenoic acid in human mast cells.
Biochimica et biophysica acta. Molecular and cell biology of lipids.
2021 05; 1866(5):158886. doi:
10.1016/j.bbalip.2021.158886
. [PMID: 33450390] - Laura Niederstaetter, Benjamin Neuditschko, Julia Brunmair, Lukas Janker, Andrea Bileck, Giorgia Del Favero, Christopher Gerner. Eicosanoid Content in Fetal Calf Serum Accounts for Reproducibility Challenges in Cell Culture.
Biomolecules.
2021 01; 11(1):. doi:
10.3390/biom11010113
. [PMID: 33467719] - Miriam C Wolters, Julia Schmetzer, Christine V Möser, Lisa Hahnefeld, Carlo Angioni, Dominique Thomas, Nerea Ferreirós, Gerd Geisslinger, Ellen Niederberger. Exercise-Induced Changes in Bioactive Lipids Might Serve as Potential Predictors of Post-Exercise Hypotension. A Pilot Study in Healthy Volunteers.
Cells.
2020 09; 9(9):. doi:
10.3390/cells9092111
. [PMID: 32948055] - Elżbieta Cecerska-Heryć, Rafał Heryć, Magda Wiśniewska, Natalia Serwin, Bartłomiej Grygorcewicz, Barbara Dołęgowska. Effect of renal replacement therapy on selected arachidonic acid derivatives concentration.
BMC nephrology.
2020 09; 21(1):394. doi:
10.1186/s12882-020-02053-8
. [PMID: 32917166] - Grégoire Ruffenach, Ellen O'Connor, Mylène Vaillancourt, Jason Hong, Nancy Cao, Shervin Sarji, Shayan Moazeni, Jeremy Papesh, Victor Grijalva, Christine M Cunningham, Le Shu, Arnab Chattopadhyay, Shuchita Tiwari, Olaf Mercier, Frédéric Perros, Soban Umar, Xia Yang, Aldrin V Gomes, Alan M Fogelman, Srinivasa T Reddy, Mansoureh Eghbali. Oral 15-Hydroxyeicosatetraenoic Acid Induces Pulmonary Hypertension in Mice by Triggering T Cell-Dependent Endothelial Cell Apoptosis.
Hypertension (Dallas, Tex. : 1979).
2020 09; 76(3):985-996. doi:
10.1161/hypertensionaha.120.14697
. [PMID: 32713273] - Alaleh Bayat Barooni, Mohammad Ghorbani, Vahid Salimi, Alimohammad Alimohammadi, Mohammad E Khamseh, Hamideh Akbari, Mehrnaz Imani, Mitra Nourbakhsh, Alireza Sheikhi, Farzad Izak Shirian, Maryam Ameri, Masoumeh Tavakoli-Yaraki. Up-regulation of 15-lipoxygenase enzymes and products in functional and non-functional pituitary adenomas.
Lipids in health and disease.
2019 Jul; 18(1):152. doi:
10.1186/s12944-019-1089-1
. [PMID: 31288808] - Amanda H Kahn-Kirby, Akiko Amagata, Celine I Maeder, Janet J Mei, Steve Sideris, Yuko Kosaka, Andrew Hinman, Stephanie A Malone, Joel J Bruegger, Leslie Wang, Virna Kim, William D Shrader, Kevin G Hoff, Joey C Latham, Euan A Ashley, Matthew T Wheeler, Enrico Bertini, Rosalba Carrozzo, Diego Martinelli, Carlo Dionisi-Vici, Kimberly A Chapman, Gregory M Enns, William Gahl, Lynne Wolfe, Russell P Saneto, Simon C Johnson, Jeffrey K Trimmer, Matthew B Klein, Charles R Holst. Targeting ferroptosis: A novel therapeutic strategy for the treatment of mitochondrial disease-related epilepsy.
PloS one.
2019; 14(3):e0214250. doi:
10.1371/journal.pone.0214250
. [PMID: 30921410] - Lin Yang, Cui Ma, Lixin Zhang, Min Zhang, Fei Li, Chen Zhang, Xiufeng Yu, Xiaoying Wang, Siyu He, Daling Zhu, Yinli Song. 15-Lipoxygenase-2/15(S)-hydroxyeicosatetraenoic acid regulates cell proliferation and metastasis via the STAT3 pathway in lung adenocarcinoma.
Prostaglandins & other lipid mediators.
2018 09; 138(?):31-40. doi:
10.1016/j.prostaglandins.2018.07.003
. [PMID: 30110652] - Dorottya Nagy-Szakal, Dinesh K Barupal, Bohyun Lee, Xiaoyu Che, Brent L Williams, Ellie J R Kahn, Joy E Ukaigwe, Lucinda Bateman, Nancy G Klimas, Anthony L Komaroff, Susan Levine, Jose G Montoya, Daniel L Peterson, Bruce Levin, Mady Hornig, Oliver Fiehn, W Ian Lipkin. Insights into myalgic encephalomyelitis/chronic fatigue syndrome phenotypes through comprehensive metabolomics.
Scientific reports.
2018 07; 8(1):10056. doi:
10.1038/s41598-018-28477-9
. [PMID: 29968805] - C Morgantini, S Trifirò, D Tricò, D Meriwether, S Baldi, A Mengozzi, S T Reddy, A Natali. A short-term increase in dietary cholesterol and fat intake affects high-density lipoprotein composition in healthy subjects.
Nutrition, metabolism, and cardiovascular diseases : NMCD.
2018 06; 28(6):575-581. doi:
10.1016/j.numecd.2018.03.005
. [PMID: 29699812] - Mikael Sandstedt, Victoria Rotter Sopasakis, Annika Lundqvist, Kristina Vukusic, Anders Oldfors, Göran Dellgren, Joakim Sandstedt, Lillemor Mattsson Hultén. Hypoxic cardiac fibroblasts from failing human hearts decrease cardiomyocyte beating frequency in an ALOX15 dependent manner.
PloS one.
2018; 13(8):e0202693. doi:
10.1371/journal.pone.0202693
. [PMID: 30138423] - Scott H Randell, Darryl C Zeldin. A Slippery Cause of a Slimy Problem: Mucin Induction by an Esterified Lipid.
American journal of respiratory cell and molecular biology.
2017 12; 57(6):633-634. doi:
10.1165/rcmb.2017-0275ed
. [PMID: 29192828] - Keng Po Lai, Jetty Chung-Yung Lee, Hin Ting Wan, Jing Woei Li, Aman Yi-Man Wong, Ting Fung Chan, Camille Oger, Jean-Marie Galano, Thierry Durand, Kin Sum Leung, Cherry C Leung, Rong Li, Chris Kong-Chu Wong. Effects of in Utero PFOS Exposure on Transcriptome, Lipidome, and Function of Mouse Testis.
Environmental science & technology.
2017 Aug; 51(15):8782-8794. doi:
10.1021/acs.est.7b02102
. [PMID: 28654245] - Nicoletta Basilico, Yolanda Corbett, Sarah D' Alessandro, Silvia Parapini, Mauro Prato, Daniela Girelli, Paola Misiano, Piero Olliaro, Donatella Taramelli. Malaria pigment stimulates chemokine production by human microvascular endothelium.
Acta tropica.
2017 Aug; 172(?):125-131. doi:
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Cancer prevention research (Philadelphia, Pa.).
2010 Sep; 3(9):1132-40. doi:
10.1158/1940-6207.capr-09-0264
. [PMID: 20668019] - Shanshan Li, Yajuan Ran, Xiaodong Zheng, Xiaoping Pang, Zhigang Wang, Rong Zhang, Daling Zhu. 15-HETE mediates sub-acute hypoxia-induced TRPC1 expression and enhanced capacitative calcium entry in rat distal pulmonary arterial myocytes.
Prostaglandins & other lipid mediators.
2010 Sep; 93(1-2):60-74. doi:
10.1016/j.prostaglandins.2010.06.007
. [PMID: 20599518] - Lei Zhang, Jun Ma, Yaqian Li, Lei Guo, Yajuan Ran, Shulin Liu, Chun Jiang, Daling Zhu. 15-Hydroxyeicosatetraenoic acid (15-HETE) protects pulmonary artery smooth muscle cells against apoptosis via HSP90.
Life sciences.
2010 Aug; 87(7-8):223-31. doi:
10.1016/j.lfs.2010.06.019
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PloS one.
2010 Aug; 5(8):e11979. doi:
10.1371/journal.pone.0011979
. [PMID: 20694143] - Satoshi Imaizumi, Victor Grijalva, Mohamad Navab, Brian J Van Lenten, Alan C Wagner, G M Anantharamiah, Alan M Fogelman, Srinivasa T Reddy. L-4F differentially alters plasma levels of oxidized fatty acids resulting in more anti-inflammatory HDL in mice.
Drug metabolism letters.
2010 Aug; 4(3):139-48. doi:
10.2174/187231210791698438
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Malaria journal.
2010 Jul; 9(?):208. doi:
10.1186/1475-2875-9-208
. [PMID: 20642847] - Michal Laniado Schwartzman, Pavel Iserovich, Katherine Gotlinger, Lars Bellner, Michael W Dunn, Mauro Sartore, Maria Grazia Pertile, Andrea Leonardi, Sonal Sathe, Ann Beaton, Lynn Trieu, Robert Sack. Profile of lipid and protein autacoids in diabetic vitreous correlates with the progression of diabetic retinopathy.
Diabetes.
2010 Jul; 59(7):1780-8. doi:
10.2337/db10-0110
. [PMID: 20424229] - D Somjen, S Katzburg, E Knoll, O Sharon, G H Posner, N Stern. Vitamin D analogs induce lipoxygenase mRNA expression and activity as well as reactive oxygen species (ROS) production in human bone cells.
The Journal of steroid biochemistry and molecular biology.
2010 Jul; 121(1-2):265-7. doi:
10.1016/j.jsbmb.2010.03.047
. [PMID: 20307663] - Mireille Basselin, Hyung-Wook Kim, Mei Chen, Kaizong Ma, Stanley I Rapoport, Robert C Murphy, Santiago E Farias. Lithium modifies brain arachidonic and docosahexaenoic metabolism in rat lipopolysaccharide model of neuroinflammation.
Journal of lipid research.
2010 May; 51(5):1049-56. doi:
10.1194/jlr.m002469
. [PMID: 20040630] - Sebastiano Banni, Roberto Montisci, Roberto Sanfilippo, Gabriele Finco, Daniela Sanna, Elena Giordano, Elisabetta Murru, Lina Cordeddu, Gianfranca Carta, Donata Banni, Antonio Marchi. Physiological response to lipid peroxidation in ischemia and reperfusion during carotid endarterectomy.
Lipids in health and disease.
2010 Apr; 9(?):41. doi:
10.1186/1476-511x-9-41
. [PMID: 20409338] - Yael Riahi, Yoav Sin-Malia, Guy Cohen, Evgenia Alpert, Arie Gruzman, Juergen Eckel, Bart Staels, Michel Guichardant, Shlomo Sasson. The natural protective mechanism against hyperglycemia in vascular endothelial cells: roles of the lipid peroxidation product 4-hydroxydodecadienal and peroxisome proliferator-activated receptor delta.
Diabetes.
2010 Apr; 59(4):808-18. doi:
10.2337/db09-1207
. [PMID: 20107107] - Christopher P Thomas, Lloyd T Morgan, Benjamin H Maskrey, Robert C Murphy, Hartmut Kühn, Stanley L Hazen, Alison H Goodall, Hassan A Hamali, Peter W Collins, Valerie B O'Donnell. Phospholipid-esterified eicosanoids are generated in agonist-activated human platelets and enhance tissue factor-dependent thrombin generation.
The Journal of biological chemistry.
2010 Mar; 285(10):6891-903. doi:
10.1074/jbc.m109.078428
. [PMID: 20061396] - Shuang Wang, Yali Wang, Jing Jiang, Ruifang Wang, Lisa Li, Zhaoping Qiu, Hong Wu, Daling Zhu. 15-HETE protects rat pulmonary arterial smooth muscle cells from apoptosis via the PI3K/Akt pathway.
Prostaglandins & other lipid mediators.
2010 Feb; 91(1-2):51-60. doi:
10.1016/j.prostaglandins.2009.12.007
. [PMID: 20060487] - Antush Mittal, V Ranganath, Ashish Nichani. Omega fatty acids and resolution of inflammation: A new twist in an old tale.
Journal of Indian Society of Periodontology.
2010 Jan; 14(1):3-7. doi:
10.4103/0972-124x.65426
. [PMID: 20922071] - Jun Ma, Shujun Liang, Zhigang Wang, Lei Zhang, Jing Jiang, Jinhua Zheng, Lei Yu, Xiaodong Zheng, Ruifang Wang, Daling Zhu. ROCK pathway participates in the processes that 15-hydroxyeicosatetraenoic acid (15-HETE) mediated the pulmonary vascular remodeling induced by hypoxia in rat.
Journal of cellular physiology.
2010 Jan; 222(1):82-94. doi:
10.1002/jcp.21923
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