Biogenic synthesis, purification, and chemical characterization of anti-inflammatory resolvins derived from docosapentaenoic acid (DPAn-6).
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15-lipoxygenase metabolites of docosahexaenoic acid inhibit prostate cancer cell proliferation and survivalA review of the biologic and pharmacologic role of docosapentaenoic acid n-3Specialized pro-resolving lipid mediators in the inflammatory response: An updateNovel lipid mediators and resolution mechanisms in acute inflammation: to resolve or not?Lithium modifies brain arachidonic and docosahexaenoic metabolism in rat lipopolysaccharide model of neuroinflammation.Omega-6 docosapentaenoic acid-derived resolvins and 17-hydroxydocosahexaenoic acid modulate macrophage function and alleviate experimental colitis.Finding homes for orphan cytochrome P450s: CYP4V2 and CYP4F22 in disease states.Resolvins and protectins in inflammation resolution.Regulation of rat brain polyunsaturated fatty acid (PUFA) metabolism during graded dietary n-3 PUFA deprivation.(n-3) fatty acids and cardiovascular health: are effects of EPA and DHA shared or complementary?Fifteen weeks of dietary n-3 polyunsaturated fatty acid deprivation increase turnover of n-6 docosapentaenoic acid in rat-brain phospholipids.Omega-3 fatty acids cause dramatic changes in TLR4 and purinergic eicosanoid signaling.Red Blood Cell Docosapentaenoic Acid (DPA n-3) is Inversely Associated with Triglycerides and C-reactive Protein (CRP) in Healthy Adults and Dose-Dependently Increases Following n-3 Fatty Acid Supplementation.Increased ω6-Containing Phospholipids and Primary ω6 Oxidation Products in the Brain Tissue of Rats on an ω3-Deficient DietLipidomics of essential fatty acids and oxygenated metabolites.LC/ESR/MS study of pH-dependent radical generation from 15-LOX-catalyzed DPA peroxidation.Controlled formation of mono- and dihydroxy-resolvins from EPA and DHA using soybean 15-lipoxygenaseDietary PUFAs attenuate NLRP3 inflammasome activation via enhancing macrophage autophagy.Orally administered [¹⁴C]DPA and [¹⁴C]DHA are metabolised differently to [¹⁴C]EPA in rats.ALOX15 oxidises DPAn-6 to 17(S)-HDPAn-6 and 10(S);17(S)-diHDPAn-6ALOX12:Fe2+ oxidises DPAn-6 to 14(S)-HDPAn-6
P2860
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P2860
Biogenic synthesis, purification, and chemical characterization of anti-inflammatory resolvins derived from docosapentaenoic acid (DPAn-6).
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 26 March 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Biogenic synthesis, purificati ...... ocosapentaenoic acid (DPAn-6).
@en
Biogenic synthesis, purificati ...... ocosapentaenoic acid (DPAn-6).
@nl
type
label
Biogenic synthesis, purificati ...... ocosapentaenoic acid (DPAn-6).
@en
Biogenic synthesis, purificati ...... ocosapentaenoic acid (DPAn-6).
@nl
prefLabel
Biogenic synthesis, purificati ...... ocosapentaenoic acid (DPAn-6).
@en
Biogenic synthesis, purificati ...... ocosapentaenoic acid (DPAn-6).
@nl
P2093
P2860
P921
P356
P1476
Biogenic synthesis, purificati ...... ocosapentaenoic acid (DPAn-6).
@en
P2093
Bindi Dangi
Julie M Nauroth
Krishna Raman
Linda M Arterburn
Mah Teymourlouei
Marcus Obeng
Micah Needham
P2860
P304
14744-14759
P356
10.1074/JBC.M809014200
P407
P577
2009-03-26T00:00:00Z