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1. Full Text Eicosanoid storm in infection and inflammation
by Dennis, Edward A and Norris, Paul C
Nature Reviews Immunology, ISSN 1474-1733, 08/2015, Volume 15, Issue 8, pp. 511 - 523
Controlled immune responses to infection and injury involve complex molecular signalling networks with coordinated and often opposing actions. Eicosanoids and... 
SOLUBLE EPOXIDE HYDROLASE | IN-VIVO | PRO-RESOLVING MEDIATORS | PPAR-GAMMA | ACTIVATED RECEPTOR-ALPHA | ANTIINFLAMMATORY LIPID MEDIATORS | ARACHIDONIC-ACID | IMMUNOLOGY | TERMINAL PROSTANOID SYNTHASES | MASS-SPECTROMETRY | PROSTAGLANDIN D-2 RECEPTOR | Inflammation - pathology | Humans | Eicosanoids - biosynthesis | Cytochrome P-450 Enzyme System - immunology | Lipid Metabolism - immunology | Phospholipases - genetics | Prostaglandin-Endoperoxide Synthases - immunology | Bacterial Infections - genetics | Bacterial Infections - immunology | Inflammation Mediators - metabolism | Eicosanoids - immunology | Bacterial Infections - microbiology | Cytokines - immunology | Inflammation Mediators - immunology | Prostaglandin-Endoperoxide Synthases - genetics | Phospholipases - immunology | Cytokines - metabolism | Signal Transduction | Gene Expression Regulation | Inflammation - immunology | Immunity, Innate | Animals | Bacterial Infections - pathology | Cytochrome P-450 Enzyme System - genetics | Inflammation - genetics | Development and progression | Genetic aspects | Inflammation | Communicable diseases
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2. Full Text Cyclooxygenase Isozymes: The Biology of Prostaglandin Synthesis and Inhibition
by Daniel L. Simmons and Regina M. Botting and Timothy Hla
Pharmacological Reviews, ISSN 0031-6997, 09/2004, Volume 56, Issue 3, pp. 387 - 437
Nonsteroidal anti-inflammatory drugs (NSAIDs) represent one of the most highly utilized classes of pharmaceutical agents in medicine. All NSAIDs act through... 
VESICULAR GLAND MICROSOMES | LIPID BODY FORMATION | TUMOR-NECROSIS-FACTOR | NONSTEROIDAL ANTIINFLAMMATORY DRUGS | ENDOPEROXIDE-H SYNTHASE-1 | NITRIC-OXIDE SYNTHASE | FATTY-ACID CYCLOOXYGENASE | PHARMACOLOGY & PHARMACY | FAMILIAL ADENOMATOUS POLYPOSIS | RANDOMIZED CONTROLLED-TRIAL | ASPIRIN-INDUCED ASTHMA | Prostaglandin-Endoperoxide Synthases - genetics | Amino Acid Sequence | Prostaglandin-Endoperoxide Synthases - pharmacology | Isoenzymes - genetics | Cyclooxygenase 2 | Humans | Cyclooxygenase 1 | Molecular Sequence Data | Isoenzymes - chemistry | Prostaglandins, Synthetic - antagonists & inhibitors | Membrane Proteins | Animals | Prostaglandin-Endoperoxide Synthases - chemistry | Prostaglandins, Synthetic - therapeutic use | Isoenzymes - pharmacology | Models, Genetic | Prostaglandins, Synthetic - chemical synthesis
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3. Full Text Cyclooxygenases: Structural and functional insights
by Rouzer, Carol A and Marnett, Lawrence J
Journal of Lipid Research, ISSN 0022-2275, 04/2009, Volume 50, Issue Supplement, pp. S29 - S34
Cyclooxygenase (COX; prostaglandin G/H synthase, EC 1.14.99.1) catalyzes the first two steps in the biosynthesis of prostaglandins (PGs). The two COX isoforms... 
Coxib | Nonsteroidal anti-inflammatory | Endocannabinoid | Prostaglandin | Hydroperoxide | Essential fatty acid | Inflammation | Arachidonic acid | arachidonic acid | endocannabinoid | coxib | ACTIVATION | nonsteroidal anti-inflammatory | COX-2 | prostaglandin | ENDOPEROXIDE-H SYNTHASE-1 | OXYGENATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | hydroperoxide | INHIBITION | inflammation | essential fatty acid | IN-VIVO | LIPOPOLYSACCHARIDE | MICE | EXPRESSION | Gene Expression Regulation, Enzymologic | Prostaglandin-Endoperoxide Synthases - genetics | Animals | Disease | Prostaglandin-Endoperoxide Synthases - chemistry | Prostaglandin-Endoperoxide Synthases - metabolism | Humans | Cyclooxygenase Inhibitors - pharmacology | Enzymology
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4. Full Text Fermentation product with new equol‐producing Lactobacillus paracasei as a probiotic‐like product candidate for prevention of skin and intestinal disorder
by Kwon, Jeong Eun and Lim, Jaewon and Bang, Ina and Kim, Inhye and Kim, Donghyuk and Kang, Se Chan
Journal of the Science of Food and Agriculture, ISSN 0022-5142, 07/2019, Volume 99, Issue 9, pp. 4200 - 4210
BACKGROUNDEquol is a major isoflavone metabolite, and equol-producing bacteria have been isolated and characterized; however, fermentation has been performed... 
skin moisturizing | JS1 | equol | Lactobacillus paracasei | Pueraria lobata | intestine inflammation | Lactobacillus paracasei JS1 | GEN-NOV | BACTERIA | FOOD SCIENCE & TECHNOLOGY | CASEI GROUP | IDENTIFICATION | ISOFLAVONES | IN-VITRO | DAIDZEIN | AGRICULTURE, MULTIDISCIPLINARY | CHEMISTRY, APPLIED | SOY | HISTORY | FOOD | Intestinal Diseases - prevention & control | Probiotics - administration & dosage | Hyaluronan Synthases - metabolism | Lactobacillus paracasei - metabolism | Skin Diseases - genetics | Humans | Male | Interleukin-1beta - genetics | Skin Diseases - prevention & control | Hyaluronan Synthases - genetics | Interleukin-1beta - metabolism | Collagen - genetics | Elastin - metabolism | Skin Diseases - metabolism | Equol - metabolism | Mice, Inbred C57BL | Intestinal Diseases - genetics | Fermentation | Intestinal Diseases - metabolism | Collagen - metabolism | Animals | Elastin - genetics | Nitric Oxide Synthase Type II - genetics | Mice | Nitric Oxide Synthase Type II - metabolism | Prevention | COX-2 inhibitors | Epidermal growth factor | Toiletries industry | Gastrointestinal diseases | Nitric oxide | Skin | Hyaluronic acid | Gene expression | Isoflavones | Soybeans | Interleukin | Genomes | Hyaluronan synthase | Prostaglandin endoperoxide synthase | Hyaluronan | Bacteria | Growth factors | Immune system | Immune response | Cytokines | Elastin | Inflammation | Nitric-oxide synthase | Substrates | Probiotics | Organic chemistry | Large intestine | Collagen
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5. Full Text Endometrial prostaglandin synthases, ovarian steroids, and oxytocin receptors in mares with oxytocin-induced luteal maintenance
by Rebordão, Maria R and Galvão, António and Pinto-Bravo, Pedro and Pinheiro, Joana and Gamboa, Sandra and Silva, Elisabete and Mateus, Luísa and Ferreira-Dias, Graça
Theriogenology, ISSN 0093-691X, 01/2017, Volume 87, pp. 193 - 204
Oxytocin (OXT) has been used to prolong the luteal phase in mares, but its mechanism of action is unknown. The aim of this study was to evaluate the effect of... 
Luteal phase | Mare | Oxytocin | Oxytocin receptor | Endometrium | Steroids receptors | CORPORA-LUTEA | SEX STEROIDS | IN-VITRO | REPRODUCTIVE BIOLOGY | EQUINE ENDOMETRIUM | EARLY-PREGNANCY | VETERINARY SCIENCES | PROGESTERONE-RECEPTOR | F-2 ALPHA | EXPRESSION | CORPUS-LUTEUM | ESTROUS-CYCLE | Oxytocics - pharmacology | Prostaglandin-Endoperoxide Synthases - genetics | Progestins - metabolism | Receptors, Estrogen - metabolism | Oxytocin - pharmacology | Receptors, Estrogen - genetics | Corpus Luteum - drug effects | Progestins - genetics | Receptors, Oxytocin - genetics | Ovary - physiology | Receptors, Progesterone - genetics | Horses - physiology | Corpus Luteum - physiology | Receptors, Progesterone - metabolism | Receptors, Oxytocin - metabolism | Animals | Prostaglandin-Endoperoxide Synthases - metabolism | Estrogens - genetics | Female | Estrogens - metabolism | Prostaglandins | Progesterone | Analysis | Estrogen
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6. Full Text Tumor cyclooxygenase-2/prostaglandin E2-dependent promotion of FOXP3 expression and CD4+CD25+ T regulatory cell activities in lung cancer
by Sharma, Sherven and Yang, Seok-Chul and Zhu, Li and Reckamp, Karen and Gardner, Brian and Baratelli, Felicita and Huang, Min and Batra, Raj K and Dubinett, Steven M
Cancer Research, ISSN 0008-5472, 06/2005, Volume 65, Issue 12, pp. 5211 - 5220
Cyclooxygenase (COX)-2 and its product prostaglandin (PG) E2 underlie an immunosuppressive network that is important in the pathogenesis of non-small cell lung... 
Dinoprostone - physiology | Cyclooxygenase 2 | Lung Neoplasms - metabolism | Carcinoma, Lewis Lung - immunology | Dinoprostone - immunology | Prostaglandin-Endoperoxide Synthases - immunology | CD4-Positive T-Lymphocytes - immunology | Receptors, Prostaglandin E, EP4 Subtype | Transfection | Lung Neoplasms - genetics | Prostaglandin-Endoperoxide Synthases - genetics | Gene Expression | Lung Neoplasms - enzymology | Lymphocyte Activation | Mice, Inbred C57BL | Mice, Transgenic | Carcinoma, Lewis Lung - metabolism | DNA-Binding Proteins - genetics | Receptors, Interleukin-2 - immunology | Cyclooxygenase Inhibitors - pharmacology | Mice, Knockout | Dinoprostone - metabolism | Lung Neoplasms - immunology | Animals | Carcinoma, Lewis Lung - genetics | Cyclooxygenase 2 Inhibitors | Prostaglandin-Endoperoxide Synthases - metabolism | Receptors, Prostaglandin E - agonists | Receptors, Prostaglandin E, EP2 Subtype | Mice | Mice, Inbred BALB C | DNA-Binding Proteins - biosynthesis | Forkhead Transcription Factors | Prostaglandin-Endoperoxide Synthases - physiology
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7. Full Text COX-3, a Cyclooxygenase-1 Variant Inhibited by Acetaminophen and Other Analgesic/Antipyretic Drugs: Cloning, Structure, and Expression
by N. V. Chandrasekharan and Hu Dai and K. Lamar Turepu Roos and Nathan K. Evanson and Joshua Tomsik and Terry S. Elton and Daniel L. Simmons
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2002, Volume 99, Issue 21, pp. 13926 - 13931
Two cyclooxygenase isozymes, COX-1 and -2, are known to catalyze the rate-limiting step of prostaglandin synthesis and are the targets of nonsteroidal... 
Biological Sciences | Cerebral cortex | Nonsteroidal antiinflammatory agents | Messenger RNA | Pain | Canines | Analgesics | RNA | Introns | Cyclooxygenase inhibitors | Fever | SYNTHASE | FEBRILE RESPONSE | PROFILE | NIMESULIDE | NONSTEROIDAL ANTIINFLAMMATORY DRUG | MESSENGER-RNA | ACUTE PAIN | MULTIDISCIPLINARY SCIENCES | INVOLVEMENT | LIPOPOLYSACCHARIDE | ROFECOXIB | Cyclooxygenase 2 | Humans | Analgesics, Non-Narcotic - pharmacology | Cyclooxygenase 1 | Molecular Sequence Data | RNA, Messenger - metabolism | Genetic Variation | Tissue Distribution | Prostaglandin-Endoperoxide Synthases - chemistry | Acetaminophen - pharmacology | Isoenzymes - metabolism | Cloning, Molecular | Molecular Structure | Aorta - enzymology | Prostaglandin-Endoperoxide Synthases - genetics | Recombinant Proteins - metabolism | Cerebral Cortex - enzymology | Isoenzymes - genetics | RNA, Messenger - genetics | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Cyclooxygenase Inhibitors - pharmacology | Membrane Proteins | Animals | Cyclooxygenase 2 Inhibitors | Prostaglandin-Endoperoxide Synthases - metabolism | Dogs | Mice | Physiological aspects | Cyclooxygenases | Acetaminophen | Antipyretics
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8. Full Text Gene expression changes of prostanoid synthases in endothelial cells and prostanoid receptors in vascular smooth muscle cells caused by aging and hypertension
by Eva H. C. Tang and Paul M. Vanhoutte
Physiological Genomics, ISSN 1094-8341, 02/2008, Volume 32, Issue 3, pp. 409 - 418
The present study was designed to assess whether or not changes in genomic expression of cyclooxygenases (COX-1, COX-2), endothelial nitric oxide synthase... 
Prostacyclin | Prostacyclin synthase | Real-time quantitative polymerase chain reaction | Endothelium-dependent contractions | Endothelium-derived contracting factors | RAT SPINAL-CORD | PHYSIOLOGY | prostacyclin | ACETYLCHOLINE | real-time quantitative polymerase chain reaction | DEPENDENT CONTRACTIONS | KNOCKOUT MICE | endothelium-derived contracting factors | CELL BIOLOGY | SIGNAL-TRANSDUCTION | IMMUNOCYTOCHEMICAL LOCALIZATION | CALCIUM | GENETICS & HEREDITY | NITRIC-OXIDE | SHR AORTA | prostacyclin synthase | endothelium-dependent contractions | PROSTAGLANDIN-F SYNTHASE | Prostaglandin-Endoperoxide Synthases - biosynthesis | Nitric Oxide Synthase Type II - biosynthesis | Rats, Inbred WKY | Gene Expression Profiling | Receptors, Prostaglandin - biosynthesis | Muscle Proteins - biosynthesis | Phenylephrine - pharmacology | Receptors, Prostaglandin - genetics | Aging - genetics | Aorta, Thoracic - drug effects | Hypertension - genetics | Myocytes, Smooth Muscle - metabolism | Muscle, Smooth, Vascular - drug effects | Prostaglandin-Endoperoxide Synthases - genetics | Rats, Inbred SHR | Cyclooxygenase 1 - genetics | Cyclooxygenase 1 - biosynthesis | Acetylcholine - pharmacology | Endothelial Cells - metabolism | Membrane Proteins - genetics | Gene Expression Regulation | Nitric Oxide Synthase Type III | Enzyme Induction | Rats | Prostaglandins - biosynthesis | Muscle Proteins - genetics | Membrane Proteins - biosynthesis | Muscle, Smooth, Vascular - pathology | Animals | Nitric Oxide Synthase Type II - genetics
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9. Full Text Cardioprotective signature of short-term caloric restriction
by Noyan, Hossein and El-Mounayri, Omar and Isserlin, Ruth and Arab, Sara and Momen, Abdul and Cheng, Henry S and Wu, Jun and Afroze, Talat and Li, Ren-Ke and Fish, Jason E and Bader, Gary D and Husain, Mansoor
PLoS ONE, ISSN 1932-6203, 06/2015, Volume 10, Issue 6, p. e0130658
Objective To understand the molecular pathways underlying the cardiac preconditioning effect of short-term caloric restriction (CR). Background Lifelong CR has... 
CARDIOMYOCYTE CIRCADIAN CLOCK | LIFE-SPAN | OXIDATIVE STRESS | ACTIVATED PROTEIN-KINASE | MITOCHONDRIAL BIOGENESIS | RHESUS-MONKEYS | MULTIDISCIPLINARY SCIENCES | DISEASE | MYOCARDIAL-ISCHEMIA | DIETARY RESTRICTION | MEDIATES CARDIOPROTECTION | AMP-Activated Protein Kinases - metabolism | Caloric Restriction | Transcriptome | Glycogen Synthase Kinase 3 beta | Male | Cytochromes c - genetics | Proto-Oncogene Proteins c-akt - genetics | Mitogen-Activated Protein Kinase 1 - genetics | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | p38 Mitogen-Activated Protein Kinases - metabolism | Nitric Oxide Synthase Type III - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Prostaglandin-Endoperoxide Synthases - genetics | Cytochromes c - metabolism | Mice, Inbred C57BL | p38 Mitogen-Activated Protein Kinases - genetics | Transcription Factors - genetics | Glycogen Synthase Kinase 3 - metabolism | Nitric Oxide Synthase Type III - genetics | Transcription Factors - metabolism | Myocardial Reperfusion Injury - metabolism | Animals | Glycogen Synthase Kinase 3 - genetics | Mitogen-Activated Protein Kinase 3 - metabolism | Prostaglandin-Endoperoxide Synthases - metabolism | Mice | AMP-Activated Protein Kinases - genetics | Myocardial Reperfusion Injury - prevention & control | Mitogen-Activated Protein Kinase 1 - metabolism | Proteins | RNA | Gene expression | Analysis | Heart attack | Myocardial infarction | Short term | Cytochrome | Heart | Oxidative stress | Laboratories | AKT protein | Cardiovascular disease | Caspase-3 | Western blotting | Prostaglandin endoperoxide synthase | Dietary restrictions | Angiogenesis | Mitochondria | Pathways | Ischemia | Health care networks | Aging | Extracellular matrix | Physiology | Heart diseases | Circadian rhythms | Stroke | Immune response | MiRNA | Extracellular signal-regulated kinase | Caspase | MAP kinase | Cardiomyocytes | Abundance | Circadian rhythm | Metabolism | Ribonucleic acid--RNA | Molecular chains | Cytochrome c | Diet | MicroRNAs | Cytoskeleton | Infarction | Hemodynamics | Cardiovascular diseases | Preconditioning | Apoptosis | Ribonucleic acid
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10. Full Text Expression of interferon‐stimulated gene 15‐kDa protein, cyclooxygenase (COX) 1, COX‐2, aldo‐keto reductase family 1, member B1, and prostaglandin E synthase in the spleen during early pregnancy in sheep
by Yang, Ling and Liu, Yong and Lv, Wan and Wang, Pengda and Wang, Bin and Xue, Jie and Zhang, Leying
Animal Science Journal, ISSN 1344-3941, 11/2018, Volume 89, Issue 11, pp. 1540 - 1548
The spleen is a unique lymphoid organ that plays a key role in immune regulation. Interferon‐tau induces upregulation of interferon‐stimulated gene 15‐kDa... 
prostaglandin synthase | ISG15 | spleen | sheep | pregnancy | CELLS | AGRICULTURE, DAIRY & ANIMAL SCIENCE | PROGESTERONE | UTERUS | BONE-MARROW | TAU | RECEPTOR | MECHANISMS | MATERNAL RECOGNITION | IDENTIFICATION | Up-Regulation | Aldehyde Reductase - genetics | Spleen - immunology | Ubiquitins - genetics | Uterus - metabolism | Pregnancy, Animal - genetics | Cyclooxygenase 2 - genetics | Prostaglandin-E Synthases - genetics | Pregnancy, Animal - immunology | Aldehyde Reductase - metabolism | Female | Placentation - genetics | Sheep - genetics | Cytokines - genetics | Ubiquitins - metabolism | Cyclooxygenase 1 - genetics | Gene Expression | Cytokines - metabolism | Prostaglandin-E Synthases - metabolism | Placentation - physiology | Pregnancy | Animals | Spleen - metabolism | Cyclooxygenase 2 - metabolism | Sheep - metabolism | Cyclooxygenase 1 - metabolism | COX-2 inhibitors | Pregnant women | Prostaglandins E | Genes | Genetic research | Interferon | Biological response modifiers | Spleen | Immunohistochemistry | Estrus | Immune response | Immunoregulation | Paracrine signalling | mRNA | Estrus cycle | Gene expression | Prostaglandin endoperoxide synthase | Proteins | Cords | Prostaglandins | Uterus | Cyclooxygenase-1 | Sheep | Dimers | Prostaglandin E |