نتایج جستجو برای: cox 2 inhibitor

تعداد نتایج: 2692087  

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2005
U Ruth Michaelis John R Falck Ronald Schmidt Rudi Busse Ingrid Fleming

OBJECTIVE Cytochrome P450 (CYP) epoxygenases metabolize arachidonic acid to epoxyeicosatrienoic acids (EETs). CYP2C9-derived EETs elicit endothelial cell proliferation and angiogenesis, but the signaling pathways involved are incompletely understood. Because cyclooxygenase-2 (COX-2) is involved in angiogenesis, we determined whether a link exists between CYP2C9 and COX-2 expression. METHODS A...

2012
J Huh J Kang Y Baek D Choi D Park J Lee

Results Injection of 0.5mg/kg and 5mg/kg of melittin suppressed tumor growth by 25.30% and 56.92%, respectively; these results are superior to those obtained for mice treated with the COX-2 inhibitor, NS398. Melittin reduced tumor cell proliferation (PCNA), microvessel density (MVD), expression of cyclooxygenase-2 (COX2), VEGF-A, and VEGFR-2, but did not affect VEGFR-1, in VEGF-A-induced hm LLC...

Journal: :Neuroscience letters 2003
Lisa A Teather Richard J Wurtman

The phospholipid mediator platelet-activating factor (PAF), and its non-hydrolyzable analog methylcarbamyl-PAF (mc-PAF) increase prostaglandin E(2) (PGE(2)) release from astrocyte-enriched cortical cell cultures. Cyclooxygenase (COX) enzymes--of which there are two known isoforms--convert arachidonic acid to prostaglandin (PG) H(2) (PGH(2)), which is further metabolized to various PGs, includin...

2005
M Fornai S Barogi P Berti R Spisni M Del Tacca

Background: Cyclooxygenase isoforms (COX-1, COX-2) may exert differential regulatory actions on enteric motor functions under normal or pathological conditions. Aims: To examine the occurrence and functions of COX-1 and COX-2 in the neuromuscular compartment of normal distal colon using human and murine tissue. Methods: Gene expression (human, mouse), protein expression (human), gene deletion (...

2002
D. A. BRADBURY J. STOCKS L. CORBETT E. D. HOLLAND L. H. PANG A. J. KNOX

Bradbury, D. A., R. Newton, Y.-M. Zhu, J. Stocks, L. Corbett, E. D. Holland, L. H. Pang, and A. J. Knox. Effect of bradykinin, TGF1, IL-1 , and hypoxia on COX-2 expression in pulmonary artery smooth muscle cells. Am J Physiol Lung Cell Mol Physiol 283: L717–L725, 2002. First published May 10, 2002; 10.1152/ajplung.00070.2002.—Prostanoids are major regulators of smooth muscle function that are g...

Journal: :physiology and pharmacology 0
elham norouzi department of biology, faculty of basic sciences, islamic azad university, damghan branch, damghan, semnan, iran keyvan keramati department of biology, faculty of basic sciences, islamic azad university, damghan branch, damghan, semnan, iran morteza zendehdel section of physiology, department of basic sciences, faculty of veterinary medicine, univercity of tehran, tehran, iran

introduction: ketoprofen is an nsaid and selective cox-1 inhibitor. in our previous study the role of flunixin meglumine, a nonselective cox inhibitor was studied on seizure and its anticonvulsant effects were confirmed. therefore this research is performed to assess the role of a selective cox-1 inhibitor, ketoprofen in treatment of seizures induced by ptz. methods: in this research, male wist...

Journal: :The Biochemical journal 1995
M Ouellet M D Percival

Cyclooxygenase (Cox) is a key enzyme in the biosynthesis of prostaglandins and, as such, is the target of non-steroidal anti-inflammatory drugs (NSAIDs). Two isoforms exist, being expressed constitutively (Cox-1), or inducibly in response to inflammatory mediators (Cox-2). Currently available NSAIDs inhibit both isoforms somewhat equipotently but selective Cox-2 inhibition may eliminate unwante...

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