نتایج جستجو برای: cox 2 inhibitor

تعداد نتایج: 2692087  

Journal: :research in pharmaceutical sciences 0

celecoxib is a non-steroidal anti-inflammatory drug (nsaid) developed as a selective inhibitor of cyclooxygenase-2 (cox-2) for the treatment of rheumatoid arthritis disease. recently some other mechanisms have been identified for anti cancer activity of these agents including induction of apoptosis, inhibition of tumor vascularization, stimulation of antitumor immune responses and inhibition of...

2014
Yuzhong Duan Fanglin Chen Anmei Zhang Bo Zhu Jianguo Sun Qichao Xie Zhengtang Chen

Aspirin has been demonstrated to be effective in inhibiting COX-2 and PGE(2) in Alveolar macrophages (AMs). However, the mechanisms have not been fully understood. In the present study, we found that pretreatment with aspirin inhibited LPS-induced COX-2 and PGE(2) upregulation, IκBα degradation, NFκB activation and the increase of PKC activity, but elevated LPS-induced the decrease of PTP activ...

Journal: :Archives of internal medicine 2005
Carolanne Dai Randall S Stafford G Caleb Alexander

BACKGROUND The withdrawal of rofecoxib has highlighted concerns regarding the safety of cyclooxygenase-2 (COX-2) inhibitors. In some patients COX-2 inhibitors may be safer than nonselective nonsteroidal anti-inflammatory drugs (NSAIDs); however, the public health benefit of COX-2 inhibitors depends on their use in patients at higher than normal risk from NSAIDs. We examined trends in COX-2 inhi...

Journal: :journal of reports in pharmaceutical sciences 0
mahnaz norouzi saeed irian adeleh divsalar mona salimi physiology & pharmacology department, pasteur institute of iran, tehran, iran

celecoxib, a specific cyclooxygenase-2 (cox-2) inhibitor, has been shown to possess antitumor activity in a variety of cancer cells. however, the antitumor activity of two synthesized cox-2 inhibitor derivatives ( a and b ) on human myeloid leukemia (k562) and breast adenocarcinoma (mcf-7) cancer cells has not been well established. this study was designed to investigate the morphological chang...

Journal: :The Journal of pharmacology and experimental therapeutics 2002
Elizabeth Connolly David J Bouchier-Hayes Elaine Kaye Austin Leahy Desmond Fitzgerald Orina Belton

Prostaglandin formation is enhanced in vascular disease, in part through induction of cyclooxygenase (COX-2) in vascular smooth muscle cells. Because COX regulates cell growth and migration, we examined whether the COX expression plays a role in the development of intimal hyperplasia after vascular injury. Rats undergoing balloon angioplasty of the carotid artery were randomized to receive a se...

تاتار, منیره , احمدیان مقدم, مریم , بخردنیا, احمدرضا,

Background and purpose: 1,2 diarylethylene or stilbenes are hydrocarbon derivatives with two phenyl group bonded to the double bond carbons. There are two isomers of stilbenes that Z-isomer is less stable than E-isomer. However, the Z-isomer is stronger than E-isomer as potent cyclooxygenase-2 (COX-2) inhibitor. E and Z isomers are interconverted through photochemical irradiation. In this resea...

Journal: :middle east journal of digestive diseases 0
ashraf mohamadkhani mohammad reza akbari reza ghanbari elnaz naderi parisa rezanejad-asl akram pourshams

background there are hoarding documents for the biological importance of cyclooxygenase-2 (cox-2) in pancreatic carcinogenesis. we aimed to thoroughly investigate the dna sequence variations of whole cox-2 exons in a large case-control study of pancreatic cancer by direct sequencing.   methods the entire exonic regions of cox-2 including 10 exons were sequenced in the germline dna of 96 patient...

Journal: :The Journal of pharmacology and experimental therapeutics 2012
Rocchina Colucci Luca Antonioli Nunzia Bernardini Chiara Ippolito Cristina Segnani Oriana Awwad Marco Tuccori Corrado Blandizzi Carmelo Scarpignato Matteo Fornai

Nonsteroidal anti-inflammatory drugs (NSAIDs) can impair gastric ulcer healing. This study investigates the involvement of NSAID-activated gene-1 (NAG-1) in ulcer repair impairment by cyclooxygenase (COX) inhibitors. Gastric ulcers were induced in rats by acetic acid. Four days later, animals received daily intragastric indomethacin (nonselective COX-1/COX-2 inhibitor; 1 mg/kg), 5-(4-chlorophen...

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