نتایج جستجو برای: phospholipase a2 pla2 neurotoxins

تعداد نتایج: 44682  

Journal: :FEBS letters 1999
T Kambe M Murakami I Kudo

By analyzing human embryonic kidney 293 cell transfectants stably overexpressing various types of phospholipase A2 (PLA2), we have shown that polyunsaturated fatty acids (PUFAs) preferentially activate type IIA secretory PLA2 (sPLA2-IIA)-mediated arachidonic acid (AA) release from interleukin-1 (IL-1)-stimulated cells. When 293 cells prelabeled with 13H]AA were incubated with exogenous PUFAs in...

2011
Yeyi Gu William J. Hurst David A. Stuart Joshua D. Lambert

We determined the in vitro inhibitory effects of cocoa extracts and procyanidins against pancreatic α-amylase (PA), pancreatic lipase (PL) and secreted phospholipase A2 (PLA2), and characterized the kinetics of such inhibition. Lavado, regular and Dutch-processed cocoa extracts as well as cocoa procyanidins (degree of polymerization (DP) = 2 to 10) were examined. Cocoa extracts and procyanidins...

Journal: :International Journal of Applied Pharmaceutics 2021

Objective: This research investigates the antibacterial, anticancer, antioxidant, and antiretroviral activities of lionfish spine poison extract.
 Methods: Isolation purification phospholipase A2 (PLA2) protein obtained from were conducted through following stages, including, extraction venom by sonication, heating, using gradual saturation levels ammonium sulfate. Furthermore, purity conc...

Journal: :The Journal of biological chemistry 2006
Rao Muralikrishna Adibhatla James F Hatcher Eric C Larsen Xinzhi Chen Dandan Sun Francis H C Tsao

Phosphatidylcholine (PtdCho) is a major membrane phospholipid, and its loss is sufficient in itself to induce cell death. PtdCho homeostasis is regulated by the balance between hydrolysis and synthesis. PtdCho is hydrolyzed by phospholipase A2 (PLA2), PtdChospecific phospholipase C (PtdCho-PLC), and phospholipase D (PLD). PtdCho synthesis is rate-limited by CTP:phosphocholine cytidylyltransfera...

Journal: :Science 1990
S P White D L Scott Z Otwinowski M H Gelb P B Sigler

The crystal structure of a complex between a phosphonate transition-state analogue and the phospholipase A2 (PLA2) from Naja naja atra venom has been solved and refined to a resolution of 2.0 angstroms. The identical stereochemistry of the two complexes that comprise the crystal's asymmetric unit indicates both the manner in which the transition state is stabilized and how the hydrophobic fatty...

Journal: :The Journal of biological chemistry 1999
S A Farber E S Olson J D Clark M E Halpern

We have developed a simple fluorescent assay for detection of phospholipase A2 (PLA2) activity in zebrafish embryos that utilizes a fluorescent phosphatidylcholine substrate. By using this assay in conjunction with selective PLA2 inhibitors and Western blot analysis, we identified the principal activity in zebrafish embryogenesis as characteristic of the Ca2+-dependent cytosolic PLA2 (cPLA2) su...

Journal: :Journal of neurochemistry 1999
H C Yang M Mosior B Ni E A Dennis

We purified an 80-kDa Ca2+-independent phospholipase A2 (iPLA2) from rat brain using octyl-Sepharose, ATP-agarose, and calmodulin-agarose column chromatography steps. This procedure gave a 30,000-fold purification and yielded 4 microg of a near-homogeneous iPLA2 with a specific activity of 4.3 micromol/min/mg. Peptide sequences of the rat brain iPLA2 display considerable homology to sequences o...

2010
Vasilis Tsimihodimos Alexandros D. Tselepis

Several lines of evidence suggest that the lipoprotein-associated phospholipase A2 (Lp-PLA2) plays an important role in the pathogenesis of atherosclerotic disease. From a pathophysiological point of view the enzyme bound to apolipoprotein-B-containing lipoproteins (which corresponds to more than 90% of plasma enzymatic activity) may play a proatherogenic role since it generates lysophosphatidy...

2012
Isabel Gonçalves Andreas Edsfeldt Na Young Ko Helena Grufman Katarina Berg Harry Björkbacka Mihaela Nitulescu Ana Persson Marie Nilsson Cornelia Prehn Jerzy Adamski Jan Nilsson

A rterial inflammation is the principal driving force responsible for atherosclerotic plaque development and destabilization. There is strong evidence that this inflammation is induced by the retention and oxidation of low-density lipo-protein (LDL) in the subendothelial space. Oxidized LDL is cytotoxic and may induce inflammation by causing arterial cell injury and by recruiting oxidized LDL-s...

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