151. Immuno-Inflammatory Response after Scorpion Envenomation: Potential Role of Eïcosanoids and Histamine H1-Receptor

Toxicon ◽  
2012 ◽  
Vol 60 (2) ◽  
pp. 172 ◽  
Author(s):  
Sonia Adi-Bessalem ◽  
Amina Ladjal-Mendil ◽  
Djelila Hammoudi-Triki ◽  
Fatima Laraba-Djebari
2001 ◽  
Vol 59 (5) ◽  
pp. 1012-1021 ◽  
Author(s):  
A. C. Megson ◽  
E. M. Walker ◽  
S. J. Hill

1994 ◽  
Vol 64 ◽  
pp. 168
Author(s):  
Kazumi Ota ◽  
Katsumi Fujimoto ◽  
Ikuo Imamura ◽  
Hideyuki Hayashi ◽  
Hiroyuki Kagamiyama ◽  
...  

2018 ◽  
Vol 1437 (1) ◽  
pp. 15-21 ◽  
Author(s):  
Rosanna Ramhorst ◽  
Guillermina Calo ◽  
Daniel Paparini ◽  
Daiana Vota ◽  
Vanesa Hauk ◽  
...  

2020 ◽  
Vol 11 (10) ◽  
pp. 9252-9262 ◽  
Author(s):  
Zhigang Zhang ◽  
Changming Guo ◽  
Huijie Jiang ◽  
Bing Han ◽  
Xiaoqiao Wang ◽  
...  

Schematic diagram of the mechanism of post treatment with natural astaxanthin attenuating arsenic-induced inflammatory response in rat liver.


1975 ◽  
Vol 142 (3) ◽  
pp. 709-721 ◽  
Author(s):  
J Siegel ◽  
A P Osmand ◽  
M F Wilson ◽  
H Gewurz

Cationic homopolymers of poly-L-lysine were found to activate complement (C) via C-reactive protein (CRP) and deplete C3 and C5 as well as early-acting C components. Maximum C consumption was obtained with polymers of 2,000-8,000 daltons; polymers of 1,700, 11,000, and 23,000 daltons were intermediate in reactivity, while L-lysine, lysyl-L-lysine, tetra-L-lysine, and polymers of 70,000-400,000 daltons lacked significant C-consuming activity. Naturally occurring polycations which consumed C in the presence of CRP included myelin basic proteins, cationic proteins of rabbit leukocytes, and both lysine- and arginine-rich histones; poly-L-arginine polymers of 17,000 but not 65,000 daltons also were C-consuming. Polycations without such reactivity included poly-L-orithine (5,000 and 165,000 daltons), egg white and human lysozymes, and Polybrene. The polycations which failed to induce C consumption via CRP, inhibited its consumption by both active polycations and by C-polysaccharide (CPS). The relative inhibitory capacity of phosphorylcholine and polycations in CPS- and polycations-CRP systems was consistent with the concept that phosphate esters and polycations react at the same or an overlapping combining site. The ability of certain polycations to activate C via CRP increases the potential for initiation of host reactions via C. The capacity of other polycations to inhibit C activation via CRP introduces a potential for physiologic or pharmacologic manipulation. These considerations would seem to expand the potential role of CRP in the initiation and modulation of the inflammatory response.


2016 ◽  
Vol 244 ◽  
pp. 187-194 ◽  
Author(s):  
Nachimuthu Maithilikarpagaselvi ◽  
Magadi Gopalakrishna Sridhar ◽  
Rathinam Palamalai Swaminathan ◽  
Bobby Zachariah

2019 ◽  
Vol 27 (3) ◽  
pp. 589-601 ◽  
Author(s):  
Amal Megdad-Lamraoui ◽  
Sonia Adi-Bessalem ◽  
Fatima Laraba-Djebari

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