Curcumin: An Antiinflammatory Compound From Turmeric and Its Role in Alleviating Arthritis

Author(s):  
Shalini Pareek ◽  
Meenal Dixit ◽  
Sumit Govil ◽  
Indrani Jadhav ◽  
Divya Shrivastava ◽  
...  
1977 ◽  
Author(s):  
I.B. Holmes

The effect on circulating platelet count of repeated intravenous infusions of collagen fibrils was measured in male OFA Sprague-Dawley rats (400-550 g). Citrated blood was pumped from the left carotid artery of anaesthetized animals, via a siliconized double-lumen cannula, into the manifold of a Technicon Autocounter, for continuous registration of platelet count. Native collagen fibrils (Collagenreagent ‘Horm’) were infused intravenously for 1 min at 15 min intervals. Successive increasing collagen doses (20-320 pg/kg) induced dose-dependent reduction in platelet count, measured as absolute platelet number disappearing from the circulation. Repeated infusion of collagen 160 pg/kg produced constant, partially reversible, reduction in platelet count. Several known inhibitors of platelet aggregation were investigated in the described test system. Collagen effects were inhibited in a dose-dependent manner to a maximum of 50-60 %, and drug activity was thus quantitated on the basis of dose producing 30 % inhibition (ID30): prostaglandin E1 (1.6 pg/kg/min i.v. infusion), SH-869 (1.1 mg/kg i.v.), aspirin (33.1 mg/kg p.o.), proquazone, a new non-steroidal antiinflammatory compound (5.0 mg/kg p.o.). That part of the collagen response not inhibited might be attributed to the initial phase of platelet adhesion to collagen, known to be relatively refractive to platelet function inhibitors.


Endocrinology ◽  
2003 ◽  
Vol 144 (12) ◽  
pp. 5227-5231 ◽  
Author(s):  
David T. Bolick ◽  
Melissa E. Hatley ◽  
Suseela Srinivasan ◽  
Catherine C. Hedrick ◽  
Jerry L. Nadler

1979 ◽  
Vol 10 (38) ◽  
Author(s):  
S. TRICERRI ◽  
E. PANTO ◽  
A. BIANCHETTI ◽  
G. BOSSONI ◽  
R. VENTURINI

Author(s):  
Rocío Sancho ◽  
Concepción Lucena ◽  
Antonio Macho ◽  
Marco A. Calzado ◽  
Magdalena Blanco-Molina ◽  
...  

1995 ◽  
Vol 25 (6) ◽  
pp. 930-939 ◽  
Author(s):  
J. E. Low ◽  
A. L. Metz ◽  
T. E. Mertz ◽  
S. P. Henry ◽  
P. Knowlton ◽  
...  

2002 ◽  
Vol 30 (Supplement) ◽  
pp. A33
Author(s):  
Rajesh Aneja ◽  
Kelli Odoms ◽  
Hector R Wong

Blood ◽  
2009 ◽  
Vol 113 (2) ◽  
pp. 328-337 ◽  
Author(s):  
Jovanka Bestebroer ◽  
Kok P. M. van Kessel ◽  
Hafida Azouagh ◽  
Annemiek M. Walenkamp ◽  
Ingrid G. J. Boer ◽  
...  

Abstract Staphylococcus aureus secretes several virulence factors modulating immune responses. Staphylococcal superantigen-like (SSL) proteins are a family of 14 exotoxins with homology to superantigens, but with generally unknown function. Recently, we showed that SSL5 binds to P-selectin glycoprotein ligand 1 dependently of sialyl Lewis X and inhibits P-selectin–dependent neutrophil rolling. Here, we show that SSL5 potently and specifically inhibits leukocyte activation by anaphylatoxins and all classes of chemokines. SSL5 inhibited calcium mobilization, actin polymerization, and chemotaxis induced by chemokines and anaphylatoxins but not by other chemoattractants. Antibody competition experiments showed that SSL5 targets several chemokine and anaphylatoxin receptors. In addition, transfection studies showed that SSL5 binds glycosylated N-termini of all G protein–coupled receptors (GPCRs) but only inhibits stimuli of protein nature that require the receptor N-terminus for activation. Furthermore, SSL5 increased binding of chemokines to cells independent of chemokine receptors through their common glycosaminoglycan-binding site. Importance of glycans was shown for both GPCR and chemokine binding. Thus, SSL5 is an important immunomodulatory protein of S aureus that targets several crucial, initial stages of leukocyte extravasation. It is therefore a potential new antiinflammatory compound for diseases associated with chemoattractants and their receptors and disorders characterized by excessive recruitment of leukocytes.


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