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Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 J+Pharmacol+Exp+Ther 2010 ; 335 (3): 735-42 Nephropedia Template TP
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Anti-inflammatory and analgesic effect of plumbagin through inhibition of nuclear factor-kappaB activation #MMPMID20858709
Luo P; Wong YF; Ge L; Zhang ZF; Liu Y; Liu L; Zhou H
J Pharmacol Exp Ther 2010[Dec]; 335 (3): 735-42 PMID20858709show ga
Plumbagin (5-hydroxy-2-methyl-1,4-naphthoquinone) (PL) is a naturally occurring yellow pigment found in the plants of the Plumbaginaceae, Droseraceae, Ancistrocladaceae, and Dioncophyllaceae families. It has been reported that PL exhibits anticarcinogenic, anti-inflammatory, and analgesic activities. However, the mechanism underlying its anti-inflammatory action remains unknown. In the current study, we investigated and characterized the anti-inflammatory and analgesic effects of PL orally administrated in a range of dosages from 5 to 20 mg/kg. We also examined the role of nuclear factor kappaB (NF-kappaB) and proinflammatory cytokines and mediators in this effect. The results showed that PL significantly and dose-dependently suppressed the paw edema of rats induced by carrageenan and various proinflammatory mediators, including histamine, serotonin, bradykinin, and prostaglandin E(2). PL reduced the number of writhing episodes of mice induced by the intraperitoneal injection of acetic acid, but it did not reduce the writhing episode numbers induced by MgSO(4) in mice or prolong the tail-flick reaction time of rats to noxious thermal pain. Mechanistic studies showed that PL effectively decreased the production of the proinflammatory cytokines interleukin 1beta, interleukin 6, and tumor necrosis factor alpha. It also inhibited the expression of the proinflammatory mediators inducible nitric-oxide synthase and cyclooxygenase 2, whereas it did not inhibit the expression of cyclooxygenase 1. Further studies demonstrated that PL suppressed inhibitor of kappaBalpha phosphorylation and degradation, thus inhibiting the phosphorylation of the p65 subunit of NF-kappaB. This study suggests that PL has a potential to be developed into an anti-inflammatory agent for treating inflammatory diseases.
J+Pharmacol+Exp+Ther 2010 ; 335 (3): 735-42
