Indexed by Science Citation Index (SciSearch), International Pharmaceutical Abstract, Chemical Abstracts, Embase, Index Copernicus, EBSCO, African Index Medicus, JournalSeek, Journal Citation Reports/Science Edition, Directory of Open Access Journals (DOAJ), African Journal Online, Bioline International, Open-J-Gate

ISSN: 1596-5996 (print); 1596-9827 (electronic)-


Home | Back Issues | Current Issue | Review manuscript | Submit manuscript

 
 

This Article

 

Abstract

 

Full-Text (PDF)

 

Table of contents

 

Comments

 

Letters

 

Comments to Editor

 

e-mail Alert

 

Sign Up

 

Original Research Article


 

Total Glucosides of Paeonia lactiflora Pall Suppress Nitric Oxide Production and iNOS Expression in Lipopolysaccharide-Stimulated RAW264.7 Macrophages

 

Gang Chen1*, Ming-Liang Tan2, Xue Gao2 and Shu-Zhen Kong2

1School of Environmental and Biological Engineering, 2Chongqing Key Laboratory of Nature Medicine Research, Chongqing Technology and Business University, Chongqing 400067, China

 

*For correspondence: Email: gangch_tcm@hotmail.com; Tel: +86-23-6276-8059; Fax: +86-23-6276-9652

 

Received: 19 December 2013                                               Revised accepted: 2 June 2014

 

Tropical Journal of Pharmaceutical Research, August 2014; 13(8): 1273-1278

http://dx.doi.org/10.4314/tjpr.v13i8.11   

Abstract

 

Purpose: To investigate the effect of total glucosides of Paeonia lactiflora (TGPL) on nitric oxide (NO) production and its potential mechanism in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophage cells.

Methods: RAW264.7 cells were treated with 10 - 300 μg/ml TGPL and 1 μg/ml LPS. Cell survival was determined by MTT assay. NO level was determined by Griess reaction assay. Inducible NO synthase (iNOS) expression and inhibitor-κBα (IκBα) degradation were determined by Western blot assay. DNA binding activity of NF-κB was determined by ELISA assay using Trans AM™ kit for p65.

Results:  The concentrations of TGPL (10 - 300 μg/ml) used in this study did not affect cell survival of RAW264.7 cells, which suggest that 10-300 μg/ml TGPL did not show cytotoxic effect on RAW264.7 cells. NO level and iNOS protein expression significantly increased in LPS-stimulated RAW264.7 cells compared to the unstimulated cells. However, 10 - 300 μg/ml TGPL significantly decreased LPS-induced NO level and iNOS protein expression compared to LPS-stimulated RAW264.7 cells alone. Furthermore, 10 - 300 μg/mL TGPL significantly reduced the content of IκBα protein in LPS-stimulated RAW264.7 cells, which suggests that TGPL inhibited LPS-induced degradation of IκBα protein. TGPL remarkably repressed LPS-induced DNA binding activity of P65 in RAW264.7 cells.

Conclusion: These findings suggest that TGP inhibits NO production and iNOS expression through suppression of NF-κB activation in LPS-stimulated RAW264.7 cells.

 

Keywords: Total glucosides, Paeonia lactiflora, Nitric oxide, iNOs, Nuclear factor-κB

Copyright@2002-2010. Pharmacotherapy Group, Faculty of Pharmacy, University of Benin, Benin City. All rights reserved.

Powered by Poracom E-mail: jmanager@poracom.net