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Compounds from Geijera parviflora with prostaglandin E2 inhibitory activity may explain its traditional use for pain relief

Authors :
Linda K. Banbury
Eleanore H. Lambley
Hans Wohlmuth
Dane E. Renshaw
Qingyao Shou
Htwe Mon
Hans J. Griesser
Banbury, Linda K
Shou, Qingyao
Renshaw, Dane E
Lambley, Eleanore H
Griesser, Hans J
Mon, Htwe
Wohlmuth, Hans
Source :
Journal of Ethnopharmacology. 163:251-255
Publication Year :
2015
Publisher :
Elsevier BV, 2015.

Abstract

Ethnopharmacological relevance Australian Aboriginal people used crushed leaves of Geijera parviflora Lindl. both internally and externally for pain relief, including for toothache ( Cribb and Cribb, 1981 ). This study tested the hypothesis that this traditional use might be at least in part explained by the presence of compounds with anti-inflammatory activity. Materials and methods A crude extract (95% EtOH) was prepared from powdered dried leaves. From the CH 3 Cl fraction of this extract compounds were isolated by bioassay-guided fractionation and tested for: (1) cytotoxicity in RAW 264.7 murine leukemic monocyte–macrophages, (2) prostaglandin E 2 (PGE 2 ) inhibitory activity in 3T3 Swiss albino mouse embryonic fibroblast cells, as well as (3) nitric oxide (NO) and (4) tumour necrosis factor alpha (TNFα) inhibitory activity in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. Isolated compounds were also tested for (5) antibacterial activity against a panel of Gram-positive ( Staphylococcus aureus ATCC 29213 and ATCC 25923, Staphylococcu s epidermidis ATCC 35984, biofilm-forming) and Gram-negative ( Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853) strains by broth microdilution. Results Eleven compounds were isolated, including one new flavone and one new natural product, with a further four compounds reported from this species for the first time. Some of the compounds showed good anti-inflammatory activity in vitro . In particular, flindersine ( 1 ) and N-(acetoxymethyl) flindersine ( 3 ) inhibited PGE 2 release with IC 50 values of 5.0 μM and 4.9 μM, respectively, without any significant cytotoxicity. Several other compounds showed moderate inhibition of NO ( 5 , 6 , 7 ) and TNF-α ( 6) , with IC 50 in the low micromolar range; however much of this apparent activity could be accounted for by the cytotoxicity of these compounds. None of the compounds showed anti-bacterial activity. Conclusions The inhibition of PGE 2 , an important mediator of inflammation and pain, by flindersine and a derivative thereof, along with the moderate anti-inflammatory activity shown by several other compounds isolated from Geijera parviflora leaf extract, support the traditional use of this plant for pain relief by Australian Aboriginal people.

Details

ISSN :
03788741
Volume :
163
Database :
OpenAIRE
Journal :
Journal of Ethnopharmacology
Accession number :
edsair.doi.dedup.....440dd764cd098a70c0a45d457d959f19
Full Text :
https://doi.org/10.1016/j.jep.2015.01.033