Anti-inflammatory Effects of Pelargonium endlicherianum Fenzl. Extracts in Lipopolysaccharide-stimulated Macrophages

被引:2
|
作者
Cumaoglu, Ahmet [1 ]
Karatoprak, Gokce Seker [2 ]
Yerer, Mukerrem Betul [3 ]
Kosar, Muberra [2 ]
机构
[1] Erciyes Univ, Fac Pharm, Dept Biochem, Kayseri, Turkey
[2] Erciyes Univ, Fac Pharm, Dept Pharmacognosy, Kayseri, Turkey
[3] Erciyes Univ, Fac Pharm, Dept Pharmacol, Kayseri, Turkey
关键词
Pelargonium species; inflammation; cytokines; cyclooxygenase-2; macrophages;
D O I
10.4274/tjps.86580
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objectives: This study was designed to investigate the anti-inflammatory effects of Pelargonium endlicherianum Fenzl. and Pelargonium quercetorum Agnew. root extracts compared with the effects of commercial Pelargonium sidoides root extract by production of pro-inflammatory substances and inflammatory signal transduction on LPS-stimulated macrophages. Materials and Methods: To measure the effects of root extracts on pro-inflammatory mediators, we used the following methods: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay (cell viability or cytotoxcicity), enzyme-linked immunosorbent assay (cytokine production, prostoglandin E2 production), reverse transcriptase-polymerase chain reaction (COX-2, iNOS mRNA), Western blotting analysis [MAPK activation and NE-kappa B (p65) traslocation] and the Griess reaction (NO production). Results: Stimulation of the RAW 264.7 cells with LPS (0.5 mu g/mL, 6 hrs treatment) caused an elevated production of pro-inflammatory cytokines (TNF-alpha and IL-6), increased mRNA expression of COX-2 and inducible NO synthase with release of PGE2 and NO, activated MAPK (phosphorylation of c-Jun N-terminal kinase, extracellular signal-regulated kinase, P38) signalling pathway, and nuclear translocation of NF-kappa B (p65), which were markedly inhibited by the pre-treatment with 11% ethanol and 70% methanol root extracts of P. endlicherianum without causing any cytotoxic effects. P. quercetorum root extract only decreased TNF-alpha production and P. sidoides root extract alleviated P38/MAPK activation and COX-2 mRNA expression with PGE2 production. Conclusion: Our data indicate that especially 11% ethanol root extract of P. endlicherianum targets the inflammatory response of macrophages via inhibition of COX-2, IL-6, and TNF-alpha through inactivation of the NE-kappa B signalling pathway, supporting the pharmacologic basis of P. endlicherianum as a traditional herbal medicine for the treatment of inflammation and its associated disorders.
引用
收藏
页码:107 / 115
页数:9
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