Abstract
Geranium oil has been used traditionally for diarrhea, dermatitis, and intestinal
inflammation in East Asia. The aim of this study was to determine the effects of geranium
oil's characteristic components, citronellol and geraniol, on lipopolysaccharide (LPS)-induced
nitric oxide (NO) and prostaglandin E2 (PGE2) production in RAW 264.7 macrophages. Citronellol and geraniol suppressed NO and
PGE2 production in a dose-dependent manner. The inhibitory efficacy of geraniol was concomitant
with decreases in protein and mRNA expression levels of inducible nitric oxide synthase
(iNOS), whereas citronellol inhibited only iNOS enzymatic activity. By adding citronellol
and geraniol, the LPS-induced cyclooxygenase-2 (COX-2) protein and mRNA expression
levels were significantly attenuated, whereas cytosolic degradation of IκBα and upregulation of NF-κB p65 in the nucleus were reversed. These results suggested that citronellol and geraniol
exhibit anti-inflammatory activities, supporting their common use and demonstrating
their therapeutic potential for inflammation-associated disorders.
Key words
geraniol - citronellol - anti‐inflammatory - nitric oxide - prostaglandin E2
- macrophage
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Prof. Ying-Chieh Tsai
Institute of Biochemistry and Molecular Biology
National Yang-Ming University
155 Li-Nong St., Sec. 2
Pei-Tou,Taipei 11221
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