TY - JOUR
T1 - In vitro and in vivo anti-inflammatory effects of ethanol extract from Acer tegmentosum
AU - Yu, Tao
AU - Lee, Jaehwi
AU - Lee, Yong Gyu
AU - Byeon, Se Eun
AU - Kim, Min Ho
AU - Sohn, Eun Hwa
AU - Lee, Yong Jin
AU - Lee, Sun Gu
AU - Cho, Jae Youl
PY - 2010/3
Y1 - 2010/3
N2 - Aim of study: Acer tegmentosum has been traditionally used for folk medicine to treat hepatic disorders such as hepatitis, hepatic cancer, and hepatic cirrhosis. In this study, we demonstrate the ethno-pharmacological activity of Acer tegmentosum in in vitro and in vivo inflammatory conditions. Results: The 70% ethanol extract (At-EE) of Acer tegmentosum dose-dependently diminished the production of nitric oxide (NO), tumour necrosis factor (TNF)-α, and prostaglandin (PG)E2, in lipopolysaccharide (LPS)-activated RAW264.7 cells and peritoneal macrophages, by a transcriptional mechanism. At-EE also suppressed the activation of nuclear factor (NF)-κB, activator protein (AP)-1, and cAMP-responsive element binding (CREB), and simultaneously blocked their upstream inflammatory signalling cascades, including Akt, p38, and JNK. Furthermore, At-EE protected against LPS-induced cell death induced by reactive oxygen species (ROS) and reactive nitrogen species (RNS) and neutralized reactive species generation. In agreement with the in vitro results, orally administered At-EE strongly ameliorated ear oedema formation induced by arachidonic acid. Conclusion: At-EE displays strong anti-inflammatory activities in vitro and in vivo, contributing to its major ethno-pharmacological role such as anti-hepatitis remedy and may be applicable to novel anti-inflammatory therapeutics.
AB - Aim of study: Acer tegmentosum has been traditionally used for folk medicine to treat hepatic disorders such as hepatitis, hepatic cancer, and hepatic cirrhosis. In this study, we demonstrate the ethno-pharmacological activity of Acer tegmentosum in in vitro and in vivo inflammatory conditions. Results: The 70% ethanol extract (At-EE) of Acer tegmentosum dose-dependently diminished the production of nitric oxide (NO), tumour necrosis factor (TNF)-α, and prostaglandin (PG)E2, in lipopolysaccharide (LPS)-activated RAW264.7 cells and peritoneal macrophages, by a transcriptional mechanism. At-EE also suppressed the activation of nuclear factor (NF)-κB, activator protein (AP)-1, and cAMP-responsive element binding (CREB), and simultaneously blocked their upstream inflammatory signalling cascades, including Akt, p38, and JNK. Furthermore, At-EE protected against LPS-induced cell death induced by reactive oxygen species (ROS) and reactive nitrogen species (RNS) and neutralized reactive species generation. In agreement with the in vitro results, orally administered At-EE strongly ameliorated ear oedema formation induced by arachidonic acid. Conclusion: At-EE displays strong anti-inflammatory activities in vitro and in vivo, contributing to its major ethno-pharmacological role such as anti-hepatitis remedy and may be applicable to novel anti-inflammatory therapeutics.
KW - Acer tegmentosum Maxim
KW - Aceraceae
KW - Anti-inflammatory effects
KW - Nitric oxide
KW - Prostaglandin E
KW - Tumour necrosis factor-α
UR - https://www.scopus.com/pages/publications/76749164790
U2 - 10.1016/j.jep.2009.12.042
DO - 10.1016/j.jep.2009.12.042
M3 - Article
C2 - 20045722
AN - SCOPUS:76749164790
SN - 0378-8741
VL - 128
SP - 139
EP - 147
JO - Journal of Ethnopharmacology
JF - Journal of Ethnopharmacology
IS - 1
ER -