Anti-inflammatory activity of cinnamon water extract in vivo and in vitro LPS-induced models

• Published in: BMC complementary and alternative medicine Vol. 12; no. 1; p. 237
• Main Authors: Hong, Joung-Woo, Yang, Ga-Eun, Kim, Yoon Bum, Eom, Seok Hyun, Lew, Jae-Hwan, Kang, Hee
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 28.11.2012; BioMed Central; BMC
• Subjects: Animals; Anti-inflammatory activity; Anti-Inflammatory Agents - administration & dosage; Anti-inflammatory drugs; Antibacterial agents; Antiviral agents; Cardiovascular diseases; Care and treatment; Cells, Cultured; Cinnamomum zeylanicum - chemistry; Cinnamon; Cold (Disease); Cytokines; Health aspects; Humans; Inflammation - drug therapy; Inflammation - immunology; Interleukin-6 - immunology; Interleukins; Lipopolysaccharides - adverse effects; Macrophages - drug effects; Macrophages - immunology; Macrophages, Peritoneal - drug effects; Macrophages, Peritoneal - immunology; Male; Medicine, Botanic; Medicine, Herbal; Metabolic disorders; Mice; Mice, Inbred BALB C; Mitogens; Plant Extracts - administration & dosage; Polyphenols; Proteins; Signaling; Studies; TNF-α; Tumor necrosis factor; Tumor Necrosis Factor-alpha - immunology; Water
• ISSN: 1472-6882; 1472-6882
• DOI: 10.1186/1472-6882-12-237

Cinnamon bark is one of the most popular herbal ingredients in traditional oriental medicine and possesses diverse pharmacological activities including anti-bacterial, anti-viral, and anti-cancer properties. The goal of this study is to investigate the in vivo and in vitro inhibitory effect of cinnamon water extract (CWE) on lipopolysaccharide (LPS)-induced tumor necrosis factor (TNF)-α and its underlying intracellular mechanisms. CWE was orally administrated to mice for 6 days prior to intraperitoneal injection of LPS. Serum levels of TNF-α and interleukin (IL)-6 were determined 1 hour after LPS stimulation. Peritoneal macrophages from thioglycollate-injected mice were isolated and assayed for viability, cytokine expression and signaling molecules upon LPS stimulation. CWE was further fractioned according to molecular size, and the levels of total polyphenols and biological activities of each fraction were measured. The oral administration of CWE to mice significantly decreased the serum levels of TNF-α and IL-6. CWE treatment in vitro decreased the mRNA expression of TNF-α. CWE blocked the LPS-induced degradation of IκBα as well as the activation of JNK, p38 and ERK1/2. Furthermore, size-based fractionation of CWE showed that the observed inhibitory effect of CWE in vitro occurred in the fraction containing the highest level of total polyphenols. Treatment with CWE decreased LPS-induced TNF-α in serum. In vitro inhibition of TNF-α gene by CWE may occur via the modulation of IκBα degradation and JNK, p38, and ERK1/2 activation. Our results also indicate that the observed anti-inflammatory action of CWE may originate from the presence of polyphenols.