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Abstract Title:

The effect of a minor constituent of essential oil from Citrus aurantium: the role ofβ-myrcene in preventing peptic ulcer disease.

Abstract Source:

Chem Biol Interact. 2014 Apr 5 ;212:11-9. Epub 2014 Jan 27. PMID: 24480520

Abstract Author(s):

Flavia Bonamin, Thiago M Moraes, Raquel C Dos Santos, Hélio Kushima, Felipe M Faria, Marcos A Silva, Ivan V Junior, Leonardo Nogueira, Tais M Bauab, Alba R M Souza Brito, Lucia R M da Rocha, Clélia A Hiruma-Lima

Article Affiliation:

Flavia Bonamin

Abstract:

The monoterpeneβ-myrcene has been widely used in cosmetics, food and beverages, and it is normally found in essential oil from citrus fruit. The aim of this study was to investigate the anti-ulcer effects of β-myrcene on experimental models of ulcers that are induced by ethanol, NSAIDs (non-steroidal anti-inflammatory drugs), stress, Helicobacter pylori, ischaemia-reperfusion injury (I/R) and cysteamine in order to compare with the essential oil of Citrus aurantium and its major compound limonene. The results indicate that the oral administration of β-myrcene at a dose of 7.50mg/kg has important anti-ulcer activity with significantly decreased gastric and duodenal lesions as well as increased gastric mucus production. The results showed treatment with β-myrcene caused a significant increase in mucosal malondialdehyde level (MDA), an important index of oxidative tissue damage. The β-myrcene was also endowed with marked enhancement of antioxidant enzyme activity from GR system as evidenced by the decreased activity of superoxide dismutase (SOD) and increased levels of glutathione peroxidase (GPx), glutathione reductase (GR), and total glutathione in gastric tissue. Our results also shown thattreatment with β-myrcene is not involved with thioredoxin reductase (TrxR) activity. Our results reveal, for the first time, the importance of β-myrcene as an inhibitor of gastric and duodenal ulcers and demonstrate that an increase in the levels of gastric mucosa defence factors is involved in the anti-ulcer activity of β-myrcene.

Study Type : Animal Study
Additional Links
Pharmacological Actions : Anti-Ulcer Agents : CK(390) : AC(140)
Additional Keywords : Essential Oils : CK(181) : AC(69)

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