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1.
J Sci Food Agric ; 93(11): 2707-14, 2013 Aug 30.
Article in English | MEDLINE | ID: mdl-23553824

ABSTRACT

BACKGROUND: There is a growing interest in industry to replace synthetic chemicals by natural products with bioactive properties. Aromatic plants are excellent sources of bioactive compounds that can be extracted using several processes. As far as oregano is concerned, studies are lacking addressing the effect of extraction processes in bioactivity of extracts. This study aimed to characterise the in vitro antioxidant and antibacterial properties of oregano (Origanum vulgare) essential oil and extracts (in hot and cold water, and ethanol), and the chemical composition of its essential oil. RESULTS: The major components of oregano essential oil were carvacrol, ß-fenchyl alcohol, thymol, and γ-terpinene. Hot water extract had the strongest antioxidant properties and the highest phenolic content. All extracts were ineffective in inhibiting the growth of the seven tested bacteria. In contrast, the essential oil inhibited the growth of all bacteria, causing greater reductions on both Listeria strains (L. monocytogenes and L. innocua). CONCLUSION: O. vulgare extracts and essential oil from Portuguese origin are strong candidates to replace synthetic chemicals used by the industry.


Subject(s)
Oils, Volatile/chemistry , Origanum/chemistry , Plant Extracts/chemistry , Plant Oils/chemistry , Antioxidants/chemistry
2.
Clin Dev Immunol ; 2012: 236564, 2012.
Article in English | MEDLINE | ID: mdl-22162714

ABSTRACT

We investigated the effect of dietary supplementation with n-3 PUFA (fish oil source) in an experimental model of food allergy. Mice were sensitized (allergic group) or not (nonallergic group) with OVA and were fed with OVA diet to induce allergy signals. Mice were fed with regular diet in which 7% of lipid content was provided by soybean (5% of n-3 PUFA) or fish (25% of n-3 PUFA) oil. Allergic group mice had increased serum levels of antiovalbumin IgE and IgG1 and changes in small intestine, characterized by an increased edema, number of rolling leukocytes in microcirculation, eosinophil infiltration, mucus production, and Paneth cell degranulation, in comparison to non-allergic group. All these inflammatory parameters were reduced in mice fed high-n-3-PUFA diet. Our data together suggest that diet supplementation with n-3 PUFA from fish oil may consist of a valid adjuvant in food allergy treatment.


Subject(s)
Fatty Acids, Omega-3/pharmacology , Fish Oils/pharmacology , Food Hypersensitivity/metabolism , Ovalbumin/immunology , Animals , Dietary Supplements , Fatty Acids, Omega-3/administration & dosage , Female , Fish Oils/administration & dosage , Food Hypersensitivity/immunology , Intestinal Mucosa/pathology , Mice , Mice, Inbred BALB C
3.
J Sci Food Agric ; 91(9): 1554-60, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21445865

ABSTRACT

BACKGROUND: This study aimed to evaluate the antioxidant and antimicrobial activity of extracts (aqueous, ethanolic and essential oil) from Satureja montana and to characterise the chemical composition of its essential oil. RESULTS: Satureja montana L. essential oil had relatively high antimicrobial activities against the seven species of bacteria tested. In contrast, aqueous extracts did not reveal antibacterial activity, and the ethanol extract was not effective against Salmonella typhimurium. The major volatile constituents of the essential oil were carvacrol (306 g L(-1)), thymol (141 g L(-1)), and carvacrol methyl ether (63 g L(-1)). The strongest antioxidant capacity was obtained with the hot water extracts of S. montana, whereas the plant essential oil revealed the highest phenolic content. CONCLUSION: The findings indicate that the bioactive extracts of S. montana have strong potential for use as natural antimicrobials and antioxidants in the preservation of processed food.


Subject(s)
Anti-Bacterial Agents/pharmacology , Antioxidants/pharmacology , Monoterpenes/pharmacology , Oils, Volatile/chemistry , Phenols/pharmacology , Plant Extracts/pharmacology , Satureja/chemistry , Anti-Bacterial Agents/analysis , Antioxidants/analysis , Bacteria/drug effects , Cymenes , Monoterpenes/analysis , Phenols/analysis , Plant Extracts/chemistry , Thymol/analysis , Thymol/pharmacology
4.
J Photochem Photobiol B ; 70(1): 51-4, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12745247

ABSTRACT

Seeds of Thevetia peruviana were screened for their antifungal photoactivity. Extracts obtained either with n-hexane or dichloromethane were fractionated by column chromatography and further analysed by thin-layer chromatography. All seed extracts and fractions were tested for inhibition of the fungus Cladosporium cucumerinum for the evaluation of photoactive inhibitory effects. Antifungal light-dependent activity was observed for some of the fractions and both crude extracts. The most photoactive fraction was analysed by capillary gas chromatography with mass spectrometry in order to identify its constituents. Two major groups of compounds were identified, terpenes and fatty acids and derivatives. Pulegone, linoleic acid and palmitic acid were the major compounds. Terpenes seem to be the major substances with antifungal photoactivity.


Subject(s)
Antifungal Agents/pharmacology , Cladosporium/drug effects , Plant Extracts/pharmacology , Thevetia , Hexanes/pharmacology , Methylene Chloride/pharmacology , Microbial Sensitivity Tests , Plant Leaves
5.
Photochem Photobiol ; 75(2): 97-106, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11883609

ABSTRACT

Flavothione (FT) and a series of 18 hydroxy- and methoxy-substituted flavothiones were screened for photobiological activity. The 5-hydroxy-substituted compounds (group 3) and the methoxy-substituted flavothiones were inactive. FT and the remaining hydroxy-substituted compounds, all displayed photobiological activity. Among these, the 3-hydroxy-substituted compounds (group 2) were the most efficient photosensitizers overall in spite of their concurrent fast photodegradation. FT and all other hydroxyflavothiones, not substituted in the 3- or 5-positions (group 1), were inefficient compared with group 2. Detailed photobiological tests were carried out for four flavothiones of groups 1 and 2. The biological tests included fungi, several strains of Escherichia coli, Salmonella typhimurium and mammalian cells. In addition, the ability of these flavothiones to perform lipid peroxidation was evaluated. FT and 6-hydroxyflavothione (group 1) induce DNA damage via H-atom abstraction from the lowest n, pi* triplet state of the thione (oxygen independent). For 3-hydroxy and 3,6-dihydroxyflavothione (group 2), both DNA and the membrane are targets. The mechanism likely involves both energy transfer and electron transfer from the lowest pi, pi* triplet state to oxygen, to form singlet oxygen and the superoxide anion. Some of these compounds could be considered as models for environmentally safe photopesticides.


Subject(s)
Flavonoids/toxicity , Photosensitizing Agents/toxicity , Bacteria/drug effects , Bacteria/radiation effects , Cell Survival/drug effects , Cell Survival/radiation effects , Flavonoids/chemistry , Flavonoids/radiation effects , Fungi/drug effects , Fungi/radiation effects , HeLa Cells/drug effects , HeLa Cells/radiation effects , Humans , Hydroxylation , Lipid Peroxidation/drug effects , Lipid Peroxidation/radiation effects , Mutagenicity Tests , Photosensitizing Agents/chemistry , Photosensitizing Agents/radiation effects , Structure-Activity Relationship , Thiones/chemistry , Thiones/radiation effects , Thiones/toxicity , Ultraviolet Rays
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