Allelopathic effect of some essential oils and components on germination of weed species

In this study, allelopathic effects of some essential oil plants (Carum carvi L., Coriandrum sativum L., Foeniculum vulgare Mill., Lavandula stoechas L., Mentha spicata L.,Origanum onites L., Pimpinella anisum L., Rosmarinus officinalis L., Salvia officinalis L. and Thymbra spicata L.) were investigated against some common weed species (Alcea pallida Waldst. & Kit., Amaranthus retroflexus L., Centaurea salsotitialis L., Raphanus raphanistrum L., Rumex nepalensis Spreng., Sinapis arvensis L. and Sonchus oleraceus L.) that grow in field and horticultural crops. Different concentrations (3, 6, 10 and 20 µl) of the essential oils were tested against weed seeds in vitro and their effect on germination was determined. Inhibitory effects of essential oils and concentrations were analysed with Freadman's test and they were found significant. Essential oils from Carum carvi, Mentha spicata, Origanum onites and Thymbra spicata showed high inhibitory effect against weed seeds at lower concentrations. The main components (carvacrol, thymol, carvone, limonene) of these four essential oils were tested for seed germination at four different concentrations (500, 250, 125 and 62.5 µg/ml) against the same weeds.Thymol, carvacrol and carvone showed high inhibition even at low concentrations against weed seeds. Only Alcea pallida seeds showed resistance against all essential oils and components. © 2008 Taylor & Francis

The in vivo genotoxic effects of carvacrol and thymol in rat bone marrow cells

PubMedID: 18361405The aim of this study was to investigate the in vivo genotoxic effects of carvacrol and thymol in bone marrow cells of rats. In the present study, both carvacrol (10, 30, 50, and 70 mg/kg b.w.) and thymol (40, 60, 80, and 100 mg/kg b.w.) significantly induced the structural and total chromosome abnormalities (CA) for all treatment periods (6, 12, and 24 h) when compared with control in bone marrow cells of rats intraperitonally administered. Both carvacrol and thymol showed similar effects with the positive control urethane on induction of the percentage of structural and total CA at the highest concentrations except the effects of carvacrol for 6 h treatment (70 mg/kg b.w. and 100 mg/kg b.w., respectively). In addition, carvacrol induced the numerical CA at all concentrations when compared to control and at two highest concentrations (50 and 70 mg/kg b.w.) when compared to solvent control. Thymol also induced the numerical CA especially at the highest concentration (100 mg/kg b.w.) for all treatment periods. It was shown that there was a dose-dependent effect on induction of structural, numerical and total CA for both carvacrol and thymol. Carvacrol and thymol decreased the mitotic index (MI) in all the concentrations and treatment times when compared with control. Carvacrol showed the similar effects with EC on decreasing the MI at 70 mg/ kg b.w. for 6 h, at 30 and 50 mg/kg b.w. for 12 h and at all concentrations for 24 h treatment periods. Thymol also showed a similar effect with urethane (ethyl carbamate, EC) on decreasing the MI at 60, 80, and 100 mg/kg b.w. for 6 h and at all concentrations for 24 h treatment periods. Test substances decreased the MI in a dose-dependent manner. © 2008 Wiley Periodicals, Inc

Effects of natamycin on sister chromatid exchanges, chromosome aberrations and micronucleus in human lymphocytes

PubMedID: 19514938Natamycin (pimaricin) (E235) is an antifungal that can be used as an antibiotic to treat most fungus infections. It has been globally used in a variety of foods and beverages. In the present study, the effects of natamycin on chromosome aberrations (CAs), sister chromatid exchanges (SCEs), and micronucleus (MN) formation in human lymphocytes cells were investigated. The human lymphocytes were treated with 13, 18, 23, and 28 µg/mL of natamycin for 24 and 48 h. Natamycin induced the SCE frequency at the highest concentration for 48 h only; however, it induced the structural CA and MN frequency at all concentrations when compared to control and at all concentrations, except the lowest concentration (13 µg/mL), when compared to solvent control. Natamycin showed a cytotoxic effect by decreasing the replication index, mitotic index, and nuclear division index (NDI), especially at the highest concentrations for two treatment periods. © 2009 Informa UK Ltd

The genotoxic and antigenotoxic effects of tannic acid in human lymphocytes

PubMedID: 21774736The genotoxicity of tannic acid (TA, tannin) were investigated using chromosome aberration (CA), sister chromatid exchange (SCE), and micronucleus (MN) test systems in human peripheral lymphocytes. Also, the antigenotoxicity of TA against known mutagen EMS was also examined. The lymphocytes were treated with 1.74×10 -5, 3.49×10 -5, and 6.98×10 -5 µM of TA for 24- and 48-hour treatment periods. For the antigenotoxicity of TA, the lymphocytes were treated with three different concentrations of TA and 2.71 µM of EMS. TA synergically induced the CA alone and with the mixture of EMS. However, TA did not induce the SCE alone, whereas TA and EMS as a mixture also synergically induced SCE. TA alone showed no clear effect on micronucleus formation, and it did not induce the MN when used with EMS as a mixture. In addition, TA showed a synergistic cytotoxic effect by decreasing the mitotic and nuclear division indices. The replication index was decreased at all concentrations for 48 hours of treatment time by TA and EMS as a mixture. © 2012 Informa Healthcare USA, Inc.FEF2007BAP4This study was funded by the Cukurova University Research Fund (FEF2007BAP4)