Literature DB >> 21067261

Ex vivo assessment of protective effects of carvacrol against DNA lesions induced in primary rat cells by visible light excited methylene blue (VL+MB).

D Slamenova1, E Horvathova, I Chalupa, L Wsolova, J Navarova.   

Abstract

Carvacrol belongs to frequently occurring phenolic components of essential oils (EOs) and it is present in many kinds of plants. Biological effect of this phenol derivative on human beings is however not sufficiently known. The present study was undertaken to evaluate the level of VL+MB-induced oxidative DNA lesions in hepatocytes and testicular cells (freshly isolated from control or carvacrol-watered rats) by the modified single cell gel electrophoresis (SCGE). The results showed that carvacrol significantly reduced the level of VL+MB-induced oxidized bases (EndoIII- and Fpg-sensitive sites) only in hepatocytes but not in testicular cells. Chromosomal aberration assay of primary hepatocytes, isolated from control or carvacrol-watered rats did not testify any genotoxic activity of carvacrol. We suggest that in vivo applied synthetic carvacrol, whose antioxidative activity was confirmed by DPPH assay, exhibits primarily a strong hepatoprotective activity against oxidative damage to DNA.

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Year:  2011        PMID: 21067261     DOI: 10.4149/neo_2011_01_14

Source DB:  PubMed          Journal:  Neoplasma        ISSN: 0028-2685            Impact factor:   2.575


  3 in total

1.  The effect of carvacrol on healthy neurons and N2a cancer cells: some biochemical, anticancerogenicity and genotoxicity studies.

Authors:  Elanur Aydın; Hasan Türkez; M Sait Keleş
Journal:  Cytotechnology       Date:  2013-04-04       Impact factor: 2.058

2.  Genotoxic and oxidative damage potentials in human lymphocytes after exposure to terpinolene in vitro.

Authors:  Hasan Turkez; Elanur Aydın; Fatime Geyikoglu; Damla Cetin
Journal:  Cytotechnology       Date:  2014-03-04       Impact factor: 2.058

3.  Carvacrol and rosemary oil at higher concentrations induce apoptosis in human hepatoma HepG2 cells.

Authors:  Martina Melušová; Soňa Jantová; Eva Horváthová
Journal:  Interdiscip Toxicol       Date:  2015-03-04
  3 in total

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