In vitro studies on protective effect of Glycyrrhiza glabra root extracts against cadmium-induced genetic and oxidative damage in human lymphocytes

被引:26
作者
Dirican, Ebubekir [1 ,2 ]
Turkez, Hasan [3 ]
机构
[1] Mustafa Kemal Univ, Fac Med, Dept Med Biol, TR-31034 Antakya, Turkey
[2] Marmara Univ, Fac Med, Dept Med Biol, TR-34668 Istanbul, Turkey
[3] Erzurum Tech Univ, Dept Mol Biol & Genet, Fac Sci, TR-25240 Erzurum, Turkey
关键词
Cadmium; Glycyrrhiza glabra; Genotoxicity; Human lymphocytes; Oxidative stress; Protective effect; INDUCED DNA; TOXICITY; LICORICE; ANTIOXIDANT; STRESS; GENOTOXICITY; ABERRATIONS; MECHANISMS; LEAVES; CELLS;
D O I
10.1007/s10616-012-9531-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cadmium is a modern environmental contaminant that is toxic and carcinogenic. Glycyrrhiza glabra is a traditional medicinal herb which grows in the various parts of the World. Recent studies demonstrated that G. glabra has antifungal, antimicrobial, antioxidant, and powerful antiinflammatory features. The purpose of this study was to investigate the genetic safety of extracts from G. glabra and its effects on cadmium (as CdCl2) induced genotoxicity. Therefore we evaluated the capability of G. glabra extract to inhibit the rate of micronucleus (MN), sister chromatid exchange (SCE) formations induced by CdCl2. Moreover, to assess the effects of G. glabra on cell viability and oxidative status, we performed 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) and total antioxidant capacity (TAC) assays. Our results showed that there were significant increases (P\0.05) in both SCE and MN frequencies of cultures treated with CdCl2 (5 ppm) as compared to controls. However, co-application of G. glabra extract (5, 10 and 20 ppm) and CdCl2 resulted in decreases of MN and SCE rates as compared to the group treated with CdCl2 alone. Again, the results of MTT and TAC assays clearly indicated dose dependent ameliorative effects of G. glabra extracts against CdCl2 toxicity. In conclusion, this study demonstrated for the first time that G. glabra extracts provided increased resistance of DNA against CdCl2 induced genetic and oxidative damage in human lymphocytes. So, the risk on target tissues of CdCl2 could be reduced and ensured early recovery from its toxicity.
引用
收藏
页码:9 / 16
页数:8
相关论文
共 73 条
[61]   The effects of some boron compounds against heavy metal toxicity in human blood [J].
Turkez, Hasan ;
Geyikoglu, Fatime ;
Tatar, Abdulgani ;
Keles, M. Sait ;
Kaplan, Ibrahim .
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2012, 64 (1-2) :93-101
[62]   The role of ascorbic acid on titanium dioxide-induced genetic damage assessed by the comet assay and cytogenetic tests [J].
Turkez, Hasan .
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2011, 63 (05) :453-457
[63]   Boric acid: a potential chemoprotective agent against aflatoxin b1 toxicity in human blood [J].
Turkez, Hasan ;
Geyikoglu, Fatime .
CYTOTECHNOLOGY, 2010, 62 (02) :157-165
[64]   Metals, toxicity and oxidative stress [J].
Valko, M ;
Morris, H ;
Cronin, MTD .
CURRENT MEDICINAL CHEMISTRY, 2005, 12 (10) :1161-1208
[65]   Molecular and cellular mechanisms of cadmium carcinogenesis [J].
Waisberg, M ;
Joseph, P ;
Hale, B ;
Beyersmann, D .
TOXICOLOGY, 2003, 192 (2-3) :95-117
[66]   Cadmium is acutely toxic for murine hepatocytes:: Effects on intracellular free Ca2+ homeostasis [J].
Wang, S. S. ;
Chen, L. ;
Xia, S. K. .
PHYSIOLOGICAL RESEARCH, 2007, 56 (02) :193-201
[67]  
Wang Z Y., 2000, Herbs, Botanicals Teas, P321
[68]   AN EXPERIMENTAL-STUDY ON THE LONG-TERM EFFECT OF CADMIUM IN MICE FED CADMIUM-POLLUTED RICE WITH SPECIAL REFERENCE TO THE EFFECT OF REPEATED REPRODUCTIVE-CYCLES [J].
WATANABE, M ;
SHIROISHI, K ;
NISHINO, H ;
SHINMURA, T ;
MURASE, H ;
SHOJI, T ;
NARUSE, Y ;
KAGAMIMORI, S .
ENVIRONMENTAL RESEARCH, 1986, 40 (01) :25-46
[69]   Cadmium-induced apoptosis in C6 glioma cells:: Influence of oxidative stress [J].
Wätjen, W ;
Beyersmann, D .
BIOMETALS, 2004, 17 (01) :65-78
[70]   Protective effects of HFE7A, mouse anti-human/mouse Fas monoclonal antibody against acute and lethal hepatic injury induced by Jo2 [J].
Yoshida, Hiroko ;
Watanabe, Kenji ;
Takahashi, Shu ;
Ichikawa, Kimihisa .
CYTOTECHNOLOGY, 2010, 62 (04) :313-323