Your browser doesn't support javascript.
loading
Protection by Panax ginseng C.A. Meyer against the genotoxicity of doxorubicin in somatic cells of Drosophila melanogaster
Pereira, Denise G; Antunes, Lusânia M. G; Graf, Ulrich; Spanó, Mário A.
Affiliation
  • Pereira, Denise G; Universidade Federal de Uberlândia. Instituto de Genética e Bioquímica. Laboratório de Mutagênese. Uberlândia. BR
  • Antunes, Lusânia M. G; Universidade de São Paulo. Faculdade de Ciências Farmacêuticas de Ribeirão Preto. Departamento de Análises Clínicas, Toxicológicas e Bromatológicas. Ribeirão Preto. BR
  • Graf, Ulrich; ETH Zurich. Institute of Animal Sciences. Physiology and Animal Husbandry. Schwerzenbach. CH
  • Spanó, Mário A; Universidade Federal de Uberlândia. Instituto de Genética e Bioquímica. Laboratório de Mutagênese. Uberlândia. BR
Genet. mol. biol ; 31(4): 947-955, Sept.-Dec. 2008. tab
Article in En | LILACS | ID: lil-501453
Responsible library: BR26.1
ABSTRACT
Panax ginseng is one of the most widely prescribed herbal medicines for the treatment of cancer, diabetes, chronic inflammation, and neurodegenerative and cardiovascular diseases. Since the use of alternative medicines in combination with conventional therapy may increase the risk of unwanted interactions, we investigated the possible genotoxicity of a water-soluble form of the dry root of P. ginseng (2.5, 5.0 or 10.0 mg/mL) and its ability to protect against the genotoxicity of doxorubicin (DOX; 0.125 mg/mL) by using the Drosophila melanogaster wing somatic mutation and recombination test (SMART) with standard and high-bioactivation crosses of flies. Panax ginseng was not genotoxic at the concentrations tested, whereas DOX-induced genotoxicity in marker-heterozygous flies resulted mainly from mitotic recombination. At low concentrations, P. ginseng had antirecombinogenic activity that was independent of the concentration of extract used. Recombination events may promote cancer, but little is known about the ability of P. ginseng to inhibit such recombination or modulate DNA repair mechanisms.
Subject(s)
Key words
Full text: 1 Index: LILACS Main subject: Doxorubicin / Drosophila melanogaster / Panax Limits: Animals Language: En Journal: Genet. mol. biol Journal subject: GENETICA Year: 2008 Type: Article
Full text: 1 Index: LILACS Main subject: Doxorubicin / Drosophila melanogaster / Panax Limits: Animals Language: En Journal: Genet. mol. biol Journal subject: GENETICA Year: 2008 Type: Article