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Macleaya cordata extract and Sangrovit genotoxicity. Assessment in vivo
Marie Stiborova, Jitka Vostalova, Adela Zdarilova, Jitka Ulrichova, Jiri Hudecek, Kathrin Tschirner, Vilim Simanek
Jazyk angličtina Země Česko
NLK
Directory of Open Access Journals
od 2001
Free Medical Journals
od 1998
Medline Complete (EBSCOhost)
od 2007-06-01
ROAD: Directory of Open Access Scholarly Resources
od 2001
- MeSH
- barvení a značení metody využití MeSH
- benzofenantridiny aplikace a dávkování diagnostické užití toxicita MeSH
- financování organizované MeSH
- hepatocyty účinky léků MeSH
- isochinoliny aplikace a dávkování diagnostické užití toxicita MeSH
- játra účinky léků MeSH
- kometový test metody využití MeSH
- léky rostlinné čínské farmakologie toxicita MeSH
- lymfocyty účinky léků MeSH
- Papaveraceae genetika toxicita MeSH
- potkani Wistar MeSH
- potravinářské přísady MeSH
- rostlinné extrakty genetika toxicita MeSH
- testy genotoxicity metody využití MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
Background: Sanguinarine (SG) has been reported to form DNA adducts in vitro and increase the levels of DNAsingle strand breaks in the blood and bone marrow of mice treated intraperitoneally with SG. Recently, we showedno genotoxic eff ects of orally administrated 120 mg/kg feed Macleaya cordata extract (a mixture of sanguinarineand chelerythrine) in pigs or rats in 90-day studies. The goal of this paper was to assess the possible genotoxicity ofM. cordata extract when included as a dietary admixture to rodents at concentrations providing 600 mg/kg feed and100, 7000 or 14000 mg/kg feed Sangrovit® (natural feed additive containing M. cordata extract and powdered M.cordata) in a 90-day pilot study.Methods and Results: The rats consumed ad libitum either the standard diet or the diets containing 367 ppm of sanguinarineand chelerythrine in M. cordata extract, and 5, 330, or 660 ppm of total alkaloids in Sangrovit® for 90 days.The DNA adducts formation in liver was analyzed by 32P-postlabeling technique and DNA single strand breaks inlymphocytes were evaluated by Comet assay. The results showed that M. cordata extract and/or Sangrovit® inducedno DNA damage to rat lymphocytes or hepatocytes after 90-days oral administration.Conclusions: Data from the studies described in this paper and the fact that Sangrovit® given to the rats in ourexperiments were higher than the recommended dose (50 to 100 mg/kg feed), argue strongly in favour of the use of Sangrovit® in live stock.
Citace poskytuje Crossref.org
Lit.: 17
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- $a Background: Sanguinarine (SG) has been reported to form DNA adducts in vitro and increase the levels of DNAsingle strand breaks in the blood and bone marrow of mice treated intraperitoneally with SG. Recently, we showedno genotoxic eff ects of orally administrated 120 mg/kg feed Macleaya cordata extract (a mixture of sanguinarineand chelerythrine) in pigs or rats in 90-day studies. The goal of this paper was to assess the possible genotoxicity ofM. cordata extract when included as a dietary admixture to rodents at concentrations providing 600 mg/kg feed and100, 7000 or 14000 mg/kg feed Sangrovit® (natural feed additive containing M. cordata extract and powdered M.cordata) in a 90-day pilot study.Methods and Results: The rats consumed ad libitum either the standard diet or the diets containing 367 ppm of sanguinarineand chelerythrine in M. cordata extract, and 5, 330, or 660 ppm of total alkaloids in Sangrovit® for 90 days.The DNA adducts formation in liver was analyzed by 32P-postlabeling technique and DNA single strand breaks inlymphocytes were evaluated by Comet assay. The results showed that M. cordata extract and/or Sangrovit® inducedno DNA damage to rat lymphocytes or hepatocytes after 90-days oral administration.Conclusions: Data from the studies described in this paper and the fact that Sangrovit® given to the rats in ourexperiments were higher than the recommended dose (50 to 100 mg/kg feed), argue strongly in favour of the use of Sangrovit® in live stock.
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