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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
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- MeSH
- Staining and Labeling methods utilization MeSH
- Benzophenanthridines administration & dosage diagnostic use toxicity MeSH
- Financing, Organized MeSH
- Hepatocytes drug effects MeSH
- Isoquinolines administration & dosage diagnostic use toxicity MeSH
- Liver drug effects MeSH
- Comet Assay methods utilization MeSH
- Drugs, Chinese Herbal pharmacology toxicity MeSH
- Lymphocytes drug effects MeSH
- Papaveraceae genetics toxicity MeSH
- Rats, Wistar MeSH
- Food Additives MeSH
- Plant Extracts genetics toxicity MeSH
- Mutagenicity Tests methods utilization MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals 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.
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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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