Sanguinarine and chelerythrine: assessment of safety on pigs in ninety days feeding experiment
Language English Country Great Britain, England Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
14630132
DOI
10.1016/j.fct.2003.08.007
PII: S0278691503002424
Knihovny.cz E-resources
- MeSH
- DNA Adducts drug effects MeSH
- Alkaloids pharmacokinetics toxicity MeSH
- Anti-Bacterial Agents pharmacokinetics toxicity MeSH
- Benzophenanthridines MeSH
- Phenanthridines pharmacokinetics toxicity MeSH
- Isoquinolines MeSH
- Liver drug effects MeSH
- Blood Cell Count MeSH
- Animal Feed MeSH
- Food Additives toxicity MeSH
- Swine MeSH
- Growth drug effects MeSH
- Tissue Distribution MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- DNA Adducts MeSH
- Alkaloids MeSH
- Anti-Bacterial Agents MeSH
- Benzophenanthridines MeSH
- chelerythrine MeSH Browser
- Phenanthridines MeSH
- Isoquinolines MeSH
- Food Additives MeSH
- sanguinarine MeSH Browser
Sanguinaria canadesis, Chelidonium majus and Macleya cordata have been used for centuries as alternative medicines. Currently the extracts from these medicinal plants are components of veterinary and human phytopreparations, and of oral-hygiene agents. Sanguinarine and chelerythrine (SA/CHE) are biologically active components of these extracts. They display distinct antibacterial and anti-inflammatory properties, but, on the other hand, they have been reported as having adverse effects - genotoxicity and hepatotoxicity. This paper is aimed at evaluation of the effects of daily administration of the extract from Macleya cordata (2 mg and 100 mg in 1 kg feed, sanguinarine:chelerythrine 3:1) in the diet on the health status of swine. After 90-day administration, alkaloids were retained to a different extent in tissues. The highest SA/CHE retention was detected in the gingiva (0.55 microg/g) and liver (0.15 microg/g), no SA/CHE were detected in muscles. Plasma SA levels attained 0.11 microg/ml. Treated animals did not display any results of hematological, biochemical or histological assay different from controls. A (32)P-postlabeling assay proved that no DNA-adducts with SA/CHE were detected in pig livers. We did not observe any symptom linked to epidemic dropsy syndrome often attributed to sanguinarine. In conclusion, an average daily oral dose of alkaloids up to 5 mg per 1 kg animal body weight proved to be safe.
References provided by Crossref.org
Seasonal variation of bioactive alkaloid contents in Macleaya microcarpa (Maxim.) Fedde