Characterization of the cytotoxicity of selected Chelidonium alkaloids in rat hepatocytes.
Alkaloids
/ chemistry
Animals
Benzophenanthridines
/ toxicity
Berberine
/ analogs & derivatives
Cells, Cultured
Chelidonium
/ chemistry
Chemical and Drug Induced Liver Injury
/ etiology
Dose-Response Relationship, Drug
Glutathione
/ metabolism
Hepatocytes
/ drug effects
Isoquinolines
/ toxicity
Male
Molecular Structure
Primary Cell Culture
Rats, Wistar
Structure-Activity Relationship
Alkaloids
Chelidonium majus
Glutathione
Hepatotoxicity
Papaveraceae
Rat hepatocytes
Sanguinarine
Journal
Toxicology letters
ISSN: 1879-3169
Titre abrégé: Toxicol Lett
Pays: Netherlands
ID NLM: 7709027
Informations de publication
Date de publication:
01 Sep 2019
01 Sep 2019
Historique:
received:
18
01
2019
revised:
22
04
2019
accepted:
29
04
2019
pubmed:
6
5
2019
medline:
14
6
2019
entrez:
5
5
2019
Statut:
ppublish
Résumé
Phytomedicinal preparations containing extracts of the plant Chelidonium majus (Greater Celandine) have been used in the therapy of upper abdominal disorders. C. majus alkaloids (CAL) were suspected to be responsible for reported cases of liver symptoms including cases of acute liver failure in patients upon treatment with certain C. majus preparations. Based on these reports, a safe oral daily dose limit of not more than 2.5 mg CAL was established in the EU. However, C. majus extracts and individual CAL were not able to elicit similar adverse effects when given orally to pigs or rats. We found that CAL differ considerably in their cytotoxicity in rat hepatocytes in culture. The cationic congeners chelerythrine, coptisine and sanguinarine were the most toxic ones (EC
Identifiants
pubmed: 31054355
pii: S0378-4274(19)30121-3
doi: 10.1016/j.toxlet.2019.04.031
pii:
doi:
Substances chimiques
Alkaloids
0
Benzophenanthridines
0
Isoquinolines
0
coptisine
0GCL71VN14
Berberine
0I8Y3P32UF
dihydrosanguinarine
3H1ZKG80F7
sanguinarine
AV9VK043SS
chelerythrine
E3B045W6X0
Glutathione
GAN16C9B8O
Types de publication
Comparative Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
91-97Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.