Subchronic oral toxicity study of rhubarb extract in Sprague-Dawley rats.
No observed adverse effect level
Rhubarb extract
Subchronic oral toxicity
Journal
Regulatory toxicology and pharmacology : RTP
ISSN: 1096-0295
Titre abrégé: Regul Toxicol Pharmacol
Pays: Netherlands
ID NLM: 8214983
Informations de publication
Date de publication:
Jul 2021
Jul 2021
Historique:
received:
20
10
2020
revised:
09
03
2021
accepted:
16
03
2021
pubmed:
25
4
2021
medline:
15
12
2021
entrez:
24
4
2021
Statut:
ppublish
Résumé
The study was primarily used to evaluate subchronic oral toxicity of rhubarb extract. The rhubarb extract was orally administered to rats at doses of 0.00, 0.65, 1.62 and 4.05 g/kg BW/day for 13 weeks with a recovery period of 4 weeks. The weight and the relative organ weight of the kidney in the 0.65 g/kg BW group were significantly increased but no significant changes were seen in renal histopathology. When the rats received rhubarb extract at 1.62 g/kg BW or above, the relative weight of the spleen and kidney were significantly increased; the kidney was also swollen and black with hydronephrosis. Histologic examination showed that there was an obvious increase in pigment deposition in renal tubular epithelial cells. No toxic related changes were observed in the 0.65 g/kg BW group, even though organ weight was increased and relative ratio to body weight of kidney were observed at 0.65 g/kg BW dosage, no significant renal histopathologic changes were detected at this dose. Based on the current study conditions and results, the no observed adverse effect level (NOAEL) of rhubarb extract in rats is 0.65 g/kg BW/day.
Identifiants
pubmed: 33894279
pii: S0273-2300(21)00061-1
doi: 10.1016/j.yrtph.2021.104921
pii:
doi:
Substances chimiques
Plant Extracts
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
104921Informations de copyright
Copyright © 2021 Elsevier Inc. All rights reserved.