A comparative study on the tissue distributions of rhubarb anthraquinones in normal and CCl4-injured rats orally administered rhubarb extract
- PMID: 21884773
- DOI: 10.1016/j.jep.2011.08.028
A comparative study on the tissue distributions of rhubarb anthraquinones in normal and CCl4-injured rats orally administered rhubarb extract
Abstract
Aim of the study: The present study comparatively investigated the tissue distributions of rhubarb anthraquinone derivatives (AQs) to examine whether they undergo different uptakes in normal or CCl(4)-induced liver-damaged rats, to explore possible reasons for the different toxicities of AQs in pathological model rats and normal rats at the tissue distribution level.
Materials and methods: The total rhubarb extract (14.49 g kg(-1) of body weight per day based on the quantity of crude material) was administrated orally to normal and model rats for 12 weeks. The concentrations of free AQs in tissues were quantitated by liquid chromatography-tandem mass spectrometry (LC-MS). After drug withdrawal for 4 weeks, tissue distributions were again determined.
Results: The five free AQs-aloe-emodin, rhein, emodin, chrysophanol and physcion--were detected in the liver, kidney and spleen, while only rhein, aloe-emodin and emodin reached the quantitative limit. The tissue distributions of rhein (p < 0.001), aloe-emodin (p < 0.001) and emodin (p < 0.05) in normal rats were higher than those in model rats with rhein>aloe-emodin>emodin in kidney and spleen tissues and aloe-emodin > rhein > emodin in liver tissues. Free AQs were not detected in the tissues after drug withdrawal for 4 weeks.
Conclusions: These results suggest that the tissue toxicity of AQs in normal animals is higher than that in pathological model animals with little accumulative toxicity of rhubarb. The results are concordant with the traditional Chinese theory of You Gu Wu Yun recorded first in Su Wen, a classical Chinese medical treatise.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.
Similar articles
-
[Tissue distribution of free anthraquinones in SD rats after orally administered extracts from raw and prepared rhubarbs].Yao Xue Xue Bao. 2011 Mar;46(3):350-4. Yao Xue Xue Bao. 2011. PMID: 21626793 Chinese.
-
Pharmacokinetics and pharmacodynamics of rhubarb anthraquinones extract in normal and disease rats.Biomed Pharmacother. 2017 Jul;91:425-435. doi: 10.1016/j.biopha.2017.04.109. Epub 2017 May 2. Biomed Pharmacother. 2017. PMID: 28475921
-
[Pharmacological study on free anthraquinones compounds in rhubarb in rats with experimental acute pancreatitis].Zhongguo Zhong Yao Za Zhi. 2014 Jan;39(2):304-8. Zhongguo Zhong Yao Za Zhi. 2014. PMID: 24761651 Chinese.
-
Research Progress on the Anti-Liver Cancer Mechanism and Toxicity of Rhubarb Anthraquinone.Drug Des Devel Ther. 2024 Dec 18;18:6089-6113. doi: 10.2147/DDDT.S489377. eCollection 2024. Drug Des Devel Ther. 2024. PMID: 39717199 Free PMC article. Review.
-
Anti-cancer properties of anthraquinones from rhubarb.Med Res Rev. 2007 Sep;27(5):609-30. doi: 10.1002/med.20094. Med Res Rev. 2007. PMID: 17022020 Review.
Cited by
-
Oral colon-specific drug delivery system reduces the nephrotoxicity of rhubarb anthraquinones when they produce purgative efficacy.Exp Ther Med. 2017 Oct;14(4):3589-3601. doi: 10.3892/etm.2017.4959. Epub 2017 Aug 17. Exp Ther Med. 2017. PMID: 29042953 Free PMC article.
-
Rhein protects pancreatic β-cells from dynamin-related protein-1-mediated mitochondrial fission and cell apoptosis under hyperglycemia.Diabetes. 2013 Nov;62(11):3927-35. doi: 10.2337/db13-0251. Epub 2013 Aug 6. Diabetes. 2013. PMID: 23919963 Free PMC article.
-
San Huang Shel Shin Tang beta-cyclodextrin complex augmented the hepatoprotective effects against carbon tetrachloride-induced acute hepatotoxicity in rats.BMC Complement Altern Med. 2016 May 27;16:150. doi: 10.1186/s12906-016-1127-8. BMC Complement Altern Med. 2016. PMID: 27234802 Free PMC article.
-
Rheum australe, an endangered high-value medicinal herb of North Western Himalayas: a review of its botany, ethnomedical uses, phytochemistry and pharmacology.Phytochem Rev. 2018;17(3):573-609. doi: 10.1007/s11101-018-9551-7. Epub 2018 Feb 21. Phytochem Rev. 2018. PMID: 32214920 Free PMC article. Review.
-
Inflammatory stress potentiates emodin-induced liver injury in rats.Front Pharmacol. 2015 Oct 23;6:233. doi: 10.3389/fphar.2015.00233. eCollection 2015. Front Pharmacol. 2015. PMID: 26557087 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials