Antioxidant Extract from Cleistocalyx nervosum var. paniala Pulp Ameliorates Acetaminophen-Induced Acute Hepatotoxicity in Rats.
Arpamas ChariyakornkulWaristha JuengwirojJetsada RuangsuriyaRawiwan WongpoomchaiPublished in: Molecules (Basel, Switzerland) (2022)
The indigenous purplish red fruit, Cleistocalyx nervosum var. paniala (CN), is grown in northern Thailand. The aqueous extract of CN pulp is known to exhibit antioxidant and anticarcinogenic properties. To search for an antioxidant fraction separated from CN, various hydroalcoholic extractions were performed. The acidified ethanolic extract of CN obtained from 0.5% ( v / v ) citric acid in 80% ( v / v ) ethanol yielded greater polyphenol content and DPPH radical scavenging activity when compared with other hydroethanolic extracts. Cyanidin-3-glucoside is a major anthocyanin present in the acidified ethanolic extract of CN (AECN). At a dose of 5000 mg/kg bw, an anthocyanin-rich extract was found to be safe when given to rats without any acute toxicity. To examine the hepatoprotective properties of AECN, an overdose of acetaminophen (APAP) was induced in a rat model, while silymarin was used as a standard reference. The administration of AECN at a dose of 300 mg/kg bw for 28 days improved hepatocyte architecture and modulated serum alanine aminotransferase levels in APAP-induced rats. Furthermore, it significantly decreased serum and hepatic malondialdehyde levels but increased hepatic glutathione content, as well as glutathione peroxidase and UDP-glucuronosyltransferase activities. In conclusion, AECN may effectively reduce oxidative stress induced acute hepatotoxicity in overdose APAP-treated rats through the suppression of oxidative stress and the enhancement of the antioxidant system in rat livers.
Keyphrases
- oxidative stress
- diabetic rats
- drug induced
- liver injury
- lymph node metastasis
- anti inflammatory
- dna damage
- ischemia reperfusion injury
- induced apoptosis
- high glucose
- squamous cell carcinoma
- liver failure
- hydrogen peroxide
- mouse model
- ionic liquid
- endothelial cells
- acute respiratory distress syndrome
- hepatitis b virus
- heat shock protein