Protective Effects of Ammannia baccifera Against CCl4-Induced Oxidative Stress in Rats

• Published in: International journal of environmental research and public health Vol. 16; no. 8; p. 1440
• Main Authors: Goodla, Lavanya, Manubolu, Manjunath, Pathakoti, Kavitha, Jayakumar, Thanasekaran, Sheu, Jeon-Rong, Fraker, Mike, Tchounwou, Paul B., Poondamalli, Parthasarathy R.
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 23-04-2019; MDPI
• Subjects: Acids; Ammannia baccifera; Animals; Antioxidants; Carbon tetrachloride; Catalase; Chromatography; Drug dosages; Enzymes; Gene expression; Glutathione peroxidase; High performance liquid chromatography; Ions; Lipid peroxidation; Lipids; Liquid chromatography; Liver; Mass spectrometry; Mass spectroscopy; Metabolites; Organic chemistry; Oxidation; Oxidative stress; Peroxidase; Proteins; Quadrupoles; Scientific imaging; Superoxide dismutase; China; India
• ISSN: 1660-4601; 1661-7827; 1660-4601
• DOI: 10.3390/ijerph16081440

Ammannia baccifera Linn. is commonly used as a traditional medicine in India and China. The antioxidant potential of an ethanolic extract of A. baccifera (EEAB; 250 mg/kg and 500 mg/kg) was evaluated against CCL4-induced toxicity in rats. Antioxidant activity was assessed by measuring the enzymatic and non-enzymatic antioxidants. Phytochemical constituents of EEAB were also analyzed by using UHPLC-QTOF-MS. EEAB treatment markedly reduced CCl4 effects on lipid peroxidation, cholesterol, triacylglycerides, and protein carbonyls. It increased the levels of phospholipids, total sulfhydryl, and antioxidant enzymes, which were reduced by CCl4 intoxication. Treatment with EEAB significantly alleviated the CCl4 effect on non-enzymatic antioxidants. Isoenzyme pattern analyses revealed that significant alterations in superoxide dismutase (SOD1), glutathione peroxidase (GPx2, GPx3), and catalase (CAT) occurred in rats that were exposed to CCl4 and restored post EEAB treatment. Moreover, CCl4-induced down regulation of SOD, CAT, and GPx gene expression was conversely counteracted by EEAB. Its bioactivity may be due to its incorporation of major compounds, such as chlorogenic acid, quercetin, protocatechuic acid, lamioside, crocetin, and khayasin C. These results suggest that EEAB may be used as a potent antioxidant and hepatoprotective agent since it is a rich source of flavonoids and phenolic compounds.