Hepatoprotective and antioxidant activity of Melaleuca styphelioides on carbon tetrachloride-induced hepatotoxicity in mice. (December 2014)
- Record Type:
- Journal Article
- Title:
- Hepatoprotective and antioxidant activity of Melaleuca styphelioides on carbon tetrachloride-induced hepatotoxicity in mice. (December 2014)
- Main Title:
- Hepatoprotective and antioxidant activity of Melaleuca styphelioides on carbon tetrachloride-induced hepatotoxicity in mice
- Authors:
- Al-Sayed, Eman
El-Lakkany, Naglaa M.
Seif el-Din, Sayed H.
Sabra, Abdel-Nasser A.
Hammam, Olfat A. - Abstract:
- <abstract> <title>Abstract</title> <p> <italic>Context</italic>: Liver disease is a serious problem. Polyphenolic compounds have marked antioxidant effect and can prevent the liver damage caused by free radicals. <italic>In vitro</italic> studies have revealed the strong antioxidant activity of an ellagitannin-rich plant, namely, <italic>Melaleuca styphelioides</italic> Sm. (Myrtaceae).</p> <p> <italic>Objective</italic>: In view of the limited therapeutic options available for the treatment of liver diseases, the hepatoprotective potential of the methanol extract of <italic>M. styphelioides</italic> leaves (MSE) was investigated against CCl<sub>4</sub>-induced liver injury in mice.</p> <p> <italic>Materials and methods</italic>: MSE was administered (500 and 1000 mg/kg/d p.o.) along with CCl<sub>4</sub> for 6 weeks. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) were determined in the serum. Glutathione (GSH), superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione reductase (GR), glutathione transferase (GST), and malondialdehyde (MDA) were estimated in the liver homogenate. The bioactive components of MSE were identified by NMR, UV and HRESI-MS/MS data.</p> <p> <italic>Results</italic>: MSE treatment (500 and 1000 mg/kg/d) markedly inhibited the CCl<sub>4</sub>-induced increase in the levels of AST (31 and 38%), ALT (29 and 32%), ALP (13 and 19%), and MDA (22 and 37%) at the tested doses, respectively. MSE<abstract> <title>Abstract</title> <p> <italic>Context</italic>: Liver disease is a serious problem. Polyphenolic compounds have marked antioxidant effect and can prevent the liver damage caused by free radicals. <italic>In vitro</italic> studies have revealed the strong antioxidant activity of an ellagitannin-rich plant, namely, <italic>Melaleuca styphelioides</italic> Sm. (Myrtaceae).</p> <p> <italic>Objective</italic>: In view of the limited therapeutic options available for the treatment of liver diseases, the hepatoprotective potential of the methanol extract of <italic>M. styphelioides</italic> leaves (MSE) was investigated against CCl<sub>4</sub>-induced liver injury in mice.</p> <p> <italic>Materials and methods</italic>: MSE was administered (500 and 1000 mg/kg/d p.o.) along with CCl<sub>4</sub> for 6 weeks. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) were determined in the serum. Glutathione (GSH), superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione reductase (GR), glutathione transferase (GST), and malondialdehyde (MDA) were estimated in the liver homogenate. The bioactive components of MSE were identified by NMR, UV and HRESI-MS/MS data.</p> <p> <italic>Results</italic>: MSE treatment (500 and 1000 mg/kg/d) markedly inhibited the CCl<sub>4</sub>-induced increase in the levels of AST (31 and 38%), ALT (29 and 32%), ALP (13 and 19%), and MDA (22 and 37%) at the tested doses, respectively. MSE treatment markedly increased the levels of GSH (29 and 57%) and antioxidant enzymes compared with the CCl<sub>4</sub>-treated group. MSE was more effective than silymarin in restoring the liver architecture and reducing the fatty changes, central vein congestion, Kupffer cell hyperplasia, inflammatory infiltration, and necrosis induced by CCl<sub>4</sub>. The LD<sub>50</sub> of MSE was more than 5000 mg/kg.</p> <p> <italic>Conclusion</italic>: MSE confers potent antioxidant and hepatoprotective effects against CCl<sub>4</sub>-induced toxicity.</p> </abstract> … (more)
- Is Part Of:
- Pharmaceutical biology. Volume 52:Number 12(2014:Dec.)
- Journal:
- Pharmaceutical biology
- Issue:
- Volume 52:Number 12(2014:Dec.)
- Issue Display:
- Volume 52, Issue 12 (2014)
- Year:
- 2014
- Volume:
- 52
- Issue:
- 12
- Issue Sort Value:
- 2014-0052-0012-0000
- Page Start:
- 1581
- Page End:
- 1590
- Publication Date:
- 2014-12
- Subjects:
- Pharmacognosy -- Periodicals
Materia medica, Vegetable -- Periodicals
615.321 - Journal URLs:
- http://www.tandfonline.com/toc/iphb20/current ↗
http://informahealthcare.com/journal/phb ↗
http://informahealthcare.com ↗ - DOI:
- 10.3109/13880209.2014.908398 ↗
- Languages:
- English
- ISSNs:
- 1388-0209
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6442.767000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3492.xml