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1.
Biochem Biophys Rep ; 10: 208-214, 2017 Jul.
Article in English | MEDLINE | ID: mdl-29114574

ABSTRACT

The aim of this study was to investigate beneficial effect of aqueous extract of Phyllanthus fraternus (AEPF) on bromobenzene (BB) induced changes on cytosolic glutathione S-transferase (GST) isozymes in rat liver. Administration of BB significantly decreased the activity of GST, however, prior administration of AEPF prevented the BB induced decrease in GST activity. Further the cytosolic GSTs were purified from 3 groups of animals (control, BB and AEPF+BB administered) and resolved into three protein bands on SDS-PAGE. Densitometric analysis showed a significant decrease in BB group compared to control. Further, 2D PAGE analysis resolved these proteins into 8 bands which were identified as five isozymes of alpha, two of Mu and one of theta by MALDI-TOF MS and also observed decreased levels of isozymes in BB group. However, on prior administration of AEPF significantly prevented the BB induced decrease in GSTs and restored to normal levels.

2.
Am J Chin Med ; 40(3): 567-80, 2012.
Article in English | MEDLINE | ID: mdl-22745071

ABSTRACT

Hemidesmus indicus (HI) is used in ancient Indian traditional herbal medicine to treat hepatic and renal disorders. The present study was designed to investigate the protective effect of HI aqueous extract against bromobenzene induced mitochondrial dysfunction in rat kidneys. Rats were administered bromobenzene with or without prior administration of HI or vitamin E. At the end of the experiment animals were sacrificed and kidneys were obtained to study mitochondrial function, oxidative stress parameters and histopathology. Administration of bromobenzene caused significant changes like: decrease in the mitochondrial respiration and P/O ratios, increase in lipid peroxidation and protein oxidation, and decrease in the activities of antioxidant enzymes (catalase, glutathione reductase, glutathione peroxidase and superoxide dismutase) in mitochondria with significant histopathological changes in the kidney. Prior administration of HI extract showed a significant protection against bromobenzene induced changes in the kidney and this effect is attributed to the antioxidant and free radical scavenging potential of the HI. The protection was much better with HI compared to vitamin E.


Subject(s)
Hemidesmus , Kidney Diseases/prevention & control , Kidney/drug effects , Mitochondria/drug effects , Oxidative Stress/drug effects , Phytotherapy , Plant Extracts/therapeutic use , Animals , Antioxidants/metabolism , Antioxidants/pharmacology , Antioxidants/therapeutic use , Bromobenzenes , Cell Respiration/drug effects , Enzymes/metabolism , Kidney/pathology , Kidney/physiopathology , Kidney Diseases/pathology , Kidney Diseases/physiopathology , Lipid Peroxidation/drug effects , Male , Mitochondria/metabolism , Mitochondria/physiology , Plant Extracts/pharmacology , Protein Carbonylation/drug effects , Rats , Rats, Wistar , Vitamin E/pharmacology , Vitamin E/therapeutic use
3.
J Med Food ; 14(1-2): 62-8, 2011.
Article in English | MEDLINE | ID: mdl-21138366

ABSTRACT

The fruit of Emblica officinalis has been used in the Ayurvedic system of medicine for the treatment of different ailments and is also an ingredient of various traditional medicinal herbal formulations in India and other countries. To investigate the protective effect of Emblica officinalis fruit extract (EFE) against alcohol-induced brain mitochondrial dysfunction, male Wistar rats were orally administered 20% alcohol (5 g/kg of body weight/day) and EFE (250 mg/kg of body weight/day) for 60 days. Alcohol-treated rats showed significantly lowered activities of mitochondrial antioxidant enzymes (superoxide dismutase and glutathione peroxidase) and reduced glutathione compared with those of experimental control rats. Furthermore, alcohol feeding lowered the activities of NADH dehydrogenase, succinate dehydrogenase (SDH), and cytochrome c oxidase and the content of cytochromes followed by increased levels of nitric oxide (NO), thiobarbituric acid-reactive substances, and protein carbonyls. No significant change was observed in membrane potential. Administration of EFE to alcohol-treated rats, lowered the levels of NO, protein carbonyls, and lipid peroxidation and elevated the activities of the antioxidant enzymes SDH, NADH dehydrogenase, and cytochrome c oxidase and the content of cytochromes. The active tannoid principles present in EFE with its antioxidant as well as NO scavenging properties might have contributed to the observed protection against alcohol-induced brain mitochondrial dysfunction.


Subject(s)
Alcohol Drinking/drug therapy , Ethanol/adverse effects , Mitochondria/metabolism , Phyllanthus emblica/chemistry , Plant Extracts/administration & dosage , Alcohol Drinking/metabolism , Animals , Ethanol/metabolism , Glutathione Peroxidase/metabolism , Humans , Male , Mitochondria/drug effects , Mitochondria/enzymology , Models, Animal , Nitric Oxide/metabolism , Rats , Rats, Wistar , Superoxide Dismutase/metabolism
4.
Food Chem Toxicol ; 48(8-9): 2170-5, 2010.
Article in English | MEDLINE | ID: mdl-20488219

ABSTRACT

The objective of the current study was to investigate the protective effect of an aqueous extract of Phyllanthus fraternus (AEPF) against bromobenzene induced mitochondrial dysfunction in rat liver mitochondria. Administration of bromobenzene (10 mmol/kg body wt.) significantly decreased the rate of respiration (with glutamate+malate or succinate as substrates), abolished respiratory control ratio (RCR) and P/O ratios completely. There was a significant increase in the levels of lipid peroxides and protein carbonyls and a significant decrease in the total sulphydryl groups. The activities of antioxidant enzymes like catalase, glutathione peroxidase (GPx), glutathione reductase (GR) and superoxide dismutase (SOD) were decreased. The levels of antioxidants like reduced and oxidized glutathione were significantly decreased compared to control. Administration of rats with an AEPF (100mg/kg body wt.) prior to bromobenzene administration showed several beneficial effects like: (i) complete protection on mitochondrial respiration, RCR and P/O ratios (ii) lipid peroxides and protein carbonyl levels were significantly lowered (iii) increased the levels of sulphydryl groups and the activity of antioxidant enzymes and (iv) significant increase in the levels of reduced and oxidized glutathione. Vitamin E was used as positive control and bromobenzene induced mitochondrial dysfunction was protected better with AEPF compared to vitamin E.


Subject(s)
Bromobenzenes/antagonists & inhibitors , Bromobenzenes/toxicity , Chemical and Drug Induced Liver Injury/prevention & control , Mitochondria, Liver/drug effects , Phyllanthus/chemistry , Protective Agents/pharmacology , Animals , Catalase/chemistry , Chemical and Drug Induced Liver Injury/pathology , Glutathione Peroxidase/metabolism , Glutathione Reductase/metabolism , In Vitro Techniques , Lipid Peroxidation/drug effects , Liver/pathology , Male , Mitochondria, Liver/pathology , Oxidative Phosphorylation/drug effects , Oxidative Stress/drug effects , Plant Extracts/pharmacology , Protein Carbonylation/drug effects , Rats , Rats, Wistar , Sulfhydryl Compounds/metabolism , Superoxide Dismutase/metabolism , Thiobarbituric Acid Reactive Substances/metabolism
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