Rat liver mitochondrial damage under acute or chronic carbon tetrachloride-induced intoxication: Protection by melatonin and cranberry flavonoids
Creators
- 1. Department of Biochemistry, Yanka Kupala Grodno State University, Len. Kom. Blvd. - 50, 230017 Grodno (Belarus)
- 2. Institute for Pharmacology and Biochemistry, National Academy of Sciences of Belarus, Len. Kom. Blvd. - 50, 230017 Grodno (Belarus)
- 3. Department of Cellular and Structural Biology, University of Texas Health Science Center, 7703 Floyd Curl Drive, San Antonio, TX 78229–3900 (United States)
- 4. Grodno State Medical University, Gorkogo - 80, 230015 Grodno (Belarus)
Description
In current societies, the risk of toxic liver damage has markedly increased. The aim of the present work was to carry out further research into the mechanism(s) of liver mitochondrial damage induced by acute (0.8 g/kg body weight, single injection) or chronic (1.6 g/ kg body weight, 30 days, biweekly injections) carbon tetrachloride – induced intoxication and to evaluate the hepatoprotective potential of the antioxidant, melatonin, as well as succinate and cranberry flavonoids in rats. Acute intoxication resulted in considerable impairment of mitochondrial respiratory parameters in the liver. The activity of mitochondrial succinate dehydrogenase (complex II) decreased (by 25%, p < 0.05). Short-term melatonin treatment (10 mg/kg, three times) of rats did not reduce the degree of toxic mitochondrial dysfunction but decreased the enhanced NO production. After 30-day chronic intoxication, no significant change in the respiratory activity of liver mitochondria was observed, despite marked changes in the redox-balance of mitochondria. The activities of the mitochondrial enzymes, succinate dehydrogenase and glutathione peroxidase, as well as that of cytoplasmic catalase in liver cells were inhibited significantly. Mitochondria isolated from the livers of the rats chronically treated with CCl4 displayed obvious irreversible impairments. Long-term melatonin administration (10 mg/kg, 30 days, daily) to chronically intoxicated rats diminished the toxic effects of CCl4, reducing elevated plasma activities of alanine aminotransferase and aspartate aminotransferase and bilirubin concentration, prevented accumulation of membrane lipid peroxidation products in rat liver and resulted in apparent preservation of the mitochondrial ultrastructure. The treatment of the animals by the complex of melatonin (10 mg/kg) plus succinate (50 mg/kg) plus cranberry flavonoids (7 mg/kg) was even more effective in prevention of toxic liver injury and liver mitochondria damage. Highlights: ► After 30-day chronic CCl4 intoxication mitochondria displayed considerable changes. ► The functional parameters of mitochondria were similar to the control values. ► Melatonin + succinate + flavonoids prevented mitochondrial ultrastructure damage. ► The above complex enhanced regenerative processes in the liver.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.taap.2012.04.007Additional details
Identifiers
- DOI
- 10.1016/j.taap.2012.04.007;
- PII
- S0041-008X(12)00135-4;
Publishing Information
- Journal Title
- Toxicology and Applied Pharmacology
- Journal Volume
- 261
- Journal Issue
- 3
- Journal Page Range
- p. 271-279
- ISSN
- 0041-008X
- CODEN
- TXAPA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45036300
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ALANINES; ANTIOXIDANTS; BILIRUBIN; CARBON TETRACHLORIDE; CATALASE; FLAVONOIDS; GLUTATHIONE; INJECTION; LIVER; LIVER CELLS; MELATONIN; MITOCHONDRIA; NITRIC OXIDE; RATS; TOXICITY
- Descriptors DEC
- AMINES; AMINO ACIDS; ANIMAL CELLS; ANIMALS; AROMATICS; AZAARENES; AZOLES; BODY; CARBOXYLIC ACIDS; CELL CONSTITUENTS; CHALCOGENIDES; CHLORINATED ALIPHATIC HYDROCARBONS; DIGESTIVE SYSTEM; DRUGS; ENZYMES; GLANDS; HALOGENATED ALIPHATIC HYDROCARBONS; HETEROCYCLIC ACIDS; HETEROCYCLIC COMPOUNDS; INDOLES; INTAKE; MAMMALS; NITROGEN COMPOUNDS; NITROGEN OXIDES; ORGANIC ACIDS; ORGANIC CHLORINE COMPOUNDS; ORGANIC COMPOUNDS; ORGANIC HALOGEN COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC OXYGEN COMPOUNDS; ORGANS; OXIDES; OXIDOREDUCTASES; OXYGEN COMPOUNDS; PEPTIDES; PEROXIDASES; PIGMENTS; POLYPEPTIDES; PROTEINS; PYRROLES; RADIOPROTECTIVE SUBSTANCES; RESPONSE MODIFYING FACTORS; RODENTS; SOMATIC CELLS; TRYPTAMINES; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.