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1.
Food Chem Toxicol ; 105: 44-51, 2017 Jul.
Article in English | MEDLINE | ID: mdl-28344087

ABSTRACT

The aim of the study was to investigate if alcohol and disulfiram (DSF) individually and in combination affect bioelements' and red-ox homeostasis in testes of the exposed rats. The animals were divided into groups according to the duration of treatments (21 and/or 42 days): C21/C42 groups (controls); OL21 and OL22-42 groups (0.5 mL olive oil intake); A1-21 groups (3 mL 20% ethanol intake); DSF1-21 groups (178.5 mg DSF/kg/day intake); and A21+DSF22-42 groups (the DSF ingestion followed previous 21 days' treatment with alcohol). The measured parameters in testes included metals: zinc (Zn), copper (Cu), iron (Fe), magnesium (Mg) and selenium (Se); as well as oxidative stress (OS) parameters: superoxide anion radical (O2•-), glutathione reduced (GSH) and oxidized (GSSG), malondialdehyde (MDA), hydrogen peroxide (H2O2) decomposition and activities of total superoxide dismutase (tSOD), glutathione-S-transferase (GST) and glutathione reductase (GR). Metal status was changed in all experimental groups (Fe rose, Zn fell, while Cu increased in A21+DSF24-32 groups). Development of OS was demonstrated in A1-21 groups, but not in DSF1-21 groups. In A21+DSF22-42 groups, OS was partially reduced compared to A groups (A1-21>MDA>C; A1-21

Subject(s)
Disulfiram/metabolism , Ethanol/adverse effects , Oxidative Stress , Testis/metabolism , Animals , Disulfiram/adverse effects , Ethanol/metabolism , Glutathione/metabolism , Glutathione Transferase/metabolism , Male , Malondialdehyde/metabolism , Oxidation-Reduction , Rats , Rats, Wistar , Selenium/metabolism , Superoxide Dismutase/metabolism , Superoxides/metabolism , Testis/enzymology
2.
J Med Food ; 17(2): 254-61, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24325457

ABSTRACT

Development of nonalcoholic fatty liver disease (NAFLD) occurs through initial steatosis and subsequent oxidative stress. The aim of this study was to examine the effects of α-lipoic acid (LA) on methionine-choline deficient (MCD) diet-induced NAFLD in mice. Male C57BL/6 mice (n=21) were divided into three groups (n=7 per group): (1) control fed with standard chow, (2) MCD2 group--fed with MCD diet for 2 weeks, and (3) MCD2+LA group--2 weeks on MCD receiving LA i.p. 100 mg/kg/day. After the treatment, liver samples were taken for pathohistology, oxidative stress parameters, antioxidative enzymes, and liver free fatty acid (FFA) composition. Mild microvesicular hepatic steatosis was found in MCD2 group, while it was reduced to single fat droplets evident in MCD2+LA group. Lipid peroxidation and nitrosative stress were increased by MCD diet, while LA administration induced a decrease in liver malondialdehyde and nitrates+nitrites level. Similary, LA improved liver antioxidative capacity by increasing total superoxide dismutase (tSOD), manganese SOD (MnSOD), and copper/zinc-SOD (Cu/ZnSOD) activity as well as glutathione (GSH) content. Liver FFA profile has shown a significant decrease in saturated acids, arachidonic, and docosahexaenoic acid (DHA), while LA treatment increased their proportions. It can be concluded that LA ameliorates lipid peroxidation and nitrosative stress in MCD diet-induced hepatic steatosis through an increase in SOD activity and GSH level. In addition, LA increases the proportion of palmitic, stearic, arachidonic, and DHA in the fatty liver. An increase in DHA may be a potential mechanism of anti-inflammatory and antioxidant effects of LA in MCD diet-induced NAFLD.


Subject(s)
Choline/adverse effects , Diet/adverse effects , Fatty Acids, Nonesterified/chemistry , Fatty Liver/drug therapy , Fatty Liver/metabolism , Methionine/adverse effects , Thioctic Acid/administration & dosage , Animals , Choline/analysis , Fatty Acids, Nonesterified/metabolism , Humans , Lipid Peroxidation , Liver/drug effects , Liver/metabolism , Male , Methionine/analysis , Mice , Mice, Inbred C57BL , Non-alcoholic Fatty Liver Disease , Oxidative Stress/drug effects
3.
Chem Biol Interact ; 206(2): 309-18, 2013 Nov 25.
Article in English | MEDLINE | ID: mdl-24070732

ABSTRACT

The aim of the study was to investigate the hypothesis that agmatine (AGM) provides protection against oxidative stress in experimental autoimmune encephalomyelitis (EAE). Wild-type (WT) and knockout (KO) CBA/H iNOS-/- 3 months old (15 ± 5 g) mice, were used for EAE induction by myelin basic protein (MBP), dissolved in Complete Freund's Adjuvant (CFA). The animals were divided into control, EAE, CFA, EAE+AGM and AGM groups. After the development of full clinical remission, animals were decapitated and oxidative stress parameters were determined in whole encephalitic mass (WEM) and cerebellum homogenates. The EAE clinical expression manifested to greater extent in WT than KO mice, was significantly decreased during AGM treatment. We demonstrated significant elevations of superoxide dismutase activity in WT and KO EAE animals, in WEM and cerebellum tissues, which were decreased during AGM treatment in both groups. Superoxide anion content was increased in WEM of both study groups, with a decrease during AGM treatment. The observed changes were more pronounced in WT than in KO animals. Also, the increased expressions of transferrin receptor and glial fibrillary acidic protein observed in WT and KO EAE mice were significantly decreased during AGM treatment. The results suggest potentially beneficial AGM effects in EAE, which might be used for a modified antioxidative approach in MS therapy.


Subject(s)
Agmatine/therapeutic use , Encephalomyelitis, Autoimmune, Experimental/drug therapy , Nitric Oxide Synthase Type II/genetics , Agmatine/pharmacology , Animals , Cerebellum/drug effects , Cerebellum/enzymology , Cerebellum/metabolism , Encephalomyelitis, Autoimmune, Experimental/pathology , Mice , Mice, Inbred CBA , Mice, Knockout , Nitric Oxide Synthase Type II/deficiency , Nitric Oxide Synthase Type II/metabolism , Receptors, Transferrin/metabolism , Superoxide Dismutase/metabolism , Superoxides/metabolism
4.
Biol Trace Elem Res ; 114(1-3): 281-91, 2006.
Article in English | MEDLINE | ID: mdl-17206009

ABSTRACT

In this report, we present the results of our investigations on the effect of Mg pretreatment on Cd and bioelements (Cu and Zn) contents in kidney of mice exposed to acute and subacute Cd intoxication. Acute intoxication was performed on male Swiss mice given a single oral dose of 20 mg Cd/kg body weight and mice given the same dose of Cd but pretreated with 40 mg Mg/kg body weight. For subacute intoxication one group of mice was given 10 mg Cd/kg body weight every day, for 2 wk, and the other one received the same dose of Cd after oral Mg intake of 20 mg/kg body weight. Cd, Cu, and Zn content was determined in kidney by atomic absorption spectrophotometry. In acute Cd intoxication, Mg pretreatment resulted in significant decrease of Cd in kidney after 4 and 6 h, compared with animals given only Cd. Under the condition of subacute Cd intoxication, Mg supplementation reduced Cd kidney content after 2 wk for about 30%, compared with animals treated with Cd only. The effect of Mg on Cu and Zn kidney content was also beneficial.


Subject(s)
Cadmium/metabolism , Copper/metabolism , Kidney/drug effects , Magnesium/administration & dosage , Zinc/metabolism , Analysis of Variance , Animals , Cadmium/toxicity , Kidney/metabolism , Male , Mice
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