Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 20
Filter
1.
Biol Trace Elem Res ; 197(2): 431-439, 2020 Oct.
Article in English | MEDLINE | ID: mdl-31898306

ABSTRACT

The current study evaluated levels of macro-/trace elements, select cytokines, and sperm quality, in the semen of men with abnormal spermograms. The study population of men with abnormal spermograms was divided into three groups, i.e., oligospermic, asthenozoospermic, and oligoasthenozoospermic. The control group was fertile men with normal semen parameters. Analyses showed that in comparison with that in the semen of the fertile men, levels of calcium, magnesium, and selenium were significantly lower in men with all three groups. Semen levels of zinc were significantly lower in men with asthenospermia as compared with that in control. GGT (gamma-glutamyltranspeptidase) activity in semen was significantly higher in men in any of the three states as compared with that seen in control semen. In contrast, semen ALT (alanine aminotransferase) activity was reduced in men with any of these abnormalities compared with that in the controls. Semen cholesterol levels were significantly lower in men with asthenospermia as compared with control semen. Of all the measured cytokines, only IL-5 levels were reduced in the semen of the men with any of the conditions as compared with control semen. The semen of infertile males is characterized by reduced levels of calcium, magnesium, and trace metals such as zinc and selenium. The study also indicated that measures of cholesterol and of GGT/ALT activities could serve as supplementary parameters indicative of semen quality. Further investigations are needed to clarify the role of the measured parameters in sperm physiology.


Subject(s)
Infertility, Male , Trace Elements , Cytokines , Humans , Male , Semen , Semen Analysis , Sperm Motility , Spermatozoa
2.
Molecules ; 23(12)2018 Dec 13.
Article in English | MEDLINE | ID: mdl-30551667

ABSTRACT

Coffee is one of the most popular beverages worldwide. Coffee contains bioactive compounds that affect the human body such as caffeine, caffeic acid, chlorogenic acids, trigonelline, diterpenes, and melanoidins. Some of them have demonstrated potential anticarcinogenic effects in animal models and in human cell cultures, and may play a protective role against colorectal cancer. Colorectal cancer (CRC) is the third leading cause of cancer-related mortality in the USA and other countries. Dietary patterns, as well as the consumption of beverages, may reduce the risk of CRC incidence. In this review, we focus on published epidemiological studies concerning the association of coffee consumption and the risk of development of colorectal cancer, and provide a description of selected biologically active compounds in coffee that have been investigated as potential cancer-combating compounds: Caffeine, caffeic acid (CA), chlorogenic acids (CGAs), and kahweol in relation to colorectal cancer progression in in vitro settings. We review the impact of these substances on proliferation, viability, invasiveness, and metastasis, as well as on susceptibility to chemo- and radiotherapy of colorectal cancer cell lines cultured in vitro.


Subject(s)
Carcinogenesis/pathology , Coffee/chemistry , Colorectal Neoplasms/pathology , Disease Progression , Animals , Anticarcinogenic Agents/pharmacology , Humans , Risk Factors
3.
Arch Environ Occup Health ; 72(3): 153-158, 2017 May 04.
Article in English | MEDLINE | ID: mdl-27120705

ABSTRACT

To investigate whether α-tocopherol supplementation in workers exposed to lead would reduce the oxidative stress intensity and decrease homocysteine level, the examined population was randomly divided into two groups. Workers in the first group (n = 49, reference group) were not administered any drugs. Workers in the second group (n = 34) were administered orally α-tocopherol, 200 mg per day for 12 weeks. The level of α-tocopherol significantly increased compared to the baseline and the reference group. The level of thiol groups significantly increased compared to the reference group. However, the levels of malondialdehyde and homocysteine did not significantly change. Animal studies suggest the ability of α-tocopherol administration to reverse adverse health effects of lead exposure, such as oxidative stress; however, the results of this study on humans do not confirm these protective effects.


Subject(s)
Antioxidants/administration & dosage , Antioxidants/pharmacology , Homocysteine/drug effects , Lead Poisoning/complications , Occupational Exposure , Oxidative Stress/drug effects , alpha-Tocopherol/administration & dosage , alpha-Tocopherol/pharmacology , Adult , Homocysteine/blood , Humans , Middle Aged
4.
J Vet Res ; 61(4): 517-525, 2017 Dec.
Article in English | MEDLINE | ID: mdl-29978118

ABSTRACT

INTRODUCTION: The aim of the study was to assess the influence of α-lipoic acid (ALA) on the morphology of the aorta and liver of rabbits fed high fat diet with addition of oxidised (ORO) and non-oxidised rapeseed oil (N-ORO). MATERIAL AND METHODS: The study was conducted on male chinchilla rabbits divided into six groups. The control group (C) was fed a breeding standard diet (BSD), group I received BSD with the addition of ALA in the dose of 10 mg/kg b.w., groups II and III received BSD enriched with 10% addition of N-ORO or ORO, whereas rabbits from groups IV and V received BSD with 10% addition of N-ORO or ORO and ALA. RESULTS: Addition of ORO caused necrosis and steatosis of hepatocytes, as well as atherosclerotic plaques of various intensification in the aorta. In the liver of rabbits from group II (N-ORO) infiltrations of mononuclear cells was observed in the area of liver triads and between liver lobules. The beneficial influence of ALA was demonstrated in rabbits fed a diet containing N-ORO or ORO. In case of ORO, the activity of ALA was not fully effective. CONCLUSION: Diet supplementation with ALA counteracts the changes generated in the liver and aorta under increased exposure to higher fat content in diet, in particular thermally treated fats.

5.
Environ Toxicol Pharmacol ; 43: 175-81, 2016 Apr.
Article in English | MEDLINE | ID: mdl-27002494

ABSTRACT

The aim of the study was to investigate whether α-tocopherol supplementation for workers who are chronically exposed to lead would normalize/improve the values of parameters that are associated with the lead-induced oxidative stress. Study population included chronically lead exposed males who were divided into two groups. Workers in the first group (reference group) were not given any antioxidants, while workers in the second group (αT group) received supplementation with α-tocopherol. After treatment, the blood lead and leukocyte malondialdehyde levels decreased significantly in the αT group compared to the baseline levels and reference group. However, the erythrocyte malondialdehyde, conjugated dienes, and lipofuscin levels significantly increased compared to the baseline levels. The glutathione level significantly increased compared with the baseline. Effects of supplementation with α-tocopherol on oxidative damage were not satisfactory. Therefore, there is no reason to administer α-tocopherol to workers chronically exposed to lead as a prophylaxis of lead poisoning.


Subject(s)
Antioxidants/pharmacology , Lead Poisoning/drug therapy , Occupational Exposure/statistics & numerical data , alpha-Tocopherol/pharmacology , Dietary Supplements , Glutathione/metabolism , Humans , Male , Malondialdehyde/blood
6.
Toxicol Ind Health ; 32(9): 1607-18, 2016 Sep.
Article in English | MEDLINE | ID: mdl-25731901

ABSTRACT

N-Acetylcysteine (NAC) could be included in protocols designed for the treatment of lead toxicity. Therefore, in this study, we decided to investigate the influence of NAC administration on homocysteine (Hcy) levels, oxidative damage to proteins, and the levels of iron (Fe), transferrin (TRF), and haptoglobin (HPG) in lead (Pb)-exposed workers. The examined population (n = 171) was composed of male employees who worked with Pb. They were randomized into four groups. Workers who were not administered any antioxidants, drugs, vitamins, or dietary supplements were classified as the reference group (n = 49). The remaining three groups consisted of workers who were treated orally with NAC at three different doses (1 × 200, 2 × 200, or 2 × 400 mg) for 12 weeks. After the treatment, blood Pb levels significantly decreased in the groups receiving NAC compared with the reference group. The protein concentration was not affected by NAC administration. In contrast, Hcy levels significantly decreased or showed a strong tendency toward lower values depending on the NAC dose. Levels of the protein carbonyl groups were significantly decreased in all of the groups receiving NAC. Conversely, glutamate dehydrogenase activity was significantly elevated in all of the groups receiving NAC, while the level of protein thiol groups was significantly elevated only in the group receiving 200 mg of NAC. Treatment with NAC did not significantly affect Fe and TRF levels, whereas HPG levels showed a tendency toward lower values. Treatment with NAC normalized the level of Hcy and decreased oxidative stress as measured by the protein carbonyl content; this effect occurred in a dose-dependent manner. Moreover, small doses of NAC elevated the levels of protein thiol groups. Therefore, NAC could be introduced as an alternative therapy for chronic Pb toxicity in humans.


Subject(s)
Acetylcysteine/therapeutic use , Anemia, Iron-Deficiency/prevention & control , Antioxidants/therapeutic use , Dietary Supplements , Hyperhomocysteinemia/prevention & control , Lead Poisoning/prevention & control , Occupational Diseases/prevention & control , Acetylcysteine/administration & dosage , Adult , Air Pollutants, Occupational/toxicity , Anemia, Iron-Deficiency/etiology , Antioxidants/administration & dosage , Haptoglobins/analysis , Homocysteine/blood , Humans , Hyperhomocysteinemia/etiology , Inhalation Exposure/adverse effects , Iron/blood , Lead/blood , Lead/toxicity , Lead Poisoning/blood , Lead Poisoning/physiopathology , Male , Middle Aged , Occupational Diseases/blood , Occupational Diseases/physiopathology , Occupational Exposure/adverse effects , Oxidative Stress/drug effects , Poland , Protein Carbonylation , Protoporphyrins/blood , Transferrin/analysis
7.
Biomed Res Int ; 2015: 827879, 2015.
Article in English | MEDLINE | ID: mdl-26634212

ABSTRACT

We hypothesized that addition of substances with antioxidant activity could decrease the concentrations of biomarkers of oxidative stress and inflammatory process, thus inhibiting nonalcoholic steatohepatitis development. We investigated the influence of α-lipoic acid (ALA) and garlic administration on the development of adverse changes in rabbit liver and serum under oxidative stress conditions induced with HFD from oxidized oils. We determined 8-hydroxy-2'-deoxyguanosine (8 OHdG) and malondialdehyde (MDA) in liver homogenates, total oxidant status (TOS), lipid peroxides (LOO) and tumor necrosis factor alpha (TNFα) in blood serum, and TNFα and IL-1α genes expression in liver. The results indicate that the intake of dietary ALA and garlic was significantly associated with decreases of 8 OHdG and MDA levels in rabbits' liver tissue as well as TOS and LOO levels in rabbits' serum. Similarly, TNFα and IL-1α gene expressions were suppressed due to ALA and garlic supplementation. The histopathological analysis confirmed that HFD results in liver disorder leading to steatosis. This adverse effect of HFD was ameliorated by the supplementation of ALA and garlic. The obtained results indicate a beneficial effect of ALA and garlic administration by reducing the oxidative stress intensity and the levels of some proinflammatory cytokines in rabbits fed HFD.


Subject(s)
Garlic/chemistry , Inflammation Mediators/immunology , Inflammation/immunology , Oxidative Stress/immunology , Plant Extracts/administration & dosage , Thioctic Acid/administration & dosage , Administration, Oral , Animals , Antioxidants/administration & dosage , Biomarkers/blood , Cytokines/immunology , Dietary Supplements , Inflammation/chemically induced , Inflammation/prevention & control , Male , Oxidation-Reduction , Plant Oils , Rabbits
8.
Med Pr ; 65(3): 309-16, 2014.
Article in English | MEDLINE | ID: mdl-25230559

ABSTRACT

BACKGROUND: Oxidative stress is involved in lead toxicity. This suggests that some antioxidants may play a role in the treatment of lead poisoning. In the light of this, the aim of the study was to determine whether beta-carotene administration reduces oxidative stress and homocysteine level in workers chronically exposed to lead. MATERIAL AND METHODS: The exposed population included healthy male workers exposed to lead who were randomly divided into 2 groups (mean blood lead level ca. 44 microg/dl). Workers in the 1st group (N = 49, reference group) had no antioxidants, drugs, vitamins or dietary supplements administered, while workers in the 2nd group (N = 33) had beta-carotene administered in a dose of 10 mg per day for 12 weeks. Biochemical analysis included markers of lead-exposure and the level of malondialdehyde (MDA), an oxidative stress biomarker. We also measured the level of homocysteine (Hcy) and thiol groups as well as the activity of superoxide dismutase (SOD) and its isoenzyme EC-SOD in serum. RESULTS: After supplementation, the level of MDA significantly decreased, compared to baseline, by 16%, and to the reference group. When compared to the reference group, Hcy level was also significantly decreased. However, the level of thiol groups was significantly higher after supplementation with beta-carotene compared to the reference group. Analogically, the activity of SOD and EC-SOD was significantly higher compared to the baseline and to the reference group. CONCLUSIONS: Despite some controversies over antioxidant properties of beta-carotene, our results indicate that its antioxidant action could provide some beneficial effects in lead poisoning independent of chelation.


Subject(s)
Homocysteine/blood , Lead Poisoning/blood , Lead Poisoning/drug therapy , Occupational Diseases/blood , Occupational Diseases/drug therapy , Oxidative Stress/drug effects , beta Carotene/therapeutic use , Antioxidants/therapeutic use , Humans , Male , Malondialdehyde/blood , Middle Aged , Poland , Sulfhydryl Compounds/blood , Superoxide Dismutase/blood
9.
Toxicol Appl Pharmacol ; 280(1): 36-41, 2014 Oct 01.
Article in English | MEDLINE | ID: mdl-25038314

ABSTRACT

The aim of this study was to determine whether beta-carotene administration reduces oxidative stress and influences antioxidant, mainly glutathione-related, defense systems in workers chronically exposed to lead. The population consisted of two randomly divided groups of healthy male volunteers exposed to lead. Workers in the first group (reference group) were not administered any antioxidants, while workers in the second group (CAR group) were treated orally with 10mg of beta-carotene once a day for 12weeks. Biochemical analysis included measuring markers of lead-exposure and oxidative stress in addition to the levels and activities of selected antioxidants. After treatment, levels of malondialdehyde, lipid hydroperoxides and lipofuscin significantly decreased compared with the reference group. However, the level of glutathione significantly increased compared with the baseline. Treatment with beta-carotene also resulted in significantly decreased glutathione peroxidase activity compared with the reference group, while the activities of other glutathione-related enzymes and of superoxide dismutase were not significantly changed. However, the activities of glucose-6-phosphate dehydrogenase and catalase, as well as the level of alpha-tocopherol, were significantly higher after treatment compared with the baseline. Despite controversy over the antioxidant properties of beta-carotene in vivo, our findings showed reduced oxidative stress after beta-carotene supplementation in chronic lead poisoning.


Subject(s)
Antioxidants/metabolism , Glutathione/metabolism , Lead Poisoning/drug therapy , Occupational Diseases/drug therapy , Oxidative Stress/physiology , beta Carotene/therapeutic use , Adult , Humans , Lead Poisoning/blood , Male , Middle Aged , Occupational Diseases/blood , Oxidative Stress/drug effects , Young Adult , beta Carotene/pharmacology
10.
Pol Orthop Traumatol ; 78: 173-81, 2013 Aug 16.
Article in English | MEDLINE | ID: mdl-23959433

ABSTRACT

BACKGROUND: The development of gonarthrosis (GA) involves inflammatory processes; the role of reactive oxygen species (ROS) is being increasingly mentioned. The body is protected from oxidative damage by the antioxidative barrier with fundamental role being played by antioxidative enzymes, such as superoxide dismutase (SOD), catalase (CAT) and enzymes involved in glutathione transformations, particularly glutathione peroxidase (GPx). The methods of treatment of cartilage depend on the disease advancement, patient's reactions to pain, disease-related impairment in daily activities, as well as the age and overall health of the patient. Viscosupplementation involving intra-articular injection of agents that increase the viscosity of the articular fluid is aimed at reducing the friction between articular surfaces and thus at reducing pain and excessive wear of the remaining articular cartilage. The objective of the study was to examine whether intra-articular administration of a hyaluronic acid agent has any effect on the function of the knee and on the selected biochemical parameters of the articular fluid and blood in gonarthrosis, as well as to demonstrate of correlation or no correlation between the effects of viscosupplementation and administration of hyaluronic acid into a knee containing articular fluid or a "dry" knee. MATERIAL AND METHODS: The study group consisted of 22 gonarthrosis patients who received hyaluronic acid into the knee containing the articular fluid (group PS) as per the study protocol and 27 gonarthrosis patients who received hyaluronic acid into the "dry" knee (group PPI). The study lasted about 40 weeks and involved 10 visits at the study site. Hyaluronic acid was administered intra-articularly upon the first three visits held in one-week intervals, as well as on visit 4 (12 weeks after visit 3). The study knee was assessed clinically at all visits using the osteoarthritis WOMAC scale, visual assessment scale (0-10) for the assessment of pain intensity and HHS questionnaire for clinical assessment of the knee function. Blood for study-related analyses was collected at study start and 12 weeks after administration of the third dose of hyaluronic acid. The activity of superoxide dismutase (SOD) within the articular fluid and plasma and plasma levels of MDA were determined. Results Worse WOMAC-scale quality of life was observed in patients with osteoarthrosis and "dry" knee, mostly due to higher joint stiffness. Following viscosupplementation treatment, improvement in all tested WOMAC scores was observed in both groups, and no significant differences between groups was observed. The SOD activity and the MDA levels in plasma did not differ between the study groups, both before the study and after viscosupplementation. No statistically significant changes were observed in the biochemical parameters following viscosupplementation in both groups other than for reduced articular fluid MDA levels in the PS group. CONCLUSIONS: Viscosupplementation with hyaluronic acid administration is an effective method of conservative treatment in patients with gonarthrosis. Its beneficial effect consists mostly of pain reduction and knee function improvement both in patients with articular fluid present within the knee joints as in patients with "dry" knee joints.


Subject(s)
Hyaluronic Acid/administration & dosage , Knee Joint/physiopathology , Osteoarthritis, Knee/drug therapy , Osteoarthritis, Knee/physiopathology , Synovial Fluid/metabolism , Viscosupplements/administration & dosage , Activities of Daily Living , Arthralgia/diagnosis , Arthralgia/etiology , Arthralgia/prevention & control , Cartilage, Articular/drug effects , Female , Humans , Injections, Intra-Articular , Male , Malondialdehyde/blood , Middle Aged , Osteoarthritis, Knee/blood , Osteoarthritis, Knee/complications , Pain Measurement , Range of Motion, Articular/drug effects , Superoxide Dismutase/blood , Synovial Fluid/drug effects , Treatment Outcome
11.
Clin Toxicol (Phila) ; 51(6): 480-6, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23731375

ABSTRACT

CONTEXT AND OBJECTIVE: The aim of the study was to investigate whether treatment with N-acetylcysteine (NAC) is able to restore erythrocyte glutathione (GSH) content in workers exposed to lead. Additionally, we measured the leukocyte and erythrocyte activities of GSH-related enzymes, such as glutathione reductase (GR), glutathione-S-transferase (GST), and glucose-6-phosphate dehydrogenase (G6PD), and estimated the influence of NAC administration on oxidative stress intensity, which was measured as the lipofuscin (LPS) level in erythrocytes. METHODS: The exposed population consisted of 171 healthy males randomly divided into four groups. Workers in the first group (n = 49) were not administered any antioxidants, drugs, vitamins, or dietary supplements, while workers in the remaining groups were treated with NAC at three doses for 12 weeks (1 × 200 mg per day, 2 × 200 mg per day, and 2 × 400 mg per day). All workers continued to work during the study. The blood of all examined workers was drawn two times: at the beginning of the study and after 12 weeks of treatment. RESULTS AND CONCLUSION: Blood lead levels decreased significantly in all groups receiving NAC compared to those in baseline. Erythrocyte GSH concentrations were significantly elevated in workers receiving 400 and 800 mg of NAC compared to those in baseline by 5% and 6%, respectively. Erythrocyte G6PD activity was significantly elevated in workers receiving 200, 400, and 800 mg of NAC compared to those in baseline by 24%, 14%, and 14%, respectively. By contrast, there were no significant differences in leukocyte G6PD or leukocyte and erythrocyte glutathione reductase (GR) activities before and after treatment. Leukocyte GST activities decreased significantly after treatment in workers receiving 200 mg of NAC by 34%, while LPS levels decreased significantly in workers receiving 200, 400, and 800 mg of NAC compared to those in baseline by 5%, 15%, and 13%, respectively. In conclusion, NAC decreases oxidative stress in workers exposed to lead via stimulating GSH synthesis.


Subject(s)
Acetylcysteine/therapeutic use , Antioxidants/therapeutic use , Erythrocytes/drug effects , Glutathione/metabolism , Lead Poisoning/drug therapy , Occupational Exposure , Oxidative Stress/drug effects , Adult , Erythrocytes/metabolism , Glucosephosphate Dehydrogenase/drug effects , Glucosephosphate Dehydrogenase/metabolism , Glutathione Reductase/drug effects , Glutathione Reductase/metabolism , Glutathione Transferase/drug effects , Glutathione Transferase/metabolism , Humans , Lead/blood , Lead Poisoning/blood , Lead Poisoning/metabolism , Male , Middle Aged , Young Adult
12.
Electromagn Biol Med ; 32(4): 463-70, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23323798

ABSTRACT

The aim of this study was to evaluate the activity of the antioxidant enzymes mitochondrial and cytosolic superoxide dismutase (EC 1.15.1.1), glutathione peroxidase (POX, EC 1.11.1.9) and glutathione S-transferase (EC 3.1.2.7), as well as the concentration of malone dialdehyde (MDA), as an indicator of lipid peroxidation rate in the liver tissue homogenates and blood serum of male rats exposed to extremely low-frequency magnetic field (ELF-MF) in order to improve the healing process of an experimental cut wound on the back of each animal. The exposure to ELF-MF with frequency 40 Hz and magnetic flux density 10 mT induced an increase in POX serum activity and a decrease in MDA contents in the liver tissue, which suggests the inhibition of phospholipid peroxidation and subsequent stabilization of cellular membranes, as a result of ELF-MF action. Based on the results obtained, it seems that ELF-MF could be a useful supplement in the complex treatment of prolonged wound healing, due to the activation of endogenous enzymatic antioxidant system.


Subject(s)
Antioxidants/metabolism , Glutathione Peroxidase/metabolism , Glutathione Transferase/metabolism , Magnetic Fields , Skin , Superoxide Dismutase/metabolism , Wound Healing , Animals , Cytosol/enzymology , Lipid Peroxidation , Liver/cytology , Liver/metabolism , Male , Malondialdehyde/blood , Malondialdehyde/metabolism , Mitochondria/enzymology , Rats , Rats, Sprague-Dawley
13.
Int J Toxicol ; 29(2): 221-30, 2010.
Article in English | MEDLINE | ID: mdl-20335516

ABSTRACT

This study examines the effects of vitamin E and an extremely low frequency electromagnetic field (ELF-EMF) and their combination in different time intervals of exposure of vitamin E (tocopherol) on the AT478 murine squamous cell carcinoma line. This study provides insight into the influence of correlations between ELF-EMF and vitamin E supplementation on antioxidant enzyme activity in malignant cells in vitro. Following vitamin E treatment, activity of the antioxidant enzymes is increased in an exposure-dependent manner compared with the untreated group. Application of ELF-EMF alone or with vitamin E increases both superoxide dismutase isoenzymes and glutathione peroxidase activities in comparison to the control group. The results suggest that ELF-EMF alters antioxidative activities of vitamin E in AT478 tumor cells. This study confirms the role of vitamin E in decreasing susceptibility to lipid peroxidation in AT478 tumor cells.


Subject(s)
Antioxidants/metabolism , Carcinoma, Squamous Cell/metabolism , Magnetics , Vitamin E/metabolism , Animals , Carcinoma, Squamous Cell/enzymology , Carcinoma, Squamous Cell/pathology , Cell Line, Tumor , Glutathione Peroxidase/metabolism , In Vitro Techniques , Malondialdehyde/metabolism , Mice , Superoxide Dismutase/metabolism
14.
Biol Trace Elem Res ; 120(1-3): 179-94, 2007.
Article in English | MEDLINE | ID: mdl-17916970

ABSTRACT

Significant disorders of liver metabolic pathways enzymes after high-cholesterol diet could give information on liver steatosis development. This process could probably also be inhibited by some compounds, as examined in rabbits. Forty-two male rabbits were served a high-cholesterol diet (2 g%) (0.67 g/kg b.m./24 h) with addition of d,l-methionine (70 mg/kg b.m./24 h) or seleno-d,l-methionine (12.5 microg/kg b.m./24 h) or alpha-tocopherol (10 mg/kg b.m./24 h) for 3 months to compare the protection effect of used compounds on liver metabolism and steatosis. At the beginning and every month, blood was taken. After the experiment was completed, livers were dissected for histological examinations. The concentration of total cholesterol (t-CH), triacylglycerol (TG), and the activities of aldolase (ALD), sorbitol dehydrogenase (SDH), glutamate dehydrogenase (GLDH), lactate dehydrogenase (LDH), aspartate aminotransferase (AST), and alanine aminotransferase (ALT) were determined. Plasma t-CH and TG concentrations were significantly higher in all experimental groups vs control group. Blood serum AST and ALT activities did not undergo change but there were observed not significant increase in the CH group vs control group. Activities of SDH, GLDH, and LDH increased in blood serum and decreased in the liver in all experimental groups. Activities of LDH and SDH increased in the liver in the CH+Met group vs CH group. ALD activity decreased in the liver only in the CH and CH+Se groups. This data support a lipotoxic model of cholesterol-mediated hepatic steatosis. Prolonged administration of high-cholesterol diet not only disturbs the structure of cell membranes, which is expressed by decreased activity of enzymes in the liver and the migration of those enzymes to plasma but as well leads to steatosis of the liver, which has been confirmed by histological examinations. The applied compounds appear to have a varying influence upon the activity of enzymes determined in serum and liver. Obtained results showed a beneficial influence of methionine and vitamin E supplementation on liver steatosis development.


Subject(s)
Cholesterol, Dietary/administration & dosage , Fatty Liver/prevention & control , Liver/metabolism , Methionine/pharmacology , Selenomethionine/pharmacology , Vitamin E/pharmacology , Alanine Transaminase , Animals , Aspartate Aminotransferases/metabolism , Cholesterol/blood , Fatty Liver/chemically induced , Fatty Liver/pathology , Fructose-Bisphosphate Aldolase/metabolism , Glutamate Dehydrogenase/metabolism , L-Iditol 2-Dehydrogenase/metabolism , L-Lactate Dehydrogenase/metabolism , Liver/drug effects , Liver/pathology , Male , Rabbits , Triglycerides/blood
15.
Biol Trace Elem Res ; 120(1-3): 195-204, 2007.
Article in English | MEDLINE | ID: mdl-17916971

ABSTRACT

Effect of garlic supplementation on blood antioxidant status, lipid peroxidation, and coronary plaque formation process was investigated in oxidized oil-fed rabbits. Eighteen adult male mixed European rabbits were given a balanced diet (21 g% protein, 34 g% fat, 45 g% carbohydrate), which contained isocaloristic addition of nonoxidized or oxidized rapeseed oil in the presence and absence of garlic. The experiment lasted 24 weeks. At the beginning and every 6 weeks, rabbits were weighed, and blood was taken. To evaluate the antioxidant status of the rabbits, erythrocytes malondialdehyde (MDA) concentration, total superoxide dismutase (t-SOD), and glutathione peroxidase (GPX) activations were determined. After the experiment was completed, aortas were dissected for histological examinations. Changes in the contents of the above parameters and histological examinations showed that oxidized rapeseed, oil administered to rabbits, caused the development of atherosclerotic changes and disturbed antioxidant status. The addition of garlic in such diets inhibited atherosclerotic changes in the aorta wall, and it is related to the homeostatic activity of antioxidative enzymes and lipid peroxidation.


Subject(s)
Antioxidants/analysis , Coronary Artery Disease/prevention & control , Erythrocytes/metabolism , Garlic , Animals , Brassica rapa , Fatty Acids, Monounsaturated , Glutathione Peroxidase/blood , Lipid Peroxidation , Male , Malondialdehyde/blood , Oxidation-Reduction , Plant Oils , Rabbits , Rapeseed Oil , Superoxide Dismutase/blood
16.
J Orthop Res ; 25(6): 804-12, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17318890

ABSTRACT

It has been suggested that patients with knee post-traumatic arthritis (PA), associated or not to haemarthrosis (HA), display altered oxidant and anti-oxidant systems in their synovial fluid. This study aimed to establish whether this is really the case. Synovial fluid samples were obtained by transdermal arthrocentesis from 69 patients with PA (36 of them had HA) and 22 control subjects. The activities of synovial fluid zinc-copper superoxide dismutase (ZnCuSOD) and manganese superoxide dismutase (MnSOD) isoenzymes, catalase (CAT), glutathione peroxidase (GPX), glutathione reductase (GR) and glutathione-S-transferase (GST) enzymes, and malondialdehyde (MDA) concentration and synovial fluid viscosity were measured in the study groups. Patients with PA had significantly increased activities of all antioxidant enzymes, except CAT, and MDA concentration than did the controls. However, synovial fluid viscosity was found to be decreased in the study group, mainly in the HA subgroup. Results suggest that excessive free radicals production may exist in synovial fluid of PA patients and may contribute to knee joint destruction.


Subject(s)
Arthritis/metabolism , Knee Injuries/metabolism , Lipid Peroxidation , Oxidants/metabolism , Synovial Fluid/enzymology , Adult , Arthritis/etiology , Arthritis/pathology , Catalase/metabolism , Female , Free Radicals/metabolism , Glutathione Peroxidase/metabolism , Glutathione Reductase/metabolism , Glutathione Transferase/metabolism , Hemarthrosis/complications , Hemarthrosis/metabolism , Hemarthrosis/pathology , Humans , Knee Injuries/complications , Knee Injuries/pathology , Knee Joint/metabolism , Knee Joint/pathology , Male , Malondialdehyde/metabolism , Superoxide Dismutase/metabolism , Viscosity
17.
Biol Trace Elem Res ; 112(2): 169-74, 2006 Aug.
Article in English | MEDLINE | ID: mdl-17028382

ABSTRACT

The aim of the study was examining the effect of fluoride ions and caffeine administration on glucose and urea concentration in blood serum and the activity of protein metabolism enzymes and selected enzymes of the urea cycle in rat liver. The study was carried out using 18 male Sprague-Daowley rats (4.5 mo old). Rats were divided into three groups. Group I received distilled water ad libitum. Group II received 4.9 mg F-/kg body mass/d of sodium fluoride in the water, and group III received sodium fluoride (in the above-mentioned dose) and 3 mg/kg body mass/d of caffeine in the water. After 50 d, the rats were anesthetized with thiopental and fluoride ions, glucose, and urea concentration in blood serum were determined. Also determined were the activities of aspartate aminotransferase, alanine aminotransferase glutamate dehydrogenase, ornithine carbamoylotransferase and arginase in liver homogenates. Liver was taken for pathomorphological examinations. The applied doses of F- (4.9 mg/kg body mass/d) and F- + caffeine (4.9 mg F-/kg body mass/d + 3 mg caffeine/kg body mass/d) resulted in a statistically significant increase of fluoride ion concentration in blood serum, a slight increase of the glucose concentration, and no changes in the concentration of urea in blood serum. This might testify to the absence of kidney lesions for the applied concentrations of F-. No change in the functioning of hepatocytes was observed; however, slight disturbances have been noted in the functioning of the liver, connected with the activation of urea cycle, increase of arginase activity, and accumulation of F- in this organ. There was no observed significant influence of caffeine supplementation on the obtained results.


Subject(s)
Blood Glucose/analysis , Caffeine/pharmacology , Fluorides/blood , Liver/drug effects , Sodium Fluoride/pharmacology , Urea/blood , Alanine Transaminase/metabolism , Animals , Arginase/metabolism , Aspartate Aminotransferases/metabolism , Glutamate Dehydrogenase/metabolism , Liver/enzymology , Male , Ornithine Carbamoyltransferase/metabolism , Rats , Rats, Sprague-Dawley
18.
Biol Trace Elem Res ; 111(1-3): 137-49, 2006.
Article in English | MEDLINE | ID: mdl-16943602

ABSTRACT

The aim of this study was to investigate the effect of combined therapy of vitamin E and selenomethionine to pro/antioxidant status in experimental hypercholesterolemia. Thirty male rabbits were included in the study and randomized into five groups consisting of the control group (standard diet) and four experimental groups staying on a diet rich in cholesterol (0.5 g/100 g diet): cholesterol group and groups supplemented cholesterol with selenomethionine (12.5 microg/kg body mass/24 h) or vitamin E (10 mg of DL-alpha-tocopherol/kg body mass/24 h) or combination of the above antioxidants for 3 mo. The activity of superoxide dismutase (SOD), glutathione peroxidase (GPX), and catalase (CAT) as well as the concentration of malondialdehyde (MDA) was estimated in the blood during every month of experiment. Increased activity of SOD and GPX with a decreased concentration of MDA in comparison to the cholesterol diet was found mainly in the combination of study antioxidants. The supplementation of the cholesterol diet with combined doses of vitamin E and selenomethionine appears to prevent the lesions induced by experimental hypercholesterolemia much more efficiently than single doses of the above.


Subject(s)
Antioxidants/metabolism , Hypercholesterolemia/metabolism , Selenomethionine/administration & dosage , Vitamin E/administration & dosage , Animals , Male , Rabbits , Selenomethionine/pharmacology , Vitamin E/physiology
19.
Ann Acad Med Stetin ; 52 Suppl 1: 97-101, 2006.
Article in Polish | MEDLINE | ID: mdl-17469511

ABSTRACT

PURPOSE: The aim of this study was to examine the effect of sodium fluoride and caffeine on concentrations of calcium, phosphorus, and magnesium in rat serum. MATERIAL AND METHODS: The experiment was carried out in adult male Sprague-Dawley rats. Rats were divided into three groups of six rats. In the control group, animals received distilled water. In study group I, water was supplemented with sodium fluoride (4.9 mg F-/kg b.m./24 h), while study group II received sodium fluoride (4.9 mg F-/kg b.m./24 h) and caffeine (3 mg/kg b.m./24 h). RESULTS: Significantly higher calcium concentrations in serum were noted after exposure to NaF and caffeine. There was a tendency to higher levels of calcium in group I. Biochemical analysis of rat serum showed unchanged concentrations of magnesium and phosphorus vs. control. In conclusion, the dose of caffeine used by us had no effect on serum markers of mineral metabolism in hard tissues.


Subject(s)
Caffeine/pharmacology , Calcium/blood , Magnesium/blood , Phosphorus/blood , Sodium Fluoride/pharmacology , Analysis of Variance , Animals , Calcium/chemistry , Drug Interactions , Magnesium/chemistry , Male , Phosphorus/chemistry , Rats , Rats, Sprague-Dawley , Serum/chemistry
20.
Postepy Hig Med Dosw (Online) ; 58: 264-9, 2004 Jun 18.
Article in Polish | MEDLINE | ID: mdl-15224008

ABSTRACT

Oxidative stress has been implicated in the pathogenesis of certain diseases, such as Alzheimer's disease. Disturbance in the prooxidant/antioxidant balance increases during aging moreover the production of free radicals is alleged to play a significant role in this neurodegenerative process. Because Alzheimer's disease applies to elderly people, the aim of this publication was to explore the connection between oxidative stress and its influence on the aging process. This study refers to recent studies and publications on Alzheimer's disease and particularly the oxidative stress processes connected with this illness. These processes suggest that oxidative damage is one of the factors in the neuronal death underlying the loss of cognition. Researchers involved in these studies describe oxidative damage as increases or decreases in antioxidant enzyme activity, the role of antioxidant vitamin supplementation, and alternative medications targeting other specific areas of activity in Alzheimer's disease prevention and treatment.


Subject(s)
Alzheimer Disease/enzymology , Alzheimer Disease/prevention & control , Antioxidants/therapeutic use , Vitamins/therapeutic use , Aged , Aging/physiology , Humans , Oxidative Stress/drug effects , Oxidative Stress/physiology
SELECTION OF CITATIONS
SEARCH DETAIL