scholarly journals Effects of copper deficiency on hepatic and cardiac antioxidant enzyme activities in lactose- and sucrose-fed rats

1989 ◽  
Vol 61 (2) ◽  
pp. 345-354 ◽  
Author(s):  
S. M. Lynch ◽  
J. J. Strain
Keyword(s):  
Superoxide Dismutase ◽  
Antioxidant Enzyme ◽  
Enzyme Activities ◽  
Manganese Superoxide Dismutase ◽  
Copper Deficiency ◽  
Cell Damage ◽  
Thiobarbituric Acid ◽  
Antioxidant Enzyme Activities ◽  
Cu Deficiency ◽  
Glucose 6 Phosphate Dehydrogenase

1. A number of dietary sugars are known to mediate the effects of copper deficiency. The effects of lactose (compared with sucrose) and a dietary Cu deficiency on hepatic and cardiac antioxidant enzyme activities and tissue mineral element status were investigated in the rat.2. Groups (n 6) of male weanling Wistar rats were provided ad lib. with deionized water and diets containing sucrose (580 g/kg) or sucrose and lactose (387 g/kg and 193 g/kg respectively) with either control (12.0 mg/kg) or deficient (1.5 mg/kg) quantities of Cu for 77 d.3. Animals consuming the low-Cu diets exhibited significantly decreased tissue Cu levels (P < 0.01), hepatic and cardiac cytochrome c oxidase (EC 1.9.3.1, CCO) activities (P < 0.01 and P < 0.001 respectively) and hepatic Cu-zinc superoxide dismutase (EC 1.15.1.1, CuZnSOD) activity (P < 0.05). The low-Cu diets also significantly decreased cardiac manganese superoxide dismutase (EC 1.15.1.1, MnSOD), catalase (EC 1.11.1.6) and glutathione peroxidase (EC 1.11.1.9, GSH-Px) activities (P < 0.01, P < 0.05 and P < 0.001 respectively).4. Hepatic Mn was significantly increased in both lactose-fed (P < 0.001) and Cu-deficient (P < 0.01) animals. These increases were unrelated to hepatic MnSOD activity. Cardiac Zn was significantly (P < 0.01) increased in Cu-deficient animals.5. Lactose feeding resulted in significantly increased cardiac CCO activity (P < 0.001) but significantly decreased hepatic CuZnSOD (P < 0.05), catalase (P < 0.01) and GSH-Px (P < 0.001) activities.6. The activities of lactose dehydrogenase (EC 1.1.1.27, LDH) and glucose-6-phosphate dehydrogenase (EC 1.1.1.49, G6PDH) were found to be significantly (P < 0.05 and P < 0.01 respectively) increased in Cu-deficient animals and G6PDH activity was significantly (P < 0.01) decreased as a result of lactose consumption.7. The observed changes in antioxidant enzyme activities associated with both Cu deficieny and lactose consumption may have important implications for the development of free radical mediated cell damage. However, no significant differences in either hepatic or cardiac levels of thiobarbituric acid reactive substances, a measure of lipid peroxidation, were found.

Cytokines increase rat lung antioxidant enzymes during exposure to hyperoxia

1989 ◽  
Vol 66 (2) ◽  
pp. 1003-1007 ◽  
Author(s):  
C. W. White ◽  
P. Ghezzi ◽  
S. McMahon ◽  
C. A. Dinarello ◽  
J. E. Repine
Keyword(s):  
Superoxide Dismutase ◽  
Antioxidant Enzymes ◽  
Antioxidant Enzyme ◽  
Enzyme Activities ◽  
Tumor Necrosis ◽  
Interleukin 1 ◽  
Antioxidant Enzyme Activities ◽  
Rat Lung ◽  
Glucose 6 Phosphate Dehydrogenase ◽  
Necrosis Factor

Pretreatment with the combination of tumor necrosis factor/cachectin (TNF/C) and interleukin 1 (IL-1) increased glucose-6-phosphate dehydrogenase (G6PDH), glutathione reductase (GR), glutathione peroxidase (GPX), catalase (CAT), and superoxide dismutase (SOD) activities in lungs of rats continuously exposed to hyperoxia for 72 h, a time when all untreated rats had already died. Pretreatment with TNF/C and IL-1 also increased, albeit slightly, lung G6PDH and GR activities of rats exposed to hyperoxia for 4 or 16 h. By comparison, no differences occurred in lung antioxidant enzyme activities of TNF/C and IL-1- or saline-pretreated rats exposed to hyperoxia for 36 or 52 h; the latter is a time just before untreated rats began to succumb during exposure to hyperoxia. The results raise the possibility that TNF/C and IL-1 treatment can increase lung antioxidant enzyme activities and that increased lung antioxidant enzymes may contribute to the increased survival of TNF/C and IL-1-pretreated rats in hyperoxia for greater than 72 h.

Superoxide dismutase, catalase, and glutathione peroxidase during epididymal maturation and prolonged storage of spermatozoa in the Mexican big-eared bat (Corynorhinus mexicanus)

2005 ◽  
Vol 83 (12) ◽  
pp. 1556-1565 ◽  
Author(s):  
E Arenas-Ríos ◽  
M A León-Galván ◽  
P E Mercado ◽  
A Rosado
Keyword(s):  
Superoxide Dismutase ◽  
Antioxidant Enzyme ◽  
Reproductive Cycle ◽  
Enzyme Activities ◽  
Storage Period ◽  
Prolonged Storage ◽  
Ros Generation ◽  
Antioxidant Enzyme Activities ◽  
Ros Scavenging ◽  
Epididymal Spermatozoon

We studied the activities of reactive oxygen species (ROS) scavenging enzymes during epididymal spermatozoon maturation and storage in Corynorhinus mexicanus (G.M. Allen, 1916), a vespertilionid bat that stores spermatozoa in the epididymides for several months after regression of the testes. Depending on the phase of the epididymal reproductive cycle, two different patterns of antioxidant enzyme activities were observed in C. mexicanus. Catalase activity is clearly present in both caput and cauda epididymides throughout the entire annual reproductive cycle, being particularly high during the post-testicular phase of epididymal function. Superoxide dismutase (SOD) activity, present during the testicular phase of epididymal transport and maturation of spermatozoa, is almost completely absent or inhibited in both epididymal segments during the post-testicular epididymal storage period. GPx activity is low during the testicular phase of epididymal spermatozoon maturation and is high in both epididymal segments during the storage phase of epididymal function. From our results, we postulate that (i) the pattern of epididymal antioxidant enzyme activities in C. mexicanus is significantly different from the pattern that is proposed to be unique for mammals; (ii) epididymal function in these species of bats can be clearly divided into two phases, a testicular-dependent phase that is related to the spermatozoon maturation function of the epididymides and a testicular-independent phase that is related to the long-term spermatozoon storage function observed in these mammals; (iii) the study of the regulation of the redox potential of the microenvironment, associated with mammalian spermatozoa as they transit through the epididymides, must be particularly focused on the anatomical region where ROS generation scavenging and spermatozoon maturation storage processes take place.

scholarly journals Synergistic Effects of Zn, Cu, and Ni and Bacillus Thuringiensis On the Hemocyte Count and the Antioxidant Activities of Hyphantria Cunea Drury (Lepidoptera: Arctiidae) Larvae

2021 ◽  
Author(s):  
Oğuzhan Yanar ◽  
Elif F. Topkara ◽  
Fatma G. Solmaz ◽  
Sevcan Mercan
Keyword(s):  
Superoxide Dismutase ◽  
Bacillus Thuringiensis ◽  
Glutathione Peroxidase ◽  
Antioxidant Enzyme ◽  
Enzyme Activities ◽  
Antioxidant Activities ◽  
Model Organisms ◽  
Metal Exposure ◽  
Antioxidant Enzyme Activities ◽  
Hyphantria Cunea

Abstract Insects are model organisms for immunological studies. The cellular and the antioxidant enzyme responses of insects are major bioindicators against environmental stresses (metal exposure, infection, etc.). In our study, the differences in the hemocyte counts and the antioxidant enzyme activities of Hyphantria cunea larvae exposed to the different amounts of zinc, copper, and nickel and Bacillus thuringiensis infection were determined. With metal exposure, the superoxide dismutase, catalase, and glutathione peroxidase activities increased, but the hemocyte counts decreased. Additionally, both the hemocyte counts and the enzyme activities increased with Bacillus thuringiensis infection. As a result of this study, we found that the superoxide dismutase, catalase, and glutathione peroxidase and the hemocyte counts varied in response to both metal exposure and bacterial infection.

scholarly journals Investigation of Some Antioxidant Enzyme Activities in Cherry Fruit

2019 ◽  
Vol 16 (04) ◽  
pp. 725-729
Author(s):  
Tuğba Gür ◽  
Fatih Karahan ◽  
Halit Demir ◽  
Canan Demir
Keyword(s):  
Superoxide Dismutase ◽  
Enzyme Activity ◽  
Antioxidant Enzyme ◽  
Enzyme Activities ◽  
Prunus Avium ◽  
Antioxidant Activities ◽  
Antioxidant Properties ◽  
Antioxidant Enzyme Activities ◽  
Fruit Extract ◽  
The Family

Superoxide dismutase (SOD) and catalase enzyme (CAT) activities with strong antioxidant properties were determined in cherry fruits obtained from different regions such as Aegean, Mediterranean and Marmara. The cherry fruit extract was prepared and some antioxidant activities were determined. Cherry (prunus avium) is a fruit belonging to the family of rosaceae. Its homeland is asia minor. Many varieties are grown in Turkey. There are more than a hundred culture forms grown in north america with temperate regions of europe and asia. Its body is in the form of a flat-shell tree. Cherry is a fruit rich in vitamin C. They do not contain fat and cholesterol. It contains essential minerals such as fiber, vitamin A, iron, calcium, protein as well as abundant potassium. Red cherries also contain melatonin, which helps combat harmful toxins. Due to its antioxidant properties, it has many benefits such as prevention of some types of cancer, reduction of inflammation, prevention of gout and removal of muscle pain. For this purpose, it is aimed to determine some enzyme activities which are thought to be found in cherry fruit. In this study, antioxidant enzyme activities in cherry fruit were determined by spectrophotometric method. Additonaly the findings were analyzed by using multidimensional statistical methods and the results were discussed in a multidimensional manner. It is obtained that the highest catalase enzyme activity was determined in the Aegean region (4.330 U/L), while the highest superoxide dismutase enzyme activity was found in the Mediterranean region (7.176 U/L).

scholarly journals Drought Stress Responses of Sunflower Germplasm Developed after Wide Hybridization

2016 ◽  
Vol 4 (10) ◽  
pp. 859
Author(s):  
Roumiana Dimova Vassilevska-Ivanova ◽  
Lydia Shtereva ◽  
Ira Stancheva ◽  
Maria Geneva
Keyword(s):  
Oxidative Stress ◽  
Superoxide Dismutase ◽  
Drought Stress ◽  
Antioxidant Enzyme ◽  
Ascorbate Peroxidase ◽  
Enzyme Activities ◽  
Antioxidant Enzyme Activities ◽  
Guaiacol Peroxidase ◽  
Fresh Weight ◽  
Breeding Lines

Response of sunflower germplasms viz. cultivated sunflower H. annuus and two breeding lines H. annuus x T. rotundifolia and H. annuus x V. encelioides developed after wide hybridization were used for identification of drought tolerant sunflower genotypes at the seedling growth stage. Three water stress levels of zero (control), -0.4, and -0.8 MPa were developed using polyethyleneglycol-6000 (PEG-6000). Physiological and biochemical stress determining parameters such as root and shoots length, fresh weight, antioxidant enzyme activities (superoxide dismutase (SOD), catalase (CAT), guaiacol peroxidase (GPO), ascorbate peroxidase (APX) and antioxidant metabolite content (total antioxidant capacity, total phenols and total flavonoids content) were compared between seedlings of all three genotypes. Results revealed that sunflower genotypes have similar responses at two osmotic potentials for shoot and root length and fresh weight. The data also showed that drought stresss could induce oxidative stress, as indicated by the increase level of ascorbate peroxidase and guaiacol peroxidase at -04 MPa in H. annuus cv 1114. Although the activity of ascorbate peroxidase and guaiacol peroxidase was differentially influenced by drought, the changes of antioxidant enzyme activities such as catalase, superoxide dismutase, guaiacol peroxidase, and ascorbate peroxidase subjected to drought stress follow a similar pattern in both breeding lines, indicating that similar defense systems might be involved in the oxidative stress injury in sunflowers. Increase in content of phenols and flavonoids were detected for all three genotypes under stress, which showed that these were major antioxidant metabolites in scavenging cellular H2O2.

scholarly journals The comparison of antioxidant enzyme activities in Quince Fruit (Cydonia Oblonga) grown in Van, Ankara and İzmir

2019 ◽  
Vol 6 (11) ◽  
pp. 301-304
Author(s):  
Halit Demir ◽  
Canan Demir
Keyword(s):  
Superoxide Dismutase ◽  
Antioxidant Enzymes ◽  
Glutathione Reductase ◽  
Antioxidant Enzyme ◽  
Spectrophotometric Method ◽  
Enzyme Activities ◽  
Antioxidant Property ◽  
Antioxidant Enzyme Activities ◽  
Cydonia Oblonga ◽  
The Difference

Objective: In this study, it was aimed to determine the activity of some antioxidant enzymes in the quince fruit (Cydonia Oblonga) which grown in different regions of Turkey. Materials and Methods: For this study, firstly, quince fruit grown in different provinces such as Van, Ankara and İzmir was obtained for this study. Then, extracts of quince fruit were prepared and antioxidant enzyme activities were determined by spectrophotometric method. The findings were analyzed using statistical methods and the results were interpreted. Results: The difference between the means in terms of Superoxide Dismutase, Catalase and Glutathione Reductase (SOD, CAT and GR) enzyme levels was found to be statistically significant for quince fruit grown in Van, Ankara and İzmir (p <0.05). Accordingly, CAT, SOD and GR levels in quince fruit grown in İzmir were significantly higher than other regions. Conclusion: As a result, the antioxidant property of quince fruit seems to be very important. The consumption of quince fruit especially in winter can be protective against some diseases, especially winter diseases. Further research on quince fruit should be done.

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