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1.
Climacteric ; 18(3): 379-88, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25236970

ABSTRACT

OBJECTIVE: This cross-sectional study aimed to evaluate the behavior of blood antioxidant enzymes (superoxide dismutase (SOD), catalase and glutathione peroxidase), plasma total antioxidant capacity and oxidative damage (lipid oxidation and protein carbonyl levels) and their relationship with the serum levels of steroid hormones in premenopausal and postmenopausal women without and with estrogen alone (ET) or estrogen plus progestin therapy (EPT). METHODS: Blood was collected from four groups of subjects: premenopausal women (n = 24), postmenopausal women without hormone therapy (n = 31), postmenopausal women with ET (n = 12) and postmenopausal women with EPT (n = 16). RESULTS: The activities of the different SOD isoforms (CuZnSOD and MnSOD) and the plasma total antioxidant power were significantly higher in the postmenopausal women under EPT than in the postmenopausal women without hormone replacement therapy (HRT). Only CuZnSOD activity was increased in women receiving ET compared to the postmenopausal women without HRT. However, no differences were observed in the levels of lipid or protein oxidation or in the non-enzymatic plasma antioxidants (uric acid and albumin) among the groups. The duration of HRT and serum estrogen levels were positively correlated to the blood CuZnSOD activity and to plasma total antioxidant power, whereas the serum progesterone levels were positively correlated to CuZnSOD activity and negatively correlated to protein carbonyl groups. Interestingly, the total antioxidant power of plasma was positively correlated to CuZnSOD and glutathione peroxidase activities. CONCLUSION: We conclude that EPT increases blood MnSOD and CuZnSOD activity in postmenopausal women, leading to an increased plasma total antioxidant capacity. This finding may be relevant to the prevention of oxidative stress-related disorders in postmenopausal women.


Subject(s)
Antioxidants/metabolism , Estrogen Replacement Therapy/methods , Estrogens/therapeutic use , Postmenopause/blood , Progestins/therapeutic use , Superoxide Dismutase/blood , Adult , Aged , Catalase/blood , Cross-Sectional Studies , Estradiol/blood , Female , Glutathione Peroxidase/blood , Humans , Middle Aged , Oxidation-Reduction , Premenopause/blood
2.
Free Radic Res ; 47(3): 219-32, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23297859

ABSTRACT

This study aimed to evaluate whether natural or synthetic steroid hormones could directly modulate the activity of the different superoxide dismutase (SOD) isoforms found in human blood fractions without changing enzyme expression. Enzyme samples of human erythrocytes, the human platelet-rich plasma fraction (PRP) or isolated CuZnSOD, which was purified from human erythrocytes were pre-incubated with natural steroids (17ß-estradiol 17-acetate and progesterone) and their synthetic derivatives (ß-estradiol 3-benzoate and medroxyprogesterone 17-acetate). Then, CuZn and MnSOD activities were measured using the xanthine/xanthine oxidase/nitroblue tetrazolium method. Hormones had no effect on MnSOD activity from the PRP, but we show for the first time that natural and synthetic steroid hormones have a direct, bell-shaped effect on the activity of CuZnSOD from both male and female human erythrocytes. Low (physiological) hormone concentrations caused a dose-dependent increase in enzyme activity, which disappeared at higher hormone concentrations. In addition, the combination of synthetic and natural estrogens and progestins had a synergistic stimulatory effect on the activity of CuZnSOD from human erythrocytes. The molecular interaction between CuZnSOD and steroid hormones was preliminarily studied. Natural hormones did not change the electrophoretic mobility of SOD under denaturing conditions, but they did increase the absorption spectra of SOD in the 230-290 nm range. These data suggest that hormone-mediated modulation of CuZnSOD is related to subtle changes in protein conformation, possibly related to Trp and Phe residues. We propose that this effect may account for the physiological regulation of enzyme activity during conditions where steroid hormones undergo alterations as the ovulatory cycle.


Subject(s)
Erythrocytes/enzymology , Estradiol/analogs & derivatives , Medroxyprogesterone Acetate/pharmacology , Superoxide Dismutase/blood , Adult , Enzyme Assays , Erythrocytes/drug effects , Estradiol/chemistry , Estradiol/pharmacology , Estradiol/physiology , Female , Humans , Isoenzymes/blood , Isoenzymes/chemistry , Male , Medroxyprogesterone Acetate/chemistry , Progesterone/chemistry , Progesterone/pharmacology , Progesterone/physiology , Protein Binding , Superoxide Dismutase/chemistry , Superoxide Dismutase-1 , Young Adult
3.
Hum Exp Toxicol ; 30(8): 981-91, 2011 Aug.
Article in English | MEDLINE | ID: mdl-20876162

ABSTRACT

Dietary fiber can affect cadmium (Cd) absorption and toxicity, but the effect appears to depend on the type of dietary fiber. The aim of the present study was to compare the effect of dietary sources containing distinct amounts of soluble and insoluble fiber on Cd absorption, accumulation and toxicity in growing rats. The absorption of essential macrominerals (Ca, P and Mg) was also evaluated. Animals received a nutritionally balanced diet with cellulose (cel - control), wheat bran or flaxseed as the fiber source with 0 or 50 mg Cd kg(-1) diet, during 30 days. Cd exposure reduced body weight gain, feed efficiency ratio, epididymal fat relative weight and liver relative weight, and increased plasma alanine aminotransferase activity in all fiber groups. The apparent Cd absorption was similar among Cd-groups, but the flax-Cd group had a higher hepatic and renal Cd concentration. Cd decreased the absorption of Ca and P, and increased Mg absorption in the wheat bran and flaxseed groups, but not in the cel group. Although the different fiber sources investigated had no effect on Cd toxicity, the major soluble fiber source, flaxseed, increased Cd retention. Thus, caution should be taken in the intake of flaxseed by Cd-exposed populations.


Subject(s)
Cadmium Chloride , Dietary Fiber/therapeutic use , Environmental Pollutants , Flax/chemistry , Plant Preparations/therapeutic use , Seeds/chemistry , Absorption , Animals , Body Weight/drug effects , Cadmium Chloride/pharmacokinetics , Cadmium Chloride/poisoning , Cadmium Poisoning/diet therapy , Cadmium Poisoning/metabolism , Environmental Pollutants/pharmacokinetics , Environmental Pollutants/poisoning , Kidney/drug effects , Kidney/metabolism , Kidney Function Tests , Liver/drug effects , Liver/metabolism , Liver Function Tests , Male , Organ Size/drug effects , Plant Preparations/chemistry , Rats , Rats, Wistar , Solubility
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