Antioxidant vitamin supplementation focuses one's attention on the prevention of age-related diseases. This study was conducted to investigate the antioxidant status and lipid profiles and to look into the antioxidant vitamin supplementation that affects lipid metabolism in 20 elderly non-smoking Korean women (placebo group: n = 6, vitC suppl: n = 7, vitE suppl: n = 7). Age, height, weight, muscle, percent of fat and WHR were not significantly different among the groups, however % of fat was above 33% and WHR was above 0.9. And blood pressure of the placebo group was 131.7/81.7 (border line hypertension), that of vitamin C supplement was 141.4/87.1 (hypertension) and that of vitamin E supplement was 151.4/92.9 (hypertension). Although nutrient intakes of all groups were poor, antioxidant status (blood vitamins C, E, A, and beta-carotene) and lipid profile (TG, total-cholesterol, VLDL-cholesterol, LDL-cholesterol, HDL-cholesterol) were normal. For nutritional intervention, the vitamin C supplement group received L-ascorbic acid 1,000 mg, and vitamin E supplement group received d-alpha-tocopherol 400IU for 4 weeks, showing the effects of vitamin E supplementation. Response total cholesterol of HDL-cholesterol (T-Chol/HDL) in vitamin E supplement group was significantly decreased from 4.3 to 3.2. And response LDL-cholesterol of HDL-cholesterol (LDL/HDL) in the vitamin E supplement group was also significantly decreased from 2.6 to 1.7. In addition, after the adjustment for plasma lipids (TG, total cholesterol), plasma vitamin A levels in vitamin E supplement group were significantly increased from 7.89 mg/g to 14.91 mg/g. And systolic blood pressure in vitamin E supplement group was significantly reduced. These results suggested that vitamin E supplementation affects the lipid profiles and blood pressure in elderly non-smoking women. So various nutrition programs must be implemented against age-related diseases and further studies are needed regarding sorts and amounts of antioxidant nutrients and supplementation periods.
Aged* ; Ascorbic Acid ; Blood Pressure ; Cholesterol ; Female ; Humans ; Lipid Metabolism ; Plasma ; Vitamin A ; Vitamin E ; Vitamins

PURPOSE: To evaluate whether alterations in plasma vitamin A and E levels in patients with psoriasis have an effect on tear film changes. METHODS: Sixty-two eyes of 31 patients with psoriasis vulgaris (Group A) and 74 eyes of 37 age- and gender-matched control subjects (Group B) were included in the study. Ocular and medical histories and dietary habits were obtained from each patient. The tear film break-up time (TBUT), the Schirmer 1 test results and plasma vitamin A and E levels were evaluated. RESULTS: The mean Schirmer 1 test score was 14.76 +/- 6.12 mm/5 min in Group A and 15.69 +/- 3.10 mm/5 min in Group B. The mean plasma levels of vitamins A and E in Groups A and B were 1.86 +/- 0.62 micromol/L and 1.88 +/- 0.65 micromol/L vs. 26.21 +/- 5.13 micromol/L and 27.19 +/- 8.89 micromol/L, respectively. The Schirmer 1 test results and plasma vitamin A and E levels were not found to be significantly different between the groups (p > 0.05). The mean TBUT was 9.94 +/- 6.18 seconds in Group A and 14.47 +/- 5.65 seconds in Group B, a significant difference (p < 0.05). No correlation existed between plasma vitamin A and E levels, TBUT or the severity and duration of the disease (p > 0.05). CONCLUSIONS: Plasma vitamin A and E levels do not seem to be related to tear film changes in patients with psoriasis vulgaris.
Adolescent ; Adult ; Female ; Humans ; Male ; Middle Aged ; Mucins/*metabolism ; Psoriasis/*metabolism ; Tears/*metabolism ; Vitamin A/*blood ; Vitamin E/*blood ; Young Adult

Alpha-tocopherol transfer protein (alpha-TTP) is a liver cytosolic transport protein that faciliates alpha-tocopherol (alpha-T) transfer into liver secreted plasma lipoproteins. Genetic defects in alpha-TTP, like dietary vitamin E deficiency, are associated with infertility, muscular weakness and neurological disorders. Both human and alpha-TTP deficient (alpha-TTP-/-) mice exhibit severe plasma and tissue vitamin E deficiency that can be attenuated by sufficient dietary alpha-T supplementations. In this review, we summarize the literature concerning studies utilizing the alpha-TTP-/- mice. Levels of vitamin E in the alpha-TTP-/- mice do not appear to be directly related to the amounts of dietary alpha-T or to the levels of alpha-TTP protein in tissues. The alpha-TTP-/- mice appear to present a good model for investigating the specific role of alpha-T in tissue vitamin E metabolism. Furthermore, alpha-TTP-/- mice appear to be useful to elucidate functions of alpha-TTP beyond its well recognized functions of transferring alpha-T from liver to plasma lipoprotein fractions.
alpha-Tocopherol* ; Animals ; Cytosol ; Humans ; Infertility ; Lipoproteins ; Liver ; Metabolism ; Mice ; Mice, Knockout* ; Muscle Weakness ; Nervous System Diseases ; Plasma ; Vitamin E ; Vitamin E Deficiency ; Vitamins

The Protective effect of vitamin E and selenium against peroxidative damage in white blood cells was studied. Forty-eight male rats (~100g BW) were divided into four groups and were fed with a torula yeast based diet deficient in Vit.E and Se. Vit.E (100IU/Kg diet) and Se (0.3ppm) supplementation increased the total peritoneal cell (P.C) population and cell survival rate. Selenium supplementation decreased the hydrogen peroxide generation (half of the control) significantly and Vit.E supplementation reduced the malonaldehyde production during phagocytosis in vitro. However, superoxide generation was not affected by the supplementation of Vit.E or Se. There were no significant differences in catalase activity between groups but glutathione peroxidase activity was increased about twofold by Se supplementation with no effect of Vit.E. In a separate experiment, activated alveolar macrophages were obtained from BCG infected rabbits fed a diet supplemented with Vit.E (100 IU/Kg diet) or Se (0.3 ppm). Se supplementation increased glutathione peroxidase in cells, and both Vit.E and Se increased the cell survival rate during phagocytosis as compared to the control. Both Vit.E and Se are necessary to protect host cells from peroxidative damage during phagocytosis.
Animal ; Macrophages/drug effects ; Macrophages/physiology* ; Male ; Peroxides/metabolism* ; Phagocytosis/drug effects* ; Rats ; Selenium/pharmacology* ; Vitamin E/pharmacology*

Animals ; Apolipoproteins E ; deficiency ; Female ; Hyperlipoproteinemia Type III ; blood ; metabolism ; Lipid Metabolism, Inborn Errors ; blood ; metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Receptors, Calcitriol ; metabolism ; Vitamin D ; blood

AIMTo observe the expression of Presenilin-1 (PS-1) and production of amyloid beta-protein (Abeta) in hippocampus of female senile rats and to investigate the effect of vitamin E(VE) on preventing Alzheimer's disease after menopause.

METHODSThe animal model was established using female senile rats. Experimental groups (n=8) were respectively given different doses of VE(5 mg/kg, 15 mg/kg, 60 mg/kg) per day. The expression of PS-1 in hippocampus was detected by immunohistochemistry, the level of Abeta in hippocampus was measured by Radioimmunoassay, and neuronal ultrastructure in hippocampal DG area was observed using transmission electron microscope.

RESULTSThe expression of PS-1 in rat hippocampus of senile control group was stronger than that of adult control group. PS-1 expressed weakly in three medication groups along with augmentation of dosage. The levels of Abeta were found to correlate statistically with the expression of PS-1. The content of Abeta in VE groups was significantly decreased compared to that in senile control group (P < 0.01). There were some changes in the neuronal ultrastructure of senile rats. Neurons were gradually recovered in VE groups.

CONCLUSIONVE may depress the production of Abeta by regulating the expression of PS-1, reducing neuronal injuries. VE may play a role in neuronal protection.

Aging ; Alzheimer Disease ; metabolism ; Amyloid beta-Peptides ; metabolism ; Animals ; Female ; Hippocampus ; drug effects ; metabolism ; Presenilin-1 ; metabolism ; Rats ; Rats, Wistar ; Vitamin E ; pharmacology

OBJECTIVETo investigate oxidative stress in chronic hepatitis B (CHB) patients with elevated serum total bilirubin (TBIL).

METHODS75 CHB patients with elevated serum TBIL were enrolled in the present study. A, B, C, D and E group were defined. Serum Malondialdehyde (MDA), Xanthine Oxidase (XOD), Vitamin C (V(C)) and Vitamin E (V(E)) were determined. The control group contained 11 healthy donors and the carrier group contained 16 Hepatitis B surface antigen (HBsAg) carriers.

RESULTSThe concentrations of MDA and XOD were significantly higher in each group of patients than in the control (P < 0.05), while V(C) and V(E) were significantly lower (P < 0.05). The concentration of XOD was significantly higher in the carrier group than in the control (P < 0.05), while MDA, V(C) and V(E) were not significantly different (P > 0.05). The concentrations of MDA and XOD were significantly positively correlated with TBIL (r = 0.670, P < 0.01; r = 0.737, P < 0.01, respectively) in the patients, while V(C) and V(E) were significantly negatively correlated with TBIL (r = -0.463, P < 0.01; r = -0.247, P < 0.05, respectively). The concentration of MDA was significantly different among all the groups in the patients except the comparison between group A and group B. The concentration of XOD was significantly different between group A, B, C and group D, E (P < 0.05). The concentration of V(C) was significantly different between group A and group D, E and between group B, C, D and group E (P < 0.05). The concentration of V(E) was significantly different between group A, B and group E (P < 0.05).

CONCLUSIONThere was a disturbance between oxidative stress and anti-oxidative ability in CHB patients with elevated serum TBIL. Oxidative stress became more serious along with the increasing of serum TBIL. In HBsAg carriers, oxidative stress level was low. The results suggest antioxidant treatment for CHB patients with elevated serum TBIL may help to improve the effect of therapy.

Adolescent ; Adult ; Bilirubin ; blood ; Female ; Hepatitis B, Chronic ; blood ; metabolism ; Humans ; Male ; Malondialdehyde ; metabolism ; Middle Aged ; Oxidative Stress ; physiology ; Reactive Oxygen Species ; metabolism ; Vitamin E ; metabolism ; Young Adult

OBJECTIVETo investigate the dynamic changes of lipoprotein lipase (LPL) expression in the hippocampus of epileptic rats and to study its effect on vitamin E levels in rats following status epilepticus (SE).

METHODSRat model of SE was induced by intraperitoneal injection of pilocarpine. The rats receiving an injection of normal saline were used as a control group. The expression of LPL in the hippocampal tissue was determined using immunofluorescent methods and the level of vitamin E was examined by the colormeric method 12 hrs, 24 hrs, 3 days, 7 days and 14 days after SE.

RESULTSLPL was expressed in the control and SE groups. In the SE group, the LPL expression began to increase 24 hr after SE (P<0.05), reached a peak 3 days after SE (P<0.01), and kept at a high level 7 days after SE (P<0.01). By 14 days, the LPL expression was reduced to the level similar to the control group. The level of vitamin E began to decline 12 hrs after SE (P<0.01), and decreased to a nadir 24 hrs after SE (P<0.01). At 3 and 7 days after SE, the levels of vitamin E were still significantly lower than the controls (P<0.05). By 14 days, the vitamin E level increased to the level similar to the control group.

CONCLUSIONSThe over-expression of LPL in the hippocampus may play an important role in the oxidative stress mechanisms following SE by regulating the uptake of vitamin E.

Animals ; Fluorescent Antibody Technique ; Hippocampus ; metabolism ; Lipoprotein Lipase ; analysis ; physiology ; Male ; Oxidative Stress ; Rats ; Rats, Sprague-Dawley ; Status Epilepticus ; metabolism ; Vitamin E ; analysis ; metabolism

OBJECTIVETo investigate the potential protective effect of water-soluble vitamin E (Trolox) against oxidative stress injury in post-thawing human sperm and its mechanism.

METHODSSemen samples from 16 fertile men were mixed with modified cryoprotectant and each sample was equally divided into groups 0 (G0), 1 (G1), 2 (G2) and 3 (G3) according to the concentration of Trolox measured by computer-assisted semen analysis (CASA). G0, with no Trolox in the mixed cryoprotectant, served as the control, while G1, G2 and G3 contained 50, 100 and 200 micromol/L of Trolox, respectively. Before and after thawing, the semen samples were subjected to CASA for sperm kinematics, flow cytometry for reactive oxygen species (ROS), and thiobarbituric acid assay for the concentration of malondialdehyde (MDA).

RESULTSAfter cryopreservation, sperm motility was markedly decreased in all the groups (P < (0.01), but less in G2 than in the control ([53.33 +/- 5.63]% vs [47.85 +/- 5.09]%, P < 0.05). Curvilinear velocity and average path velocity were remarkably higher in G2 (P < 0.05), and ROS and MDA significantly lower in G2 and G3 than in the control (P < 0.05).

CONCLUSIONAddition of vitamin E (Trolox) to freezing extender at a moderate concentration may decrease surplus ROS in the freezing-thawing process, ease ROS-induced oxidative stress injury to the plasma membrane, and improve sperm motility and kinematic parameters after cryopreservation.

Antioxidants ; pharmacology ; Cryopreservation ; Humans ; Male ; Oxidative Stress ; drug effects ; Reactive Oxygen Species ; metabolism ; Semen ; drug effects ; metabolism ; Semen Preservation ; Vitamin E ; pharmacology

OBJECTIVETo investigate the effect of Vitamin E (VitE) on memory and brain monoaminergic neurotransmitter level in chronic episodic hypoxia (EHYP) rat.

METHODSVitE [50 IU/ (250 g.d) or 5 IU/ (250 g.d)] was given to the EHYP rat model. The memory was evaluated by the passive avoidance test and the levels of monoaminergic neurotransmitter, including norepinephrine (NE), dopamine (DA) and 5-hydroxytryptamine (5-HT), were determined in three different brain regions (including cerebral cortex, hippocampus and striatum) using high performance liquid chromatography and electrochemical detection (HPLC-ECD).

RESULTSThe performance on passive avoidance test of EHYP rats was worse than that of controlled rats (P < 0.01). The performance of rats in two different treatment groups was better than that of EHYP rats (P < 0.05), the performance of rats in high-dose group was worse than that of rats in low-dose group (P < 0.05). Compared with controlled rats, levels of monoaminergic neurotransmitters in different brain regions of EHYP rats decreased significantly (P < 0.05). Compared with EHYP rats, level of NE and DA in cerebral cortex and level of monoamine (NE, DA, and 5-HT) in hippocampus and striatum of low-dose treated rats were increased significantly (P < 0.05). Different with low-dose treated rats, only level of monoamine (NE, DA, and 5-HT) in striatum and level of 5-HT in hippocampus in high-dose treated rats were increased significantly (P < 0.05), as compared with the EHYP rats.

CONCLUSIONSvitE can improve memory and increase brain monoaminergic neurotransmitter of EHYP rats. Moreover, the effect of low-dose vitE is better than that of high-dose VitE.

Animals ; Avoidance Learning ; Biogenic Monoamines ; metabolism ; Brain ; metabolism ; Dopamine ; metabolism ; Ischemic Attack, Transient ; metabolism ; physiopathology ; Male ; Memory ; drug effects ; Norepinephrine ; metabolism ; Rats ; Rats, Sprague-Dawley ; Serotonin ; metabolism ; Vitamin E ; pharmacology