,d,l-a-Tocopherol (vitamin E) isfound to be synthesized by condensingtrimethylhydroquinone with isophytol catalyzed by heteropoly acids (HPA) H3:PW12O40 andH3PMo12O40 at room temperature. These HPA are efficient cata...,d,l-a-Tocopherol (vitamin E) isfound to be synthesized by condensingtrimethylhydroquinone with isophytol catalyzed by heteropoly acids (HPA) H3:PW12O40 andH3PMo12O40 at room temperature. These HPA are efficient catalysts for the synthesis of d l-a-Tocopherol and can easily be separated from the reaction mixture and roused,展开更多
Lipid peroxidation mediated by oxygen radical is one of the main mechanisms underlying secondary brain injury. Among all vitamin E compounds, α-tocopherol shows the most prominent antioxidative effects. It plays an i...Lipid peroxidation mediated by oxygen radical is one of the main mechanisms underlying secondary brain injury. Among all vitamin E compounds, α-tocopherol shows the most prominent antioxidative effects. It plays an important role in cell aging and injury. However, there has been no report regarding the effects of α-tocopherol on changes in brain tissue morphology after intracerebral hemorrhage (ICH), cerebral edema, or the expression of Bax and Bcl-2 proteins. We use SD rats to carry out the related studies;based on the atlas of SD rats, the caudate nucleus was positioned using a stereotaxic apparatus, and 50 μl autologous tail artery blood was injected to caudate nucleus in the ICH and α-tocopherol groups to establish ICH model. Rats in the sham surgery group received the same volume of saline in the caudate nucleus. Rats in the α-tocopherol group received intraperitoneal injections of α-tocopherol at 600 mg/kg every day. Rats in the ICH group and sham surgery group received the same amount of saline at the same times as those in the α-tocopherol group. We observed some interesting results: comparisons of brain tissue sections of rats from different groups showed that brain tissue damage and functional neurological deficits among rats from the α-tocopherol group were less pronounced than in the ICH group. Wet weight/ dry weight measurement showed that rats from the α-tocopherol group exhibited less cerebral edema than those in the ICH group. Rats from the α-tocopherol group showed less Bax expression and more Bcl-2 expression than those in the ICH group.展开更多
Aim: To examine the impact and prognostic significance of α-tocopherol associated protein (TAP) expression in a series of prostate cancer patients. Methods: Tissues from 87 patients underwent radical prostatectom...Aim: To examine the impact and prognostic significance of α-tocopherol associated protein (TAP) expression in a series of prostate cancer patients. Methods: Tissues from 87 patients underwent radical prostatectomy were examined for TAP expression by immunohistochemistry. The relationships of the staining results, the clinic pathological characteristics and the recurrence times were analyzed. Results: Compared with the adjacent areas of normal and benign glands, immunoreactivity of TAP was reduced in areas of prostate cancer. A lower TAP-positive cell number per mm^2 of the largest cancer area (defined as TAP-PN) was associated with higher clinical stage (r = -0.248, P = 0.0322). Inverse associations were found among the TAP-PN and positive lymph nodes (r = -0.231, P = 0.0325), preoperative prostatespecific antigen (PSA) levels (r = -0.423, P = 0.0043), tumor size (r = -0.315, P = 0.0210) and elevated tumor cell proliferation, which was indicated by the staining of Ki-67 (r = -0.308, P = 0.0026). TAP-PN was a significant predictor of recurrence univariately (P = 0.0006), as well as multivariately, adjusted for known markers including preoperative PSA, clinical stage, Gleason score, surgical margin, extra-prostatic extension, seminal vesicle invasion and lymph node metastasis (P = 0.0012). Conclusion: Reduced expression of TAP was associated with the cell proliferation status of prostate cancer, adverse pathological parameters and the increased risk of recurrence.展开更多
Objective:To investigate if the protective effect ofα-tocopherol against the impact of ethanol on brain morphogenesis involved the activity of the selenoproteins phospholipid hydroperoxide glutathione peroxidase (PHG...Objective:To investigate if the protective effect ofα-tocopherol against the impact of ethanol on brain morphogenesis involved the activity of the selenoproteins phospholipid hydroperoxide glutathione peroxidase (PHGPx;GPx4) and selenoprotein P (SelPP) that have roles against oxidative stress.Methods:Forty female mice were randomly assigned into natural control (CON), positive control (ETOH), low-, medium-, and high-α-tocopherol-supplemented-ethanol groups (LTOC, MTOC, HTOC, respectively). CON received drinking water without ethanol while ETOH, LTOC, MTOC and HTOC groups received 20% ethanol in drinking water. The supplemented groups were given respective dosages ofα-tocopherol, 0.410, 0.819, and 1.640 mg/g body weight, at day 14 before mating onwards to the day 9 of gestation. At 10.5 ED of gestation (1100 h), the pregnant females were sacrificed by cervical dislocation and the embryos were harvested. Total RNA were extracted, cDNA synthesis and qRT- PCR analyses were carried out.Results: The level of expression of PHGPx in the positive control was significantly lower than that of the natural control. Among the threeα-tocopherol-supplemented groups, only the medium dose- group was significantly higher than the positive control. The level of expression of SelPP in the positive control was significantly lower than those of the natural control, the low- and medium- dose -tocopherol supplemented groups. In the high dose-α-tocopherol supplemented group, the level of expression was not significantly different from the positive control but significantly lower than the natural control.Conclusions: The activity of the selenoproteins PHGPx and SelPP are involved in the internetwork of antioxidative enzymes with vitamin E when given up to a medium dose only and is one of the possible pathways of shielding embryonic development against the impact of ethanol on brain morphogenesis. This study strengthens the impact of dietaryα-tocopherol and Selenium supplement during the critical period of pregnancy.展开更多
Methylene blue sensitized singlet oxygen oxidation of dl-α-tocopherol in dodecylsulfate (SDS) or cetyl trimethyl ammonium brondde (CTAB) ndcelles led to the formation, besidesα-tocopherol quinone and its epoxide, of...Methylene blue sensitized singlet oxygen oxidation of dl-α-tocopherol in dodecylsulfate (SDS) or cetyl trimethyl ammonium brondde (CTAB) ndcelles led to the formation, besidesα-tocopherol quinone and its epoxide, of a hitherto unknown spiro compound 6-hydroxy-2,6,8,9-tetramethyl-2-phytyl- 1-oxaspiro [4, 5] dec -8 - en - 7, 10-dione.展开更多
A crosslinked chitosan film with α-tocopherol was produced by a solution casting method. The appearance, mechanical properties, morphology, barrier properties and release kinetics of the α-tocopherol were evaluated....A crosslinked chitosan film with α-tocopherol was produced by a solution casting method. The appearance, mechanical properties, morphology, barrier properties and release kinetics of the α-tocopherol were evaluated. The addition of glutaraldehyde and α-tocopherol decreased the lightness and greenness and increased the yellowness of the chitosan-based film. Moreover, it also affected the compatibility of the film due to a decrease in the opacity values. The elongation at break(EB) and tensile strength(TS) values of the film decreased when the glutaraldehyde and α-tocopherol were added. In contrast, the Young’s modulus(YM) values increased. SEM micrographs showed coarse spots and pores on the surface and cross-section of the film when compared with the chitosan film. Based on the results, it was indicated that the chitosan structure was disconnected by the α-tocopherol, and the glutaraldehyde as a crosslinking agent generated a link between the chitosan network, which could be the cause of the reduced flexibility and the increased surface roughness of the film. However, the glutaraldehyde and α-tocopherol did not result in a significant difference in water vapour permeability(WVP) values. The glutaraldehyde influenced the release kinetics of the α-tocopherol as seen by the decrease of the diffusion coefficient values that were calculated using the Fickian diffusion model.展开更多
Membrane damage is one of the important consequence of chromium, an environmental toxicant, to produce cytotoxicity. α-tocopherol, a membrane protectant can be used to reduce the chromium-induced membrane damage. In...Membrane damage is one of the important consequence of chromium, an environmental toxicant, to produce cytotoxicity. α-tocopherol, a membrane protectant can be used to reduce the chromium-induced membrane damage. In the present study, the impact of chromium in presence and absence of α-tocopherol was studied on plasma membrane of liver and kidney in male Wistar rats (80—100 g body weight). Significant increase in membrane cholesterol level as well as significant decrease in membrane phospholipid level in chromium exposed ( 0.8 mg /100 g body weight/d, i.p., for 4 weeks) animals suggest structural alteration of both liver and kidney plasma memebrane. The alkaline phosphatase, total ATPase and Na +-K +-ATPase activities of plasma membrane were significantly decreased in both liver and kidney after chromium treatment. However, α-tocopherol (30 mg/100 g diet) supplementation can restrict the changes in these membrane-bound enzyme activities. Thus, the usefulness of dietary supplementation of α-tocopherol to restrain the chromium-induced membrane damage is suggested.展开更多
Vitamin E is a group of naturally-occurring compounds often chemically elucidated as a series of homologues mainly consisting of α-, β-, γ- and δ-tocopherols. All of those compounds show the biological function o...Vitamin E is a group of naturally-occurring compounds often chemically elucidated as a series of homologues mainly consisting of α-, β-, γ- and δ-tocopherols. All of those compounds show the biological function of tocopherol while α-tocopherol exhibits the strongest. To improve its biological function, non-α-tocopherol can be successfully converted into α-tocopherol by methylation. A novel process was developed to efficiently convert non-α-tocopherol (in this case γ-tocopherol) into α-tocopherol by methylolation-reduction. The conversion was confirmed by NMR-H(nuclear magnetic resonance-H) spectroscopy on the final product and the reactants. The NMR-H analysis of the material and specific product contents shows that the non-α-tocopherol methylation of mixture of all four tocopherols proceeds as expected with no intermediate materials remaining in the product.展开更多
We studied the effect of the simultaneous treatment withα-tocopherol(100 mg / kg;im) and nickel sulfate (20 mg/kg,ip) on nickel-induced changes in serum lipid profiles.Nickel-treated rats showed a significant increas...We studied the effect of the simultaneous treatment withα-tocopherol(100 mg / kg;im) and nickel sulfate (20 mg/kg,ip) on nickel-induced changes in serum lipid profiles.Nickel-treated rats showed a significant increase in serum LDL cholesterol,total cholesterol,triglycerides,and a significant decrease in serum HDL cholesterol. Simultaneous administration ofα-tocopherol with nickel sulfate improved LDL-cholesterol and HDLcholesterol level when compared with rats receiving nickel sulfate alone.The results indicate thatα-tocopherol is beneficial in preventing nickel-induced lipid profile alterations.展开更多
BACKGROUND: Alpha-tocopherol ( α-tocopherol) can effectively relieve neuronal damage induced by oxygen-centered free radicals. However, the effective dose remains controversial. OBJECTIVE: To evaluate the protect...BACKGROUND: Alpha-tocopherol ( α-tocopherol) can effectively relieve neuronal damage induced by oxygen-centered free radicals. However, the effective dose remains controversial. OBJECTIVE: To evaluate the protective effects of low-concentration α-tocopherol on neuronal membranes. DESIGN, TIME AND SETTING: Contrast observation and in vitro study, performed at Laboratory of Neurosurgery, Tianjin Huanhu Hospital between April and September 2006. MATERIALS: Fetal cortical neurons were derived from two 14-day pregnant SD rats, and α-tocopherol was provided by Sigma, USA. METHODS: The neurons were randomly assigned to six groups: (1) normal: neurons were cultured under normal conditions; (2) oxidative damage: oxidative free radicals was damaged using the Fenton reaction; (3) α-tocopherol: neurons were cultured in different concentrations of -tocopherol 10, 20, 40, and 80 mg/L for 2 hours, respectively. MAIN OUTCOME MEASURES: Neuronal membrane damage was observed using a confocal laser microscope, and malonaldehyde production was detected using the thiobarbituric acid method. RESULTS: At normal, biological concentrations (10 mg/L), α-tocopherol induced no change in the damaged neurons (P 〉 0.05). However, at a concentration of 80 mg/L, the number of damaged neurons was significantly reduced, compared with the damage group (P 〈 0.05). Malonaldehyde levels following 80 mg/L α-tocopherol treatment were less than the oxygen free radical damage group (P 〈 0.05), but greater than the control group (P 〈 0.01). CONCLUSION: A concentration of 80 mg/L α-tocopherol can effectively protect the neuronal cell membrane from oxidative damage展开更多
The objectives of the present study were to identify a suitable parameter to assess the oil oxidation and to study the possibilities of delaying the oxidation of moderately oxidized unrefined almond oil by adding supp...The objectives of the present study were to identify a suitable parameter to assess the oil oxidation and to study the possibilities of delaying the oxidation of moderately oxidized unrefined almond oil by adding supplementary amounts of α-tocopherol. Three oil samples, with initial peroxide values of 13.3, 19.5 (moderately oxidized oils), and 28.9 (oxidized oil), were supplemented with 100, 250 and 500 ppm of α-tocopherol and subjected to the oxidation at 50°C for 9 days. The level of oxidation was determined by measuring peroxide value (PV), conjugated dienes (CD) and thiobarbituric acid reactive substances (TBARS). Chemometric analysis indicated that, under the conditions of the present study, PV was the most suitable indicator of oil oxidation. The results have shown that the α-tocopherol could have an anti- oxidant or pro-oxidant effects, depending on its concentration and initial level of oil oxidation. Results also show that α-tocopherol addition at all the concentrations tested resulted in pro-oxidation of the moderately oxidized oils;hence additional supplementation with α-tocopherol could not be recommended to delay oxidation of unrefined almond oil.展开更多
Alginate capsules containing α-tocopherol were prepared adding polysaccharide species such as κ-carrageenan, gellan gum, pectin, curdlan and ghatti gum. The effects of polysaccharide species and the diameters of α-...Alginate capsules containing α-tocopherol were prepared adding polysaccharide species such as κ-carrageenan, gellan gum, pectin, curdlan and ghatti gum. The effects of polysaccharide species and the diameters of α-tocopherol on storage stability of the capsules were investigated and characterized in detail. As the contact angle of α-tocopherol to the capsule shell strongly affected storage stability, the contact angle was measured on the model sheet made of calcium alginate with polysaccharide species. The leakage ratio decreased with the contact angle and increased with the diameter of α-tocopherol. The capsules made of calcium alginate with gellan gum showed the largest contact angle and the highest storage stability. The capsules made of calcium alginate with curdlan, ghatti gum and pectin were harder than other capsules and showed higher storage stability. All the capsules showed the almost similar swelling ratio in the acidic solution with pH 4, but showed the different swelling ratios according to the polysaccharide species in the alkali solution with pH 9. The tablets were prepared with the wet and the dried capsules. The tablets prepared with the dried capsules showed higher storage stability.展开更多
文摘,d,l-a-Tocopherol (vitamin E) isfound to be synthesized by condensingtrimethylhydroquinone with isophytol catalyzed by heteropoly acids (HPA) H3:PW12O40 andH3PMo12O40 at room temperature. These HPA are efficient catalysts for the synthesis of d l-a-Tocopherol and can easily be separated from the reaction mixture and roused,
文摘Lipid peroxidation mediated by oxygen radical is one of the main mechanisms underlying secondary brain injury. Among all vitamin E compounds, α-tocopherol shows the most prominent antioxidative effects. It plays an important role in cell aging and injury. However, there has been no report regarding the effects of α-tocopherol on changes in brain tissue morphology after intracerebral hemorrhage (ICH), cerebral edema, or the expression of Bax and Bcl-2 proteins. We use SD rats to carry out the related studies;based on the atlas of SD rats, the caudate nucleus was positioned using a stereotaxic apparatus, and 50 μl autologous tail artery blood was injected to caudate nucleus in the ICH and α-tocopherol groups to establish ICH model. Rats in the sham surgery group received the same volume of saline in the caudate nucleus. Rats in the α-tocopherol group received intraperitoneal injections of α-tocopherol at 600 mg/kg every day. Rats in the ICH group and sham surgery group received the same amount of saline at the same times as those in the α-tocopherol group. We observed some interesting results: comparisons of brain tissue sections of rats from different groups showed that brain tissue damage and functional neurological deficits among rats from the α-tocopherol group were less pronounced than in the ICH group. Wet weight/ dry weight measurement showed that rats from the α-tocopherol group exhibited less cerebral edema than those in the ICH group. Rats from the α-tocopherol group showed less Bax expression and more Bcl-2 expression than those in the ICH group.
文摘Aim: To examine the impact and prognostic significance of α-tocopherol associated protein (TAP) expression in a series of prostate cancer patients. Methods: Tissues from 87 patients underwent radical prostatectomy were examined for TAP expression by immunohistochemistry. The relationships of the staining results, the clinic pathological characteristics and the recurrence times were analyzed. Results: Compared with the adjacent areas of normal and benign glands, immunoreactivity of TAP was reduced in areas of prostate cancer. A lower TAP-positive cell number per mm^2 of the largest cancer area (defined as TAP-PN) was associated with higher clinical stage (r = -0.248, P = 0.0322). Inverse associations were found among the TAP-PN and positive lymph nodes (r = -0.231, P = 0.0325), preoperative prostatespecific antigen (PSA) levels (r = -0.423, P = 0.0043), tumor size (r = -0.315, P = 0.0210) and elevated tumor cell proliferation, which was indicated by the staining of Ki-67 (r = -0.308, P = 0.0026). TAP-PN was a significant predictor of recurrence univariately (P = 0.0006), as well as multivariately, adjusted for known markers including preoperative PSA, clinical stage, Gleason score, surgical margin, extra-prostatic extension, seminal vesicle invasion and lymph node metastasis (P = 0.0012). Conclusion: Reduced expression of TAP was associated with the cell proliferation status of prostate cancer, adverse pathological parameters and the increased risk of recurrence.
基金De La Sale University-University Research Coordination OficeUniversity Science Foundation(USF)under project#43FU/S309 and partly from the Department of Science and Technology.
文摘Objective:To investigate if the protective effect ofα-tocopherol against the impact of ethanol on brain morphogenesis involved the activity of the selenoproteins phospholipid hydroperoxide glutathione peroxidase (PHGPx;GPx4) and selenoprotein P (SelPP) that have roles against oxidative stress.Methods:Forty female mice were randomly assigned into natural control (CON), positive control (ETOH), low-, medium-, and high-α-tocopherol-supplemented-ethanol groups (LTOC, MTOC, HTOC, respectively). CON received drinking water without ethanol while ETOH, LTOC, MTOC and HTOC groups received 20% ethanol in drinking water. The supplemented groups were given respective dosages ofα-tocopherol, 0.410, 0.819, and 1.640 mg/g body weight, at day 14 before mating onwards to the day 9 of gestation. At 10.5 ED of gestation (1100 h), the pregnant females were sacrificed by cervical dislocation and the embryos were harvested. Total RNA were extracted, cDNA synthesis and qRT- PCR analyses were carried out.Results: The level of expression of PHGPx in the positive control was significantly lower than that of the natural control. Among the threeα-tocopherol-supplemented groups, only the medium dose- group was significantly higher than the positive control. The level of expression of SelPP in the positive control was significantly lower than those of the natural control, the low- and medium- dose -tocopherol supplemented groups. In the high dose-α-tocopherol supplemented group, the level of expression was not significantly different from the positive control but significantly lower than the natural control.Conclusions: The activity of the selenoproteins PHGPx and SelPP are involved in the internetwork of antioxidative enzymes with vitamin E when given up to a medium dose only and is one of the possible pathways of shielding embryonic development against the impact of ethanol on brain morphogenesis. This study strengthens the impact of dietaryα-tocopherol and Selenium supplement during the critical period of pregnancy.
文摘Methylene blue sensitized singlet oxygen oxidation of dl-α-tocopherol in dodecylsulfate (SDS) or cetyl trimethyl ammonium brondde (CTAB) ndcelles led to the formation, besidesα-tocopherol quinone and its epoxide, of a hitherto unknown spiro compound 6-hydroxy-2,6,8,9-tetramethyl-2-phytyl- 1-oxaspiro [4, 5] dec -8 - en - 7, 10-dione.
基金Supported by Tianjin Science and Technology Planning Project(No.18PTSYJC00140)
文摘A crosslinked chitosan film with α-tocopherol was produced by a solution casting method. The appearance, mechanical properties, morphology, barrier properties and release kinetics of the α-tocopherol were evaluated. The addition of glutaraldehyde and α-tocopherol decreased the lightness and greenness and increased the yellowness of the chitosan-based film. Moreover, it also affected the compatibility of the film due to a decrease in the opacity values. The elongation at break(EB) and tensile strength(TS) values of the film decreased when the glutaraldehyde and α-tocopherol were added. In contrast, the Young’s modulus(YM) values increased. SEM micrographs showed coarse spots and pores on the surface and cross-section of the film when compared with the chitosan film. Based on the results, it was indicated that the chitosan structure was disconnected by the α-tocopherol, and the glutaraldehyde as a crosslinking agent generated a link between the chitosan network, which could be the cause of the reduced flexibility and the increased surface roughness of the film. However, the glutaraldehyde and α-tocopherol did not result in a significant difference in water vapour permeability(WVP) values. The glutaraldehyde influenced the release kinetics of the α-tocopherol as seen by the decrease of the diffusion coefficient values that were calculated using the Fickian diffusion model.
文摘Membrane damage is one of the important consequence of chromium, an environmental toxicant, to produce cytotoxicity. α-tocopherol, a membrane protectant can be used to reduce the chromium-induced membrane damage. In the present study, the impact of chromium in presence and absence of α-tocopherol was studied on plasma membrane of liver and kidney in male Wistar rats (80—100 g body weight). Significant increase in membrane cholesterol level as well as significant decrease in membrane phospholipid level in chromium exposed ( 0.8 mg /100 g body weight/d, i.p., for 4 weeks) animals suggest structural alteration of both liver and kidney plasma memebrane. The alkaline phosphatase, total ATPase and Na +-K +-ATPase activities of plasma membrane were significantly decreased in both liver and kidney after chromium treatment. However, α-tocopherol (30 mg/100 g diet) supplementation can restrict the changes in these membrane-bound enzyme activities. Thus, the usefulness of dietary supplementation of α-tocopherol to restrain the chromium-induced membrane damage is suggested.
文摘Vitamin E is a group of naturally-occurring compounds often chemically elucidated as a series of homologues mainly consisting of α-, β-, γ- and δ-tocopherols. All of those compounds show the biological function of tocopherol while α-tocopherol exhibits the strongest. To improve its biological function, non-α-tocopherol can be successfully converted into α-tocopherol by methylation. A novel process was developed to efficiently convert non-α-tocopherol (in this case γ-tocopherol) into α-tocopherol by methylolation-reduction. The conversion was confirmed by NMR-H(nuclear magnetic resonance-H) spectroscopy on the final product and the reactants. The NMR-H analysis of the material and specific product contents shows that the non-α-tocopherol methylation of mixture of all four tocopherols proceeds as expected with no intermediate materials remaining in the product.
基金Defence Institute of Physiology and Allied Sciences,New Delhi,DRDO,Ministry of Defence,Government of India No.TC/ 260/ TASK- 91(KKD) / DIPAS/2004 dt.07/06/2004.
文摘We studied the effect of the simultaneous treatment withα-tocopherol(100 mg / kg;im) and nickel sulfate (20 mg/kg,ip) on nickel-induced changes in serum lipid profiles.Nickel-treated rats showed a significant increase in serum LDL cholesterol,total cholesterol,triglycerides,and a significant decrease in serum HDL cholesterol. Simultaneous administration ofα-tocopherol with nickel sulfate improved LDL-cholesterol and HDLcholesterol level when compared with rats receiving nickel sulfate alone.The results indicate thatα-tocopherol is beneficial in preventing nickel-induced lipid profile alterations.
基金Supported by:the 211 Key Subject Construction Foundation of Tianjin,No. 05YFGD5F02500
文摘BACKGROUND: Alpha-tocopherol ( α-tocopherol) can effectively relieve neuronal damage induced by oxygen-centered free radicals. However, the effective dose remains controversial. OBJECTIVE: To evaluate the protective effects of low-concentration α-tocopherol on neuronal membranes. DESIGN, TIME AND SETTING: Contrast observation and in vitro study, performed at Laboratory of Neurosurgery, Tianjin Huanhu Hospital between April and September 2006. MATERIALS: Fetal cortical neurons were derived from two 14-day pregnant SD rats, and α-tocopherol was provided by Sigma, USA. METHODS: The neurons were randomly assigned to six groups: (1) normal: neurons were cultured under normal conditions; (2) oxidative damage: oxidative free radicals was damaged using the Fenton reaction; (3) α-tocopherol: neurons were cultured in different concentrations of -tocopherol 10, 20, 40, and 80 mg/L for 2 hours, respectively. MAIN OUTCOME MEASURES: Neuronal membrane damage was observed using a confocal laser microscope, and malonaldehyde production was detected using the thiobarbituric acid method. RESULTS: At normal, biological concentrations (10 mg/L), α-tocopherol induced no change in the damaged neurons (P 〉 0.05). However, at a concentration of 80 mg/L, the number of damaged neurons was significantly reduced, compared with the damage group (P 〈 0.05). Malonaldehyde levels following 80 mg/L α-tocopherol treatment were less than the oxygen free radical damage group (P 〈 0.05), but greater than the control group (P 〈 0.01). CONCLUSION: A concentration of 80 mg/L α-tocopherol can effectively protect the neuronal cell membrane from oxidative damage
文摘The objectives of the present study were to identify a suitable parameter to assess the oil oxidation and to study the possibilities of delaying the oxidation of moderately oxidized unrefined almond oil by adding supplementary amounts of α-tocopherol. Three oil samples, with initial peroxide values of 13.3, 19.5 (moderately oxidized oils), and 28.9 (oxidized oil), were supplemented with 100, 250 and 500 ppm of α-tocopherol and subjected to the oxidation at 50°C for 9 days. The level of oxidation was determined by measuring peroxide value (PV), conjugated dienes (CD) and thiobarbituric acid reactive substances (TBARS). Chemometric analysis indicated that, under the conditions of the present study, PV was the most suitable indicator of oil oxidation. The results have shown that the α-tocopherol could have an anti- oxidant or pro-oxidant effects, depending on its concentration and initial level of oil oxidation. Results also show that α-tocopherol addition at all the concentrations tested resulted in pro-oxidation of the moderately oxidized oils;hence additional supplementation with α-tocopherol could not be recommended to delay oxidation of unrefined almond oil.
文摘Alginate capsules containing α-tocopherol were prepared adding polysaccharide species such as κ-carrageenan, gellan gum, pectin, curdlan and ghatti gum. The effects of polysaccharide species and the diameters of α-tocopherol on storage stability of the capsules were investigated and characterized in detail. As the contact angle of α-tocopherol to the capsule shell strongly affected storage stability, the contact angle was measured on the model sheet made of calcium alginate with polysaccharide species. The leakage ratio decreased with the contact angle and increased with the diameter of α-tocopherol. The capsules made of calcium alginate with gellan gum showed the largest contact angle and the highest storage stability. The capsules made of calcium alginate with curdlan, ghatti gum and pectin were harder than other capsules and showed higher storage stability. All the capsules showed the almost similar swelling ratio in the acidic solution with pH 4, but showed the different swelling ratios according to the polysaccharide species in the alkali solution with pH 9. The tablets were prepared with the wet and the dried capsules. The tablets prepared with the dried capsules showed higher storage stability.