• 한국식품과학회지
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• 제4권4호
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• pp.245-251
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• 1972

BHA (0.05%), ascorbic acid (0.1%) 그리고. BHA (0.05%)+ascorbic acid (0.1%)를 각각 첨가시킨 감자튀김을 여러 조건하에서 저장할 때 이들 BHA, As.A 및 BHA+As. A의 상대적인 산패억제 효과를 비교 관찰하였다. 즉 감자튀김을 암소(暗所)에서 $33{\pm}0.5^{\circ}C$로 저장하였을 때는 감자튀김의 산패억제에 대한 BHA의 효과는 매우 컸다. Ascorbic acid도 상당한 항산화 효과를 보였으나 BHA 보다는 약하였으며, 한편 BHA와 ascorbic acid를 동시에 처리하였을 때에는 그 효과는 BHA 단독의 경우와 거의 같았다. 투명, 무색 Polypropylene film으로 덮은 감자튀김을 하루 6시간씩 일사광선에 조사(照射)시키면서 저장하였을 때는 BHA의 항산화력은 상당히 감소되었으며, 한편 ascorbic acid의 항산화력은 거의 완전히 상실되었다. 그러나 황색으로 착색된 투명 polypropylene film을 대신 사용하였을 경우에는 BHA는 그 항산화력을 상당히 잘 유지하였다. 한편, ascorbic acid는 이와 같은 조건하에서도 그 항산화력을 거의 상실하였다.

• 한국환경과학회지
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• 제17권10호
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• pp.1139-1146
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• 2008

To investigate the functional properties and the antioxidant effect of pine needle(Pinus densiflora), the pine needle extract was obtained with methanol and its functionality was measured by spectrophotometric method, and the antioxidant experiment on soybean oil was carried out by the active oxygen method. The extraction yield of pine needle with 99% methanol was about 19%, the total flavonoid content of the pine needle-methanol extract was 11.32 mg/g on dry basis and the superoxide dismutase-like activity was 94.3%. The nitrite scavenging ability of the extract was pH dependent with the values of 77.44% at pH 1.2, 48.45% at pH 3.0 and 11.04% at pH 6.0, respectively. The peroxide value was 92.6 meq/kg at 5% dosage, 138.4 meq/kg at 2% dosage of the extract on 8 oxidation days. The period of the peroxide value to be 100 mg/kg was 4.9, 6.3 and 8.5 days at control, 2% and 5% dosage of extract, respectively. And the relative antioxidant effectiveness of the extract was 27.9% and 72.3% increase at 2% and 5% dosage, respectively, compared to control. The thiobarbituric acid value showed few differences within 4 oxidation days, but with the dosage of the extract it fairly decreased with considerable antioxidant effect to control above 4 days.

• Journal of Nutrition and Health
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• 제30권9호
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• pp.1102-1108
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• 1997

The purpose of this study was to find the extent of lipid peroxidation of erythrocytes in cigarette smokers, and to determine the relative effectiveness of $\beta$-carotene, canthaxanthin , and $\alpha$-tocopherol as antioxidants. Thirty smokers and 30 nonsmokers participated in this study . No significant differences according to age, sex, and height were shown. Cigarette smokers in this study had higher hemoglobin concentrations and more oxidation of hemoglobin than non-smokers. In addition, the erythrocytes of cigarette smokers had significantly higher MDA concentrations than crythrocytes of nonsmokers, which suggests that smokers may have tocopherol were studied in vitro by measuring the concentration of malondialdehyde(MDA) and precent hemolysis of erythrocytes. The addition of any antioxidant to erythrocytes significantly decreased MDA concentrations(p<0.05) while antioxidants showed nonsignificant inhibition of hemolysis. Among the antioxidant used in this study, canthaxanthin showed the greatest inhibition of both lipid peroxidationand hemolysis. Meanwhile, $\alpha$-tocopherol showed potent inhibition of lipid peroxidation, but not of hemolysis.

• Nutritional Sciences
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• 제9권4호
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• pp.288-294
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• 2006

In this study, the effects of smoking cessation and relative antioxidant activities on the oxidative stress were determined by using in vitro method. Thirty healthy smokers who were free of any disease and smoked more than 1 pack per day for the past 10 years participated in this study. For smoking cessation, smokers were asked to wear nicotine patch (21mg nicotine/ patch) everyday for 30 days and then to replace at the same time of the day. Smoking cessation program in conjunction with nicotine patch replacement was also conducted every week, one hour/each session, for 4 weeks. Canthaxanthin, $\beta-carotene$, and $\alpha-tocopherol$ were added into red blood cells at pre and post smoking cessation. As indicators of oxidative stress, hemoglobin degradation, lipid peroxidation, and percent hemolysis were determined at both pre and post smoking cessation. After 30 days of smoking cessation, the subjects gained an average of 5 pounds, varying 2 to 8 pounds, by suggesting that behavioral problems rather than nicotine itself are more important for gaining weight in ex-smokers. The total hemoglobin concentrations in blood were similar in pre and post smoking cessation, but smoking cessation resulted in a decrease in the percentage of methemoglobin from 0.96% to 0.85% Smoking cessation also caused to decease malondialdehyde (MDA) values ($26.7{\pm}7.8$ vs. $23.6{\pm}4.5$ (without oxidation), $179.3{\pm}21$ vs. $161.2{\pm}28$ nmol/ml (with oxidation) (p<0.05)), not percent hemolysis. Various antioxidants with smoking cessation significantly decreased MDA values(p<0.05), in contrast to marginal decrease of MDA in smoking cessation only. Three antioxidants used in this stu study were similarly effective in inhibiting MDA production, but relative effectiveness of canthaxanthin or $\alpha-tocopherol$ was greater than that of $\beta-carotene$ (p<0.05), in case of oxidation induced. The percent hemolysis was greatly decreased when antioxidants were added into the blood of ex-smokers (p<0.05) but no statistical significance in relative effectiveness of antioxidants was observed.

• 한국식품조리과학회지
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• 제10권1호
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• pp.63-70
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• 1994

Oleoresin, 6-gingerol and 6,10-gingerol: 6-paradol= 1 : 1 mixture were extracted from ginger (Zingi-her of ficinale Roscoe) and changes of its antioxidant activity by heat-treatment were studed. Oleoresin was extracted with Ethanol-Ether and 6,10-gingerol : 6-paradol(1 : 1) and 6-gingerol were extracted with Hexane and Hexan : Ether= 1 : 1, respectively, and identified on the Thin-layer Chromatograpy (TLC) plate with the solvent system of Hexane Ether(1 : 4, v/v). And oleoresin was heat-treated during 0, 10, 30, 60, 120 minutes, and 6-gingercl and 6,10-gingerol . 6-paradol=1 : 1 were heat-treated during 0, 5, 10, 20, 40 minutes, respectively, at 140$^{\circ}C$ dry oven. To compare with antioxidant activity, oleoresins were added into soybean oil at 3fo level, 6-gingerol and 6,10-gingerol : 6-paradol= 1 : 1 at 0.1% level, BHT and TBHQ at 0.02% level, respectively. All the substrates treated were stored in a incubator at 45 2$^{\circ}C$ condition. The oxidative stability was estimated by the analysises of peroxide value and conjugated diene value during storage. The results were as follows: Antioxidant activity of oleoresins were considerably high and by heat-treatment were not decreased. 6-paradol was not show the antioxidant activity. 6,10-gingerol : 6-paradol=1 : 1 provided poor protection for soybean oil. Antioxidant activity of 6-gingerol was higher than 6,10-gingerol : 6-paradol=1 : 1 and by heat-treat-ment antioxidant activity was directly decreased. Relative antioxidant effectiveness(RAE) of each antio-xidant was compared. RhR was found to decrease as follow : TBHQ>oleoresin》BHT TBHQ》BHT>6-gingerol》6,10-gingerol : 6-paradol=1 : 1.

• 한국식품조리과학회지
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• 제9권4호
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• pp.298-302
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• 1993

항산화제가 첨가되지 않은 유지의 $85^{\circ}C$저장중에 과산화물가 측정에 의한 유도기간은 어유, 대두유, 돈지 및 팜유에 대하여 5.0, 17.0, 38.4 및 57.6시간으로 어유의 산화가 가장 먼저 일어났다. Gingerol이 첨가된 각 유지의 상대적항산화 효과는 돈지,대두유, 어유 및 팜유에 대하여 219, 176, 160 및 146%로 나타나 gingerol은 돈지의 산화를 가장 안정시켰으며, 대두유 및 어유에 대하여 BHT보다 산화를 안정시켰다.

• 동아시아식생활학회지
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• 제4권3호
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• pp.97-102
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• 1994

The oxidative stability of perilla oil were examined by measuring peroxide value. The induction period of perilla oil for each storage temperature was measured by POV and indicated that it was 80 days for 45$^{\circ}C$, 22.5 days for 65$^{\circ}C$, 9.5 days for 85$^{\circ}C$ and 5 days for 105$^{\circ}C$ respectively. Also, the induction period of the perilla oil with different concentration of ginger powder at 85$^{\circ}C$was studied and has been found that 9.4 days for 6% ginger powder, 11.9 days for 4% and 11days for 2% ginger power. The relative antioxidant effectiveness of ginger power was 99% for 6% ginger power, 125% for 4% ginger power, 122% for 2% ginger power. The induction period of perilla oil with gingerol at 85$^{\circ}C$ was 13.5days for 2% crude gingerol, 11.7days for 0.2% crude gingerol and 12.0 days for 0.02% BHT. The elativi antroxidant effectiveness of perilla oil gingerol at 85$^{\circ}C$was 142% for 2% crude gingerol, 123% for 0.2% crude gingerol, 126% for 0.02% BHT.

• 한국식품조리과학회지
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• 제10권2호
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• pp.121-125
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• 1994

Gingerol, BHT 및 tocopherol이 첨가된 대두유의 산화중에 gingerol 첨가군이 45~105$^{\circ}C$ 모든 온도에서 대두유의 산화를 안정시켰으며,무첨가군의 유도기간은45, 65, 85 및 105$^{\circ}C$에서 276.0 48.0, 17.0 및 4.7시간으로, 특히 45$^{\circ}C$에서 $65^{\circ}C$로 온도 상승에 따른 유도기간의 차이가 큰 것으로 나타났다. Gingrol의 상대적 항산화효과는 45, 65, 85 및 105$^{\circ}C$에서 191, 200, 176 및 181%로서 45~105$^{\circ}C$ 온도 범위에서는 지속적인 항산화 효과를 보였으며, 반면 BHT는 174, 150, 132 및 106%로서 105$^{\circ}C$에서는 상대적항산화 효과가 감소됨을 나타냈다. 한편, gingerol, BHT 및 tocopherol이 첨가된 대두유의 산화중에 온도의 영향을 반응속도론적 측면에서 해석하기 위하여, Arrhenius 방정식, 찰성화 에너지(Ea) 및 온도계수(Q10)를 구한 결과, 대두유의 산화 반응속도는 45~$65^{\circ}C$ 범위에서 활성화 에너지가 높은 것으로 나타나 반응속도가 급격히 가속화되는 경향이 있었으며 첨가된 항산화제의 종류에 따라서도 활성화 에너지의 차이를 보여서 산화 반응속도에 영향을 주는 것으로 나타났다. BHT가 첨가된 대두유는 105$^{\circ}C$가까이에서 급속히 활성화 에너지가 높아져서 온도의 영향을 받아 반응속도가 증가된 반면 gingerol은 비교적 온도의 영향을 받지 않는 것으로 보여진다.

• 동아시아식생활학회지
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• 제9권1호
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• pp.100-106
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• 1999

본 연구는 참죽나무 잎의 기능성을 검토하기 위하여 참죽나무 잎 용매 추출물의 항산화 효과를 합성항산화제인 BHA $\alpha$-tocopherol의 항산화 효과와 비교하였다. 본 실험에서 얻어진 결과를 요약하면 다음과 같다. 1. 참죽나무잎 추출물을 0.1M linoleic acid에 농도별(0.02, 0.1, 0.5, 1 및 3%)로 첨가한 것을 5$0^{\circ}C$에서 20시간 항온 저장시 기존의 항산화제와 비교하여 항산화력은 참죽나무 잎 methanol추추물(CME) 3%＞참죽나무 잎 methanol 추출물 1%＞ BHT 0.02%＞참죽나무 잎 ethyl acetate 추출물(CEAC) 3%＞CME 0.5%＞$\alpha$-tocopherol 0.02%＞CME 0.1과 0.02%＞CEAC 1, 0.5, 0.1 및 0.02%＞대조군 순으로 CME 1%가 BHT 0.02%보다도 높은 항산화력을 보였으나, CME 0.5%와 CEAC에서는 CME 1%와 3%에 비해 약간 낮은 항산화 효과를 보였다. 2. CME를 첨가한 대두유를 60$\pm$1$^{\circ}C$에서 30일간 항온저장시 항산화 효과는 CME 1%＞BHT 0.02%＞CME 3%＞$\alpha$-tocopherol 0.02%＞대조군 순이었으며, CME l% 항산화 효과는 BHT보다 더 우수하였다. 3. CME의 상대적 항산화력(RAE)는 CME 1% 첨가시료가 가장 높은 항산화 효과를 보였다.

• Journal of Nutrition and Health
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• 제36권9호
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• pp.908-917
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• 2003

It has been proposed that oxidative modification of LDL (oxLDL) plays a significant role in the pathogenicity of atherogenesis. We tested the hypothesis that chitin and chitosan may function as antioxidants with respect to 0.1 mg cholesterol/ml LDL incubated with 5 $\mu$ M Cu$^2$$^{+}$alone or in the P338Dl mouse macrophage system using L-ascorbic acid as a standard classical antioxidant. The degree of oxLDL formation was ascertained by the relative electrophoretic mobility (rEM) in the combination of thiobarbituric acid reactive substances (TBARS) levels, and the cytotoxicity of oxLDL was detected by macrophage viability. The oxLDL uptake and foam cell formation of macrophages were measured by Oil Red O staining. Incubation with Cu$^2$$^{+}$and macrophages increased rEM of LDL and stimulated TBARS formation. Culture of macrophages with LDL in the presence 5 $\mu$ M Cu$^2$$^{+}$induced macrophage death. In cell-free system 200 $\mu$g/ml water-soluble chitosan and chitosan-oligosaccharide blocked oxLDL formation. Water-soluble chitosan and chitosan-oligosaccharide blocked oxLDL formation near-completely relative to L-ascorbic acid, whereas water-soluble chitin and chitin-oligosaccharide had no measurable antioxidant effect. In macrophage system water-soluble chitosan and chitosan-oligosaccharide blocked oxidation of LDL with a significant increase in cell viability, and decreased TBARS in medium. As for the inhibitory effect on macrophage foam cell formation, chitosan and its oligosaccharide, but not watersoluble chitin, revealed the effectiveness. The endothelial expression of lectin-like oxLDL receptor-1 (LOX-1) was tested by Western blot analysis, and chitosan, chitosan-oligosaccharide and chitin-oligosaccharide blocked LOX-1 expression. These results indicate that water-soluble chitosan and its oligosaccharide showed the inhibitory effect on Cu$^2$$^{+}$-induced LDL oxidation of macrophages, and chitosan, chitosan-oligosaccharide and chitin-oligosaccharide had blocking effect on oxLDL receptor expression in the human umbilical vein endothelial system. Thus, water-soluble chitosan and its oligosaccharides possess anti-atherogenic potentials possibly through the inhibition of macrophage LDL oxidation or endothelial oxLDL receptor expression depending on chemical types.l types.