• 한국식생활문화학회지
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• 제31권5호
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• pp.481-488
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• 2016

The objective of this study was to investigate the antioxidant and anti-inflammatory activities of Eugenia caryophyllata Thunb. water and 70% ethanol extracts. The content of total polyphenol was significantly higher in water extract than in 70% ethanol extract. The DPPH radical scavenging activity of water extract was similar to that of Vit. C at a concentration of $1,000{\mu}g/mL$. The ABTS radical scavenging activities of water and 70% ethanol extract were similar to that of Vit. C at a concentration of $1,000{\mu}g/mL$. SOD-like activity of water extract was higher than that of 70% ethanol extract at a concentration of $1,000{\mu}g/mL$ but lower than that of Vit. C. The DPPH radical scavenging activity, ABTS radical scavenging activity, and SOD-like activity increased as concentrations of water and 70% ethanol extracts increased. Cell cytotoxicity was not observed at all concentrations except at $100{\mu}g/mL$ concentration of water extract. Inhibitory activity on NO production effect of water extract was significantly higher than that of 70% ethanol extract. These results show that E. caryophyllata Thunb. has potent biological activities, and their activities were different depending on extraction solvent.

• 생명과학회지
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• 제21권6호
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• pp.811-818
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• 2011

해조류 매생이의 기능성을 증명하기 위하여 열수 또는 에탄올 추출하여 여러 가지 생리활성에 대하여 조사하였다. 우선, 매생이 열수와 에탄올 추출물의 항산화능을 조사하기 위하여 DPPH radical 소거능, SOD 유사활성을 측정하였다. 그 결과, 매생이 열수와 에탄올 추출물의 농도가 증가함에도 불구하고 낮은 증가율을 보였는데, 10 mg/ml에서 DPPH radical 소거능은 각각 10.8, 62.4%, SOD 유사활성은 각각 13.8, 27.1%로 나타났다. 항고혈압 활성 측정에서는 1 mg/ml의 매생이 열수와 에탄올 추출물이 각각 5.9, 49.7%의 활성을 보여 비교적 높은 효능이 매생이 에탄올 추출물에서 나타났다. 매생이 열수와 에탄올 추출물의 혈당 강하 효과는 ${\alpha}$-glucosidase 저해능 분석으로 측정하였는데, 1 mg/ml 농도의 매생이 열수와 에탄올 추출물은 각각 1.4, 67.3%로써 비교적 높은 효능을 매생이 에탄올 추출물에서 보였다. 매생이의 숙취해소 효능은 ADH와 ALDH 활성증진에 매생이 열수와 에탄올 추출물이 미치는 영향을 조사함으로써 증명하고자 하였다. 그 결과, 매생이 열수와 에탄올 추출물의 농도가 증가함에도 불구하고 알콜 분해능 증가율이 낮게 나타났으며, 심지어 acetaldehyde 분해능은 관찰되지 않았다. Elastase 억제 효능 분석에서는 매생이 열수와 에탄올 추출물 10 mg/ml에서 각각 75.9, 51.2%로 나타났다.

• Toxicological Research
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• 제16권2호
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• pp.125-131
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• 2000

The ethanol extract of Rhus verniciflua Stokes (RVS), the Korean Lacquer tree, was subsequentely isolated and fractioned into two portions using distilled water (SED) and 99% ethanol (SEE) as elution buffers through silica gel column (4x28 em, 22 $\AA$. 28~200 mesh). To know the antioxidative effect of the RVS extracts, primary hepatocytes were exposed to hydroxyl radical generated by 20 mU/$m\ell$ glucose oxidase with SED or SEE for 4 hr. The addition of 100$\mu\textrm{g}$/$m\ell$ SED in culture medium showed good protection from glucose oxidase (GO)-mediated cytotoxicity of hepatocytes, showing approximately equivalent to control. When the hepatocytes were incubated with 100 $\mu\textrm{g}$/$m\ell$ SED or SEE only for 4 hr. the activities of cell-associated superoxide dismutase (SOD) and catalase were elevated up to 1.22 fold and 1.4 fold, respectively, compared to control. Further increase, 1.88fold in SOD activity or 1.64fold in catalase activity, was also observed when the hepatocytes were incubated with 100 units/$m\ell$ of commercial SOD or catalase for 4 hr. Moreover. the glucose oxidase-mediated cytotoxicity in cultured hepatocytes was generally reduced upon addition of lysate obtained from SED or SEE-stimulated hepatocytes in a dose-dependent manner. From these results, we suggest that, in cultured hepatocytes, RVS ethanol extract can efficiently reduce cytotoxicity induced by glucose oxidase and may increase the activity of cell-associated SOD and/or catalase, thereby preventing and/or scavenging superoxides and hydroxyl radicals in this experiment.

• Asian-Australasian Journal of Animal Sciences
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• 제19권9호
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• pp.1328-1334
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• 2006

This paper aimed to study the toxicity of arsanilic acid on rat primary hepatocytes in vitro by a modification of the perfusion method. The conditions included concentrations of 0, 1.085, 10.85, 108.5, 1,085 and 10,850 mg/kg arsanilic acid in RPMI 1,640 medium at rat hepatocytes plates respectively, each group had five repeats at $37^{\circ}C$ for 48 h. The rat primary hepatocytes survival ratio, DNA Ladder, activities of glutathione peroxidase (GSH-px), superoxide dismutase (SOD) and catalase (CAT) in hepatocytes, activity of SOD in the medium and the expression of gene bax in hepatocytes were measured at 12 h, 24 h and 48 h respectively. The results showed that arsanilic acid decreased the activities of GSH-px and SOD, and increased the activity of CAT in all dosages, and affected as positive DNA ladder. Although the SOD activities of both hepatocytes and medium in 1.085 mg/L arsanilic acid were significantly lower than the base line at 12 h, CAT activity in 10.85 mg/L arsanilic acid was significantly higher than the base line at 48 h, and all of the DNA ladders were positive, which means 1.085 mg/L arsanilic acid induced apoptosis at 24 h. The gene expression of bax was significantly upregulated in 1.085 mg/L arsanilic acid or higher for 24 h.The parameters in 1,085 mg/L and 10,850 mg/L arsanilic acid had more severe changes than the others at any time indicating that these levels of arsanilic acid were toxic hazards for hepatocyte survival. It was concluded that arsanilic acid induced a dosage- and time-dependent gene expression of bax, 1.085 mg/L arsanilic acid could be involved in rat liver cell apoptosis at 24 h. Arsanilic acid as additives in livestock feed could present potential toxic implications for farm animals.

• Asian-Australasian Journal of Animal Sciences
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• 제17권8호
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• pp.1162-1167
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• 2004

The present study was designed to define whether dietary conjugated linoleic acid (CLA) could affect antioxidant enzymes including superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), catalase (CAT), and glutathione S transferase (GST), and the level of malondialdehyde (MDA), a marker of lipid peroxidation, in the small intestine and liver from broiler chickens. A total of twenty-four 3 wk-old male broiler chickens were assigned to three dietary treatments (1.5% corn oil, 0.75% corn oil plus 0.75% CLA, and 1.5% CLA, isocalorically), and fed a grower-finisher diet from 22 to 35 days. In the small intestinal mucosae, the specific activities of SOD, GSH-Px, CAT, and GST, and the level of MDA were not substantially influenced by dietary CLA. In the liver, the specific activities of SOD, GSH-Px, and GST, and the level of MDA were also unaffected by dietary CLA at the level of either 0.75% or 1.5% compared with corn oil at the level of 1.5%. However, the broiler chickens fed the diet containing 1.5% CLA resulted in a significant increase in peroxisomal CAT activity and a marked decrease in total lipid and non-esterified fatty acids (NEFA) from liver tissues compared with those fed the diet containing 1.5% corn oil. In conclusion, ability of CLA to increase hepatic CAT activity suggest that dietary CLA may affect, at least in part, antioxidant defense system as well as lipid metabolism in the liver of broiler chickens.

• 미생물학회지
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• 제51권2호
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• pp.108-114
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• 2015

본 연구에서는 Streptomyces subrutilus P5의 생장과 세포내 외 철 함유 superoxide dismutase 활성을 비교 분석하여 철함유 superoxide dismutase의 분비 시점을 확인하고 분자 수준에서 이 효소의 분비에 관여하는 유전정보를 확인하고자 하였다. Streptomyces subrutilus P5의 균체 생장은 건체 중량을 측정하여 결정하였다. Glucose는 log phase에서 급격히 소모되어 24시간 후에 이르러 완전히 고갈되었다. 세포내의 철 함유 superoxide dismutase는 배양 후 3시간에 나타나며 세포외 철 함유 superoxide dismutase는 배양 후 7.5시간부터 나타난다. 따라서 superoxide dismutase는 용균에 의해서가 아니라 능동적인 분비기작에 의해서 세포 외로 분비된 것으로 추측할 수 있다. Streptomyces subrutilus P5의 sodF에는 signal peptide 유전정보가 존재하지 않았다. 그러나 sodF의 상류지역에서 다른 세균의 type III 분비단백질 유전자와 유사한 type III 분비상자가 발견되었다. Streptomyces 균주에서 type III 분비단백질이 존재할 가능성이 있음을 처음으로 제시하였다.

• 대한화장품학회지
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• 제48권3호
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• pp.275-285
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• 2022

본 연구에서는 감(Diospyros kaki)의 1,3-butylene glycol 추출물(DBG)과 에탄올 추출물(DET)를 이용하여 항산화, 항노화 및 미백 기능을 규명하였다. 항산화능은 DPPH와 superoxide dismutase (SOD) assay를 통해 규명하였으며, 그 결과 DBG와 DET 모두 현저한 DPPH 소거능 및 SOD-유사능을 보여주었다. 또한 elastase와 hyaluronidase 억제능 그리고 matrix metalloproteinase (MMP-1) 발현을 통해 항노화 기능을 규명하였다. DBG와 DET 모두 농도의존적으로 elastase와 hyaluronidase를 억제하였으며, MMP-1 발현 역시 저해하였다. 마지막으로 미백 기능을 규명하기 위하여 tyronisinase 억제 및 melanin 생성 저해능을 알아보았는데, DBG 추출물만이 tyrosinase를 저해할 수 있었다. 요약하면, 감 추출물은 강한 항산화, 항노화, 미백 기능을 갖고 있으며, 추후 화장품 소재로 활용이 가능할 것으로 사료된다.

• 한국식품과학회지
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• 제39권5호
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• pp.569-574
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• 2007

화살나무잎을 이용하여 열수추출물에 대한 항산화활성 및 생리 활성과 화살나무잎을 고온에서 덖음처리시 가열처리가 화살나무잎의 생리활성 물질에 미치는 영향을 검토하기 위해 덖음처리 한 것과 덖음처리하지 않은 시료에 대한 항산화 활성, ${\alpha}-amylase,\;{\alpha}-glucosidase$ 및 염증억제효과를 분석하였다. 화살나무잎 열수추출물에 대한 총폴리페놀 함량은 덖음처리하지 않은 시료 10.6 mg/g, 덖음 처리한 시료 9.6 mg/g로 덖음처리하지 않은 시료가 다소 높게 나타났다. DPPH 라디칼 소거능은 덖음처리 하지 않은 시료의 항산화 활성$(19.1{\mu}g/mL)$이 덖음처리한 시료$(21.9{\mu}g/mL)$보다도 좋은 활성을 보여주었다. Hydroxyl 라디칼 소거능은 덖음처리한 시료와 덖음처리하지 않은 시료, 모두 농도의 증가에 따라 hydroxyl radical이 감소하는 경향을 보여주어 농도 의존적인 저해효과를 나타냈다. SOD유사활성은 농도에 의존하는 경향을 보여주었고, 화살나무 잎의 열수추출물에 대한 대조구인 ascorbic acid의 경우, 3 mg/mL에서 52%의 SOD 유사활성을 보인 반면, 덖음처리하지 않은 시료가 20%, 덖음처리한 시료가 18%로 덖음처리하지 않은 시료가 다소 높은 SOD 유사활 성도를 나타내었다. ${\alpha}-Amylase$ 저해효과는 화살나무 잎의 열수추출물은 농도의 증가에 따라 효과가 낮아졌고, 덖음처리한 시료가 덖음처리하지 않은 것에 비해 다소 좋은 효과를 보여주었다. 그러나 ${\alpha}-glucosidase$ 저해효과에 대한 활성은 거의 없었다. 대식세포 Raw 264.7세포를 이용한 화살나무잎 열수추출물의 항염증활성 효과는 LPS로 활성화시킴과 동시에 화살나무잎 열수추출물을 첨가하고 18시간 경과한 후 생성된 NO의 양을 측정하여, 덖음처리한 시료와 덖음처리하지 않은 시료 모두에서 농도의존적인 NO 생성억제효과가 확인되었다. MIT를 이용한 화살나무잎 열수추출물의 세포생존율은 덖음처리하지 않은 시료의 경우, 열수추출물의 첨가량이 증가하여도 세포생존율이 일정하게 나타났지만, 덖음처리 한 시료는 열수추출물의 첨가량 증가와 함께 세포생존율이 감소하였다.

• Journal of Nutrition and Health
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• 제4권4호
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• pp.25-28
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• 1971

The effects of additives for food and drug upon the tryptic hydrolysis of casein an a Synthetic substrate, $N^{\alpha}-Benzoyl-L-arginine$ ethylester (BAEE) in vitro has been studied. The results of this study were summarized as follows 1) It was found that the action of inhibition became stronger in the following order: Methyl parabene>Rose Bengal> Phloxine> Sod. DHA> Erythrosine by the colorimetric method using BAEE. These results also showed that other additives had no effect on the activity of trypsin. 2) All samples tested showed respectively same tendency using casein in this method. But the activity by Erythrosine and Sod. DHA was slightly increased in this experiment.

• 한국잠사곤충학회지
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• 제42권2호
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• pp.93-98
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• 2000

This study was designed to investigate the effect of silkworm powder on oxygen radicals and their scavenger enzymes in brain membrances of SD rats. Hydroxyl radical (OH) levels resulted in a considerable decreases in brain mitochondria fraction. Superoxide radical (O$_2$) levels were a slightly decreased in brain cytosol fraction. Lipid peroxide (LPO) and Oxidized protein (OP) levels were significantly decreased in brain mitochondria and microsomes fraction. Mn-superoxide dismutase (SOD) activity was remarkably increased in the mitochondria fraction. Cu and Zn-SOD activities were effectively increased in brain cytosol fraction. GSHPx activity was considerably increased in brain cytosol fraction. These results suggest that anti-aging effect of silkworm plays an effective role in attenuating an oxidative stress and increasing a scravenger enzyme activity in brain membranes.