• 한국식품영양과학회지
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• 제46권1호
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• pp.10-17
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• 2017

본 연구는 유산균발효 마늘추출물의 간 보호 효능에 대해 천연보존료인 복합 황금추출물이 유산균발효 마늘추출물의 간 보호 효능에 미치는 영향 여부를 확인하기 위해 수행되었다. 복합 황금추출물은 $H_2O_2$에 의한 산화적 손상에 대한 유산균발효 마늘추출물의 간 보호 효능에 있어서 유의적인 영향을 미치지 않았으며, acetaminophen에 의한 급성 간 손상 동물 모델에서 시료에 첨가된 복합 황금추출물은 유산균 발효 마늘추출물의 간 손상 억제 효능에 있어 유의적인 영향을 미치지 않았다. 이상의 결과들을 종합 고찰할 때 복합황금추출물은 기능성 원료의 유효성에 영향을 미치지 않으면서 액상제형 건강기능성식품의 안전성을 확보할 수 있는 천연보존제로 판단되었다.

• 한국식품영양과학회지
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• 제41권11호
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• pp.1487-1492
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• 2012

본 연구는 치콘 추출물의 항산화 효능을 확인하고자 물과 에탄올로 추출하였다. 치콘에 포함된 총 폴리페놀 함량을 측정한 결과, 에탄올 추출물($37.3{\pm}5.2$ mg/GAE/g extract)과 열수 추출물($36.3{\pm}1.0$ mg/GAE/g extract)이 유사한 총 폴리페놀 함량을 포함하고 있었으며, 총 플라보노이드 함량은 물 추출물이 $47.0{\pm}3.8$ mg CE/g extract 그리고 에탄올 추출물이 $53.9{\pm}5.1$ mg CE/g extract를 나타내었다. ABTS를 이용한 라디칼 소거활성, FRAP를 이용한 환원력을 통한 항산화 활성을 측정한 결과에서도 치콘 추출물이 항산화 효과를 나타내었다. 한편, 세포 독성을 살펴보기 위하여 신경세포를 이용하여 MTT assay를 수행한 결과, 세포의 생존율은 1.0 mg/mL의 농도 이상에서는 생존에 영향을 미치지 않았고 신경세포 보호효능 실험에서는 2.5 mM의 $H_2O_2$로 유발시킨 산화적 손상에 대해 농도 의존적인 신경세포 보호 효과가 있었으며, 항산화 효소 활성을 SOD와 CAT로 분석한 결과 SOD는 0.5 mg/mL 농도에서 95% 이상의 활성과 CAT는 손상그룹에 비해 2배 이상의 활성을 각각 확인하였다. 또한 치콘 추출물이 세포사와 관련이 있는 단백질인 Bax와 Bcl-2의 발현을 조절하는 것을 확인하였다. 이와 같은 결과는 치콘 추출물이 산화적 손상의 억제를 통해 세포를 보호하는 효과가 있는 것으로 사료된다.

• Molecular & Cellular Toxicology
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• 제5권2호
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• pp.120-125
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• 2009

Alaria esculenta is a brown seaweed found in the Arctic. This study investigated the protective effect of A. esculenta extract (AEE) against oxidant-mediated injury and its mode of action in RAW264.7 macrophages. The methyl thiazolyl tetrazolium (MTT) assay showed that $H_2O_2$ treatment reduced cell viability, whereas AEE protected cells from $H_2O_2$-mediated cytotoxicity in a dose-dependent manner. Because heme oxygenase-1 (HO-1) is known to protect cells against oxidative damage, we investigated the effect of AEE on HO-1 gene expression and HO enzyme activity. The protective effect of AEE against $H_2O_2$-induced injury was correlated with increased HO enzyme activity. AEE also induced HO-1 mRNA and protein expression, as determined RT-PCR and Western blotting, respectively. To characterize the mechanisms by which AEE induces HO-1 gene expression, we examined the effect of AEE on the nuclear translocation of NF-E2-related factor-2 (Nrf2) and Akt phosphorylation. AEE treatment activated upstream signaling for HO-1 gene expression, including the nuclear translocation of Nrf2 and Akt phosphorylation. Collectively, these results suggest that AEE has anti-oxidant activity that is mediated, at least in part, via the activation of Nrf2 and Akt and the subsequent induction of HO-1 gene expression.

• 생명과학회지
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• 제20권2호
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• pp.161-168
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• 2010

White-skinned sweet potato (WSP, Ipomoea batatas L.)는 일본, 인도네시아 등에서 당뇨병과 그 치료에 민간에서 사용되고 있다. 본 실험에서는 WSP의 메탄올 추출물을 체중 1 kg 당 Dose 100, 200 mg을 투여하여 streptozotocin으로 유발된 당뇨쥐에서 손상된 신장 보호효과를 평가하였고 그 효능을 인슐린 분비촉진제인 glimepiride (45 mg/kg 체중)와 비교해 보았다. WSP 메탄올 추출물과 glimepiride를 2주 투여 한 후 혈당, 혈중 요소성 질소(BUN), 크레아티닌, 젖산 탈수소효소(LDH), 지질 과산화물(LPO) 함량, 그리고 항산화효소들인 superoxide dismutase (SOD), 카탈라아제(CAT), 글루타치온 과산화물 분해효소(GPx), 글루타치온 S-전이효소(GST) 등의 활성도를 측정하였다. BUN, 크레아티닌, LDH, 혈당, LPO 함량 등은 대조군에 비하여 그 값이 증가하였고, SOD, CAT, GPx, GST 값은 감소하였다. WSP 메탄올 추출물(200 mg/kg)을 투여한 후 측정한 값은 혈당, LPO, 신장병 표지인자인 BUN, 크레아티닌, LDH, 그리고 지질 과산화물 함량에서 의미있는 개선효과를 볼 수 있었고 항산화효소, 항산화물질의 증가도 나타났다. 따라서 WSP 메탄올 추출물은 당뇨쥐의 혈당을 낮추며 산화적 스트레스를 약화시키고 당뇨로 유발된 신장 손상을 보호해 주는 효과가 있다는 결과를 얻었다. 또한 민간에서 사용하고 있는 WSP가 실제로 당뇨 치료에 효과가 있음을 과학적 증거로 제공해 주었다고 판단된다.

• 환경위생공학
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• 제7권2호
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• pp.95-110
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• 1992

Much progress has been made in understanding the subcellular events of the human lung injuries after acute exposure to environmental air pollutants. Host of those events represent oxidative damages mediated by reactive oxygen species such as superoxide, hydrogen peroxide, and the hydroxy, free radical. Recently, nitric oxide (NO) was found to be endogenously produced by endothelial cells and cells of the reticulo-endothelial system as endothelialderived relaxation factor (EDRF) which is a vasoactive and neurotransmitter substance. Together with superoxide, NO can form another strong oxidant, peroxonitrite. The relative importance of exogenous sources of $N0/N0_2$ and endogenous production of NO by the EDRF producing enzymes in the oxidative stresses to the heman lung has to be elucidated. The exact events leading to chronic irreversible damage are still yet to be known. From chronic exposure to oxidant gases, progressive epithelial and interstitial damages develop. Type I epithelial cells become thicker and cover a smaller average alveolar surface area while thee II cells proliferate instead. Under acute damages, the extent of loss of the alveolar epithelial cell lining, especially type II cells appears to be a good predictor of the ensuing irreversible damage to alveolar compartment. Interstitial matrix undergo remodeling during chronic exposure with increased collagen fibers and interstitial fibroblasts. However, Inany of these changes can be reversed after cessation of exposure. Among chronic lung injuries, genetic damages and repair responses received particular attention in view of the known increased lung cancer risks from exposure to several air pollutants. Heavy metals from foundry emission, automobile traffics, and total suspended particulate, especially polycystic aromatic hydrocarbons have been positively linked with the development of lung cancer. Asbestos in another air pollutant with known risk of lung cancer and mesothelioma, but asbestos fibers are nonauthentic in most bioassays. Studies using the electron spin resonance spin trapping method show that the presence of iron in asbestos accelerates the production of the hydroxy, radical in vitro. Interactions of these reactive oxygen species with particular cellular components and disruption of cell defense mechanisms still await further studies to elucidate the carcinogenic potential of asbestos fibers of different size and chemical composition. The distribution of inhaled pollutants and the magnitude of their eventual effects on the respiratory tract are determined by pollutant-independent physical factors such as anatomy of the respiratory tract and level and pattern of breathing, as well as by pollutant-specific phyco-chemical factors such as the reactivity, solubility, and diffusivity of the foreign gas in mucus, blood and tissue. Many of these individual factors determining dose can be quantified in vitro. However, mathematical models based on these factors should be validated for its integrity by using data from intact human lungs.

• 한국식품영양과학회지
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• 제32권7호
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• pp.1076-1081
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• 2003

근육은 지속적인 수축운동 과정상에서 근육 세포내의 에너지원인 ATP가 고갈되고, 근육피로를 나타내는 물질이 축적되어 근력이 약해지고 피로도가 증가하게 된다. 지구력을 향상시키기 위하여 ATP의 합성 증가 및 근육내 피로 물질의 축적 방지 등이 요구되어지는데, 본 연구에서는 전통 생약재로부터 추출 증류한 조성물 JR-22를 이용하여 지구력 향상 효과를 확인하고자 하였다. JR-22를 4주간 실험 동물에게 투여한 이후 체중의 4-8%에 해당하는 무게를 부가하고 강제수영 시간을 통하여 지구력 향상효과를 확인한 결과 JR-22의 투여로 인하여 지구력이 향상되는 효과를 확인하였다 JR-22에 의한 지구력 향상효과의 기작을 관찰하기 위하여 체중의 4%에 해당하는 무게를 부가한 뒤 90분간 강제 수영시킨 실험 동물로부터 근육 피로 물질들과 근육내 ATP 함량을 측정한 결과 JR-22의 투여가 근육내 ATP 함량을 증가시키는 것으로 나타나 JR-22의 투여가 근육내 ATP를 증가시킴으로서 지구력을 향상시키는 효과를 나타내는 것으로 추측되었다. 또한 근육세포의 강화와 연관성이 있는 IGF-1과의 관련성을 알아보기 위하여 JR-22를 투여한 이후 혈액중의 IGF-1의 농도를 측정하였을 때도 JR-22에 의해서 유의성이 있는 IGF-1의 증가가 관찰되어 JR-22의 투여가 근력 강화에 도움을 줄 수 있다고 추측되었다. 이러한 운동 과정상에서 발생하는 체내의 산화적 손상은 JR-22의 투여를 통해 완화되고 있음을 확인하여 JR-22의 투여가 체내의 항산화력 증진에 도움을 줄 수 있는 것으로 추측되었다. 한편 JR-22를 4주 이상 투여하였을 경우에도 간독성 지표인 GOT, GPT를 비롯한 각종 혈액 생화학적 수치들의 변화가 나타나지 않았으며, 기타 이상 소견이 발견되지 않아 JR-22의 식용으로서의 안전성에도 문제가 없는 것으로 판단되었다. 이상의 결과에서 JR-22는 IGF-1의 증가 및 근육내 ATP 농도를 증가시킴으로서 지구력을 강화시키는 효과가 있을 뿐 아니라 운동시 발생하는 부작용중 하나인 산화적 손상을 억제시키는 항산화 효과 또한 겸비하고 있는 것으로 판단된다.

• 한국수정란이식학회지
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• 제32권4호
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• pp.257-265
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• 2017

Ferulic Acid (FA) is a metabolite of phenylalanine and tyrosine, a phenolic compound commonly found in fruits and vegetables. Several studies have shown that FA has various functions such as antioxidant effect, prevention of cell damage from irradiation, protection from cell damage caused by oxygen deficiency, anti-inflammatory action, anti-aging action, liver protective effect and anti-cancer action. In this study, we investigated the maturation rate, intracellular glutathione (GSH) and reactive oxygen species (ROS) of porcine oocytes by adding FA to the in vitro maturation (IVM) medium and examined subsequent embryonic developmental competence at 5% oxygen through parthenogenesis. There is no significant difference between the control group ($0{\mu}M$) and treatment groups ($5{\mu}M$, $10{\mu}M$, $20{\mu}M$) on maturation rates. Intracellular GSH levels in oocyte treated with $5{\mu}M$ of FA significantly increased (P < 0.05), and $20{\mu}M$ of FA revealed significant decrease (P < 0.05) in intracellular ROS levels compared with the control group. Oocytes treated with FA exhibited significantly higher cleavage rates (79.01% vs 89.19%, 92.20%, 90.89%, respectively) than the control group. Oocytes treated with $10{\mu}M$ showed significantly higher blastocyst formation rates (28.3% vs 40.3%, respectively) after PA than the control group. Total cell numbers in blastocyst of $10{\mu}M$ FA displayed significantly higher (39.4 vs 51.9, respectively) than the control group. In conclusion, these results suggested that treatment with FA during IVM improved the developmental potential of porcine embryos by increasing intracellular GSH synthesis and reducing ROS levels. Also, there was an improvement of cleavage rate, blastocyst formation and total cell numbers in blastocysts. It might be associated with Keap1-Nrf2 pathway as an antioxidant regulate pathway that plays a crucial role in determining the sensitivity of cells to oxidative damages by regulating the basal and inducible expression of enzymes which is related to detoxification and anti-oxidative effects, stress response enzymes and/or proteins and ABC transporters.

• 대한약리학회지
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• 제32권2호
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• pp.201-209
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• 1996

Restoration of the blood flow after a period of ischemia is accompanied by generation of toxic oxygen radicals. This phenomenon may account for the occurrence of reperfusion-mediated tissue injury in ischemic hearts. In in vitro studies, although oxygen radicals can be generated from a variety of sources, including xanthine oxidase system, activated leucocytes, mitochondria and others, the most important source and mechanism of oxygen radical production in the post-ischemic reperfused hearts is unclear. In the present study, we tested the hypothesis that the respiratory chain of mitochondria might be an important source of oxygen radicals which are responsible for the development of the reperfusion injury of ischemic hearts. Langendorff-perfused, isolated rat hearts were subjected to 30 min of global ischemia at $37^{\circ}C$, followed by reperfusion. Amytal, a reversible inhibitor of mitochondrial respiration, was employed to assess the mitochondrial contributions to the development of the reperfusion injury. Intact mitochonria were isolated from the control and the post-ischemic reperfused hearts. Mitochondrial oxygen radical generation was measured by chemiluminescence method and the oxidative tissue damage was estimated by measuring a lipid peroxidation product, malondialdehyde(MDA). To evaluate the extent of the reperfusion injury, post-ischemic functional recovery and lactate dehydrogenase(LDH) release were assessed and compared in Amytal-treated and -untreated hearts. Upon reperfusion of the ischemic hearts, MDA release into the coronary effluent was markedly increased. MDA content of mitochondria isolated from the post-ischemic reperfused hearts was increased to 152% of preischemic value, whereas minimal change was observed in extramitochondrial fraction. The generation of superoxide anion was increased about twice in mitochondria from the reperfused hearts than in those from the control hearts. Amytal inhibited the mitochondrial superoxide generation significantly and also suppressed MDA production in the reperfused hearts. Additionally, Amytal prevented the contractile dysfunction and the increased release of LDH observed in the reperfused hearts. In conclusion, these results indicate that the respiratory chain of mitochondria may be an important source of oxygen radical formation in post-ischemic reperfused hearts, and that oxygen radicals originating from the mitochondria may contribute to the development of myocardial reperfusion injury.

• Archives of Pharmacal Research
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• 제28권3호
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• pp.335-342
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• 2005

The effects of ginsenosides Rg$_3$(R) , Rg$_3$(S) and Rg$_5$/Rk$_1$ (a mixture of Rg$_5$ and Rk$_1$ 1:1, w/w), which are components isolated from processed Panax ginseng C.A. Meyer (Araliaceae), on memory dysfunction were examined in mice using a passive avoidance test. The ginsenosides Rg3(R), Rg3(S) or Rg$_5$/Rk$_1$, when orally administered for 4 days, significantly ameliorated the memory impairment induced by the single oral administration of ethanol. The memory impairment induced by the intraperitoneal injection of scopolamine was also significantly recovered by ginsenosides Rg3(S) and Rg$_5$/Rk$_1$. Among the three ginsenosides tested in this study, Rg$_5$/Rk$_1$ enhanced the memory function of mice most effectively in both the ethanol­and scopolamine-induced amnesia models. Moreover, the latency period of the Rg$_5$/Rk$_1$­treated mice was 1.2 times longer than that of the control (no amnesia) group in both models, implying that Rg$_5$/Rk$_1$ may also exert beneficial effects in the normal brain. We also evaluated the effects of these ginsenosides on the excitotoxic and oxidative stress-induced neuronal cell damage in primary cultured rat cortical cells. The excitotoxicity induced by glutamate or N­methyl-D-aspartate (NMDA) was dramatically inhibited by the three ginsenosides. Rg$_3$(S) and Rg$_5$/Rk$_1$ exhibited a more potent inhibition of excitotoxicity than did Rg$_3$(R). In contrast, these ginsenosides were all ineffective against the H$_2$O$_2$- or xanthine/xanthine oxidase-induced oxidative neuronal damage. Taken together, these results indicate that ginsenosides Rg$_3$(S) and Rg$_5$/Rk$_1$ significantly reversed the memory dysfunction induced by ethanol or scopolamine, and their neuroprotective actions against excitotoxicity may be attributed to their memory enhancing effects.

• 한국식품영양과학회지
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• 제31권1호
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• pp.81-86
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• 2002

에탄올 투여에 의한 산화적 손상에 대하여 비타민 A의 보충급여 영향을 조사하고자 흰쥐에게 AIN-76 요구량에 2배 수준으로 retinyl acetate와 $\beta$-carotene을 보충한 식이를 5주간 급여한 후 20% 에탄올 용액(3g/kg B.W)을 급성으로 복강내에 투여하였다. 그런 다음 간조직에서 생성되는 지질과산 화물 함량, 간조직에서의 관련 효소활성도와 항산화비타민의 함량을 분석한 결과는 다음과 같다. 간조직에서의 지질과 산화물 함량은 대조군에 비하여 $\beta$-carotene 공급군에서 유의적인 감소를 나타내었다. 그러나 retinyl acetate 공급군과 $\beta$-carotene 공급군 사이에서의 유의적인 차이를 나타내지 않았다. SOD 활성은 대조군에 비해 retinyl acetate 공급군이 높았고, catalase 활성과 GSH-Px 활성은 실험군 간에 유의적인 차이가 없었다. GST 활성은 에탄올만을 투영한 대조군에 비해 retinyl acetate와 $\beta$-carotene을 공급한 군에서 유의적으로 감소되었다. 간조직 내 retinol 함량은 대조군에 비해 retinyl acetate 공급군에서 유의적으로 높게 나타났으며, 이는 에탄올 급여로 인한 간조직 비타민 A의 소모를 retinyl acetate의 급여로 인해 완화시킨 것으로 여겨진다. 그러나 혈청에서는 실험군 간에 유의적인 차이가 없었다. 간조직내 $\alpha$-tocopherol의 함량은 retinyl acetate와 $\beta$-carotene 공급군에서 증가하는 경향을 나타내었다. 이상의 결과를 종합해 볼 때 금성적인 에탄올의 투여에 대해 retinyl acetate나 $\beta$-carotene을 보충 급여한 경우 항산화효소계 중 superoxide dismutase의 활성이 유도되는 경향을 보였으며, 대표적인 항산화비타민으로 알려진 $\alpha$-tocopherol의 간조직 내 수준이 증가하는 것으로 나타났다.