• Journal of Ginseng Research
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• 제12권1호
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• pp.76-86
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• 1988

쥐에게 물대신 12% 에탄올(대조군) 또는 인삼사포닌 분획을 포함한 12% 에탄올(시험군)을 6일간 투여한 후 간과 혈청에서의 acetaldehyde 농도와 간의 [$NAD^+$]/ [NADH] 및 [$NADP^+$]/[NADPH] 비율을 조사하였다. 대조군의 간과 혈청의 acetaldehyde 농도는 물로 사육한 정상군에 비해 훨씬 높았으나 물대신 인삼사포닌을 포함한 에탄올을 투여한 시험군의 경우는 정상군에 비해 약간 높았을 뿐이었으며 [$NAD^+$]/ [NADH] 비의 감소율도 대조군보다는 시험군이 훨씬 작았다. l-$^{l4}C$]-ethanol을 함유한 10% ethanol을 1ml 복강으로 투여하고 30분 후의 간의 지방질의 방사능을 분석한 결과 시험군의 간 지방질의 전체 방사능은 대조군보다 훨씬 낮았고 인산지방질, 콜레스테롤, 지방산, 중성지방과 같은 지방질의 분석결과는 에탄올 투여로 인한 인산지방질 생합성 저하와 지방산 및 중성지방의 생합성 증가현상이 인삼사포닌의 투여로 개선되는 것으로 관찰되었다.

• Bulletin of the Korean Chemical Society
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• 제34권8호
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• pp.2413-2418
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• 2013

Forensic and legal medicine require reliable data to indicate excessive alcohol consumption. Ethanol is oxidatively metabolized to acetate by alcohol dehydrogenase and non-oxidatively metabolized to ethyl glucuronide (EtG), ethyl sulfate (EtS), phosphatidylethanol, or fatty acid ethyl esters (FAEE). Oxidative metabolism is too rapid to provide biomarkers for the detection of ethanol ingestion. However, the non-oxidative metabolite EtG is a useful biomarker because it is stable, non-volatile, water soluble, highly sensitive, and is detected in body fluid, hair, and tissues. EtG analysis methods such as mass spectroscopy, chromatography, or enzyme-linked immunosorbent assay techniques are currently in use. We suggest that nuclear magnetic resonance (NMR) spectroscopy could be used to monitor ethanol intake. As with current conventional methods, NMR spectroscopy doesn't require complicated pretreatments or sample separation. This method has the advantages of short acquisition time, simple sample preparation, reproducibility, and accuracy. In addition, all proton-containing compounds can be detected. In this study, we performed $^1H$ NMR analyses of urine to monitor the ethanol and EtG. Urinary samples were collected over time from 5 male volunteers. We confirmed that ethanol and EtG signals could be detected with NMR spectroscopy. Ethanol signals increased immediately upon alcohol intake, but decreased sharply over time. In contrast, EtG signal increased and reached a maximum about 9 h later, after which the EtG signal decreased gradually and remained detectable after 20-25 h. Based on these results, we suggest that $^1H$ NMR spectroscopy may be used to identify ethanol non-oxidative metabolites without the need for sample pretreatment.

• The Korean Journal of Physiology
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• 제15권2호
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• pp.103-109
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• 1981

Ethanol 투여(投與) 용량(容量)에 따른 혈압(血壓)과 신기능(腎機能)의 변화(變化)를 알아보고자 흰쥐의 복부대동맥(腹部大動脈)에 catheter 를 삽입(揷入)하고 그 다른 끝을 목뒤로 끌어낸 후(後) 1주일(週日)이상 수술(手術)에서 회복(恢復)시킨 다음 실험(實驗)에 사용(使用)하였다. 실험직전(實驗直前)에 방광(膀胱)을 비운 뒤 metabolism cage에 넣어 안정(安靜)시킨 후(後) 60분(分)에 복부대동맥(腹部大動脈)의 catheter를 통(通)하여 평균동맥혈압(平均動脈血壓)(MAP)을 직접(直接) 측정(測定)하고 동맥혈액(動脈血液)과 뇨(尿)를 채취(採取)하였다. 곧 이어 ethanol 은 10 g% (저농도(低濃度)), 또는 30 g% (고농도(高濃度)) 용액(溶液)을, 대조실험(對照實驗)으로는 물을, 체중(體重) 100 g 당(當) 1 ml 씩 각각(各各) 경구(經口) 투여(投與)하였다. 용액투여후(溶液投與後) 3시간(時間)동안 MAP를 측정(測定)하고, 혈액(血液)은 매(每) 시간(時間)마다, 뇨(尿)는 90분(分) 간격(間隔)으로 채취(採取)하여 다음의 결과(結果)를 얻었다. 혈중(血中) ethanol 농도(濃度)는 ethanol 투여후(投與後) 1시간(時間)에 최고치(最高値)를 나타내고 (저농도(低濃度); $105.0{\pm}7.5,$ 고농도(高濃度); $214.7{\pm}20.2\;mg%$), 그후 직선적(直線的)으로 감소(減少)하였다. MAP는 물투여군(投與群)에서는 변화(變化)가 없었으나 ethanol 투여군(投與群)에서는 15분(分)부터 감소(減少)하기 시작(始作)하여 3시간(時間)동안 계속유의(繼續有意)하게 감소(減少)된 상웅(狀熊)를 나타내었다. 뇨량(尿量)은 ethanol 투여군(投與群)에서는 90분(分)동안에 유의(有意)한 증가(增加)를 보여주었고 (저농도(低濃度); $0.88{\pm}0.20{\rightarrow}1.04{\pm}0.22,$ 고농도(高濃度); $0.56{\pm}0.11{\rightarrow}1.35{\pm}0.18\;ml/1.5\;hr$), 180분(分)동안에는 뇨량(尿量)이 ethanol 투여전(投與前)보다 더 낮았다(저농도(低濃度); $0.25{\pm}0.06$, 고농도(高濃度); $0.22{\pm}0.06\;ml/1.5\;hr$). 물투여군(投與群)에서는 뇨량(尿量)이 계속(繼續) 감소(減少)하였다$(0.88{\pm}0.10{\rightarrow}0.59{\pm}0.09{\rightarrow}0.45{\pm}0.09\;ml/1.5\;hr)$. 이상(以上)의 결과(結果)는 ethanol의 혈중농도(血中濃度)가 높을수록 더 심(甚)한 혈압강하작용(血壓降下作用)을 나타내며, ethanol 로 인(因)한 이뇨작용(利尿作用)도 ethanol 량(量)이 증가(增加)함에 따라 뇨량(尿量)도 증가(增加)함을 보여 주었다.

• Journal of Nutrition and Health
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• 제31권4호
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• pp.708-715
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• 1998

Chronic abuse of alcohol can lead to the development of folate deficiency due to inadequate folate intaike, excessive urinary excretion and from effects of ethanol on folate absorption and metabolism . To investigate the effects of alcohol and folate intake on folate metabolism, the rates were raised for 4 and 10 weeks on experimental diets containing 0, 2 8mg folate/kg diet, and were administered 50% ethanol(1.8$m\ell$/kg body weight) three times a week intragastrically. Plasma and tissue folate concentrations were found to be significantly influenced by dietary folate level. In animals fed on folate-deficient diet, concentrations of folate in the plasma, liver and kidney were decreased by 60-89% compared to those on folate-adequate diet, and ther values were further decreased with experimental period. Folate supplementation increased plasma and tissue folate levels significantly by 16-78% compared to those on folate-adequate diet, and the folate levels in the plasma and liver were affected most by the supplementation. Alcohol administration did not seem to influence folate status in the body significantly when animals were raised on folate-deficient diet. However, when rats were fed folate-adequate or folate-supplemented diet, alcohol was shown to decrease plasma and tissue folate concentrations. Among the animals receiving alcohol, folate concentrations in the plasma and tissues were significantly higher when animals fed folate-supplemented diet compared to folate adequate diet. Alcohol seems to exert differential effects on urinary foalte excretion by experimental period it increased urinary folate in the 4-week period, but lowered foalte excretion in the urine when the experimental period was extended to 10 weeks. Alcohol did not seem to influence folate excretion in the feces. These results indicate that folate supplementation might be beneficial in ameliorating the inadequate folate status that might occur with chronic alcoholism.

• Nutrition Research and Practice
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• 제9권3호
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• pp.227-234
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• 2015

BACKGROUND/OBJECTIVES: We investigated the effects of a combination of grape pomace (Vitis labrusca, Campbell Early) and Omija fruit (Schizandra chinensis, Baillon) ethanol extracts on lipid metabolism and antioxidant defense system in diet-induced obese mice. MATERIALS/METHODS: Forty male C57BL/6J mice were divided into four groups and fed high-fat diet (control group, CON) or high-fat diet added 0.5% grape pomace extract (GPE), 0.05% Omija fruit extract (OFE) or 0.5% GPE plus 0.05% OFE (GPE+OFE) for 12 weeks. RESULTS: In contrast to the GPE- or OFE-supplemented groups, the GPE+OFE group showed significantly lower body weight and white adipose tissue weights than the CON group. Moreover, GPE+OFE supplementation significantly decreased plasma total cholesterol and increased the plasma HDL-cholesterol/total-cholesterol ratio (HTR) compared to the control diet. The hepatic triglyceride level was significantly lower in the GPE+OFE and GPE groups by increasing ${\beta}$-oxidation and decreasing lipogenic enzyme compared to the CON group. Furthermore, GPE+OFE supplementation significantly increased antioxidant enzyme activities with a simultaneous decrease in liver $H_2O_2$ content compared to the control diet. CONCLUSIONS: Together our results suggest that supplementation with the GPE+OFE mixture may be more effective in improving adiposity, lipid metabolism and oxidative stress in high-fat diet-fed mice than those with GPE and OFE alone.

• 한국식품영양과학회지
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• 제32권1호
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• pp.119-123
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• 2003

양파를 80% ethanol로 추출하여 Sephadek LH-20 column chromatography로 fraction I, II 및 III의 생리활성물질을 분리하여 angiotensin converting enzyme(ACE), xanthine oxidase, tyrosinase의 저해작용 효과와 지질대사를 검토하였다 Fraction I과 II의 ACE 저해작용은 50 ppm 농도에서 80% 이상의 효소 저해효과를 나타내었고 fraction III에서는 500 ppm 농도에서 90% 효소저해작용을 보였다. 100 ppm 농도에서 fraction III의 xantine oxidase 효소저해 효과는 82.5%로 나타났으며 tyrosinase의 저해효과는 42.6%이었다. 효소저해작용이 가장 강한 fraction III를 2개월 동안 고지방식이에 첨가하여 혈장 및 간장에서 지질대사에 미치는 영향을 분석한 결과 혈장에서는 총지질, 중성지질이 대조군에 비하여 유의성 있게 감소하였다. 간의 콜레스테롤량도 약 50% 정도 감소하는 결과를 얻었다.

• Journal of Microbiology and Biotechnology
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• 제34권3호
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• pp.606-621
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• 2024

This study evaluated the hepatoprotective effect of fermented Protaetia brevitarsis larvae (FPB) in ethanol-induced liver injury mice. As a result of amino acids in FPB, 18 types of amino acids including essential amino acids were identified. In the results of in vitro tests, FPB increased alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) activities. In addition, FPB treatment increased cell viability on ethanol- and H₂O₂-induced HepG2 cells. FPB ameliorated serum biomarkers related to hepatoxicity including glutamic oxaloacetic transaminase, glutamine pyruvic transaminase, total bilirubin, and lactate dehydrogenase and lipid metabolism including triglyceride, total cholesterol, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol. Also, FPB controlled ethanol metabolism enzymes by regulating the protein expression levels of ADH, ALDH, and cytochrome P450 2E1 in liver tissue. FPB protected hepatic oxidative stress by improving malondialdehyde content, reduced glutathione, and superoxide dismutase levels. In addition, FPB reversed mitochondrial dysfunction by regulating reactive oxygen species production, mitochondrial membrane potential, and ATP levels. FPB protected ethanol-induced apoptosis, fatty liver, and hepatic inflammation through p-AMP-activated protein kinase and TLR-4/NF-κB signaling pathways. Furthermore, FPB prevented hepatic fibrosis by decreasing TGF-β1/Smad pathway. In summary, these results suggest that FPB might be a potential prophylactic agent for the treatment of alcoholic liver disease via preventing liver injury such as fatty liver, hepatic inflammation due to chronic ethanol-induced oxidative stress.

• 대한본초학회지
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• 제29권4호
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• pp.77-82
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• 2014

Objectives : The effects of ethanol extract of Plantago asiatica L. were investgated on adipocyte differentiation, lipopogenesis, lipolysis and apoptosis using differnentiated 3T3-L1 adipocytes. Methods : Plantago asiatica L. was extracted with ethanol (CCE). We carried on MTT assay for cell proliferation, Oil Red O staining for determination of cell differentiation and intracelluar adipogenesis. TUNEL staining assay for cell apoptosis, and Western blot analysis for measurement of pAMPK and pACC, $C/EBP{\alpha}$, $PPAR{\gamma}$ protein expressions were performed. Results : The addition of CCE up to 0.2 mg/ml into cell culture media showed no cytotoxicity. Treatment of 0.2 mg/ml CCE significantly inhibited differentiation in 3T3-L1 preadipocytes. Lipid accumulation of the CCE treated cells was decreased compared with that of control. Induction of cell apoptosis was increased in CCE treated cells compared with that of control. AMPK and ACC levels of the cells with 0.2 mg/ml CCE were led to phosphorylation and also expressions of $C/EBP{\alpha}$ and $PPAR{\gamma}$, as adipogenic transcription factors, were suppressed compared with those of control. Conclusions : Taken together, these results provide evidence that CCE has a regulatory role in lipid metabolism that is related to differentiation into adipocytes, adipogenesis and apoptosis.

• 한방비만학회지
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• 제18권1호
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• pp.19-26
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• 2018

Objectives: Alcoholic fatty liver is a potentially pathologic condition which can progress to steatohepatitis, fibrosis, and cirrhosis. The objective of this study is to investigate the effects of Scutellaria Radix (SR) extract on the alcoholic fatty liver induced by long-term EtOH administration. Results: Male Sprague Dawley rats were used in this study. All animals were randomly divided into Normal group, treated with saline (n=10); EtOH group, treated with ethanol (n=10); EtOH+SR group, treated with ethanol+Scutellaria Radix extract (n=10). For oral administration of ethanol in EtOH and EtOH+SR group, the ethanol was dissolved in distilled water in concentrations of 25% (v/v). Throughout the experiment of 8 week, the rats were allowed free access to water and standard chow. Sample group were administrated by Scutellaria Radix extract daily for 8 weeks. Results: The levels of hepatic marker such as aspartate aminotransferase and alanine aminotransferase were altered. Histopathological changes such as ballooning, fatty and hydropic degeneration were reduced and the expression of tumor necrosis $factor-{\alpha}$ ($TNF-{\alpha}$) was significantly attenuated by Scutellaria Radix extract. Conclusions: These data suggest that Scutellaria Radix extract attenuated the alcoholic simple fatty liver by improving hepatic lipid metabolism via suppression of $TNF-{\alpha}$ protein. Scutellaria Radix could be effective in protecting the liver from alcoholic fatty liver.

• Journal of Nutrition and Health
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• 제36권8호
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• pp.801-810
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• 2003

본 연구는 만성적인 에탄올 섭취시 엽산 결핍이 체내 콜레스테롤 함량과 항산화계에 미치는 영향을 조사하고자 Sprague-Dawley종 흰쥐에게 총 열량의 36%에 해당하는 에탄올을 함유한 액체식이를 4주간 급여하였다. 본 실험에서 얻은 결과는 다음과 같다. 일일 체중증가량과 사료효율은 알코올 급여군이 각각의 pair-fed군보다 낮았고 엽산 공급의 유무에 따른 영향은 없었다. 총 콜레스테롤 함량은 엽산 결핍과 함께 에탄올을 급여시킨 ED군과 Pair-fed군인 PD군 사이에는 유의적인 차이가 없었으나 엽산과 함께 에탄올을 급여시킨 EF군이 pair-fed군인 PF군보다 유의적으로 높았다. HDL-콜레스테롤 함량과 HDL/총 콜레스테롤 함량은 전 군에서 유의적인 차이를 보이지 않았다. 혈장내 지질과산화물 함량은 엽산 결핍군인 PD와 ED군 모두 높았으며 엽산급여군에서는 에탄올을 급여한 EF군 pair-fed군인 PF군에 비해 유의적인 증가를 보여서 에탄올에 의한 지질과산화물 함량증가에 엽산 공급이 아무런 도움을 주지 못한 것으로 나타났다. 간 마이크로솜 내 지질과산화물 함량 역시 혈장내 지질과산화물 함량과 동일한 경향으로 에탄올 급여로 증가된 지질과산화물 함량에 대하여 엽산이 별다른 효과를 보이지 않았다. ADH 활성화는 전군에서 유의적인 차이가 없었고 catalase 활성도는 엽산을 결핍시킨 PD와 ED군과 에탄올 급여와 함께 엽산을 공급한 EF군이 pair-fed군인 PF군에 비해 유의적으로 높은 활성을 보였다. 간 세포질에서 SOD 활성은 전 군에서 유의적인 차이가 없었고 GSH-Px 활성은 에탄올 급여군이 각각의 pair-fed군에 비하여 유의적으로 낮은 활성을 보였으며 특히 에탄올과 함께 엽산을 공급한 EF군에서 가장 낮은 활성을 나타내었다. 그리고 GST 활성은 전 군에서 유의적인 차이를 보이지 않았다. 혈장내 retinol 함량은 엽산의 공급 유무와 상관없이 에탄올 급여군인 ED와 EF가 각각의 pair-fed군에 비하여 유의적으로 낮은 함량을 보였다. 간조직 내 retinol 함량은 엽산 결핍군에서는 에탄을 급여군인 ED군이 pair-fed군인 PD군에 비하여 유의적으로 낮은 함량을 보였으나 엽산 공급군에서는 에탄올에 의한 retnol 함량 저하에 대하여 엽산이 보호효과를 보였다. 간조직 내 retinyl palmitate 함량 역시 엽산의 공급 유무와 상관없이 에탄올 급여군이 비급여군에 비하여 유의적으로 낮은 함량을 나타내었다. 혈장내 비타민 E 함량은 엽산을 결핍시킨 군 중 에탄올 급여군인 ED군이 pair-fed군인 PD군에 비하여 유의적으로 비타민E 함량이 낮았으며 엽산을 공급시킨 군에서는 에탄올 급여군과 pair-fed군 사이에 유의적인 차이가 없었다. 이상의 결과를 통해서 볼 때 에탄올 급여시 혈장 내 콜레스테롤 함량은 엽산 섭취에 의해 증가되었으나 지질과산화물과 항산화 효소 및 항산화 영양소의 변화에 대하여 엽산결핍이 에탄올 섭취에 의해 변화된 항산화계의 손상을 더욱 가중시키는 경향이 있는 것으로 나타났다.