• 제목/요약/키워드: ALDH1A3

검색결과 78건 처리시간 0.033초

매생이 추출물의 angiotensin converting enzyme 및 α-glucosidase 활성 저해 효과 (Inhibitory Effects of Maesaengi (Capsosiphon fulvescens) Extracts on Angiotensin Converting Enzyme and α-Glucosidase)

  • 조은경;유슬기;최영주
    • 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.

황기(黃芪)의 재배 년수에 따른 면역 및 항산화 활성 연구 (Studies on Immunomodulatory and Antioxidant Activities of Astragali membranacei Radix according to the Cultivated Years)

  • 정철
    • 대한한방피부미용학회지
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    • 제1권1호
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    • pp.53-90
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    • 2005
  • Purpose: Contents of astragaloside I, II and IV, cytotoxicity, anticancer activity, immunomodulatory activity and antioxidant capacity were to be compared as a function of the cultivated years as one, three, five and seven years. Method: Major components of Astragali membranacei Radix were separated as astragaloside I, astragaloside II, astragaloside IV by HPLC analysis. Cytotoxicity and anticancer activities were measured by MTT and SRB assay. For immunomodulatory activity, the secretion of IL -6 and $TNF-{\alpha}$, NK cell activation and macrophage activation were observed as well as kinetics of responding to human T cells by a microphysiometer. In vitro antioxidant activities were measured by several radical scavenging activities of superoxide anion radican, DPPH, LDL and linoleic acid. For in vivo activity, the activation of SOD, GSH-px, catalase, ALDH and ADH was measured as well the relative weight of liver. Result : 1. For HPLC analysis, the contents of all of astragaloside I, astragaloside II, astragaloside IV were in order of three, five, one and seven years. 2. The cytotoxicity of normal human lung cell line, HEL299 showed lower than 18% in adding 0.25 mg/ml, and 28.9% in adding 1.0 mg/ml of water extract of seven year root. For methanol extracts, three year root showed highest cytotoxicity as 35.2 % and there was no difference between the cultivated years. 3. For anticancer activities, methanol extracts of one and three year roots showed relatively high inhibition of human stomach cancer cells, AGS, breast cancer cells, MCF-7, lung cancer cells, A549 and liver cancer cell, Hep3B as well as high selectivities. 4. The water extract of seven year root could yield high secretion of IL-6 from both human Band T cells while the methanol extracts of three and five year roots secreted high amounts of IL-6 and $TNF-{\alpha}$ from both Band T cells. 5. As a result of in vitro antioxidant activities, both water and methanol extracts from five and seven year roots showed high activities for superoxide anion radical scavenging activity, inhibiting linoleic acid peroxide and contents of total phenols. 6. For in vivo tests, Mn-SOD and GSH-px activities and weight of liver were better in adding seven year root. For ALDH activity one year root was better and for ADH activity five year root. Overall speaking, seven year root showed relatively better antioxidant activities. Conclusion:There was difference of the contents of astragaloside I, astragaloside II, astragaloside IV according to cultivation year. Methanol extract showed better activities of anticancer and immune activation rather than water extract Interestingly enough, for methanol extracts, overall activities were improved as the cultivation year increased. There might be further investigation required for the clinical uses of the results as several biological activities varied according to the cultivated year of Astragali membranacei Radix.

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흑마늘 추출물이 알코올을 투여한 흰쥐에 미치는 영향 (Effects of Aged Black Garlic Extract on Ethanol Induced Hangover in Rats)

  • 양승택
    • 생명과학회지
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    • 제20권2호
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    • pp.225-230
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    • 2010
  • 본 연구에서는 숙취용 음료를 개발하기 위하여 알코올을 투여한 흰쥐를 대상으로 흑마늘 추출물 130 mg/kg과 260 mg/kg을 각각 40% 알코올(5 g/kg, B.W.) 투여 30 분 전과 30 분 후에 경구 섭취시키고 1, 3 및 5 시간 동안 경시적으로 혈액 중의 알코올 및 아세트알데히드 농도와 간조직 중의 alcohol dehydrogenase (ADH) 및 acetaldehyde dehydrogenase (ALDH)의 활성과 간지표 효소인 alanine aminotransferase (ALT) 및 aspartate aminotransferase (AST)의 활성을 측정하였다. 알코올 투여 30 분 전에 흑마늘 추출물을 경구 섭취시켰을 때 혈 중 알코올의 농도는 시간 경과에 따라 급격하게 감소하였으며 알코올 투여 후 5 시간 경과 시 알코올 투여 대조군에 비하여 흑마늘 추출물 투여군이 28.5%로 감소하는 경향을 나타내었다. 또한 혈 중 아세트알데히드의 농도는 알코올 대조군에 비하여 흑마늘 추출물 투여군이 매우 감소하였다. 알코올 투여 30 분 후 흑마늘 추출물을 투여한 것은 알코올 투여 30 분 전의 실험군과 비슷한 경향을 나타내었다. 간 조직중의 ADH 활성은 정상군과 흑마늘 추출물 투여군 모두 큰 변화는 찾아 볼 수 없었으나 ALDH의 활성은 약간의 차이를 확인할 수 있었다. 혈청 ALT, AST 활성은 대조군과 흑마늘 추출물 간에 유의적인 차이는 나타내지 않았으나, 흑마늘 추출물의 섭취가 간 기능에 나쁜 영향을 미치지 않는 결과로 보아 안전성이 있다고 사료된다.

Genes Frequently Coexpressed with Hoxc8 Provide Insight into the Discovery of Target Genes

  • Kalyani, Ruthala;Lee, Ji-Yeon;Min, Hyehyun;Yoon, Heejei;Kim, Myoung Hee
    • Molecules and Cells
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    • 제39권5호
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    • pp.395-402
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    • 2016
  • Identifying Hoxc8 target genes is at the crux of understanding the Hoxc8-mediated regulatory networks underlying its roles during development. However, identification of these genes remains difficult due to intrinsic factors of Hoxc8, such as low DNA binding specificity, context-dependent regulation, and unknown cofactors. Therefore, as an alternative, the present study attempted to test whether the roles of Hoxc8 could be inferred by simply analyzing genes frequently coexpressed with Hoxc8, and whether these genes include putative target genes. Using archived gene expression datasets in which Hoxc8 was differentially expressed, we identified a total of 567 genes that were positively coexpressed with Hoxc8 in at least four out of eight datasets. Among these, 23 genes were coexpressed in six datasets. Gene sets associated with extracellular matrix and cell adhesion were most significantly enriched, followed by gene sets for skeletal system development, morphogenesis, cell motility, and transcriptional regulation. In particular, transcriptional regulators, including paralogs of Hoxc8, known Hox co-factors, and transcriptional remodeling factors were enriched. We randomly selected Adam19, Ptpn13, Prkd1, Tgfbi, and Aldh1a3, and validated their coexpression in mouse embryonic tissues and cell lines following $TGF-{\beta}2$ treatment or ectopic Hoxc8 expression. Except for Aldh1a3, all genes showed concordant expression with that of Hoxc8, suggesting that the coexpressed genes might include direct or indirect target genes. Collectively, we suggest that the coexpressed genes provide a resource for constructing Hoxc8-mediated regulatory networks.

흰쥐에서 어성초 열수 추출물을 포함한 혼합물의 숙취해소 효과 (Effect of Mixture Including Hot Water Extract of Houttuynia cordata Thunb on Ethanol-Induced Hangover in Rats)

  • 유양희;이현미;정창식;이민재;전우진
    • 한국식품영양과학회지
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    • 제45권10호
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    • pp.1508-1512
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    • 2016
  • 어성초 열수 추출물, 연잎 열수 추출물, 녹차씨 70% 에탄올 추출물의 혼합물인 MIX가 흰쥐에서 에탄올 투여에 따른 혈중 에탄올 및 아세트알데히드 농도와 에탄올 대사 효소들에 작용하는 효과와 직접적인 에탄올 대사 효소 활성에 미치는 영향을 확인하여 신규 숙취해소 소재로서 MIX의 활용 가능성을 연구하였다. 급성 에탄올을 투여한 EtOH군과 MIX-200군은 혈중 에탄올 농도가 에탄올을 투여하지 않은 NC군보다 높게 나타났고, MIX-200군은 EtOH군에 비교해 혈중 에탄올 농도가 에탄올 투여 3시간부터 감소하였고, 혈중 아세트알데히드의 농도는 에탄올 투여 1시간 이후부터 감소하였다. 에탄올과 아세트알데히드를 분해하는 효소인 ADH와 ALDH의 활성은 MIX-200군에서 EtOH군보다 높게 나타났다. 또한, MIX는 높은 alcohol dehydrogenase 및 acetaldehyde dehydrogenase 활성을 나타내었다. 따라서 MIX는 에탄올 대사 효소들의 활성 증가에 직 간접적으로 작용해 알코올 섭취 후 혈중 알코올 및 아세트알데히드를 감소시키는 숙취해소 작용을 갖는 신규 식품 소재로 사용될 수 있을 것으로 생각한다.

Aqueous extract of Laurus nobilis leaf accelerates the alcohol metabolism and prevents liver damage in single-ethanol binge rats

  • Jae In Jung;Yean-Jung Choi;Jinhak Kim;Kwang-Soo Baek;Eun Ji Kim
    • Nutrition Research and Practice
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    • 제17권6호
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    • pp.1113-1127
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    • 2023
  • BACKGROUND/OBJECTIVES: Excessive alcohol consumption has harmful health effects, including alcohol hangovers and alcohol-related liver disease. Therefore, methods to accelerate the alcohol metabolism are needed. Laurus nobilis is a spice, flavoring agent, and traditional herbal medicine against various diseases. This study examined whether the standardized aqueous extract of L. nobilis leaves (LN) accelerates the alcohol metabolism and protects against liver damage in single-ethanol binge Sprague-Dawley (SD) rats. MATERIALS/METHODS: LN was administered orally to SD rats 1 h before ethanol administration (3 g/kg body weight [BW]) at 100 and 300 mg/kg BW. Blood samples were collected 0.5, 1, 2, and 4 h after ethanol administration. The livers were excised 1 h after ethanol administration to determine the hepatic enzyme activity. The alcohol dehydrogenase (ADH), aldehyde dehydrogenase (ALDH), superoxide dismutase (SOD), and glutathione peroxidase (GPx) activities in the liver tissue were measured. RESULTS: LN decreased the serum ethanol and acetaldehyde levels in ethanol-administered rats. LN increased the hepatic ADH and ALDH activities but decreased the alanine aminotransferase, aspartate aminotransferase, and gamma-glutamyl transferase activities in the ethanol-administered rats. In addition, LN inhibited lipid peroxidation and increased the activities of SOD and GPx. CONCLUSIONS: LN modulates the mediators of various etiological effects of excessive alcohol consumption and enhances the alcohol metabolism and antioxidant activity, making it a potential candidate for hangover treatments.

청간해주탕(淸肝解酒湯)이 alcohol 대사관련 유전자 및 apoptosis에 미치는 영향 (Effects of Chungganhaeju-tang on Gene Expression of Alcohol-metabolizing Enzymes and Alcohol-induced Apoptosis)

  • 김영태;김영철;우홍정;이장훈
    • 대한한방내과학회지
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    • 제24권1호
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    • pp.123-133
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    • 2003
  • Objectives : This study was designed to investigate the effects of Chungganhaeju-tang on expression of alcohol metabolizing enzymes, cell viability and alcohol-induced apoptosis. Materials and Methods : For this study, the human hepatoma cell line HepG2 was used. HepG2 cells were treated with ethanol-or acetaldehyde, chungganhaeju-tang, anti-Fas neutralizing antibody and were investigated by using quantitative RT-PCR, MTT and Trypan blue exclusion assays. Results : The results are summarized as follows: 1. Quantitative RT-PCR analysis demonstrated that ethanol-or acetaldehyde-mediated increase of ALDH gene expression was not affected by Chungganhaeju-tang treatment. 2, Ethanol-or acetaldehyde-induced apoptosis was remarkably inhibited by Chungganhaeju-tang in a dose-dependent manner. 3, Ethanol-or acetaldehyde-induced apoptosis was significantly blocked by anti-FasL neutralizing antibody, suggesting apoptosis induced by alcohol might be mediated by FasL/Fas signaling pathway. Conclusions : Taken all together, these results indicate that the FasL/Fas signaling plays a critical role in alcohol-induced apoptosis and Chungganhaeju-tang increases viability of liver cells by suppression of the FasL/Fas-mediated apoptosis-signaling pathway.

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Long face를 갖는 성인과 normal face를 갖는 성인의 측모와 정모 두부방사선 사진상에서 안모유형의 차이에 관한 연구 (A STUDY ON THE MORPHOLOGIC DIFFERENCES BETWEEN LONG-FACE ADULTS AND NORMAL-FACE ADULTS ON THE LATERAL AND P-A CEPHALOGRAMS)

  • 김현도;손병화
    • 대한치과교정학회지
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    • 제20권2호
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    • pp.293-304
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    • 1990
  • The purpose of this study was to describe the morphologic differences between long-face adults and normal-face adults on the lateral and P-A cephalograms. Long-face and normal-face subifects were selected clinically, and then each of them was taken the lateral cephalogram. According to SN-MP angle and ATFH on the lateral cephalogram, long-face group and normal-face group were classified. 2 long-face adults and 18 normal-face adults were collected, and each of them was taken the P-A cephalogram. The results were as follows: 1. The morphologic differences between long-face adults and normal-face adults were closely related to mandibular morphology. 2. Long-face adults, compared with normal-face adults, demonstrated significant increase in ALFH, and significant decrease in ramus height. 3. Long-face adults, compared with normal-face adults, demonstrated significant increase in AUDH and, ALDH, especially in ALDH. 4. On the P-A cephalogram, no measures of transverse dimension demonstrated significant differences between two groups. 5. On the P-A cephalogram, facial height/facial width ratio was significantly larger than normal in the long-face adults, and in the normal-face adults, facial height/facial width ratio was approximately 90%. 6. In the correlation analysis of SN-MP angle and ATFH with all the other variables, the correlation coefficients of SN-MP angle and PTFH/ATFH that of ATFH and ALFH on the lateral cephalogram demonstrated the highest value, and on the P-A cephalogram, SN-MP angle and Cg-GA-Me (Lt.), ATFH and lower facial height demonstrated the highest value of correlation coefficients.

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Finding Genes Discriminating Smokers from Non-smokers by Applying a Growing Self-organizing Clustering Method to Large Airway Epithelium Cell Microarray Data

  • Shahdoust, Maryam;Hajizadeh, Ebrahim;Mozdarani, Hossein;Chehrei, Ali
    • Asian Pacific Journal of Cancer Prevention
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    • 제14권1호
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    • pp.111-116
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    • 2013
  • Background: Cigarette smoking is the major risk factor for development of lung cancer. Identification of effects of tobacco on airway gene expression may provide insight into the causes. This research aimed to compare gene expression of large airway epithelium cells in normal smokers (n=13) and non-smokers (n=9) in order to find genes which discriminate the two groups and assess cigarette smoking effects on large airway epithelium cells.Materials and Methods: Genes discriminating smokers from non-smokers were identified by applying a neural network clustering method, growing self-organizing maps (GSOM), to microarray data according to class discrimination scores. An index was computed based on differentiation between each mean of gene expression in the two groups. This clustering approach provided the possibility of comparing thousands of genes simultaneously. Results: The applied approach compared the mean of 7,129 genes in smokers and non-smokers simultaneously and classified the genes of large airway epithelium cells which had differently expressed in smokers comparing with non-smokers. Seven genes were identified which had the highest different expression in smokers compared with the non-smokers group: NQO1, H19, ALDH3A1, AKR1C1, ABHD2, GPX2 and ADH7. Most (NQO1, ALDH3A1, AKR1C1, H19 and GPX2) are known to be clinically notable in lung cancer studies. Furthermore, statistical discriminate analysis showed that these genes could classify samples in smokers and non-smokers correctly with 100% accuracy. With the performed GSOM map, other nodes with high average discriminate scores included genes with alterations strongly related to the lung cancer such as AKR1C3, CYP1B1, UCHL1 and AKR1B10. Conclusions: This clustering by comparing expression of thousands of genes at the same time revealed alteration in normal smokers. Most of the identified genes were strongly relevant to lung cancer in the existing literature. The genes may be utilized to identify smokers with increased risk for lung cancer. A large sample study is now recommended to determine relations between the genes ABHD2 and ADH7 and smoking.

Identification of Differentially Expressed Genes by TCDD in Human Bronchial Cells: Toxicogenomic Markers for Dioxin Exposure

  • Park, Chung-Mu;Jin, Kyong-Suk;Lee, Yong-Woo
    • 대한의생명과학회지
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    • 제18권1호
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    • pp.1-9
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    • 2012
  • Differentially expressed genes by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) were identified in order to evaluate them as dioxin-sensitive markers and crucial signaling molecules to understand dioxin-induced toxic mechanisms in human bronchial cells. Gene expression profiling was analyzed by cDNA microarray and ten genes were selected for further study. They were cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1), S100 calcium binding protein A8 (calgranulin A), S100 calcium binding protein A9 (calgranulin B), aldehyde dehydrogenase 1 family, member A3 (ALDH6) and peroxiredoxin 5 (PRDX5) in up-regulated group. Among them, CYP1B1 was used as a hallmark for dioxin and sharply increased by TCDD exposure. Down-regulated genes were IK cytokine, interferon-induced protein with tetratricopeptide repeats 1 (IFIT1), nuclease sensitive element binding protein 1 (NSEP1), protein tyrosine phosphatase type VI A, member 1 (PTP4A1), ras oncogene family 32 (RAB32). Although up-regulated 4 genes in microarray were coincided with northern hybridization, down-regulated 5 genes showed U-shaped expression pattern which is sharply decreased at lower doses and gradually increased at higher doses. These results introduce some of TCDD-responsive genes can be sensitive markers against TCDD exposure and used as signaling cues to understand toxicity initiated by TCDD inhalation in pulmonary tissues.