• 제목/요약/키워드: phase II enzyme

검색결과 102건 처리시간 0.022초

시화호에서 채집한 풀망둑 Acanthogobius hasta의 간장 약물대사효소계 및 항산화계의 반응 (Responses in Hepatic Xenobiotic Metabolizing and Antioxidant Enzymes in Javelin Goby Acanthogobius hasta Collected at Shihwa Lake)

  • 이지선;정지현;한창희;심원준;전중균
    • 환경생물
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    • 제26권2호
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    • pp.94-101
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    • 2008
  • 공장 폐수로 인한 오염이 심한 경기 시화호에서 오염정도가 다른 두 지역으로부터 풀망둑을 채집하여 이들의 해독효소계 또는 항산화효소계의 반응을 비교하였다. 해독효소계에서 I상효소로는 CYP, P450R, b5R, EROD를, II상효소로는 GST를 조사하였다. 그리고 항산화효소계로는 CAT, GR, CPx의 활성 그리고 GSH및 CSSG농도를 조사하였다. 그 결과, 오염정도가 심한 지역에서 잡은 어류가 간장 중 P450R, b5R, GST의 활성이 높았으나 EROD활성은 오히려 낮았고 CYP농도는 차이가 없었다. 그리고 이지역에서 잡은 어류는 CAT와 GR의 활성, 비효소적인 항산화계인 CSH와 GSSC농도도 더 높았으나 GTx활성은 오히려 낮았다. 이들 결과는 시화호의 오염된 곳에서 서식하는 풀망둑 Acanthogobius hasta은 상당히 해독효소계가 항진되어 있으며 산화 스트레스도 크게 받고 있음을 보여준다.

약물대사효소의 유전적 다형성 및 임상적 응용 (Clinical Pharmacogenomics of Drug Metabolizing Enzymes and its Clinical Application)

  • 김경임;김승희;박지은;채한정;최지선;신완균;손인자;오정미
    • 한국임상약학회지
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    • 제16권2호
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    • pp.155-164
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    • 2006
  • Great inter-variability in drug response and adverse drug reactions is related to inter-variability of drug bioavailability, drug interaction and patient's disease and physyological state that cause change in absorption, distribution, metabolism and excretion of drugs. However, these alone do not sufficiently predict and explain inter-variability in drug response. In recent studies, it is reported that inter-variability in drug response and adverse drug reactions may largely resulted from genetically determined differences in drug absoption, distribution, metabolism and drug target proteins. Especially, the major human drug-metabolizing enzymes such as CYP450, N-acetyl tranferase, thiopurine S-methyl transferase, glutathione S-transferase are identified as the major gene variants that cause inter-individual variability in drug's response and adverse drug reactions. These variations may have most significant implications for those drugs that have narrow therapeutic index and serious adverse drug reactions. Therefore, the genetic variation such as polymorphisms in drug metabolizing enzymes can affect the response of individuals to drugs that are used in the treatment of depression, psychosis, cancer, cardiovascular disorders, ulcer and gastrointestinal disorders, pain and epilepsy, among others. This review describes the pharmacogenomics of the drug metabolizing enzymes associated with the drug response and its clinical applications.

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Induction of Quinone Reductase, an Anticarcinogenic Marker Enzyme, by Extract from Chrysanthemum zawadskii var. latilobum K.

  • Kim, Ju-Ryoung;Kim, Jung-Hyun;Lim, Hyun-Ae;Jang, Chan-Ho;Kim, Jang-Hoon;Kwon, Chong-Suk;Kim, Young-kyun;Kim, Jong-Sang
    • Preventive Nutrition and Food Science
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    • 제10권4호
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    • pp.340-343
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    • 2005
  • Induction of NAD(P)H:(quinone-acceptor) oxidoreductase (QR) which promotes obligatory two electron reduction of quinones and prevents their participation in oxidative cycling and thereby the depletion of intracellular glutathione, has been used as a marker for chemopreventive agents. Induction of phase II enzyme is considered to be an important mechanism of cancer prevention. In our previous study, we assessed the quinone reductase QR-inducing activities of 216 kinds of medicinal herb extracts in cultured murine hepatoma cells, BPRc1 and hepalc1c7 cells. Among the 216 herbal extracts tested in that study, extracts from Chrysanthemum zawadskii showed significant induction of QR. In this study, we examined QR-inducing activity of solvent fractions of the herbal extract. The dichloromethane fraction of the herb showed the highest QR induction among the samples fractionated with four kinds of solvents with different polarity. The fraction also significantly induced the activity of glutathione S-transferase (GST), one of the major detoxifying enzymes, at $4{\mu}g/mL\;and\;2{\mu}g/mL$ in hepalc1c7 and BPRc1 cells, respectively. In conclusion, dichloromethane-soluble fraction of Chrysanthemum zawadskii which showed relatively strong induction of detoxifying enzymes merits further study to identify active components and evaluate their potential as cancer preventive agents.

Mouse hepatoma 세포를 이용한 농산부산물로부터 quinone reductase활성물질의 탐색 (Screening of Quinone Reductase Inducers from Agricultural Byproducts Using Mouse Hepatoma Cell Line)

  • 김정상;남영중;김주원
    • 한국식품과학회지
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    • 제27권6호
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    • pp.972-977
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    • 1995
  • Quinone reductase(QR)를 포함한 2상효소계를 활성화시키는 성분들은 많은 동물실험에서 발암물질의 세포내 작용을 억제함으로서 항종양효과를 나타내는 것으로 보고되어 있다. 본 연구에서는 대표적인 농산부산물로서 미강, 밀기울, 탈지대두박, 두유박, 참깨박, 들깨박등 6종의 시료에 대한 암예방효과를 갖는 물질의 존재여부를 탐색하기 위하여, mouse hepatoma cell line(Hepalclc7 cells) 을 이용하여, quinone reductase활성유도 여부를 측정하였다. 참깨박과 들깨박의 80%메탄올 추출물은 0.5mg/ml 농도에서 강력한 QR 유도활성을 나타냈으며, 같은 농도에서 다른 시료들은 거의 QR 효소활성을 증가시키지 않았다. 한편 QR효소활성을 유도하는 성분을 찾아내기 위하여 일차적으로 TLC를 수행한 결과, 참깨박과 들깨박의 메탄올 추출물 가운데 사용한 전개용매(n-butanol : n-propanol : 2N ammonium hydroxide(10 : 60 : 30)에서 가장 빨리 이동하는 분획(Rf=0.70)이 유효성분을 함유하고 있음을 확인하였으며, 현재 활성성분의 동정이 진행중에 있다.

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Cytoprotective effect exerted by geraniin in HepG2 cells is through microRNA mediated regulation of BACH-1 and HO-1

  • Aayadi, Hoda;Mittal, Smriti P.K.;Deshpande, Anjali;Gore, Makarand;Ghaskadbi, Saroj S.
    • BMB Reports
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    • 제50권11호
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    • pp.560-565
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    • 2017
  • Geraniin, a hydrolysable tannin, used in traditional medicine in Southeast Asia, is known to exhibit various biological activities. As an antioxidant it is known to up-regulate phase II enzyme Heme oxygenase-1 (HO-1). However its mechanism is not clearly understood. Nuclear factor erythroid-derived 2 related factor 2 (Nrf-2) is transcriptionally up-regulated by Extracellular signal-regulated kinase (ERK) 1/2 and retained in nucleus due to inactivated Glycogen synthase kinase 3 beta ($GSK-3{\beta}$). Geraniin additionally down-regulates expression of microRNA 217 and 377 (miR-217 and miR-377) which target HO-1 mRNA. Expression of BTB and CNC homolog 1 (BACH-1), another regulator of HO-1, is also down-regulated by up-regulating microRNA 98 (miR-98), a negative regulator of BACH-1. Thus, geraniin up-regulates HO-1 expression both through activating its positive regulator Nrf-2 and by down-regulating its negative regulator BACH-1. Up-regulation of HO-1 also confers protection to HepG2 cells from tertiary butyl hydroperoxide (TBH) induced cytotoxicity.

GSTM1 and GSTT1 Allele Frequencies among Various Indian and non-Indian Ethnic Groups

  • Senthilkumar, K.P.;Thirumurugan, R.
    • Asian Pacific Journal of Cancer Prevention
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    • 제13권12호
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    • pp.6263-6267
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    • 2012
  • Background: Glutathione-S-transferase (GST) is an important phase II xenobiotic compound metabolizing enzyme family, involved in tolerance to a particular drug or susceptibility to a diseasec. This study focused the GSTM1 and T1 null allele frequency in the Gujarat population with a comparison across other Inter- and Intra-Indian ethnic groups to predict variation in the possible susceptible status. Methods: DNA was isolated by a salting out method and GSTM1 and T1 homozygous null genotypes were detected by multiplex polymerase chain reaction in 504 unrelated individuals. The genotype distribution of null alleles was compared with Indian and non Indian ethnics reported earlier in the literature using Fisher's test. Results: The frequencies of the homozygous null genotypes of GSTM1 and GSTT1 were 20% (95%CI 16.7-23.9) and 35.5% (95%CI 31.4-39.9) respectively. GSTM1 null frequency did not deviate from most other Indian ethnic groups but differed from the majority of those of non Indian ethnicity studied. The frequency of homozygous null type of GSTT1 was significantly higher and deviated from all Indian groups and a few of non Indian ethnicity. Conclusions: Gujarat ethnicity, possibly the most susceptible for GSTT1 dependent drug disposition and diseases regarding effects of pollution. Further, the results have implications for GSTT1 dependent drugs used for treatment, a serious problem which needs to be solved by physicians and clinical researchers.

Unusual Intronic Variant in GSTP1 in Head and Neck Cancer in Pakistan

  • Masood, Nosheen;Malik, Faraz Arshad;Kayani, Mahmood Akhtar
    • Asian Pacific Journal of Cancer Prevention
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    • 제13권4호
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    • pp.1683-1686
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    • 2012
  • In the present case control study mRNA expression of the GSTP1 gene, encoding a phase II enzyme that detoxifies via glutathione conjugation, was investigated using semiquantitative PCR followed by SSCP for 49 confirmed head and neck (HN) cancer and 49 control samples. It was found that GSTP1 was upregulated in significantly higher number of cancers (OR 4.2, 95% CI 1.2-15.3). Grade wise correlation was also observed with more up regulation in patients with more advanced grades of HN carcinomas. We also found that 5 patients showed variation in mRNA with a larger product size than expected. Sequencing revealed insertion of an intronic segment between the $6^{th}$ and $7^{th}$ exon of the GSTP1 gene. Germline screening was performed showing mobility shifts which suggested mutation at the DNA level resulting in intronic portion retention. This study is of prime importance for drug design and treatment selection to overcome increased resistance of HN cancers to drugs due to alteration in the GSTP1 gene.

Effect of Variation of ABCB1 and ABCC3 Genotypes on the Survival of Bone Tumor Cases after Chemotherapy

  • Yang, Jie;Wang, Zhi-Gang;Cai, Hai-Qing;Li, Yu-Chan;Xu, Yun-Lan
    • Asian Pacific Journal of Cancer Prevention
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    • 제14권8호
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    • pp.4595-4598
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    • 2013
  • We conducted a comprehensive study to investigate the role of genes involved in transport pathways in response to chemotherapy and clinical outcome of osteosarcoma cases. Genotyping of six SNPs was performed in a 384-well plate format on the Sequenom MassARRAY platform for 208 osteosarcoma patients to reveal any correlations of the six SNPs with response to chemotherapy and clinical outcome. Individuals with the ABCB1 rs1128503 TT and ABCC3 rs4148416 TT genotypes had a higher probability of responding poorly to chemotherapy, indicated by odds ratios (ORs) of 2.46 (95%CI, 1.21-5.74) and 3.78 (95% CI, 1.20-13.85), respectively. Moreover, the ABCB1 rs1128503 TT and ABCC3 rs4148416 TT genotypes were significantly associated with shorter diseasefree survival (DFS) and overall survival (OS). Our study found the two SNPs in two transporter genes and one phase II metabolism enzyme to be associated with response to chemotherapy and overall survival in osteosarcoma patients, suggesting potential prognostic biomarker applications of the two SNPs.

(-) Epigallocatechin gallate restores ethanol-induced alterations in hepatic detoxification system and prevents apoptosis

  • Anuradha, Carani V;Kaviarasan, Subramanian
    • Advances in Traditional Medicine
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    • 제7권3호
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    • pp.311-320
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    • 2007
  • The present study was designed to estimate the protective effect of (-) epigallocatechin gallate (EGCG) on ethanol-induced liver injury in rats. Chronic ethanol administration (6 g/kg/day ${\times}$ 60 days) caused liver damage that was manifested by the elevation of markers of liver dysfunction - aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, lactate dehydrogenase, bilirubin and ${\gamma}$-glutamyl transferase in plasma and reduction in liver glycogen. The activities of alcohol metabolizing enzymes such as alcohol dehydrogenase and aldehyde dehydrogenase were found to be altered in alcohol-treated group. Ethanol administration resulted in the induction of cytochrome p450 and cytochrome-$b_{5}$ activities and reduction of cytochrome-c reductase and glutathione-S-transferase, a phase II drug metabolizing enzyme. Further, ethanol reduced the viability of isolated hepatocytes (ex vivo) as assessed by trypan blue exclusion test and induced hepatocyte apoptosis as assessed by propidium iodide staining. Treatment of alcoholic rats with EGCG restored the levels of markers of liver injury and mitigated the alterations in alcohol metabolizing and drug metabolizing enzymes and cyt-c-reductase. Increased hepatocyte viability and reduced apoptotic nuclei were observed in alcohol + EGCG-treated rats. These findings suggest that EGCG acts as a hepatoprotective agent against alcoholic liver injury.

Micrococcus sp.의 생육 및 casein 분해에 미치는 배양조건의 영향 : (II) -배양시간에 따른 casein 분해 형태에 관한 연구- (Effects of cultural conditions on growth of Micrococcus sp. and casein hydrolysis : (II) -Studies on patterns of casein hydrolysis with time during culture-)

  • 이시경;백운화;주현규
    • Applied Biological Chemistry
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    • 제35권6호
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    • pp.479-484
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    • 1992
  • Cheddar 치즈의 숙성기간을 단축시키고 flavor를 증진시킬 목적으로 단백분해력이 있는 Micrococcus sp. LL3를 Cheddar 치즈에 첨가하기 위하여 본 균의 균체생산을 위한 최적배양 온도와 pH 및 배양시간에 따른 casein의 분해형태를 관찰하였다. 본 균주의 생육을 위한 최적 배양온도는 $30^{\circ}C$, 단백분해 효과의 최적 배양온도는 $37^{\circ}C$이었으며, 초기 배양 pH 7.0에서 균의 생육과 단백분해 효과가 가장 좋았다. 배양기간 중 정지기 초기의 세포에서 aminopeptidase의 효소활성이 가장 높았으며, 본 효소의 열 안정성이 높아 $50^{\circ}C$에서 20분간 열처리 후에도 높은 효소활성을 보였다. Casein의 분해속도는 배양 24에서 36시간에서 가장 높았으며, 전기영동을 통한 casein hydrolysis patterns는 ${\alpha}-casein $뿐만 아니라 ${\beta}-casein$도 본 균주에 의해 완전히 분해되었다. 특히 본 균주는 ${\beta}-casein$의 분해력이 더욱 우수하였다.

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