• 제목/요약/키워드: cytochrome P-450

검색결과 936건 처리시간 0.04초

Expression of Cytochrome P450 1A1, 1A2, 2C8, 2E1 and 3A4 in Human Brain

  • Yoo, Min
    • 대한의생명과학회지
    • /
    • 제7권2호
    • /
    • pp.65-70
    • /
    • 2001
  • We have carried out PCR reactions to investigate if cytochrome P450 (P450) enzymes (1A1, 1A2, 2C8, 2E1 and 3A4), which are well hewn to be the key enzymes in detoxification process and/or synthesis of steroids in the liver, are expressed in the human brain, too. P450 1A1, 2C8 and 2E1 were expressed clearly. However, P450 1A2 and 3A4 were not detectable. Their expression levels in the human brain could be extremely low or they were not expressed at all. One base substitution at nucleotide 290 (A->G) was identified in P450 1A1. It is suspected to be an individual polymorphism. Our results should contribute to the better understanding of the role of cytochrome P450 enzymes in the human brain.

  • PDF

Potent inhibition of human cytochrome P450 1 enzymes by SY-081

  • Kim, Yong-Mo;Lee, Sang-Kwang;Kim, Mie-Young;Kim, Sang-Hee;Jin, Chun-Young
    • 대한약학회:학술대회논문집
    • /
    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
    • /
    • pp.148.2-149
    • /
    • 2003
  • Recently we have reported that various hydroxystilbenes show strong inhibition of human cytochrome P450 1 enzyme activities. A series of syntheic trans-stilbene derivatives were prepared and their inhibitory potentials were evaluated with the bacterial membrane of recombinant human cytochrome P450 1A1, 1A2 and 1B1 coexpressed with hyman NADPH-P450 reductase to find a new inhibitor of cytochrome P450 enzymes. Of the compounds tested, SY-081 exhibited a potent inhibition of human cytochrome P450 1B1 with an $IC_50$ value of 2.6 nM. (omitted)

  • PDF

인삼이 백서 간 약물대사효소에 미치는 효과 (The Effect of Ginseng on Hepatic Drug Metabolizing Enzyme in Rats)

  • 이태하;김낙두
    • 약학회지
    • /
    • 제25권4호
    • /
    • pp.145-151
    • /
    • 1981
  • The effect of ginseng methanol extract on hepatic drug metabolizing enzyme in rat was investigated. The ginseng methanol extract (100mg/kg) was administered orally to Sprague Dawley rats for 7days and the contents of cytochrome $P_{450}$ and NADPH cytochrome c reductase in liver were measured by the method of Stanton et al. and Mazel respectively. The content of liver cytochrome $P_{450}$ and NADPH cytochrome c reductase in the rats treated with ginseng methanol extract (100mg/kg) were increased by 21.9% and l6.6% respectively and their increases were statistically significant. Single i.p. injection of phenobarbital (100mg/kg) to the rats produced approximately 25% increase in cytochrome $P_{450}$ content in this investigation and further stimulation was produced in the rats pretreated with ginseng methanol extract (100mg/kg). On the other hand, single i.p. injection of 95% $CCl_{4}$ (0.5ml/kg) showed 29% decrease in cytochrome $P_{450}$ content and 10.5% decrease in NADPH cytochrome c reductase activity. The degree of inhibition of cytochrome $P_{450}$ content in the rats pretreated with ginseng methanol extract (100mg/kg) was similar to that observed in the $CCl_{4}$ alone treated group, but NADPH cytochrome c reductase activity was increased by 65% in the rats pretreated with ginseng methanol extract (100mg/kg). These results suggest that ginseng is the hepatic drug metabolizing enzyme inducing agent in the rat and the effect is similar to phenobarbital.

  • PDF

막지질 과산화와 간세포내 마이크로솜 및 리덕타제 기능과의 상관성에 관한 연구 (Effect of membrane lipid peroxidation on rat liver microsomal enzyme activity)

  • 박상열;조종후
    • 대한수의학회지
    • /
    • 제44권2호
    • /
    • pp.185-193
    • /
    • 2004
  • The effects of membrane lipid peroxidation and retinyl palmitate on rat liver microsomal functions were investigated in vitro. Rat liver homogenates exposed to oxygen tension for 0, 3, 6, 9 or12 hours and lipid peroxidation levels were evaluated by the measurements of fluorescence intensity, malondialdehyde (MDA) and retinyl palmitate. The fluorescence intensity of homogenates and microsomes were elevated and retinyl palmitate concentrations were decreased. But the concentration of MDA was not affected to exposure time. Therefore, fluorescence intensity and retinyl palmitate concentration were used to analyze the correlation between lipid peroxidation and microsomal functions. To investigate the liver microsomal functions, the microsome was isolated from rat liver homogenates exposed to oxygen. The concentration of cytochrome P450 and the activity of NADPH-cytochrome P450 reductase in liver microsomes were gradually decreased with increasing the exposure time. The correlation between fluorescence intensity of microsomes showed a very high inverse correlation of -0.97 and -0.93, respectively. The decrease of cytochrome P450 concentration was due to the regeneration of cytochrome P450 to cytochrome P420. Also, the activities of cytochrome P450-dependent aminopyrine demethylase and benzpyrene hydroxylase of liver microsomes were gradually decreased with increasing the exposure time. The correlation with fluorescence intensity of microsome showed a high inverse correlation of -0.97 and -0.91, respectively. The retinyl palmitate concentrations of rat liver homogenates were decreased with increasing the exposure time. The decrease of retinyl palmitate concentration was followed by a low concentration of cytochrome P450 and activity of NADPH-cytochrome P450 reductase. The correlation indicated high direct correlation of 0.92 and 0.93, respectively. The decrease of retinyl palmitate concentration was also accompanied by the reduction of aminopyrine demethylase and benzpyrene hydroxylase activities. The correlation was analyzed a high direct correlation of 0.90 and 0.85, respectively. In conclusion, these studies have shown that the membrane lipid peroxidation of rat liver microsome proportionally decreased microsomal enzyme activities in vitro experiments.

Glugathione S-transferase mu 및 theta, 그리고 cytochrome P450 1A1, cytochrome P450 2E1 다형성이 폐암발생에 미치는 영향에 대한 환자-대조군연구 (A case-control study on the effects of the genetic polymorphism of glutathione S-transferase mu and theta, cytochrome P450 1A1 and cytochrome P450 2E1 on the risk of lung cancer)

  • 남홍매;김헌
    • 대한예방의학회:학술대회논문집
    • /
    • 대한예방의학회 1998년도 제50차 추계 학술대회 연제집
    • /
    • pp.291-292
    • /
    • 1998
  • PDF

가지과식물에서 Capsidiol 생합성에 관여하는 Cytochrome P450 유전자의 발현과 효소활성 (Enzyme Activity and Gene Expression of Cytochrome P450 Involved in Capsidiol Biosynthesis in Solanaceae Plants)

  • 권순태
    • 한국자원식물학회지
    • /
    • 제21권2호
    • /
    • pp.139-143
    • /
    • 2008
  • 다섯 종류의 가지과 식물을 대상으로 elicitor에 의해 생합성 되는 capsidiol의 함량을 측정하고 생합성에 관련된 P450 효소의 활성과 관련 유전자 발현을 조사하였다. 고추, 피망 및 담배는 capsidiol의 생합성에 관련된 두개의 유전자인 cyclase와 P450 유전자가 세포내에 존재하였고, elicitor의 처리에 의하여 유전자의 발현이 유도되고 효소의 촉매가 이루어 졌다. 가지세포에는 두개의 유전자가 게놈상에 존재하지만 P450 유전자는 발현되나, cyclase 유전자의 발현은 나타나지 않았다. 감자에는 capsidiol의 생합성에 관련된 P450 및 cyclase 유전자 모두가 존재하지 않은 것으로 나타났다. 본 실험에 사용된 P450과 cyclase 유전자는 식물이 정상상태에 있을 때는 전혀 발현되지 않으나 elicitor에 의해 특이적으로 유도 되는 특징을 보였고, 식물체 조직이나 기관별로 다양한 발현 양상을 보였다.

홍삼의 장기 투여가 흰쥐 간 대사효소 유도에 미치는 영향 (Modulation of Cytochrome P-450 Induction by Long-Term Supplementation with Korean Red Ginseng to Rats)

  • 임흥빈
    • 한국약용작물학회지
    • /
    • 제15권6호
    • /
    • pp.437-443
    • /
    • 2007
  • 홍삼의 물추출물을 장기간 흰쥐에 급여했을 때 흰쥐 간의 이물질대사효소 활성도 유도에 미치는 영향을 조사하였다. 홍삼 물추출물의 급여농도는 25 mg/kg body weight이었으며, 간의 이물질대사효소 유도제는 항경련제 PB (80 mg/kg)와 발암제 3-MC (20 mg/kg)을 사용하였다. 간에서 이물질대사에 관여하는 cytochrome P-450의 함량, cytochrome P-450 dependent monooxygenase인 ECOD와 BPDM, cytochrome P-450 reductase와 GST의 활성도는 PB와 3-MC 투여에 의해서 대조군과 홍삼투여군 모두 크게 증가되었다. 흰쥐의 나이가 3개월에서는 두 유도제를 투여했을 때 이물질대사효소의 활성은 대조군이 인삼투여군에 비해 상대적으로 더 많이 유도되었다. 그러나 12개월에서는 두 시험군 모두 유도정도가 감소하였으나 홍삼투여군은 그 활성도 감소정도가 대조군에 비해 상대적으로 크지 않았다. 한편 두 그룹 모두 이물질대사 효소 중 cytochrome $B_5$ 함량과 cytochrome $b_5$ reductase의 활성도는 PB와 3-MC 투여에 의해서 뚜렷한 차이를 보이지 않았다. 따라서 이러한 결과는 흰쥐에 홍삼의 장기간 급여는 간에서 효소유도제의 이물질대사효소유도 정도를 조절하여 무독화에 기여할 수 있다는 것을 의미한다.

Benzo(a)pyrene 과 Cytochrome P-450의 대한 상호작용에 대한 이론적 연구 (Theoretical Study on The Interaction Between Benzo(a)pyrene and Cytochrome P-450)

  • 도성탁
    • 대한의생명과학회지
    • /
    • 제1권1호
    • /
    • pp.89-94
    • /
    • 1995
  • B(a)P와 cytochrome P-450의 heme부분은 구조가 평면이므로 겹침 상호작용이 가능하다. 가능성이 큰 겹침 상호작용모형을 결정하기 위해 이들 분자에 대해 MO계산을 행하였다. 이 경우 궤도함수 상호작용이 가장 중요하므로, 프론티어궤도함수의 eigen vetor값이 크며 상호 결합성을 보여야 한다. 이를 바탕으로 다섯가지 가능성이 있는 모형을 선택한 수 MN2와 MO방법을 실행하였다. 이중 B(a)P의 4, 5, 6번 위치와 heme group의 Y탄소와 III pyrrole환이 포개어지는 형태가 가장 안전하였다.

  • PDF

Production of Genistein from Naringenin Using Escherichia coli Containing Isoflavone Synthase-Cytochrome P450 Reductase Fusion Protein

  • Kim, Dae-Hwan;Kim, Bong-Gyu;Jung, Na-Ri;Ahn, Joong-Hoon
    • Journal of Microbiology and Biotechnology
    • /
    • 제19권12호
    • /
    • pp.1612-1616
    • /
    • 2009
  • Isoflavonoids are a class of phytoestrogens. Isoflavonone synthase (IFS) is responsible for the conversion of naringenin to genistein. IFS is a cytochrome P450 (CYP), and requires cytochrome P450 reductase (CPR) for its activity. Additionally, the majority of cytochrome P450s harbor a membrane binding domain, making them difficult to express in Escherichia coli. In order to resolve these issues, we constructed an inframe fusion of the IFS from red clover (RCIFS) and CPR from rice (RCPR) after removing the membrane binding domain from RCIFS and RCPR. The resultant fusion gene, RCIFS-RCPR, was expressed in E. coli. The conversion of naringenin into genistein was confirmed using this E. coli transformant. Following the optimization of the medium and cell density for biotransformation, $60\;{\mu}M$ of genistein could be generated from $80\;{\mu}M$ of naringenin. This fusion protein approach may be applicable to the expression of other P450s in E. coli.

한국인 집단에서 Cytochrome P450 2E1의 유전적 다형성 (Genetic Polymorphism of Cytochrome P450 2E1 in Korean Population)

  • 정혜광;구희경;이상섭;양규환;정태천;변부형
    • 한국환경성돌연변이발암원학회지
    • /
    • 제16권2호
    • /
    • pp.97-102
    • /
    • 1996
  • In this study, we have quantified genotype frequency of the cytochrome P450 (P450) 2E1 which codes for the P450 enzyme primarily responsible for the metabolic activation of carcinogenic nitrosamines and low molecular organic solvents, in Korean population by using PCR and RFLP at two sites previously associated with some cancers; a PstI and RsaI RFLP in the transcriptional regulatory region of the human P450 2E1 gene. The genotype frequencies of homozygous wild type (PstI site-absent) and heterozygous mutant type (PstI site-present) in PstI RFLP were 0.70 and 030, respectively. The homozygous mutant type in Pstl RFLP was not observed in Korean population. The genotype frequencies of homozygous wild type (RsaI site-present), heterozygous mutant type (RsaI site-absent), and homozygous mutant type in RsaI RFLP were 0.71, 0.26, and 0.03, respectively.

  • PDF