• 제목/요약/키워드: glutathione S-transferase activity

검색결과 453건 처리시간 0.027초

Inhibition of glutathione S-transferase omega 1-catalyzed protein deglutathionylation suppresses adipocyte differentiation

  • Sana Iram;Areeba Mashaal;Seulgi Go;Jihoe Kim
    • BMB Reports
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    • 제56권8호
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    • pp.457-462
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    • 2023
  • Glutathione S-transferase omega 1 (GstO1) is closely associated with various human diseases, including obesity and diabetes, but its functional mechanism is not fully understood. In the present study, we found that the GstO1-specific inhibitor C1-27 effectively suppressed the adipocyte differentiation of 3T3-L1 preadipocytes. GstO1 expression was immediately upregulated upon the induction of adipocyte differentiation, and barely altered by C1-27. However, C1-27 significantly decreased the stability of GstO1. Moreover, GstO1 catalyzed the deglutathionylation of cellular proteins during the early phase of adipocyte differentiation, and C1-27 inhibited this activity. These results demonstrate that GstO1 is involved in adipocyte differentiation by catalyzing the deglutathionylation of proteins critical for the early phase of adipocyte differentiation.

아세트아미노펜 유도 흰쥐에서 수산생물자원 추출물의 in vivo 간보호작용 (Protective Effect of Marine Natural Products on the Hepatic Lipid Peroxidation in Acetaminophen-treated Rats)

  • 최종원;박종철
    • 약학회지
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    • 제40권5호
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    • pp.574-581
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    • 1996
  • The study was initiated to elucidate the protective mechanism by examining in vivo effect of some marine natural products, Styela plicata, Ecklonia stolonifera and Pachymeniopsis elliptica on acetaminophen-induced lipid peroxidation. The methanol extract of S. plicata prevented acetaminophen (800mg/kg, i.p.)-induced hepatotoxicity in rats as evidenced by the decreased formation of lipid peroxide. But the methanol extracts of E. stolonifera and P. elliptica were not affected on the formation of lipid peroxidation. The activities of cytochrome P-450, animopyrine N-demethylase and aniline hydroxylase were not changed by the treatment with S. plicata in comparison with acetaminophen-teated group. In acetaminophen-treated control rats, the glutathione S-transferase activity was decreased markably. However. in S. plicata pretreated group, the effect caused by acetaminophen was markably reduced. A-cetaminophen decreased the level of hepatic, glutathione, which was restored to same degree by S. plicata pretreatment. And activity of ${\gamma}$-glutamylcystein synthetase was not changed by S. plicata pretreatment, but the activity of glutathione reductase was increased significantly.

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Glutathione-S-transferase와 esterase 효소 저해특성을 이용한 농약의 혼합 상승효과 (Synergistic action of pesticide mixtures using glutathione-s-transferase- and esterase-inhibiting properties in diamondback moth (Plutella xylostella L.))

  • 유용만;홍순성;김성문;허장현
    • 농약과학회지
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    • 제7권1호
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    • pp.38-44
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    • 2003
  • 본 연구는 다양한 계열의 농약을 대상으로 체내에서 농약을 무독화하는 효소로 알려진 glutathione-S-transferase(GST) 와 esterases 에 대한 저해정도를 조사하고, 이 중 저해력이 높은 약제를 선발하여 무독화 효소에 의하여 분해되는 것으로 보고된 약제와 혼합 처리하였을 때 나타나는 약효의 변화를 조사하고자 수행하였다. 무독화효소를 저해하는 농약을 선발하기 위하여 34종의 살충제와 31종의 살균제를 대상으로 glutathione-S-transferase와 esterases 에 대한 저해력을 측정한 결과, thiodicarb $(I_{50}:1.87{\times}10^{-4}M)$, thiocyclarn $(I_{50}:7.40{\times}10^{-4}M)$, dithianon $(I_{50}:7.55{\times}10^{-5}M)$, tolylfluanide $(I_{50}:8.66{\times}10^{-5}M)$은 glutathione-S-transferase의 활성을 강게 저해하였고, dichlorvos $(I_{50}:8.95{\times}10^{-8}M)$, pirimicarb $(I_{50}:2.74{\times}10^{-6}M)$, pyrazophos $(I_{50}:3.31{\times}10^{-5}M)$, benomyl $(I_{50}:4.96{\times}10^{-5}M)$은 esterases의 활성을 강하게 저해하였다. Glutathione-S-transferase를 저해하였던 thiodicarb, thiocyclarn, dithianon, tolylfluanide와 glutathione-S-transferase 에 의해 대사되는 것으로 알려진 aeephate를 혼합 (1:1)하여 배추좀나방 (Plutella xylostella L.) 에 처리하고 약효를 관찰한 결과, 각각의 단제를 처리하였을 때보다 약효가 상승되었다. 특히 dithianon과 thiocyclam을 acephate 와 혼합시 각각 7배와 4배 약효가 상승하였다. 그리고 esterase를 저해한 약제인 dichlorvos, pirimicarb, pyrazophos, benomyl 을 esterase 에 의해 대사되는 것으로 알려진 phenthoate 와 혼합하였을 경우에도 단제 처리시의 약효보다는 혼합처리시의 약효가 높았다. Phenthoate와 dichlorvos 혼합시 18배, phenthoate 와 benomyl 혼합처리시 12배의 약효상승효과가 나타났다. 본 연구의 결과들은 무독화과정 효소에 의해 무독화되는 약제를 무독화효소 저해제와 혼합처리시 약효상승이 유발된다는 것을 나타내는데, 이러한 결과들은 향후 혼합제 개발에 유용하게 사용될 수 있을 것이라 생각된다.

들깨유 옥수수유의 섭취가 2-Acetylaminofluorene을 투여한 쥐 간에서 소포체막의 지방산 조성과 Cytochrome P-450 함량, Glutathione S-transferase 활성도에 미치는 영향 (Effects of Perilla and Corn Oil Diets on the Hepatic Microsomal Fatty Acid Composition, Cytochrome P-450 Contents, and Glutathione S-transferase Activities in 2-Acctylaminofluorcne Treated Rats)

  • 김경민
    • Journal of Nutrition and Health
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    • 제25권1호
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    • pp.3-11
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    • 1992
  • This paper examines the effects of dietary fats on the fatty acid composition and market enzyme activites during liver damage in 2-acetylaminofluorene treated rats. Weaning Sprague-Dawley male rats were fed the diet of beef tallow(BT source of sturated fatty acid) corn oil(CO source of n-6 fatty acid) and perilla oil(PO source of n-3 fatty acid) at the level of 15% fat. Ten days after feeding 2-acetylaminofluorene(2-AAF) was injected intraperitoneally twice every week at the level of 50mg/kg body weight for 7 weeks. Liver microsomal and cytosolic fractions were collected to determine the microsomal fatty acid composition lipid peroxide(malondialdehyde MDA) contents glucose 6-phosphatase(G6 Pase) activity cytochrome(Cyt) P-450 contents and cytosolic glutathione S-transferase(G6 Pase) activity cytochrome(Cyt) P-450 contents and cytosolic glutathione S-transferase(GST) activity. The fatty acid composition in microsomal fraction was reflected by different dietary fats. By 2-AAF treatment linoleic acids were increased regardless of the diet MDA contents were higher in CO group than it was in BT group. However 2-AAF treatment decreased MDA contents in all dietary groups. G6Pase activity of BT group was higher than those of the other gropus. CO group had the highest Cyt P-450 contents and 2-AAF treatment lowered Cyt P-450 contents only in CO gropu GST activites were higher in CO than in BT group whereas the enzyme activites were increased by 20AAF treatment in all dietary groups. These results suggest that dietary fats and 2-AAF treatment in all dietary groups,. These results suggest that dietary fats and 2-AAF treatment affect microsomal fatty acid composition The enzyme activities concerned with liver damage were influenced differently by dietary fats and 2-AFF treatment Although PO diet contains much more polyunsaturated fatty acids than CO diet PO diet doesn't cause more oxidant stress compared with CO diet in these data.

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브로모벤젠으로 유도된 간독성 흰쥐에서 생열귀나무 뿌리의 간보호활성 (Hepatoprotective Activities of Rosa davurica Root Extract in Rats Intoxicated with Bromobenzene)

  • Park, Jong-Cheol;Hur, Jong-Moon;Hwang, Young-Hee;Choi, Myeong-Rak;Kim, Suk-Nam;Choi, Jong-Won
    • 생명과학회지
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    • 제13권2호
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    • pp.230-235
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    • 2003
  • Bromobenzene으로 간독성을 유발한 흰쥐에 생열귀나무 뿌리를 투여하여 bromobenzene 대사계에 미치는 효소활성을 관찰하였다. Bromobenzene은 bromobenzene 2,3-oxide와 bromobenzene-3, 4-oxide로 전환되며, 3,4-oxide는 독성물질로서 epoxide hydrolase에 의해 무독성 bromobenzene-3,4-dihyrodiol로 대사 또는 glutathione S-transferase에 의하여 배설되기도 한다. 중국 민간에서 강장제로 사용하는 생열귀나무는 한방에서 소화불량, 위통 등의 치료에 사용되는 약용식물이다. 생열귀나무의 뿌리 추출물은 흰쥐의 간 epoxide 생성계에 관여하는 aminopyrine N-demethylase, aniline hydroxylase 활성과 epoxide를 대사시키는 glutathione S-transferase 활성에는 변화를 주지 않았다. 그러나 생열귀추출물 500 mg/kg 경구투여군은 eporide를 무독화시키는 epoxide hydrolase 활성에서 bromobenzene 투여로 효소활성이 저하된 대조군보다 33% 활성을 회복시켰다. 따라서 생열귀나무 뿌리는 간독성물질인 bromobenzene 대사에 관여하는 epoxide hydrolase 활성 증가로 인해 간보호작용이 일어나는 것으로 판단된다.

추출농도에 따른 오미자 및 구기자를 첨가한 한방약술의 품질특성 (Quality Properties of Herbal Wine containing Schizandra chinensis and Lycium chinense according to Extract Concentration)

  • 오성천
    • 한국응용과학기술학회지
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    • 제36권1호
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    • pp.341-347
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    • 2019
  • 본 연구에서는 한약재의 활용도를 높이기 위한 연구로 추출물 농도에 따른 생리활성물질의 용출량을 측정하기 위해 한방약술의 품질 특성과 Glutathione S-transferase의 활성 저해능을 측정한 결과는 다음과 같다. 한방약술의 pH결과는 4.4로 발효 전의 대조구 3.9보다 증가하였다. 이러한 변화는 알코올 발효과정 중 발효부산물 및 유기산 때문으로 사료된다. 한방약술의 산도는 0.55%로 발효 전의 대조구 0.09%보다 약 6배 증가하였다. 이런 결과는 유기산이 알코올 등과 결합하여 ester와 같은 향미 형성 등에 이용되는 것을 알 수 있다. 한방약술 15%의 glutathione S-transferase의 활성 저해능 $5.1{\pm}0.3$, 한방약술 20%는 저해능 $6.5{\pm}0.5$, 한방약술 25%는 $7.6{\pm}0.6$, 한방약술 30%는 $8.4{\pm}0.2$, 최대 농도인 35%에서의 저해능은 $9.7{\pm}0.7$로 나타내었다. 추출 농도별로 glutathione S-transferase의 활성 저해능은 통계학적으로 유의한 차이가 있음을 보였다 (p<0.05).

Enhancement of Anticancer Activities of Kimchi by Manipulating Ingredients

  • Kim, Ju-Youn;Rhee, Sook-Hee;Park, Kun-Young
    • Preventive Nutrition and Food Science
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    • 제5권3호
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    • pp.126-130
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    • 2000
  • To enhance the antitumor activity of Chinese cabbage kimchi, four kinds of kimchi, which ere differently prepared in kinds and levels of sub-ingredients, were fermented at 15$^{\circ}C$ for 1 day and then at 5$^{\circ}C$ up to pH 4.3. The solid tumor formation, hepatic glutathione S-transferase activity and glutathione contents in the liver, and natural killer (NK) cell activity of spleen were determined from the sarcoma-180 cell injected Balb/c mice that were treated with methanol extracts of the kimchi samples. Kimchi IV, prepared with organically cultivated Chinese cabbage, red pepper powder, garlic, Chinese pepper powder mustard leaf and heat processed salt (Gueun salt), reduced the tumor formation by 39.3% compared to the sarcoma-180 cell treated group, resulting in the smallest tumor weight. Methanol extracts of the kimchi III and kimchi IV recovered the activities of hepatic glutathione S-transferase(GST) that was decreased by the transplantation of the sarcoma-180 cells to th mice. The injections of methanol extracts of kimchi II and kimchi IV increased glutathione contents in sarcoma-180 cells treated mice. The methanol extract of kimchi IV increased the natural killer (NK) cell activity of spleen lymphocytes a more effectively (p<0.05) than those the other kimchi samples. These results suggest that the anticancer activities of kimchi can be increased by changing the kinds and levels of sub-ingredients.

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애엽(艾葉) 약침액(藥鍼液)에 의한 Phase II 효소 활성 유도 (Induction of Phase II Enzyme Activity by Artemisia asiatica Nakai Aqua-acupuncture Solution)

  • 윤성묵;조경희;손윤희;남경수;임종국
    • Korean Journal of Acupuncture
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    • 제18권1호
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    • pp.1-9
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    • 2001
  • 애엽으로 약침액을 조제하여 암예방 효과를 살펴 본 결과 다음과 같은 결론을 얻었다. 애엽 약침액으로 10일간 전투여한 후 Ehrlich ascites tumor cell을 이식하여 복수암이 유발된 생쥐의 EATC 성장을 살펴 본 결과 약침액을 투여한 생쥐의 EATC의 성장이 크게 억제되었으며, 복수암이 유발된 생쥐의 비장 무게가 대조군에 비해 증가하였다. 또한 장기간의 관찰에 의해서도 복수암 세포의 성장 저해에 의해 생쥐의 체중변화율은 대조군에 비해 크게 억제되었으며 수명 연장 효과가 나타났다. 이와같은 생체에서의 암예방 효과를 in vitro 상에서 그 기전을 살펴본 결과 애엽 약침액은 phase II detoxification 효소인 QR의 생성을 유도하고 GSH 함량을 증가시켜서 암예방 효과를 나타내었다.

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황기(黃耆) 약침액(藥鍼液)의 Glutathione S-transferase 와 NAD(P)H: Quinone Reductase 유도 (Induction of Glutathione S-transferase and NAD(P)H:Quinone Reductase by Astragali Radix Aqua-acupuncture Solution)

  • 류준선;임종국
    • Korean Journal of Acupuncture
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    • 제18권1호
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    • pp.21-26
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    • 2001
  • 발암물질을 무독화시키는 QR 생성 유도를 살펴보기 위하여 황기 약침액 및 열수추출액을 생쥐의 간암세포인 Hepa1c1c7에 처리하여 측정한 결과, 황기 약침액의 농도를 증가시킬수록 많은 QR 생성율을 보였으며, GSH 생성이 증가하였고, GST 생성 또한 증가하였다.

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In Vitro Cancer Chemopreventive Activities of Polysaccharides from Soybeans Fermented with Phellinus igniarius or Agrocybe cylindracea

  • Shon, Yun-Hee;Nam, Kyung-Soo
    • Journal of Microbiology and Biotechnology
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    • 제11권6호
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    • pp.1071-1076
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    • 2001
  • Chemopreventive activities of polysaccharides from soybeans fermented with either Phellinus igniarius or Agrocybe cylindracea were investigated by measuring the induction of quinone reductase (QR), glutathione S-transferase (GST) activities, and glutathione (GSH) levels in the cell culture along with inhibition of polyamine biosynthesis. The polysaccharides from soybeans fermented with P. igniarius strongly (p<0.005) induced QR activity at all concentrations tested. The extract not only induced GST activity in a dose-dependent manner in the concentration range of 0.1-1.0 mg, but significantly induced GSH revels in cultured Hepa 1c1c7 cells with a maximal 1.4-fold increase at 0.1 mg. The polysaccharides from soybeans fermented with A. cylindracea were effective in inhibiting polyamine metabolism. These results suggest that polysaccharides from soybeans fermented with P. igniarius or A. cylindracea have cancer chemopreventive activities in in vitro models and, therefore, could be considered as potential agents for cancer chemoprevention.

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