• 제목/요약/키워드: damage accumulation

검색결과 454건 처리시간 0.031초

Vitamin C가 방사선과 Aflatoxin B1을 처리한 흰쥐의 간세포에서 Aflatoxin B1-DNA Adduct 형성에 미치는 영향 (Effects of vitamin C on the formation of aflatoxin B1-DNA adduct in rat livers treated with radiation and aflatoxin B1)

  • 김소영;김한수;강진순
    • 한국식품저장유통학회지
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    • 제21권5호
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    • pp.747-756
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    • 2014
  • 본 연구는 흰쥐에게 $AFB_1$을 투여하거나 방사선과 $AFB_1$을 병합처리함으로 유발된 흰쥐의 간세포에서의 $AFB_1$-DNA 부가체의 형성과 세포의 산화적 손상에 대한 vitamin C의 효과를 조사하기 위하여 수행되었다. X-ray 조사는 실험기간 내 단 1회로 실험사육기간 1일에 조사 하였고 X-ray 조사 후 vitamin C를 투여하였으며 vitamin C 투여 1시간 후 $AFB_1$을 투여하였다. Vitamin C와 $AFB_1$은 모두 복강투여로 실험 사육 첫 일부터 1회 시작하여 3일에 한번씩, 5회 반복 투였으며 실험동물 사육기간은 총 15일로 하였다. ELISA에 의한 흰쥐의 혈청 내 $AFB_1$ 잔여 농도는 $AFB_1$ 단독 투여군에서 $5.17{\pm}0.34ng/mL$이었으나 여기에 vitamin C 혼합 투여군에서는 $3.23{\pm}0.76ng/ml$가 검출되었다. 간세포의 $AFB_1$-DNA adduct 농도는 $AFB_1$ 단독 투여군에서는 $9.38{\pm}0.41ng/mL$이었으며 2군에 vitamin C를 함께 투여한 3군에서는 $5.28{\pm}0.32ng/ml$로 나타나 2군에 비해 유의적으로(p<0.001) 44% 감소한 양상을 나타내었다. 한편 X선 조사와 $AFB_1$ 병합처리한 4군에 비해 4군에 vitamin C를 투여한 5군에서 혈청 내 $AFB_1$ 함량과 간세포의 $AFB_1$-DNA adduct 함량이 다소 감소하였으나 유의적인 차이는 없었다. 또한 면역조직화학적 관찰에서 $AFB_1$ 단독 투여군에서는 중심정맥과 혈관주변에서 $AFB_1$ 축적이 관찰되었는데 이러한 현상은 vitamin C를 혼합 투여함으로써 중심정맥과 혈관 주변의 갈색 침전이 현저하게 감소한 것으로 나타났다. 그러나 X선 조사와 $AFB_1$ 병합 처리한 군에서는 그 정도가 약했다.

Paraquat 유도 산화스트레스하의 배추 잎에서 Ascorbate-Glutathione 회로 효소의 활성도에 대한 산화질소 (Nitric oxide)의 효과 (Effects of nitric oxide on ascorbate-glutathione cycle enzymes activities in chinese cabbage leaves under paraquat-induced oxidative stress)

  • 나호견;진창덕
    • Journal of Plant Biotechnology
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    • 제41권2호
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    • pp.73-80
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    • 2014
  • 산화질소(nitric oxide: NO) 공여체인 $100{\mu}M$ sodium nitroprusside (SNP)를 배추 잎에 전처리한 후 이어서 $2{\mu}M$ paraquat (PQ)처리 시, PQ에 의해 유도된 산화적 손상에 대한 잎의 내성이 효과적으로 증진되었다. 24 시간 광 배양기간 동안 PQ 단독 처리구 잎에서는 생체량, 엽록소 및 단백질 함량이 현저하게 감소하였으나 PQ 노출 전에 3시간 SNP 전처리로 이들 잎 손상이 의미 있게 완화되었다. 게다가 PQ 처리에 기인된 malondialdehyde (MDA)와 $H_2O_2$ 함량 증가도 SNP 전처리에 의해 유의하게 억제되었다. 잎에서 이들 PQ 독성에 대한 SNP의 방어효과와 관련하여 ascorbate-glutathione 회로 구성 효소의 활성도 변화를 조사하였다. PQ 단독 처리구에서 APX, DHAR 및 GR 효소 활성도는 배양 6시간후에 급격히 감소되어 대조구 잎과 비교 시 각각 대조구의 19%, 50%, 39% 수준의 활성도 값을 보였다. 그러나, 이들 효소 활성도 값 감소는 SNP 전처리에 의해 현저하게 억제되어 6시간 배양 후에 PQ 단독처리구 보다 각각 5배, 2배, 1.5배 높은 값을 나타내었다. 또한, 그 이후 24시간 배양 때까지 PQ 단독 처리구보다 계속 높은 활성도를 보이면서 점차로 감소하였다. 이들 결과로부터, PQ에 노출된 배추 잎에서 SNP 전처리에 의한 ascorbate-glutathione 회로의 활성화가 $H_2O_2$의 축적을 억제하며 그로인해 PQ에 의해 유도된 산화스트레스로부터 잎을 방어하는 것으로 생각되었다. 동시에 이 들 결과는 산화질소가 배추 잎에서 PQ 스트레스에 대한 항산화 방어자로서의 역할을 하는 것을 의미한다.

Effects of a Chelate (DTPA) on Cucumber Growth and Soil Chemical Properties in Nutrient-accumulated Soil of Polytunnel Greenhouse

  • Kim, Myung Sook;Kim, Yoo Hak;Kang, Seong Soo;Kong, Myung Suk;Hyun, Byung Keun;Lee, Chang Hoon
    • 한국토양비료학회지
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    • 제46권6호
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    • pp.665-672
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    • 2013
  • This study was conducted to evaluate the effects of a chelating agent on cucumber growth and changes in soil nutrients availability in polytunnel greenhouse fields. Diethylene triamine penta acetic acid (DTPA) was selected as a chelating agent. Two experiments were carried out as follows: i) For field experiment in the autumn season of 2010, each plot was treated by varying the concentration and the number of times being applied with DTPA; [DTPA (0.5 mM, 1 time/3 months), DTPA (0.06 mM, 1 time/1 week), DTPA (0.13 mM, 1 time/2 weeks), DTPA (0.06 mM, 1 time/1 week)+N]. Conventional practice was also investigated. ii) In the spring and summer seasons of 2011, each plot was treated by varying the concentration (0, 0.06, 0.13, 0.19 mM) of DTPA, chemical fertilizers (NPK), and combination of chemical fertilizers and DTPA 0.06 mM. The fruit yields of cucumber and soil chemical properties had no significant differences between treatments. However, in the spring season of 2011, DTPA 0.06 mM plot added 1 time per 2 weeks increased the yield of cucumber, but caused the reduction of yield in next cultivation season. This result showed that excess use of DTPA can cause the damage of crop growth. The inorgainc contents such as Ca and Mg absorbed by cucumber plant had significant differences between DTPA 0.19 mM (2 times/1 week) and fertilizers plus DTPA treatments [DTPA 0.06 mM (2 times/1 week) + 1/2 NPK, DTPA 0.06 mM (2 times/1 week) + NPK]. The input cost of fertilizers was saved when the concentration and the number of times added with DTPA was 0.06 mM and 1 time a week, respectively. This treatment used 67% less of applied fertilizers cost than the plot of conventional practice did. Thus, this research suggested that the application of DTPA 0.06 mM by 1 time a week can be effective for sustainability of crop production and reduction of fertilizers usage in polytunnel greenhouse.

김치 종류를 달리한 식이가 Hairless Mice의 간과 피부에서 산화억제 및 광산화에 미치는 영향 (Effect of Different Kimchi Diets on Oxidation and Photooxidation in Liver and Skin of Hairless Mice)

  • 류복미;류승희;이유순;전영수;문갑순
    • 한국식품영양과학회지
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    • 제33권2호
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    • pp.291-298
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    • 2004
  • 김치에는 여러 가지 항산화 물질들이 많이 함유되어 있으므로 김치의 섭취는 생체조직의 노화억제 효과가 있을 것으로 기대된다. 본 연구에서 배추김치, 갓김치, 부추김치를 동결건조하여 항산화물질의 함량을 측정한 결과 갓김치와 부추김치의 클로로필 함량이 가장 높았고 $\beta$-카로텐과 ascorbic acid 함량은 갓김치에서 가장 높았다. Hairless mouse에게 10% 동결건조 김치식이를 공급하여 20주간 사육한 후 간에서 활성산소종의 생성량을 측정한 결과 superoxide anion과hydroxyl radical 함량은 유의적인 차이가 없었고 hydrogen peroxide 함량은 갓김치군과 부추김치군에서 유의적으로 낮게 나타나 이들 김치가 활성산소를 소거하는데 효과가 있는 것으로 나타났다. 간 균질액에서 지질과산화물을 측정한 결과 대조군에 비해 김치섭취군에서 지질과산화가 낮게 나타났으며, 특히 갓김치 와 부추김 치군의 효과가 우수하였다. 피부에서 지질과산화물 함량은 김치섭취군들이 대조군보다 낮게 나타났으며, 부추김치가 유의적으로 지질과산화를 억제하였다. 김치섭취가 광산화에 미치는 영향을 규명하기 위해 간 및 피부조직에 자외선을 조사한 후 조직산화 정도를 측정한 결과 간과 피부의 지질과산화물 함량은 갓김치군과 배추김치군에서 대조군보다 낮아졌으나 부추김치군에서는 높게 나타났다. 즉, 자외선 조사 후 갓김치군과 배추김치군은 대조군보다 광산화가 억제되었으나 부추김치군에서는 산화가 촉진되었다.

납 노출에 따른 붕어(Carassius auratus) 조직의 미세구조 및 생리적 변화 (Morphological and Physiological Effects of Lead (Pb) Exposure on Tissues of Carassius auratus)

  • 김정숙;신명자;이종은;서을원
    • 생태와환경
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    • 제43권3호
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    • pp.409-417
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    • 2010
  • 본 연구는 Pb의 농도와 노출 기간이 붕어(Carassius auratus) 조직의 미세구조와 생리적 변화에 미치는 영향을 조사하였다. 아가미, 뼈와 근육 조직에서 Pb의 축적 농도는 노출 40일에 증가하였다. 아가미 조직 내 Pb의 축적량은 다른 조직에 비하여 높았으며, 아가미, 뼈 및 근육 조직에서 노출기간이 길어질수록 증가하였다. Pb에 노출된 아가미, 뼈와 근육 조직의 항산화효소 활성은 아가미와 근육 조직에서 높았으며, 신장 조직에서 가장 낮은 활성을 보였다. 또한 항산화효소 중 superoxide dismutase의 활성은 대조군에 비해 2배 정도 증가하였으나, glutathion peroxidas의 활성은 매우 낮았다. Pb에 노출된 아가미 조직에서 점액세포는 수가 증가하였으며, 곤봉화와 부종이 이차새변에서 나타났다. 또한 40일간 Pb에 노출된 아가미 조직 내 미토콘드리아와 핵에서는 막의 손상이 관찰되었으며, 신장 조직 내 사구체는 수축되어 보우만 주머니의 공간이 넓게 관찰되었다. 이러한 결과로 보아 붕어 조직 이 장기간 고농도의 Pb에 노출이 되면 비정상적인 형태로 변형되며, 이에 따라 매우 유해한 영향을 받을 수 있을 것으로 생각된다.

시령탕(柴苓湯)이 에탄올 투여로 유발된 흰쥐의 간손상에 미치는 방어효과 (Effects of Shiryung-tang Extract on the Liver Injury induced by Ethanol in Rats)

  • 김범회;최영현
    • 동의생리병리학회지
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    • 제27권5호
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    • pp.611-616
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    • 2013
  • Alcoholic liver disease (ALD) is a major cause of morbidity and mortality around the world. Although much progress has been made in understanding the pathogenesis of ALD, there remains no effective therapy for it. Accumulated evidence indicates that oxidative stress is the main pathological factors in the development of ALD. Ethanol administration causes accumulation of reactive oxygen species (ROS), including superoxide, hydroxyl radical, and hydrogen peroxide. ROS, in turn, cause lipid peroxidation of cellular membranes, and protein and DNA oxidation, which results in hepatocyte injury. In addition to pro-oxidants formation, antioxidants depletion caused by ethanol administration also results in oxidative stress. The objective of this study is to investigate the effects of Shiryung-tang extract on the chronic alcoholic liver injury induced by EtOH. Male Sprague Dawley rats were used in this study. All rats were maintained under standard laboratory conditions ($23{\pm}1^{\circ}C$, 12h light/12h dark cycles). All animals (n=30) were randomly divided into following groups: (1) Normal group, treated with distilled water (n=10); (2) Control group, treated with ethanol (n=10); (3) Sample group, treated with ethanol + pharmacopuncture (n=10). For oral administration of ethanol in Control and Sample 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 Shiryung-tang extract daily for 8 weeks. Control group were given normal saline for same weeks. As a results, the oral administration of ethanol for 8 weeks leads to hepatotoxicity. The levels of hepatic marker such as HDL-cholesterol, triglyceride, aspartate aminotransferase and alanine aminotransferase were altered. The ethanol also increased lipid peroxidation and depletion of antioxidant enzyme activities as well as hepatic tissue injury. However, the treatment of Shiryung-tang extract prevented all the alterations induced by ethanol and returned their levels to near normal. These data suggest that Shiryung-tang extract could have a beneficial effect in inhibiting the oxidative damage induced by chronic ethanol administration. Therefore, Shiryung-tang extract can be a candidate to protect against EtOH-induced liver injury.

Pharmacologic Inhibition of Autophagy Sensitizes Human Acute Leukemia Jurkat T Cells to Acacetin-Induced Apoptosis

  • Lee, Ji Young;Jun, Do Youn;Kim, Ki Yun;Ha, Eun Ji;Woo, Mi Hee;Ko, Jee Youn;Yun, Young Ho;Oh, In-Seok;Kim, Young Ho
    • Journal of Microbiology and Biotechnology
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    • 제27권1호
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    • pp.197-205
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    • 2017
  • Exposure of Jurkat T cell clone (J/Neo cells) to acacetin (5,7-dihydroxy-4'-methoxyflavone), which is present in barnyard millet (Echinochloa esculenta (A. Braun)) grains, caused cytotoxicity, enhancement of apoptotic $sub-G_1$ rate, Bak activation, loss of mitochondrial membrane potential (${\Delta}{\Psi}m$), activation of caspase-9 and caspase-3, degradation of poly(ADP-ribose) polymerase, and FITC-Annexin V-stainable phosphatidylserine exposure on the external surface of the cytoplasmic membrane without accompanying necrosis. These apoptotic responses were abrogated in Jurkat T cell clone (J/Bcl-xL) overexpressing Bcl-xL. Under the same conditions, cellular autophagic responses, including suppression of the Akt-mTOR pathway and p62/SQSTM1 down-regulation, were commonly detected in J/Neo and J/Bcl-xL cells; however, formation of acridine orange-stainable acidic vascular organelles, LC3-I/II conversion, and Beclin-1 phosphorylation (Ser-15) were detected only in J/Neo cells. Correspondingly, concomitant treatment with the autophagy inhibitor (3-methyladenine or LY294002) appeared to enhance acacetin-induced apoptotic responses, such as Bak activation, ${\Delta}{\Psi}m$ loss, activation of caspase-9 and caspase-3, and apoptotic $sub-G_1$ accumulation. This indicated that acacetin could induce apoptosis and cytoprotective autophagy in Jurkat T cells simultaneously. Together, these results demonstrate that acacetin induces not only apoptotic cell death via activation of Bak, loss of ${\Delta}{\Psi}m$, and activation of the mitochondrial caspase cascade, but also cytoprotective autophagy resulting from suppression of the Akt-mTOR pathway. Furthermore, pharmacologic inhibition of the autophagy pathway augments the activation of Bak and resultant mitochondrial damage-mediated apoptosis in Jurkat T cells.

HvIRIP 과발현 유채 형질전환체의 내한성 증진 (Overexpression of Ice Recrystallization Inhibition Protein (HvIRIP) from Barley Enhances Cold Tolerance in Transgenic rapeseed plants)

  • 노경희;박종석;강한철;김종범;장영석;김광수;이한길
    • Journal of Applied Biological Chemistry
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    • 제58권4호
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    • pp.325-332
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    • 2015
  • 유채는 월동작물로 내한성이 약해 남부지역에서만 재배가 가능하다. 따라서 재배면적 확대 및 안정적 생산성 확보를 위해 내한성 증진 품종 육성이 절실하다. 본 연구에서는 유채의 내한성을 증진시키기 위해 보리에서 유래한 HvIRIP 유전자를 CaMV35S 프로모터 조절하에서 전신발현되도록 운반체를 제작하였고, 아그로박테리움을 이용하여 유채에 형질전환하였다. Southern 분석을 통해 HvIRIP 유전자가 유채 Genome 안으로 전이 되었음을 확인하였다. 또한 Northern 분석을 통해 $4^{\circ}C$에서 2주간 처리된 유묘에서 HvIRIP 유전자의 발현이 크게 증대되는 것을 알 수 있었다. 본엽 3-4매 전개 유채 형질전환체를 영하 $5^{\circ}C$에서 2일간 저온에 노출한 후 회복여부를 조사한 결과, 대조구는 회복하지 못하고 죽은 반면, 형질전환체는 회복이 정상적으로 이루어졌다. 또한 저온스트레스가 진행되는 동안에 스트레스를 극복하는데 필요한 Proline 함량이 형질전환체에서 크게 증대되는 것이 관찰되었다. 이 외에도 저온스트레스 과정 중에 생성되는 활성산소의 독성을 감소시키는 항산화제 효소인 CAT, SOD 그리고 ADH 활성을 측정한 결과, 대조구에 비해 형질전환체에서 그 함량이 현저히 증가됨을 알 수 있었다. 따라서 이러한 결과를 통해 HvIRIP 유전자가 함유된 유채 형질전환체의 내한성이 증진되었음을 확인하였다.

Desalinated underground seawater of Jeju Island (Korea) improves lipid metabolism in mice fed diets containing high fat and increases antioxidant potential in t-BHP treated HepG2 cells

  • Noh, Jung-Ran;Gang, Gil-Tae;Kim, Yong-Hoon;Yang, Keum-Jin;Lee, Chul-Ho;Na, O-Su;Kim, Gi-Ju;Oh, Won-Keun;Lee, Young-Don
    • Nutrition Research and Practice
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    • 제4권1호
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    • pp.3-10
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    • 2010
  • This study was performed to investigate the effect of desalinated underground seawater (named as 'magma seawater', MSW) of Jeju Island in Korea on lipid metabolism and antioxidant activity. MSW was collected from underground of Han-Dong in Jeju Island, and freely given to high fat diet (HFD)-fed C57BL/6 mice for 10 weeks. Although there were no significant differences in the body weight changes and plasma lipid levels, hepatic triglyceride levels were significantly lower in the MSW group than in the normal tap water (TW)-drunken control group. Furthermore, the activity of fatty acid synthase (FAS) was significantly decreased and carnitine palmitoyltransferase (CPT) activity was increased in MSW group compared to TW group. Similarly, real-time PCR analysis revealed that mRNA expressions of lipogenic genes were lowered in MSW groups compared to the control group. In a morphometric observation on the liver tissue, accumulation of fats was remarkably reduced in MSW group. Meanwhile, in vitro assay, tree radical scavenging activity measured by using diphenylpicrylhydrazyl (DPPH) was increased in MSW group. The 2'-7'-dichlorofluorescein diacetate (DCF-DA) staining followed with fluorescent microscopy showed a low intensity of fluorescence in MSW-treated HepG2 cells, compared to TW-treated HepG2 cells, which indicated that the production of reactive oxygen species by tert-butyl hydroperoxide (t-BHP) in HepG2 cells was decreased by MSW treatment. The antioxidant effect of MSW on t-BHP-induced oxidative stress in HepG2 cells was supported by the increased activities of intracellular antioxidant enzymes such as catalase and glutathione reductase. From these results, we speculate that MSW has an inhibitory effect on lipogenesis in liver and might play a protective role against cell damage by t-BHP-induced oxidative stress.

Antioxidant and hepatoprotective effects of Korean ginseng extract GS-KG9 in a D-galactosamine-induced liver damage animal model

  • Jo, Yun Ho;Lee, Hwan;Oh, Myeong Hwan;Lee, Gyeong Hee;Lee, You Jin;Lee, Ji Sun;Kim, Min Jung;Kim, Won Yong;Kim, Jin Seong;Yoo, Dae Seok;Cho, Sang Won;Cha, Seon Woo;Pyo, Mi Kyung
    • Nutrition Research and Practice
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    • 제14권4호
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    • pp.334-351
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    • 2020
  • BACKGROUND/OBJECTIVES: This study was designed to investigate the improvement effect of white ginseng extract (GS-KG9) on D-galactosamine (Ga1N)-induced oxidative stress and liver injury. SUBJECTS/METHODS: Sixty Sprague-Dawley rats were divided into 6 groups. Rats were orally administrated with GS-KG9 (300, 500, or 700 mg/kg) or silymarin (25 mg/kg) for 2 weeks. The rats of the GS-KG9- and silymarin-treated groups and a control group were then intraperitoneally injected Ga1N at a concentration of 650 mg/kg for 4 days. To investigate the protective effect of GS-KG9 against GalN-induced liver injury, blood liver function indicators, anti-oxidative stress indicators, and histopathological features were analyzed. RESULTS: Serum biochemical analysis indicated that GS-KG9 ameliorated the elevation of aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), and lactate dehydrogenase (LDH) in GalN-treated rats. The hepatoprotective effects of GS-KG9 involved enhancing components of the hepatic antioxidant defense system, including glutathione, glutathione peroxidase (GPx), superoxide dismutase (SOD), and catalase (CAT). In addition, GS-KG9 treatment inhibited reactive oxygen species (ROS) production induced by GalN treatment in hepatocytes and significantly increased the expression levels of nuclear factor erythroid-2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1) proteins, which are antioxidant proteins. In particular, by histological analyses bases on hematoxylin and eosin, Masson's trichrome, α-smooth muscle actin, and transforming growth factor-β1 staining, we determined that the administration of 500 mg/kg GS-KG9 inhibited hepatic inflammation and fibrosis due to the excessive accumulation of collagen. CONCLUSIONS: These findings demonstrate that GS-KG9 improves GalN-induced liver inflammation, necrosis, and fibrosis by attenuating oxidative stress. Therefore, GS-KG9 may be considered a useful candidate in the development of a natural preventive agent against liver injury.