• 제목/요약/키워드: Cu,Zn-superoxide dismutase (SOD1)

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Effects of Placing Micro-Implants of Melatonin in Striatum on Oxidiative Stress and Neuronal Damage Mediated by N-Methyl-D-Aspartate (NMDA) and Non-NMDA Receptors

  • Kim, Hwa-Jung;Kwon, Jin-Suk
    • Archives of Pharmacal Research
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    • 제22권1호
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    • pp.35-43
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    • 1999
  • Overstimulation of both kainate (KA) and N-methyl-D-aspartate (NMDA) receptors has been reported to induce excitatoxicity which can be characterized by neuronal damage and formation of reactive oxygen free radicals. Neuroprotective effect of melatonin against KA-induced excitotoxicity have been documented in vitro and in vivo. It is, however, not clear whether melationin is also neuroportective against excitotoxicity mediated by NMDA receptors. In the present work, we tested the in vivo protective effects of striatally infused melatonin against the oxidative stress and neuronal damage induced by the injection of KA and NMDA receptors into the rat striatum. Melatonin implants consisting of 22-gauge stainless-steel cannule with melatonin fused inside the tip were placed bilaterally in the rat brain one week prior to intrastriatal injection of glutamate receptor subtype agonists. Melatonin showed protective effects against the elevation of lipid peroxidation induced by either KA or NMDA and recovered Cu, Zn-superoxide dismutase activities reduced by both KA and NMDA into the control level. Melatonin also clearly blocked both KA- and NMDA-receptor mediated neuronal damage assessed by the determination of choline acetyltransferase activity in striatal monogenages and by microscopic observation of rat brain section stained with cresyl violet. The protective effects of melatonin are comparable to those of DNQX and MK801 which are the KA- and NMDA-receptor antagonist, respectively. It is suggested that melatonin could protect against striatal oxidative damages mediated by glutamate receptors, both non-NMDA and NMDA receptors.

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흰쥐 간조직의 활성산소 및 제거효소에 미치는 목초액의 영향 (Effect of Pyroligneous Liquor on Oxygen Radicals and Their Scavenger Enzymes in Liver of CD Rats)

  • 최진호;조원기
    • Journal of Nutrition and Health
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    • 제40권2호
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    • pp.111-117
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    • 2007
  • 시판 목초액 A (원액 35%)을 사용하여 음용수에 0%, 1.0%, 25.0%, 50.0%, 75.0%가 되도록 조제한 다음, CD계 수컷 흰쥐 (150 ${\pm}$ 10 g)에 2개월 동안 조제사료와 함께 자유 음용케 하여 간조직 중의 활성산소로서 수퍼옥시드 라디칼(O$_{2}\;^-$), 히디록시 라디칼, 과산화수소 및 제거효소로서 수퍼옥시드 디스무타아제 (SOD), 글루타치온 퍼옥시다아제 (GPx) 및 카탈라아제 (CAT)에 미치는 영향을 평가하였다. 목초액 PL-25 및 PL-50 투여군의 간조직의 미토콘드리아 획분에서는 O$_{2}\;^-$의 생성량은 대조군 대비 12${\sim}$14%의 O$_{2}\;^-$의 생성량 억제효과가 나타났고, 간조직의 마이크로솜획분에서는 대조군 대비 각각 11.0${\sim}$15.0의 O$_{2}\;^-$의 생성량 억제효과가 나타났다. 간조직 미토콘드리아획분에서 ${\cdot}$OH 생성량이 목초액 PL-25 및 PL-50 투여군에서 대조군 대비 12${\sim}$20%의 ${\cdot}$OH 생성 억제효과가 나타났고, 간조직의 마이크로솜획분에서는 대조군 대비 17${\sim}$20%의 ${\cdot}$OH 생성 억제효과가 나타났다. 목초액 PL-25 및 PL-50 투여군의 간조직의 미토콘드리아획분에서는 대조군 대비 12${\sim}$15%의 유의적인 H$_{2}$O$_{2}$의 생성 억제효과가 나타났고, 간조직의 마이크로솜획분에서는 대조군 대비 20${\sim}$22%의 상당히 유의적인 H$_{2}$O$_{2}$의 생성 억제효과가 나타났다. 목초액 PL-25 및 PL-50 투여군의 간조직의 Mn-SOD 활성은 대조군 대비 15${\sim}$25%나 유의적인 활성 증가효과가 인정되었고, 간조직의 Cu/Zn-SOD 활성은 대조군 대비 11${\sim}$16%의 유의적인 SOD활성 증가효과가 인정되었다. 목초액 PL-25 및 PL-50 투여군의 간조직의 미토콘드리아획분의 GPx 활성은 대조군 대비 10${\sim}$17%의 GPx 활성 증가효과가 인정되었고, 간조직의 마이크로솜획분의 GPx 활성 증가효과가 인정되었다. 목초액 PL-25 및 PL-50 투여군의 간조직의 미트콘드리아획분의 CAT 활성은 대조군 대비 12${\sim}$14%의 유의적인 CAT 활성 증가효과가 나타났고, 간조직의 시토졸 1획분에서는 대조군 대비 15${\sim}$27%의 CAT 활성 증가효과가 인정되었다. 이상의 결과에서 목초액의 장기간 투여는 간조직 중의 활성산소의 억제효과뿐만 아니라 방어시스템으로서 활성산소 제거효소의 역할도 충실히 수행하여 노화를 효과적으로 예방하고 억제할 수 있을 것으로 기대된다.

Scratching Stimuli of Mycelia Influence Fruiting Body Production and ROS-Scavenging Gene Expression of Cordyceps militaris

  • Liu, Gui-Qing;Qiu, Xue-Hong;Cao, Li;Han, Ri-Chou
    • Mycobiology
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    • 제46권4호
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    • pp.382-387
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    • 2018
  • The entomopathogenic fungus Cordyceps militaris is a valuable medicinal ascomycete, which degenerates frequently during subsequent culture. To avoid economic losses during industrialized production, scratching stimuli of mycelia was introduced to improve the fruiting body production. The present results indicated that higher yields and biological efficiency were obtained from two degenerate strains (YN1-14 and YN2-7) but not from g38 (an insertional mutant in Rhf1 gene with higher yields and shorter growth periods). Furthermore, the growth periods of the fruiting bodies were at least 5 days earlier when the mycelia were scratched before stromata differentiation. Three ROS-scavenging genes including Cu/Zn superoxide dismutase (CmSod1), Glutathione peroxidase (CmGpx), and Catalase A (CmCat A) were isolated and their expression profiles against scratching were determined in degenerate strain YN1-14 and mutant strain g38. At day 5 after scratching, the expression level of CmGpx significantly decreased for strain g38, but that of CmSod1 significantly increased for YN1-14. These results indicated that scratching is an effective way to promote fruiting body production of degenerate strain, which may be related at least with Rhf1 and active oxygen scavenging genes.

Effect of troglitazone on radiation sensitivity in cervix cancer cells

  • An, Zhengzhe;Liu, Xianguang;Song, Hye-Jin;Choi, Chi-Hwan;Kim, Won-Dong;Yu, Jae-Ran;Park, Woo-Yoon
    • Radiation Oncology Journal
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    • 제30권2호
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    • pp.78-87
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    • 2012
  • Purpose: Troglitazone (TRO) is a peroxisome proliferator-activated receptor ${\gamma}$ ($PPAR{\gamma}$) agonist. TRO has antiproliferative activity on many kinds of cancer cells via G1 arrest. TRO also increases $Cu^{2+}/Zn^{2+}$-superoxide dismutase (CuZnSOD) and catalase. Cell cycle, and SOD and catalase may affect on radiation sensitivity. We investigated the effect of TRO on radiation sensitivity in cancer cells in vitro. Materials and Methods: Three human cervix cancer cell lines (HeLa, Me180, and SiHa) were used. The protein expressions of SOD and catalase, and catalase activities were measured at 2-10 ${\mu}M$ of TRO for 24 hours. Cell cycle was evaluated with flow cytometry. Reactive oxygen species (ROS) was measured using 2',7'-dichlorofluorescin diacetate. Cell survival by radiation was measured with clonogenic assay. Results: By 5 ${\mu}M$ TRO for 24 hours, the mRNA, protein expression and activity of catalase were increased in all three cell lines. G0-G1 phase cells were increased in HeLa and Me180 by 5 ${\mu}M$ TRO for 24 hours, but those were not increased in SiHa. By pretreatment with 5 ${\mu}M$ TRO radiation sensitivity was increased in HeLa and Me180, but it was decreased in SiHa. In Me180, with 2 ${\mu}M$ TRO which increased catalase but not increased G0-G1 cells, radiosensitization was not observed. ROS produced by radiation was decreased with TRO. Conclusion: TRO increases radiation sensitivity through G0-G1 arrest or decreases radiation sensitivity through catalase-mediated ROS scavenging according to TRO dose or cell types. The change of radiation sensitivity by combined with TRO is not dependent on the PPAR ${\gamma}$ expression level.

Melatonin mitigates the adverse effect of hypoxia during myocardial differentiation in mouse embryonic stem cells

  • Lee, Jae-Hwan;Yoo, Yeong-Min;Lee, Bonn;Jeong, SunHwa;Tran, Dinh Nam;Jeung, Eui-Bae
    • Journal of Veterinary Science
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    • 제22권4호
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    • pp.54.1-54.13
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    • 2021
  • Background: Hypoxia causes oxidative stress and affects cardiovascular function and the programming of cardiovascular disease. Melatonin promotes antioxidant enzymes such as superoxide dismutase, glutathione reductase, glutathione peroxidase, and catalase. Objectives: This study aims to investigate the correlation between melatonin and hypoxia induction in cardiomyocytes differentiation. Methods: Mouse embryonic stem cells (mESCs) were induced to myocardial differentiation. To demonstrate the influence of melatonin under hypoxia, mESC was pretreated with melatonin and then cultured in hypoxic condition. The cardiac beating ratio of the mESC-derived cardiomyocytes, mRNA and protein expression levels were investigated. Results: Under hypoxic condition, the mRNA expression of cardiac-lineage markers (Brachyury, Tbx20, and cTn1) and melatonin receptor (Mtnr1a) was reduced. The mRNA expression of cTn1 and the beating ratio of mESCs increased when melatonin was treated simultaneously with hypoxia, compared to when only exposed to hypoxia. Hypoxia-inducible factor (HIF)-1α protein decreased with melatonin treatment under hypoxia, and Mtnr1a mRNA expression increased. When the cells were exposed to hypoxia with melatonin treatment, the protein expressions of phospho-extracellular signal-related kinase (p-ERK) and Bcl-2-associated X proteins (Bax) decreased, however, the levels of phospho-protein kinase B (p-Akt), phosphatidylinositol 3-kinase (PI3K), B-cell lymphoma 2 (Bcl-2) proteins, and antioxidant enzymes including Cu/Zn-SOD, Mn-SOD, and catalase were increased. Competitive melatonin receptor antagonist luzindole blocked the melatonin-induced effects. Conclusions: This study demonstrates that hypoxia inhibits cardiomyocytes differentiation and melatonin partially mitigates the adverse effect of hypoxia in myocardial differentiation by regulating apoptosis and oxidative stress through the p-AKT and PI3K pathway.

Transduced HSP27 protein protects neuronal cell death by enhancing FALS-associated SOD1 mutant activity

  • An, Jae-Jin;Lee, Yeom-Pyo;Kim, Dae-Won;Sohn, Eun-Joung;Jeong, Hoon-Jae;Kang, Hye-Won;Shin, Min-Jae;Kim, Mi-Jin;Ahn, Eun-Hee;Jang, Sang-Ho;Kang, Jung-Hoon;Kang, Tae-Cheon;Won, Moo-Ho;Kwon, Oh-Shin;Cho, Sung-Woo;Lee, Kil-Soo;Park, Jin-Seu;Eum, Won-Sik;Choi, Soo-Young
    • BMB Reports
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    • 제42권3호
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    • pp.136-141
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    • 2009
  • Familial Amyotrophic lateral sclerosis (FALS) is a progressive neurodegenetative disorder induced by mutations of the SOD1 gene. Heat shock protein 27 (HSP27) is well-defined as a stress-inducible protein, however the its role in ALS protection has not yet been established. To investigate the role HSP27 may have in SOD1 mutant-mediated apoptosis, human SOD1 or HSP27 genes were fused with a PEP-1 peptide in a bacterial expression vector to produce a genetic in-frame fusion protein, which was then transduced into cells. We found the purified PEP-1-HSP27 fusion proteins can be transduced efficiently into neuronal cells and protect against cell death by enhancing mutant SOD1 activity. Moreover, transduced PEP-1-HSP27 efficiently prevents protein aggregation produced by oxidative stress. These results suggest that transduced HSP27 fusion protein may be explored as a potential therapeutic agent for FALS patients.

Antioxidant and Anti-inflammatory Effects of Yam (Dioscorea batatas Decne.) on Azoxymethane-induced Colonic Aberrant Crypt Foci in F344 Rats

  • Son, In Suk;Lee, Jeong Soon;Lee, Ju Yeon;Kwon, Chong Suk
    • Preventive Nutrition and Food Science
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    • 제19권2호
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    • pp.82-88
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    • 2014
  • Yam (Dioscorea batatas Decne.) has long been used as a health food and oriental folk medicine because of its nutritional fortification, tonic, anti-diarrheal, anti-inflammatory, antitussive, and expectorant effects. Reactive oxygen species (ROS), which are known to be implicated in a range of diseases, may be important progenitors of carcinogenesis. The aim of this study was to investigate the modulatory effect of yam on antioxidant status and inflammatory conditions during azoxymethane (AOM)-induced colon carcinogenesis in male F344 rats. We measured the formation of aberrant crypt foci (ACF), hemolysate antioxidant enzyme activities, colonic mucosal antioxidant enzyme gene expression, and colonic mucosal inflammatory mediator gene expression. The feeding of yam prior to carcinogenesis significantly inhibited AOM-induced colonic ACF formation. In yam-administered rats, erythrocyte levels of glutathione, glutathione peroxidase (GPx), and catalase were increased and colonic mucosal gene expression of Cu/Zn-superoxide dismutase (SOD), Mn-SOD, and GPx were up-regulated compared to the AOM group. Colonic mucosal gene expression of inflammatory mediators (i.e., nuclear factor kappaB, inducible nitric oxide synthase, cyclooxygenase-2, tumor necrosis factor alpha, and interleukin-1beta) was suppressed by the yam-supplemented diet. These results suggest that yam could be very useful for the prevention of colon cancer, as they enhance the antioxidant defense system and modulate inflammatory mediators.

Efficacy evaluation of novel organic iron complexes in laying hens: effects on laying performance, egg quality, egg iron content, and blood biochemical parameters

  • Jiuai Cao;Jiaming Zhu;Qin Zhou;Luyuan Zhao;Chenhao Zou;Yanshan Guo;Brian Curtin;Fei Ji;Bing Liu;Dongyou Yu
    • Animal Bioscience
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    • 제36권3호
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    • pp.498-505
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    • 2023
  • Objective: This study was conducted to determine the optimal dose of novel iron amino acid complexes (Fe-Lys-Glu) by measuring laying performance, egg quality, egg iron (Fe) concentrations, and blood biochemical parameters in laying hens. Methods: A total of 1,260 18-week-old healthy Beijing White laying hens were randomly divided into 7 groups with 12 replicates of 15 birds each. After a 2-wk acclimation to the basal diet, hens were fed diets supplemented with 0 (negative control, the analyzed innate iron content was 75.06 mg/kg), 15, 30, 45, 60, and 75 mg Fe/kg as Fe-Lys-Glu or 45 mg Fe/kg from FeSO4 (positive control) for 24 wk. Results: Results showed that compared with the negative and positive control groups, dietary supplementation with 30 to 75 mg Fe/kg from Fe-Lys-Glu significantly (linear and quadratic, p<0.05) increased the laying rate (LR) and average daily egg weight (ADEW); hens administered 45 to 75 mg Fe/kg as Fe-Lys-Glu showed a remarkable (linear, p<0.05) decrease in feed conversion ratio. There were no significant differences among all groups in egg quality. The iron concentrations in egg yolk and serum were elevated by increasing Fe-Lys-Glu levels, and the highest iron content was found in 75 mg Fe/kg group. In addition, hens fed 45 mg Fe/kg from Fe-Lys-Glu had (linear and quadratic, p<0.05) higher yolk Fe contents than that with the same dosage of FeSO4 supplementation. The red blood cell (RBC) count and hemoglobin content (linear and quadratic, p<0.05) increased obviously in the groups fed with 30 to 75 mg Fe/kg as Fe-Lys-Glu in comparison with the control group. Fe-Lys-Glu supplementation also (linear and quadratic, p<0.05) enhanced the activity of copper/zinc-superoxide dismutase (Cu/Zn-SOD) in serum, as a result, the serum malonaldehyde content (linear and quadratic, p<0.05) decreased in hens received 60 to 75 mg Fe/kg as Fe-Lys-Glu. Conclusion: Supplementation Fe-Lys-Glu in laying hens could substitute for FeSO4 and the optimal additive levels of Fe-Lys-Glu are 45 mg Fe/kg in layers diets based on the quadratic regression analysis of LR, ADEW, RBC, and Cu/Zn-SOD.

백편두의 항산화 물질 분리 및 동정 (Purification and Identification of Antioxidant Compounds from Dolichos lablab L. Seeds)

  • 권남우;김재연;조용범;황방연;김준구;우선희;이문순
    • 한국약용작물학회지
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    • 제27권6호
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    • pp.419-426
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    • 2019
  • Background: This study aimed to identify antioxidant compounds from the seeds of Dolichos lablab L. by bioassay-guided isolation and recrystallization. Methods and Results: The water layer of D. lablab L. seed extract inhibits intracellular reactive oxygen species (ROS) expressing the 2',7'-dichlorofluorescein diacetate (DCF-DA), Cu/Zn superoxide dismutase (SOD) and catalase genes, as determined by quantitative real-time PCR (qRT-PCR). Two compounds were purified from the water layer of the seeds of D. lablab L. using column chromatography and prep-high performance liquid chromatography (HPLC). Using nuclear magnetic resonance (NMR) and electrospray Ionization mass spectrometry (ESI-MS), their chemical structures were identified as 5-[(2-acetyl-2,3-dihydro-1H-indazol-1-yl)carbonyl]-4,5-dihydro-3H-furan-2-one (C14H14N2O4) and stachyose. Conclusions: Two active antioxidant compounds were purified from the seed extract of D. lablab L. seed extract and the structures of these compounds were identified as C14H14O4N2 and stachyose.

생식제품 급여가 영양불균형식이를 섭취하는 흰쥐의 항산화체계 및 혈청 무기질 농도에 미치는 영향 (Effects of Uncooked Powdered Food on Antioxidative System and Serum Mineral Concentrations in Rats Fed Unbalanced Diet)

  • 이여진;이해미;박태선
    • Journal of Nutrition and Health
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    • 제36권9호
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    • pp.898-907
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    • 2003
  • 본 연구에서는 비타민과 무기질을 sub-optimal 수준으로 섭취시키고 고콜레스테롤식이와 에탄올을 병행 섭취시키는 흰쥐를 대상으로 5주간 생식제품을 20% (생식20군) 및 40% (생식40군) 수준으로 보충 섭취시킨 후, 체내 항산화체계에 미치는 영향을 평가하여 다음과 같은 결과를 얻었다. 일일 식이섭취량, 체중증가량 및 식이효율은 일반대조군과 영양불균형대조군 간에 유의적인 차이가 관찰되지 않았고, 생식40군의 경우 영양불균형대조군에 비해 식이효율이 유의하게 향상되었다 (p < 0.05) . 간조직의 지질과 산화물농도는 일반대조군에 비해 영양불균형대조군에서 유의하게 더 낮았으며 (p < 0.05), 식이내 생식첨가에 의해 영향을 받지 않았다. 간조직의 SOD 활성은 일반대조군에 비해 영양불균형대조군에서 유의적으로 증가하였고, 생식 섭취군의 경우 영양불균형대조군에 비해 유의하게 감소하였다 (p < 0.05), 간조직의 catalase 활성은 영양불균형대조군에서 일반대조군에 비해 유의하게 더 낮았으며 (p <0.05), 생식섭취에 의해 영향을 받지 않았다. 간조직의 (GSH-Px + catalase)/SOD 비율은 영양불균형대조군에서 일반대조군보다 유의하게 더 낮았으며, 영양불균형대조식이에 생식을 20% 수준으로 첨가시킨 결과 유의하게 증가하였다 (P < 0.05). 영양불균형대조식이는 일반대조식이에 비해 혈중 Cu 농도를 유의하게 증가시켰다. 생식분말 섭취군의 경우 영양불균형대조군에 비해 Fe, Se, Mn, Zn 및 Cu 등의 무기질 섭취량이 더 많음에도 불구하고 혈중 농도는 오히려 더 낮게 나타났으며, 특히 Fe 및 Cu농도는 유의적으로 감소하였다. 이는 생식제품이 phytate 및 섬유질이 풍부한 전곡류 및 식물성식품들로 구성되어 있어 무기질의 생체이용률을 저하시키기 때문으로 사료되며, 생식제품의 장기 섭취시 이들 무기질 영양상태가 저하되지 않도록 주의가 필요할 것으로 생각된다.