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      마우스에서 사염화탄소로 유발된 급성 간독성에 대한 EDTA 및 EGTA의 보호효과 = Protective effects of EDTA and EGTA against CCl<sub>4</sub>-induced acute hepatotoxicity in mice

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      https://www.riss.kr/link?id=A105732972

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      다국어 초록 (Multilingual Abstract)

      This study investigated the protective effects of ethylene glycol-bis(${\beta}$-aminoethyl ether)-N,N,N',N'-tetraacetic acid (EGTA), an extracellular calcium chelator, and ethylenediaminetetraacetic acid (EDTA), which chelates calcium and most metal ions, against carbon tetrachloride ($CCl_4$)-induced acute hepatotoxicity in mice. Mice were treated with EGTA or EDTA at a dose of 20 (low) or 100 mg/kg (high) subcutaneously 1h before $CCl_4$ administration. The mice were fasted and sacrificed 18h after $CCl_4$ treatment. Blood samples were collected from the carotid artery by decapitation under light ether anesthesia. Serum alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), triglyceride (TG), and cholesterol levels were measured. Malondialdehyde (MDA) production was determined as an index of lipid peroxidation in the liver. The liver, kidneys, and spleen were weighed. We also evaluated the histopathological changes in the liver in each group. The relative weights of the liver were significantly higher in the $CCl_4$-treatment group than in the normal group, except in the high-EDTA treatment group. EGTA and EDTA treatment caused a significant decrease in serum ALP, ALT, and AST levels. Of all of the doses of EGTA and EDTA tested, the high-EDTA dose resulted in the most remarkable inhibitory action. The protective effect in the high-EDTA-treatment group was confirmed histopathologically. The low-EGTA-treatment group showed a significant decrease in serum TG and cholesterol levels. Liver MDA levels were significantly decreased in the EGTA (20 mg/kg) and EDTA (20, 100 mg/kg) groups. These results suggest that EDTA, which chelates both calcium and metal ions, confers better protection in $CCl_4$-induced acute liver damage than does EGTA, a calcium chelator.
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      This study investigated the protective effects of ethylene glycol-bis(${\beta}$-aminoethyl ether)-N,N,N',N'-tetraacetic acid (EGTA), an extracellular calcium chelator, and ethylenediaminetetraacetic acid (EDTA), which chelates calcium and most metal i...

      This study investigated the protective effects of ethylene glycol-bis(${\beta}$-aminoethyl ether)-N,N,N',N'-tetraacetic acid (EGTA), an extracellular calcium chelator, and ethylenediaminetetraacetic acid (EDTA), which chelates calcium and most metal ions, against carbon tetrachloride ($CCl_4$)-induced acute hepatotoxicity in mice. Mice were treated with EGTA or EDTA at a dose of 20 (low) or 100 mg/kg (high) subcutaneously 1h before $CCl_4$ administration. The mice were fasted and sacrificed 18h after $CCl_4$ treatment. Blood samples were collected from the carotid artery by decapitation under light ether anesthesia. Serum alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), triglyceride (TG), and cholesterol levels were measured. Malondialdehyde (MDA) production was determined as an index of lipid peroxidation in the liver. The liver, kidneys, and spleen were weighed. We also evaluated the histopathological changes in the liver in each group. The relative weights of the liver were significantly higher in the $CCl_4$-treatment group than in the normal group, except in the high-EDTA treatment group. EGTA and EDTA treatment caused a significant decrease in serum ALP, ALT, and AST levels. Of all of the doses of EGTA and EDTA tested, the high-EDTA dose resulted in the most remarkable inhibitory action. The protective effect in the high-EDTA-treatment group was confirmed histopathologically. The low-EGTA-treatment group showed a significant decrease in serum TG and cholesterol levels. Liver MDA levels were significantly decreased in the EGTA (20 mg/kg) and EDTA (20, 100 mg/kg) groups. These results suggest that EDTA, which chelates both calcium and metal ions, confers better protection in $CCl_4$-induced acute liver damage than does EGTA, a calcium chelator.

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      참고문헌 (Reference)

      1 배지혜, "흰쥐에 있어서 사염화탄소에 의한 간손상의 allopurinol의 영향" 11 : 247-252, 1995

      2 Boullerne AI, "of calcium in nitric oxide-induced cytotoxicity: EGTA protects mouse oligodendrocytes" 63 : 124-135, 2001

      3 Younes M, "The role of iron in the paracetamol- and CCl4-induced lipid peroxidation and hepatotoxicity" 327-334,

      4 Minotti G, "The role of iron in oxygen radical mediated lipid peroxidation" 1-19,

      5 Klaassen CD, "The pharmacological basis of therapeutics" Pergamon Press (nmetallic environmental toxicants) : 1622-1623, 1985

      6 Halliwell B, "The importance of free radicals and catalytic metal ions in human diseases" 89-193, molaspectsmed1985

      7 Fisher AEO, "Superoxide and hydrogen peroxide suppression by metal ions and their EDTA complexes" 316 : 48-51, 2004

      8 Mansour MA, "Protective effects of thymoquinone and desferrioxamine against hepatotoxicity of carbon tetrachloride in mice" 66 : 2583-2591, 2000

      9 de Ferreyra EC, "Prevention of CCl4-induced liver necrosis by the calcium chelator arsenazo III" de fe (de fe): expmolpathol1993194-204

      10 McCay PB, "Oxygen and carbon-centered free radical formation during carbon tetrachloride metabolism Observation of lipid radicals in vivo and in vitro" 2135-2143,

      1 배지혜, "흰쥐에 있어서 사염화탄소에 의한 간손상의 allopurinol의 영향" 11 : 247-252, 1995

      2 Boullerne AI, "of calcium in nitric oxide-induced cytotoxicity: EGTA protects mouse oligodendrocytes" 63 : 124-135, 2001

      3 Younes M, "The role of iron in the paracetamol- and CCl4-induced lipid peroxidation and hepatotoxicity" 327-334,

      4 Minotti G, "The role of iron in oxygen radical mediated lipid peroxidation" 1-19,

      5 Klaassen CD, "The pharmacological basis of therapeutics" Pergamon Press (nmetallic environmental toxicants) : 1622-1623, 1985

      6 Halliwell B, "The importance of free radicals and catalytic metal ions in human diseases" 89-193, molaspectsmed1985

      7 Fisher AEO, "Superoxide and hydrogen peroxide suppression by metal ions and their EDTA complexes" 316 : 48-51, 2004

      8 Mansour MA, "Protective effects of thymoquinone and desferrioxamine against hepatotoxicity of carbon tetrachloride in mice" 66 : 2583-2591, 2000

      9 de Ferreyra EC, "Prevention of CCl4-induced liver necrosis by the calcium chelator arsenazo III" de fe (de fe): expmolpathol1993194-204

      10 McCay PB, "Oxygen and carbon-centered free radical formation during carbon tetrachloride metabolism Observation of lipid radicals in vivo and in vitro" 2135-2143,

      11 "Mechanisms of lipid peroxidation dependent upon cytochrome P-450 LM2" 195-201

      12 Aurich O, "Genetic toxicology of ethylenediaminetetraacetic acid" 149-173,

      13 Agarwal AK, "Excessive hepatic accumulation of intracellular Ca2+ in chlordecone potentiated CCl4 toxicity" 17-24, toxicology1984

      14 Albano E, "Effects of carbon tetrachloride on calcium homeostasis" 2719-2725,

      15 Frezza EE, "CCl4-induced liver cirrhosis and hepatocellular carcinoma in rats relationship to plasma zinc" 367-369, hepatogastroenterology1994

      16 Yagi K, "Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction" 351-358,

      17 Cherny RA, "Aqueous dissolution of Alzheimer’s disease Aβ amyloid deposits by biometal depletion" 274 : 23223-23228, 1999

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      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-05-20 학술지명변경 외국어명 : Korean J. of Veterinary Science -> Korean J. of Veterinary Research KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-07-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.15 0.15 0.13
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.11 0.1 0.25 0.04
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