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      KCI등재후보 SCOPUS SCIE

      CJ-11555의 안전성 약리실험 = Safety Pharmacology of CJ-11555

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      https://www.riss.kr/link?id=A75919887

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      다국어 초록 (Multilingual Abstract)

      Safety pharmacological properties of CJ-11555, an anti-cirrhotic agent, were investigated in experimental animals and in vitro test system. CJ-11555 had no effects on normal body temperature in rats, motor coordination, chemoshock induced by pentetrazol, electric shock induced by electric shocker and writhing syndromes in mice at dose levels of 100, 300 and 1,000 mg/kg. CJ-11555 inhibited intestinal activity and prolonged hexobarbital-induced sleeping time in mice at the dose level of 1,000 mg/kg. CJ-11555 affected on general activity and behaviour tests in SD rats, such as<br/>
      lacrimation, ptosis, piloerection, decreased body tone, abnormal dispersion within the cage, diarrhoea, red colored faeces, slight hypothermia and decreased grooming, at the dose level of 1,000mg/kg in rats. CJ-11555 was effected on cardiovascular and respiratory system in anesthetized beagle dogs, such as tachycardia, increase of mean blood pressure and decrease of PR interval, decrease of respiratory rate and minute volume, at dose levels of 10 and <br/>
      30mg/kg. However, these effects were also observed in vehicle treated anesthetized beagle dogs. In in vitro experiments, CJ-<br/>
      11555 inhibited agonists (histamine, acetyl-choline or BaCl2) induced contraction of isolated guinea-pig at the concentration of 30x10-6 M. CJ-11555 was weekly inhibited hERG channel current at concentrations of 10 and 30x10-6 M, and IC50 was estimated to be higher than 30x10-6 M. Based on these results, it was concluded that CJ-11555 affected on cardiovascular and respiratory system, general activity and behaviour and hexobarbital-induced sleeping time at the dose level of 1,000 mg/kg and contraction of the smooth muscle and hERG channel current at the concentration of 30x10-6 M.
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      Safety pharmacological properties of CJ-11555, an anti-cirrhotic agent, were investigated in experimental animals and in vitro test system. CJ-11555 had no effects on normal body temperature in rats, motor coordination, chemoshock induced by pentetraz...

      Safety pharmacological properties of CJ-11555, an anti-cirrhotic agent, were investigated in experimental animals and in vitro test system. CJ-11555 had no effects on normal body temperature in rats, motor coordination, chemoshock induced by pentetrazol, electric shock induced by electric shocker and writhing syndromes in mice at dose levels of 100, 300 and 1,000 mg/kg. CJ-11555 inhibited intestinal activity and prolonged hexobarbital-induced sleeping time in mice at the dose level of 1,000 mg/kg. CJ-11555 affected on general activity and behaviour tests in SD rats, such as<br/>
      lacrimation, ptosis, piloerection, decreased body tone, abnormal dispersion within the cage, diarrhoea, red colored faeces, slight hypothermia and decreased grooming, at the dose level of 1,000mg/kg in rats. CJ-11555 was effected on cardiovascular and respiratory system in anesthetized beagle dogs, such as tachycardia, increase of mean blood pressure and decrease of PR interval, decrease of respiratory rate and minute volume, at dose levels of 10 and <br/>
      30mg/kg. However, these effects were also observed in vehicle treated anesthetized beagle dogs. In in vitro experiments, CJ-<br/>
      11555 inhibited agonists (histamine, acetyl-choline or BaCl2) induced contraction of isolated guinea-pig at the concentration of 30x10-6 M. CJ-11555 was weekly inhibited hERG channel current at concentrations of 10 and 30x10-6 M, and IC50 was estimated to be higher than 30x10-6 M. Based on these results, it was concluded that CJ-11555 affected on cardiovascular and respiratory system, general activity and behaviour and hexobarbital-induced sleeping time at the dose level of 1,000 mg/kg and contraction of the smooth muscle and hERG channel current at the concentration of 30x10-6 M.

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      목차 (Table of Contents)

      • ABSTRACT
      • 서론
      • 재료 및 방법
      • 시험결과
      • 고찰
      • ABSTRACT
      • 서론
      • 재료 및 방법
      • 시험결과
      • 고찰
      • 감사의 글
      • 참고문헌
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      참고문헌 (Reference)

      1 "의약품 등의 일반약리시험 지침" 식품의약품 안전청 1998.5.

      2 "quantitative procedure for assessing the behavioral and physiologic state of the mouse" 222-257, 1968

      3 "Strategies for chemoprevention of liver cancer" 2 : 58-64, 2002

      4 "Safety pharmacology study for human pharmaceuticals" ICH Harmonized Tripartite guideline (S7A) 2001

      5 "Oltipraz regenerates cirrhotic liver through CCAAT/enhancer binding protein-mediated stellate cell inactivation" 16 : 1988-1990, 2002b

      6 "Inhibition of dimethylnitrosamine-induced liver fibrosis by 5-(2-pyrazinyl)-4-methyl-1,2-dithiol-3-thione (oltipraz) in rats: suppression of transforming growth factor-beta1 and tumor necrosis factor-alpha expression." 139 : 61-67, 2002a

      7 "Improve patch clamp techniques for high-resolution current recording from cells and cell-free membrane-patches" 85-100, 1981

      8 "Chronic toxicity studies of 5-(2-pyrazinyl)-4-methyl-1,2-dithiole-3-thione, a potential chemopreventive agent." 35 : 9-21, 1997

      9 "Ann Rev Pharmacol" 25 : 485-508, 1985

      1 "의약품 등의 일반약리시험 지침" 식품의약품 안전청 1998.5.

      2 "quantitative procedure for assessing the behavioral and physiologic state of the mouse" 222-257, 1968

      3 "Strategies for chemoprevention of liver cancer" 2 : 58-64, 2002

      4 "Safety pharmacology study for human pharmaceuticals" ICH Harmonized Tripartite guideline (S7A) 2001

      5 "Oltipraz regenerates cirrhotic liver through CCAAT/enhancer binding protein-mediated stellate cell inactivation" 16 : 1988-1990, 2002b

      6 "Inhibition of dimethylnitrosamine-induced liver fibrosis by 5-(2-pyrazinyl)-4-methyl-1,2-dithiol-3-thione (oltipraz) in rats: suppression of transforming growth factor-beta1 and tumor necrosis factor-alpha expression." 139 : 61-67, 2002a

      7 "Improve patch clamp techniques for high-resolution current recording from cells and cell-free membrane-patches" 85-100, 1981

      8 "Chronic toxicity studies of 5-(2-pyrazinyl)-4-methyl-1,2-dithiole-3-thione, a potential chemopreventive agent." 35 : 9-21, 1997

      9 "Ann Rev Pharmacol" 25 : 485-508, 1985

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2010-06-22 학술지명변경 외국어명 : Journal of Toxicology and Public Health -> Toxicological Research KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2004-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2002-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.44 0.44 0.36
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.32 0.31 0.707 0.1
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