• 제목/요약/키워드: N,N-dimethylnitrosamine

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흰쥐에서 사염화탄소 또는 N,N-Dimethylnitrosamine에 의한 간경화시 Theophylline의 생체내변환 (Biotransformation of Theophylline in Cirrhotic Rats Induced by Carbon Tetrachloride or N,N-Dimethylnitrosamine)

  • 박은전;김재백;손동환;고건일
    • 한국임상약학회지
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    • 제9권1호
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    • pp.55-61
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    • 1999
  • The object of this work was to study the pharmacokinetic differences and the cause of these differences in cirrhotic rats induced by N,N-dimethylnitrosamine or carbon tetrachloride treatment when aminophylline (8 mg/kg as theophylline, i.v.) was injected. The concentrations of theophylline and its major metabolite (1,3-dimethyluric acid) in plasma were determined by HPLC. In addition, formation of 1,3-dimethyluric acid from theophylline in microsomes was determined. In cirrhotic rats, the systemic clearance of theophylline was reduced to $17\%$ of the control value while AUC (area under the plasma concentration-time curve) and $(t_{1/2})_{\beta}$ were increased to about 6 fold and 10 fold, respectively. The formation of 1,3-dimethyluric acid was decreased to $33-41\%$ of the control value in microsomes of cirrhotic rat liver. From these results, it can be concluded that in cirrhotic rats induced by N,N-dimethylnitrosamine or carbon tetrachloride the total body clearance of theophylline is markedly reduced due to a reduced hepatic metabolism.

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디메틸니트로자민에 의한 흰쥐의 간독성에 미치는 유기황화합물의 효과 (Effect of Organic Sulfur-Containing Compounds on Hepatotoxicity in Rats Induced by N, N-Dimethylnitrosamine)

  • 신혜순;강주연
    • Environmental Analysis Health and Toxicology
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    • 제20권3호
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    • pp.237-242
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    • 2005
  • This study il focused on the hepatopreventive effect in cirrhotic rats induced by N, N -dimethylnitrosamine treatment when organir Lulfur -containing compoundE were orally injected. Biochemical parameters (aspatate transaminase (AST), alanine transaminase (ALT) alkaline phosphatase (ALP), 1-protein and t-bilirubin) were measured in serum injured liver tissue. The increased AST and ALT values were significantly reduced by organic sulfur-containing compounds at the oral dotes of 50 mg/kg. The result of morphological changes have illustrated the accumulation of liver damages, Each as inflammatory cell accumulation and cirrhosis, caused by N, N-dimethylnitrosamine. Also, it was found that liver damages were prevented by the treatment of organic sulfur- containing compounds.

Streptococcus uberis에 의한 질산염의 환원및 Dimethylnitrosamine의 생성에 관한 연구 (Studies on the Reduction of Nitrate and Formation of N-Dimethylnitrosamine by Streptococcus uberis in Human Saliva)

  • 정규찬;김종협;남경수
    • 약학회지
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    • 제30권1호
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    • pp.8-13
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    • 1986
  • It has been assumed that nitrite, one of the precursor of N-nitrosamine, in human saliva must have been formed from salivary nitrate through the action of microorganism in the oral cavity. In this paper, we have tested the concentration of nitrite and nitrate in human saliva and the degrees of nitrate reduction by oral microflora and identified some bacteria which were able to reduce nitrate. The concentration of nitrite and nitrate was 1.7~9.5ppm and 9.0~28.5ppm respectively. The numbers of total bacteria and nitrate reducing bacteria in four korean human saliva sample were 15~63${\times}10^8$ CFU and 1.0~6.0${\times}10^8$ CFU and the main nitrate reducing bacteria were Streptococcus uberis which was presented in large quantities and showed remarkable reductive activity. Lastly, we knowed that N-dimethylnitrosamine was formed by the reaction between dimethylamine and nitrite in the presence of St. uberis in vitro.

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수종약물이 Dimethylnitrosamine에 의한 DNA, RNA 및 단백질 손상도에 미치는 영향 (Effect of Several Drugs of DNA, RNA and Protein Damage induced by Dimethylnitrosamine in Mouse Tissues)

  • 김재현;박정식;홍성렬;권오철;박창원;이동권
    • 약학회지
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    • 제35권6호
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    • pp.522-529
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    • 1991
  • The purpose of this research is to evaluate effects of chloramphenicol, phenobarbital and progesterone on damage of DNA, RNA and protein which was induced by dimethylnitrosamine. $N,N-Di[^{14}C]$ methyl-nitrosamine (DMN) was used as a damaging agent and levels of DNA, RNA and protein damage in liver, brain and pancreas were compared with a control group. Pretreatment of mice with chloramphenicol increased protein damage in pancreas two times more than the control level. Liver RNA damage was increased up to 5.8 times and brain DNA damage up to 6.95 times by treatment of phenobarbital but brain RNA damage was decreased significantly down to 21% of the control group. The damage of liver RNA was significantly decreased by treatment of progesterone, although liver protein damage, pancreas RNA damage and pancreas protein damage were increased.

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실험적 간경화 동물모델 비교 (Experimental Hepatic Cirrhosis in Rats)

  • 박은전;김재백;손동환;고건일
    • 약학회지
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    • 제41권5호
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    • pp.622-628
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    • 1997
  • Hepatic cirrhosis is a common response to chronic liver injury from many causes and is one of the most common cause of all deaths. This study was carried out to compare experimental hepatic cirrhosis in rats to understand this disease and to apply for the pharmacokinetics in disease state. Following three kinds of experimental models were induced; 1) Bile duct ligation/scission (BDL/S), 2) N, N-dimethylnitrosamine(DMN), 3) Carbon tetrachloride. The hepatic cirrhosis was characterized by examing the liver/body weight ratio, serum biochemical values, hydroxyproline content in liver and histopathological lesions in cirrhotic rat liver. The results are as follows : (1) In BDL/S, the liver was enlarged to 250% of normal liver. In contrast the liver was shrinked to 48% and 78% of the normal liver in DMN and carbon tetrachloride, respectively. (2) In carbon tetrachloride and BDL/S, the serum ALT, AST, ALP and total bilirubin levels were significantly increased to 200~300% of normal level, while ALT and total bilirubin levels were significantly increased in DMN group. (3) Hydroxyproline content in cirrhotic rat liver was significantly 200~500% higher than that of normal liver. (4) Nodular formation with fibrosis was observed in BDL/S, DMN, carbon tetrachloride induced cirrhotic rat liver.

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Antimutagenic Effects of Doenjang(Korean Soy Paste)

  • Park, Kun-Young;Suk-Hee;Cheigh, Hong-sik;Baik, Hyung-Suk
    • Preventive Nutrition and Food Science
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    • 제1권2호
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    • pp.151-158
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    • 1996
  • Antimutagenic effect of Doenjang (Korean soy paste) on various carcinogens in Salmonella typhimurium strains of TA98 and TA100 were studied. By the addition of methanol extract of Doenjang to aflatoxin B₁(AFB₁)in the experimental system, the mutagenicity of AFB₁ on the strains of TA98 and TA100 was com-pletely inhibited. The methenol extract of the Doenjang also inhibited the mutagencities induced by direct mutagens such as N-methy1-N'-nitro-N-nitroguanidine(MNNG)and 4-nitroquinoline-1-oxide(4-NQO), and another indirect mutagens of benzo(a) pyrene(BaP) and dimethylnitrosamine(DMN). From the solvents and thin layer chromatographic(TLC) fractionations, free fatty acid(s), especially linoleic acid in Doenjang seemed to be one of the active antimutagenic compounds.

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Ultrasonography as a Tool for Monitoring the Development and Progression of Cholangiocarcinoma in Opisthorchis viverrini/Dimethylnitrosamine-Induced Hamsters

  • Plengsuriyakarn, Tullayakorn;Eursitthichai, Veerachai;Labbunruang, Nipawan;Na-Bangchang, Kesara;Tesana, Smarn;Aumarm, Waraporn;Pongpradit, Ananya;Viyanant, Vithoon
    • Asian Pacific Journal of Cancer Prevention
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    • 제13권1호
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    • pp.87-90
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    • 2012
  • Cholangiocarcinoma (CCA) is the most common cancer in northeastern Thailand. At present, effective diagnosis of CCA either in humans or animals is not available. Monitoring the development and progression of CCA in animal models is essential for research and development of new promising chemotherapeutics. Ultrasonography has been widely used for screening of bile duct obstruction in CCA patients. In this study, we preliminarily investigated the applicability of ultrasonography to monitor the development and progression of CCA in Syrian golden hamsters (n=8) induced by Opisthorchis viverrini (OV)/dimethylnitrosamine (DMN) administration. Ultrasonography and histopathological examination of hamsters was performed at week 0, 20, 24 and 28 of OV infection or at the start of water/Tween-80 administration to controls. The ultrasonographic images of liver parenchyma and gallbladders of OV/DMN-induced CCA hamsters showed sediments in gallbladder, thickening of gallbladder wall, and hypoechogenicity of liver parenchyma cells. The ultrasonographic images of liver tissues were found to correlate well with histopathological examination. Although ultrasonography does not directly detect the occurrence of CCA, it reflects the thickening of bile ducts and abnormality of liver tissues. It may be applied as a reliable tool for monitoring the development and progression of CCA in animal models in research and development of new promising chemotherapeutics for CCA.

멸치 젓갈 숙성중의 dimethylamine의 생성 (FORMATION OF DIMETHYLAMINE IN THE COURSE OF ANCHOVY FERMENTATION WITH SALT)

  • 변재형;정보영;황금소
    • 한국수산과학회지
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    • 제9권4호
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    • pp.223-231
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    • 1976
  • 어류가공품중에 분포하는 2급 amino의 생성 원인을 구명하기 위한 연구의 일부로서, 멸치를 $22\%$의 식염을 첨가하여 $17^{\circ}C$$27^{\circ}C$의 온도별로 열성시키면서 숙성 일정별로 단백질과 TMAO의 분해생성물을 분석하여 2급 amino의 생성과 관계있는 몇가지 실험결과를 얻었기에 보고한다. 단백질 질소는 $17^{\circ}C$$27^{\circ}C$에서 숙성시켰을 때, 전숙성기간을 통하여 일률적으로 감소하는 경향을 보였으나, 아미노태 질소는 단백태 질소의 감소에 반비례하여 증가하였으며, 이때 아미노태 질소의 증가속도는 $27^{\circ}C$에서 숙성한 것이 $17^{\circ}C$에서 숙성한 것에 비하여 훨씬빨랐다. TMA는 TMAO의 감소와 더불어 증가하여 갔으며 숙성 69일까지는 계속 증가하다가 이후 서서히 감소하는 경향을 보였다. 이때 온도에 의한 차이는 보이지 않았다. DMA는 $17^{\circ}C$에서 숙성시켰을 때는 숙성 69일까지 계속 증가하다가 이후 미미한 변화를 보였으며, $27^{\circ}C$에서 열성시킨 것은 숙성 59일까지는 계속 증가하다가 그 이후는 미미한 변화를 보였다. DMA는 TMAO의 양적변화에 비추어, $17^{\circ}C$에서 숙성시켰을 때는 상관계수 r=-0.811, 그리고 $27^{\circ}C$에서 숙성시켰을 때는 상관계수 r=-0.865로서 각각 부의 상관관계를 보였다. 멸치 젓갈 숙성중의 DMA의 생성원인은 그 기여율이 $17^{\circ}C$일 때 $r^2\fallingdotseq0.75$, TMAO의 분해와 밀접한 관련이 있는 것으로 판단되었다.

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Selonsertib Inhibits Liver Fibrosis via Downregulation of ASK1/MAPK Pathway of Hepatic Stellate Cells

  • Yoon, Young-Chan;Fang, Zhenghuan;Lee, Ji Eun;Park, Jung Hee;Ryu, Ji-Kan;Jung, Kyung Hee;Hong, Soon-Sun
    • Biomolecules & Therapeutics
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    • 제28권6호
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    • pp.527-536
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    • 2020
  • Liver fibrosis constitutes a significant health problem worldwide due to its rapidly increasing prevalence and the absence of specific and effective treatments. Growing evidence suggests that apoptosis-signal regulating kinase 1 (ASK1) is activated in oxidative stress, which causes hepatic inflammation and apoptosis, leading to liver fibrogenesis through a mitogen-activated protein kinase (MAPK) downstream signals. In this study, we investigated whether selonsertib, a selective inhibitor of ASK1, shows therapeutic efficacy for liver fibrosis, and elucidated its mechanism of action in vivo and in vitro. As a result, selonsertib strongly suppressed the growth and proliferation of hepatic stellate cells (HSCs) and induced apoptosis by increasing Annexin V and TUNEL-positive cells. We also observed that selonsertib inhibited the ASK1/MAPK pathway, including p38 and c-Jun N-terminal kinase (JNK) in HSCs. Interestingly, dimethylnitrosamine (DMN)-induced liver fibrosis was significantly alleviated by selonsertib treatment in rats. Furthermore, selonsertib reduced collagen deposition and the expression of extracellular components such as α-smooth muscle actin (α-SMA), fibronectin, and collagen type I in vitro and in vivo. Taken together, selonsertib suppressed fibrotic response such as HSC proliferation and extracellular matrix components by blocking the ASK1/MAPK pathway. Therefore, we suggest that selonsertib may be an effective therapeutic drug for ameliorating liver fibrosis.