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Reversal of ethanol and indomethacin‐induced suppression of hepatic DNA synthesis by 16,16‐dimethyl prostaglandin E2

 

作者: Gloria E. McNeil,   Thomas S. Chen,   Carroll M. Leevy,  

 

期刊: Hepatology  (WILEY Available online 1985)
卷期: Volume 5, issue 1  

页码: 43-46

 

ISSN:0270-9139

 

年代: 1985

 

DOI:10.1002/hep.1840050110

 

出版商: W.B. Saunders

 

数据来源: WILEY

 

摘要:

AbstractInvestigations were undertaken to determine effectiveness of 16,16‐dimethyl prostaglandin E2(dmPGE2) in overcoming the suppressive effects of ethanol and/or indomethacin on hepatic DNA synthesis. Adult litter mate Sprague‐Dawley rats were subjected to sham operation or partial hepatectomy. Immediately after partial hepatectomy, and at 8‐hr intervals for 24 hr, the rats were given: (a) ethanol with and without dmPGE2or (b) indomethacin with and without ethanol and/or dmPGE2. DmPGE2produced a significant increase in DNA synthesis in sham‐operated (p<0.001) and untreated partially hepatectomized animals (p<0.025). Ethanol and indomethacin caused a 6‐ and 18‐fold reduction, respectively, in hepatic DNA synthesis following partial hepatectomy. DmPGE2overcame the inhibitory effect of ethanol (p<0.005) and indomethacin (p<0.0005) in partially hepatectomized animals. Mitoses were decreased concomitantly with ethanol and/or indomethacin‐induced reduction in DNA synthesis and increased with administration of dmPGE2.It is concluded that dmPGE2increases hepatic DNA synthesis and regeneration in normal rat liver and overcomes their inhibition when ethanol and/or indomethacin is given after partial hepatectomy. Timing of dmPGEz administration is crucial. When given 30 min before ethanol, it completely inhibits suppression of regenerative activity; omission of this “priming” dmPGE2dose results in only 44% of DNA synthesis obtained i

 

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