<?xml version="1.0"?>
<Articles JournalTitle="Acta Medica Iranica">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Acta Medica Iranica</JournalTitle>
      <Issn>0044-6025</Issn>
      <Volume>42</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2004</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">"EFFECT OF CIMETIDINE AND RANITIDINE ON LIPID PROFILE AND LIPID PEROXIDATION IN &#x3B3;-IRRADIATED MICE"</title>
    <FirstPage>198</FirstPage>
    <LastPage>204</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>S. Kabodanian Ardestani</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>M. Mahmood Janlow</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>A. Kariminia2  Z.Tavakoli</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>09</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Elevated amounts of free radicals due to ionizing radiation have damaging effects on the
body. H2-receptor antagonists have potential oxygen radical scavenging properties. We tried to determine the effects of two H2-receptor antagonists (cimetidine and ranitidine) on lipid peroxidation (LPO) and lipid profile (LP) in plasma and liver of &#x3B3;-irradiated (1Gy/day for 3 days) BALB/c mice. The control group of mice were fed with normal food and drinks but the experiment group of mice were fed control diet and drinking water, containing cimetidine or ranitidine (1mg/lit). After 3 days of supplementation, the animals were subjected to sublethal &#x3B3;-radiation, which caused a significant increase in cholesterol level in experimental group (100% increase in comparison with the control group), but the amount of phospholipids did not change. The ratio of cholesterol to phospholipid showed a slight increase. Also &#x3B3;-irradiation caused a significant increase in lipid fluorescence (11-48%), conjugated dienes (33-81%) in liver and increase in malondialdehyde (19-300%) in serum of mice who had received 1.09-3.1 Gy for 1-3 days. Cimetidine or ranitidine supplementation was able to restore the changes of LPO and LP in mice (1 Gy-radiated for 3 days). It is therefore concluded that the mice treated with cimetidine or ranitidine were able to tolerate biomembrane damages provoked by sublethal &#x3B3;-radiation. This supports the hypothesis that cimetidine or ranitidine may afford an efficient protection against ionizing radiation or diseases that are characterized by in vivo free radical-mediated oxidative stress mechanisms.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/2719</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/2719/2701</pdf_url>
  </Article>
</Articles>
