<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.0//EN" "http://www.ncbi.nlm.nih.gov:80/entrez/query/static/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
<PublisherName>Science and Education Publishing</PublisherName>
<JournalTitle>International Journal of Clinical Nutrition</JournalTitle>
<Volume>2</Volume>
<Issue>1</Issue>
<PubDate PubStatus="epublish">
<Year>2014</Year>
<Month>01</Month>
<Day>15</Day>
</PubDate>
</Journal>
<ArticleTitle>Protective Effects of Ruitn and / or Hesperidin Against Doxorubicin-Induced Hepatotoxicity</ArticleTitle>
<FirstPage>11</FirstPage>
<LastPage>17</LastPage>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>Walaa G.</FirstName>
<LastName>Hozayen</LastName>
<Affiliation>Biochemistry Department, Faculty of Science, Beni-Suef University</Affiliation>
</Author>
<Author>
<FirstName>Howida S. Abou</FirstName>
<LastName>Seif</LastName>
</Author>
<Author>
<FirstName>Susan</FirstName>
<LastName>Amin</LastName>
</Author>

</AuthorList>
<ArticleIdList>
<ArticleId IdType="pii">IJCN2014212</ArticleId>
<ArticleId IdType="doi">10.12691/ijcn-2-1-2</ArticleId>
</ArticleIdList>
<History>
<PubDate PubStatus="received">
<Year>2013</Year>
<Month>12</Month>
<Day>18</Day>
</PubDate>
<PubDate PubStatus="revised">
<Year>2013</Year>
<Month>12</Month>
<Day>30</Day>
</PubDate>
<PubDate PubStatus="accepted">
<Year>2014</Year>
<Month>01</Month>
<Day>15</Day>
</PubDate>
</History>
<Abstract>The present study was conducted to evaluate the protective role of rutin and hesperidin on experimental doxorubicin induced hepatotoxicity. Doxorubicin (DXR) administered rats (25 mg / kg; three times intraperitoneally / week for two weeks) were pretreated with rutin, hesperidin, or their mixture (50 mg / kg body weight) three times per week for three weeks. Results showed that DXR caused a marked rise in serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP) and gamma glutamyl transferase (GGT) activities alongside an increase in serum total bilirubin, α-fetoprotein (AFP) and sialic acid levels Concerning oxidative stress and antioxidant defense system, the depleted hepatic glutathione content of DXR-administered rats was increased above normal levels as a result of pretreatment with rutin, hesperidin and both rutin and hesperidin. However, while elevated lipid peroxidation was noticed in DXR treated rats, pretreatment with rutin, hesperidin or both produced a detectable decrease in the lipid peroxidation level. Taken these data together, it can be concluded that natural plant components such as Rutin and Hesperidin could protect the liver against DXR-induced liver toxicity.</Abstract>
</Article>
</ArticleSet>
