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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>International Journal of Preventive Medicine (Int J Prev Med)</JournalTitle><Issn>2008-7802</Issn><Volume>0</Volume><Issue>0</Issue><PubDate PubStatus="epublish"><Year>2016</Year><Month>06</Month><Day>22</Day></PubDate></Journal><title locale="en_US">Potential Effects of Pomegranate on Lipid Peroxidation and Pro‑inflammatory Changes in Daunorubicin‑induced Cardiotoxicity in Rats</title><FirstPage>1709</FirstPage><LastPage>1709</LastPage><Language>EN</Language><AuthorList><Author><affiliation locale="en_US">Department of Pharmacology, Toxicology and Medicine, College of Medicine, Al‑Mustansiriya University, Baghdad</affiliation></Author><Author><affiliation locale="en_US">Department of Pharmacology, Toxicology and Medicine, College of Medicine, Al‑Mustansiriya University, Baghdad</affiliation></Author></AuthorList><History><PubDate PubStatus="received"><Year>2016</Year><Month>06</Month><Day>22</Day></PubDate></History><abstract locale="en_US">&lt;p&gt;&lt;strong&gt;Background:&lt;/strong&gt; Daunorubicin‑induced acute cardiotoxicity caused by oxidative stress and free radical formation. Pomegranate possessed a significant in vitro free radical scavenging&lt;br /&gt;activity. Therefore, the aim of this study was estimations of the role of pomegranate effects in daunorubicin‑induced cardiotoxicity.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods:&lt;/strong&gt; A total of 21 Sprague male rats were allocated into three groups, seven animals in each group. Group A: Control group received distilled water. Group B: Treated group with daunorubicin 20 mg/kg via intraperitoneal injection daily for the 12th day for total cumulative dose of 240 mg/kg. Group C: Pretreatment group with pomegranate 25 mg/kg for 6 days orally, then daunorubicin 20 mg/kg administrated concomitantly for the next 6 days with a cumulative dose of 120 mg/kg.&lt;br /&gt;Cardiac troponin I ([cTn I] pg/ml), malondialdehyde (MDA) (ng/ml), interleukin 17 (IL‑17 pg/ml), and cardiac lactate dehydrogenase (LDH) (pm/ml), all these biomarkers were used to measure the severity of cardiotoxicity.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results:&lt;/strong&gt; Daunorubicin at a dose of 20 mg/kg lead to pronounced cardiac damage that reflected on through elevations of serum cTn and serum LDH levels significantly P &amp;lt; 0.01, it induced lipid&lt;br /&gt;peroxidation during cardiotoxicity that reflected through an elevation in the serum MDA significantly P &amp;lt; 0.01, moreover, daunorubicin induces pro‑inflammatory changes in cardiotoxicity; it raises the IL‑17 serum level significantly P &amp;lt; 0.01 as compared with control. Pomegranate pretreatment demonstrated a significant cardioprotection from daunorubicin‑induced cardiotoxicity; it attenuated the cardiac damage through reduction of cTn, LDH, MDA, and serum IL‑17 level significantly&lt;br /&gt;P &amp;lt; 0.01 as compared with daunorubicin‑treated group.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions:&lt;/strong&gt; Pomegranate demonstrated significant cardioprotection in daunorubicin‑induced cardiotoxicity through reduction of oxidative stress, lipid peroxidation, pro‑inflammatory, and cardiac injury biomarkers.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Keywords:&lt;/strong&gt; Cardiotoxicity, daunorubicin, pomegranate&lt;/p&gt;</abstract><web_url>http://ijpm.mui.ac.ir/index.php/ijpm/article/view/1709</web_url><pdf_url>http://ijpm.mui.ac.ir/index.php/ijpm/article/download/1709/1999</pdf_url></Article></Articles>
