<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Akram A Hammo</style></author><author><style face="normal" font="default" size="100%">Abdulla A Ahmad</style></author><author><style face="normal" font="default" size="100%">Zeina A Althanoon</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Role of Gender in the Protection Against Doxorubicin-Induced Oxidative Stress</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Coenzyme Q10</style></keyword><keyword><style  face="normal" font="default" size="100%">Doxorubicin</style></keyword><keyword><style  face="normal" font="default" size="100%">Gender difference</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxidative stress</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">782-788</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; There are gender differences in the oxidation-reduction reactions. Doxorubicin (Dox) is a chemotherapeutic drug that can produce oxidative stress which may require prevention by antioxidants. Aim: The study aimed to investigate the gender-dependent changes in Dox-induced oxidative stress, and the protective effects of coenzyme Q10 (CoQ10).&lt;strong&gt; Materials and Methods&lt;/strong&gt;: Rats were administered CoQ10 orally for 17 days. On day 13, some rats receiving CoQ10 received a single intraperitoneal dosage of Dox, whereas other rats received normal saline. Glutathione (GSH), malondialdehyde (MDA), and total anti-oxidant capacity (T-AOC) were measured in both genders of albino rats. &lt;strong&gt;Results&lt;/strong&gt;: Dox significantly reduced both GSH and T-AOC levels and caused a significant increase in MDA. The administration of CoQ10 significantly prevented these changes. Dox caused a larger reduction in GSH in males than in females, while CoQ10 caused more protection in females. Dox caused a higher increase in MDA levels in males.&lt;strong&gt; Conclusion:&lt;/strong&gt; Pre-treatments with CoQ10 may protect against Dox-induced oxidative stress, with gender-dependent variations in the extent of these Dox/CoQ10 effects.&lt;/p&gt;
&lt;quillbot-extension-portal&gt;&lt;/quillbot-extension-portal&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><section><style face="normal" font="default" size="100%">782</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Akram A Hammo&lt;sup&gt;1&lt;/sup&gt;, Abdulla A Ahmad&lt;sup&gt;2,*&lt;/sup&gt;, Zeina A Althanoon&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;The primary health care sector in Al-Baaj, Nineveh Health Directorate, Ministry of Health, IRAQ.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of clinical and laboratory sciences, College of Pharmacy, University of Mosul, IRAQ.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of pharmacology and toxicology, College of Pharmacy, University of Mosul, IRAQ&lt;/p&gt;
&lt;quillbot-extension-portal&gt;&lt;/quillbot-extension-portal&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Panneerselvam Punniyakotti</style></author><author><style face="normal" font="default" size="100%">Rengasamy Lakshminarayanan Rengarajan</style></author><author><style face="normal" font="default" size="100%">Shanmugam Velayuthaprabhu</style></author><author><style face="normal" font="default" size="100%">Kalaiyarasan Vijayakumar</style></author><author><style face="normal" font="default" size="100%">Ramasamy Manikandan</style></author><author><style face="normal" font="default" size="100%">Arumugam Vijaya Anand</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Protective Effect of Terminalia catappa Leaves and Terminalia chebula Fruits on the Enzymatic and Non-enzymatic Anti-oxidant Levels in the Doxorubicin Induced Toxicity Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Doxorubicin</style></keyword><keyword><style  face="normal" font="default" size="100%">Enzymatic antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Non-enzymatic antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxidative stress</style></keyword><keyword><style  face="normal" font="default" size="100%">Termianlia catappa</style></keyword><keyword><style  face="normal" font="default" size="100%">Terminalia chebulla.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">346-349</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Oxidative stress plays an important role in chronic complications of diabetes, cancer, liver disorder etc. The free radicals such as superoxide anions, hydrogen peroxides are causing the oxidative stress and it involves the cellular damage. Evidences recommended that the natural medicines from plant sources are treated to overcome the oxidative stress complications. &lt;strong&gt;Objective:&lt;/strong&gt; The aim of the present is to find the antioxidant activity of the ethanolic extract of&lt;em&gt; Terminalia catappa&lt;/em&gt; leaves and &lt;em&gt;Terminalia chebula&lt;/em&gt; fruits in the doxorubicin (DOX) induced toxicity rats. &lt;strong&gt;Methods:&lt;/strong&gt; Oxidative stress is induced with a single dose of doxorubicin and then the animals were treated with a dose of various concentration of ethanolic extract of&lt;em&gt; T. catappa&lt;/em&gt; leaves and &lt;em&gt;T. chebula&lt;/em&gt; fruits (200, 300 mg/kg/b.w) for 21 days. After the treatment, lipid peroxide (LPO), reduced glutathione (GSH), vitamin C, vitamin E, glutathiones- transferase (GST), glutathione peroxidase (GPx), superoxide dismutase (SOD), catalase levels are determined. Propranolol 25mg/kg is used as standard drug.&lt;strong&gt; Results:&lt;/strong&gt; In the present study, after the treatment of doxorubicin the levels of SOD, CAT, GSH, GST, GPX, vitamin C, vitamin E levels are decreased and LPO level is increased. After the treatment of &lt;em&gt;T. catappa&lt;/em&gt; leaves and &lt;em&gt;T. chebula&lt;/em&gt; fruits the levels were returned to the normal level. &lt;strong&gt;Conclusion:&lt;/strong&gt; The results proved that the ethanolic extract of&lt;em&gt; T. catappa&lt;/em&gt; leaves and &lt;em&gt;T. chebula&lt;/em&gt; fruits may protects the cells from oxidative stress induced by the doxorubicin induced toxicity rats.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">346</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Panneerselvam Punniyakotti&lt;sup&gt;1&lt;/sup&gt;, Rengasamy Lakshminarayanan Rengarajan&lt;sup&gt;2&lt;/sup&gt;, Shanmugam Velayuthaprabhu&lt;sup&gt;3&lt;/sup&gt;, Kalaiyarasan Vijayakumar&lt;sup&gt;4&lt;/sup&gt;, Ramasamy Manikandan&lt;sup&gt;5&lt;/sup&gt;, Arumugam Vijaya Anand&lt;sup&gt;6,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biochemistry, Manonmaniam Sundaranar University, Abishekapatti, Tirunelveli-627 012, Tamilnadu, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Animal Science, Bharathidasan University, Trichy, Tamilnadu, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biotechnology, Bharathiar University, Coimbatore- 641 046, Tamilnadu, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Assistant Professor, Department of Biochemistry, Sri Meenakshi Vidiyal College of Arts and Science, Trichy, Tamilnadu, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Biochemistry, MIET Arts and Science College, Trichy, Tamilnadu, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Human Genetics and Molecular Biology, Bharathiar University, Coimbatore-641 046, Tamilnadu, INDIA.&lt;/p&gt;
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