<?xml version="1.0" encoding="UTF-8"?>
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  <title>DSpace Collection:</title>
  <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/75" />
  <subtitle />
  <id>http://localhost:8080/xmlui/handle/123456789/75</id>
  <updated>2026-01-20T08:26:55Z</updated>
  <dc:date>2026-01-20T08:26:55Z</dc:date>
  <entry>
    <title>The Effect Of Rivaroxaban And Dabigatran On Glycemic Parameters And Lipid Profile In High Fat Diet And Low Dose Streptozotocin Induced Diabetes Mellitus In Male Wistar Rats</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/1876" />
    <author>
      <name>REG.N0: BO0121004</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/1876</id>
    <updated>2025-04-28T12:12:12Z</updated>
    <published>2024-01-01T00:00:00Z</published>
    <summary type="text">Title: The Effect Of Rivaroxaban And Dabigatran On Glycemic Parameters And Lipid Profile In High Fat Diet And Low Dose Streptozotocin Induced Diabetes Mellitus In Male Wistar Rats
Authors: REG.N0: BO0121004
Abstract: Introduction&#xD;
The current experimental study aimed to evaluate the effect of Rivaroxaban and Dabigatran on glycemic parameters in a High-fat diet and low dose Streptozotocin-induced Diabetes Mellitus in male Wistar rats. In addition, the effect on the Lipid profile and inflammatory markers were also assessed.</summary>
    <dc:date>2024-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Effect Of Cilnidipine on Depression Paradigm in Male Swiss Mice-An Experimental Study</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/1875" />
    <author>
      <name>REG.N0: BO0121003</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/1875</id>
    <updated>2025-04-28T12:11:18Z</updated>
    <published>2024-01-01T00:00:00Z</published>
    <summary type="text">Title: Effect Of Cilnidipine on Depression Paradigm in Male Swiss Mice-An Experimental Study
Authors: REG.N0: BO0121003
Abstract: Introduction&#xD;
Depression is a commonly occurring ailment that frequently coexists with cardiovascular problems, impacting approximately 16-23% of individuals. Emerging genetic, ex vivo, and clinical trial evidence suggest that Calcium channel blockers (CCB) have a positive effect on mood and cognitive performance. The hypothesis posits that calcium channel blockers (CCB) alter the release of central neurotransmitters, particularly noradrenaline (NA) and 5-hydroxytryptamine (5-HT) contribute to the occurrence of depression. Nevertheless, the therapy now accessible has limitations in terms of effectiveness and the accompanying negative consequences.&#xD;
Study Objectives:&#xD;
1.&#xD;
To evaluate the effects of Cilnidipine on depression paradigm in Male Swiss Mice using the Forced Swim Test, Tail Suspension Test and Locomotor Activity Test.&#xD;
2.&#xD;
To compare the effects of Cilnidipine and Fluoxetine on depression paradigm in Male Swiss Mice using the Forced Swim Test, Tail Suspension Test and Locomotor Activity Test.</summary>
    <dc:date>2024-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Effect Of Withania Somnifera On Selected Gene Expression In Brain Tissue Of Male Wistar Rats Subjected To Chronic Stress Induced Depression</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/1874" />
    <author>
      <name>REG.N0: BO0121002</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/1874</id>
    <updated>2025-04-28T12:10:22Z</updated>
    <published>2024-01-01T00:00:00Z</published>
    <summary type="text">Title: Effect Of Withania Somnifera On Selected Gene Expression In Brain Tissue Of Male Wistar Rats Subjected To Chronic Stress Induced Depression
Authors: REG.N0: BO0121002
Abstract: Introduction and Objective :-&#xD;
The present study was designed to evaluate the effect of Withania somnifera (WS) alone and in combination with Fluoxetine on gene expression of Neuritin, NARP &amp; BDNF Exon – III gene in hippocampus of male Wistar rats using chronic unpredictable mild stress (CUMS) as a model of depression.</summary>
    <dc:date>2024-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Investigation of Cardioprotective Potential of Remogliflozin in preventing Streptozotocin induced Diabetic Cardiomyopathy in Male Wistar Rats</title>
    <link rel="alternate" href="http://localhost:8080/xmlui/handle/123456789/1873" />
    <author>
      <name>REG.N0: BO0121001</name>
    </author>
    <id>http://localhost:8080/xmlui/handle/123456789/1873</id>
    <updated>2025-04-28T12:09:13Z</updated>
    <published>2024-01-01T00:00:00Z</published>
    <summary type="text">Title: Investigation of Cardioprotective Potential of Remogliflozin in preventing Streptozotocin induced Diabetic Cardiomyopathy in Male Wistar Rats
Authors: REG.N0: BO0121001
Abstract: Introduction and objective - One of the cardiac problems that diabetes patients face is Diabetic&#xD;
Cardiomyopathy (DCM), which can lead to heart failure and an increase in morbidity and death. The&#xD;
two main pathogenic characteristics of diabetic hearts that contribute to the development of DCM are&#xD;
inflammation and oxidative stress. Because of its anti-oxidant and anti-inflammatory qualities,&#xD;
remogliflozin, an SGLT 2 inhibitor, has been demonstrated to lessen inflammation and oxidative&#xD;
stress. The purpose of this study was to look at how Remogliflozin protects diabetic hearts and assess&#xD;
via the corresponding changes in blood marker and histological characteristics.</summary>
    <dc:date>2024-01-01T00:00:00Z</dc:date>
  </entry>
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