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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/12483" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/12483</id>
  <updated>2026-10-10T21:41:55Z</updated>
  <dc:date>2026-10-10T21:41:55Z</dc:date>
  <entry>
    <title>Effect of exposure to extremely low electro-magnetic field during  prenatal period on mice spleen</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/12529" />
    <author>
      <name>Bayat, Parvin Dokht</name>
    </author>
    <author>
      <name>Ghanbari, Ali</name>
    </author>
    <author>
      <name>Babaei, Saeid</name>
    </author>
    <author>
      <name>Khazaei, Mozafar</name>
    </author>
    <author>
      <name>Ghorbani, Rostam</name>
    </author>
    <author>
      <name>Ayubian, Mahmood</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/12529</id>
    <updated>2011-08-03T16:30:55Z</updated>
    <published>2011-08-01T00:00:00Z</published>
    <summary type="text">Title: Effect of exposure to extremely low electro-magnetic field during  prenatal period on mice spleen
Authors: Bayat, Parvin Dokht; Ghanbari, Ali; Babaei, Saeid; Khazaei, Mozafar; Ghorbani, Rostam; Ayubian, Mahmood
Abstract: Total body&#xD;
weight of newborns, the volume of spleen, and the number of megakaryocytes&#xD;
decreased following the exposure to ELF-MF (6x10&lt;sup&gt;-3&lt;/sup&gt; T and 50 Hz) at 1-5,&#xD;
6-10, 11-15, and 16-20 days of pregnancy of mice. The complete period of&#xD;
gestation was sensitive to ELF-MF exposure; the initial days were more prone to&#xD;
exposure. The results suggest that the use of ELF-MF producing instruments&#xD;
should be limited during gestation.
Page(s): 634-638</summary>
    <dc:date>2011-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Evaluation of antioxidant and neuroprotective effect of date palm (&lt;i style=""&gt;Phoenix dactylifera &lt;/i&gt;L.) against bilateral common carotid artery occlusion in rats</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/12528" />
    <author>
      <name>Pujari, Rohini R</name>
    </author>
    <author>
      <name>Vyawahare, Neeraj S</name>
    </author>
    <author>
      <name>Kagathara, Virendra G</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/12528</id>
    <updated>2011-08-05T16:30:49Z</updated>
    <published>2011-08-01T00:00:00Z</published>
    <summary type="text">Title: Evaluation of antioxidant and neuroprotective effect of date palm (&lt;i style=""&gt;Phoenix dactylifera &lt;/i&gt;L.) against bilateral common carotid artery occlusion in rats
Authors: Pujari, Rohini R; Vyawahare, Neeraj S; Kagathara, Virendra G
Abstract: The&#xD;
cerebral ischemia in rats was induced by occluding bilateral common carotid&#xD;
arteries (BCCAO) for 30 min., followed by 45 min reperfusion. BCCAO caused&#xD;
significant depletion in superoxide dismutase, catalase, glutathione,&#xD;
glutathione peroxidase, glutathione-S-transferase, glutathione reductase and&#xD;
significant increase in lipid peroxidation along with severe neuronal damage in&#xD;
the brain. All the alterations except depletion in glutathione peroxidase and&#xD;
glutathione-S-transferase levels induced by cerebral ischemia were&#xD;
significantly attenuated by 15 days pretreatment with methanolic extract of &lt;i style=""&gt;P. dactylifera&lt;/i&gt; fruits (100, 300 mg/kg),&#xD;
whereas 30 mg/kg dose was insignificant in this regard. These results suggest&#xD;
the possible use &lt;i style=""&gt;P. dactylifera&lt;/i&gt;&#xD;
against bilateral common carotid artery occlusion induced oxidative stress and&#xD;
neuronal damage
Page(s): 627-633</summary>
    <dc:date>2011-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Anti-depressant-like activity of a novel serotonin type-3 (5-HT&lt;sub&gt;3&lt;/sub&gt;) receptor antagonist in rodent models of depression</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/12527" />
    <author>
      <name>Gupta, Deepali</name>
    </author>
    <author>
      <name>Devadoss, Thangaraj</name>
    </author>
    <author>
      <name>Bhatt, Shvetank</name>
    </author>
    <author>
      <name>Gautam, Baldev</name>
    </author>
    <author>
      <name>Jindal, Ankur</name>
    </author>
    <author>
      <name>Pandey, Dilip</name>
    </author>
    <author>
      <name>Mahesh, Radhakrishnan</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/12527</id>
    <updated>2011-08-02T16:31:10Z</updated>
    <published>2011-08-01T00:00:00Z</published>
    <summary type="text">Title: Anti-depressant-like activity of a novel serotonin type-3 (5-HT&lt;sub&gt;3&lt;/sub&gt;) receptor antagonist in rodent models of depression
Authors: Gupta, Deepali; Devadoss, Thangaraj; Bhatt, Shvetank; Gautam, Baldev; Jindal, Ankur; Pandey, Dilip; Mahesh, Radhakrishnan
Abstract: &lt;i style=""&gt;N&lt;/i&gt;-Cyclohexyl-3-methoxyquinoxalin-2-carboxamide (QCM-13), a novel 5-HT&lt;sub&gt;3&#xD;
&lt;/sub&gt;antagonist identified from a series of compounds with higher pA&lt;sub&gt;2&lt;/sub&gt;&#xD;
(7.6) and good log P (2.91) value was screened in rodent models of depression&#xD;
such as forced swim test (FST), tail suspension test (TST), interaction studies&#xD;
with standard anti-depressants and confirmatory studies such as reversal of&#xD;
parthenolide induced depression and reserpine induced hypothermia. In FST (2&#xD;
and 4 mg/kg) and TST (2 and 4 mg/kg), QCM-13 significantly reduced the duration&#xD;
of immobility in mice without affecting the base line locomotion. QCM-13 (2 and&#xD;
4 mg/kg) was also found to have significant interaction with standard&#xD;
anti-depressants (fluoxetine and bupropion in FST and TST respectively).&#xD;
Further, reversal of parthenolide induced depression in mice and reserpine&#xD;
induced hypothermia in rat models indicate the serotonergic influence of QCM-13&#xD;
for anti-depressant potential.
Page(s): 619-626</summary>
    <dc:date>2011-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Possible nitric oxide mechanism in the protective effect of hesperidin against ischemic reperfusion cerebral injury in rats</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/12526" />
    <author>
      <name>Gaur, Vaibhav</name>
    </author>
    <author>
      <name>Aggarwal, Aditi</name>
    </author>
    <author>
      <name>Kumar, Anil</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/12526</id>
    <updated>2011-08-02T16:31:09Z</updated>
    <published>2011-08-01T00:00:00Z</published>
    <summary type="text">Title: Possible nitric oxide mechanism in the protective effect of hesperidin against ischemic reperfusion cerebral injury in rats
Authors: Gaur, Vaibhav; Aggarwal, Aditi; Kumar, Anil
Abstract: Stroke is the third leading cause of death&#xD;
and disability around the globe. The aim of the present investigation was to&#xD;
evaluate the protective effect of hesperidin and its nitric oxide mechanism&#xD;
against cerebral ischemia reperfusion injury. Bilateral common carotid artery&#xD;
occlusion for 30 min followed by 24 h reperfusion was given to induce ischemia&#xD;
in rats. Animals were pretreated with hesperidin (50 and 100 mg/kg, po) for 7&#xD;
days. Various behavioural tests, oxidative stress parameters, endogenous&#xD;
antioxidant system, antioxidant enzyme activity and mitochondrial enzyme&#xD;
complex (I, II, III and IV) dysfunctions in cortex and striatum were assessed&#xD;
subsequently. Hesperidin (50 and&#xD;
100 mg/kg) significantly improved neurobehavioral alterations (neurological&#xD;
score, locomotor activity, resistance to lateral push and hanging wire&#xD;
latency), attenuated oxidative damage, restored antioxidant and mitochondrial&#xD;
complex enzyme activities in cortex and in striatum regions of the brain as&#xD;
compared to their respective controls. L-arginine (100 mg/kg) or L-NAME (10&#xD;
mg/kg) pretreatment with lower dose of hesperidin (50 mg/kg) significantly&#xD;
reversed or potentiated its protective effect, respectively which was&#xD;
significant as compared to hesperidin (50 mg/kg). The results highlight the&#xD;
involvement of nitric oxide mechanism in the protective effect of hesperidin&#xD;
against ischemia reperfusion injury induced alterations.
Page(s): 609-618</summary>
    <dc:date>2011-08-01T00:00:00Z</dc:date>
  </entry>
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