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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/9070" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/9070</id>
  <updated>2026-10-10T00:25:03Z</updated>
  <dc:date>2026-10-10T00:25:03Z</dc:date>
  <entry>
    <title>Wound healing potential of ethanolic extract&lt;i style=""&gt; &lt;/i&gt;of&lt;i style=""&gt; Kalanchoe pinnata &lt;/i&gt;Lam. leaf—A preliminary study</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/9083" />
    <author>
      <name>Nayak, B Shivananda</name>
    </author>
    <author>
      <name>Marshall, Julien R</name>
    </author>
    <author>
      <name>Isitor, Godwin</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/9083</id>
    <updated>2010-05-29T16:30:29Z</updated>
    <published>2010-06-01T00:00:00Z</published>
    <summary type="text">Title: Wound healing potential of ethanolic extract&lt;i style=""&gt; &lt;/i&gt;of&lt;i style=""&gt; Kalanchoe pinnata &lt;/i&gt;Lam. leaf—A preliminary study
Authors: Nayak, B Shivananda; Marshall, Julien R; Isitor, Godwin
Abstract: The extract of &lt;i style=""&gt;K. pinnata &lt;/i&gt;was evaluated for its wound healing activity by&lt;i style=""&gt; &lt;/i&gt;using excision wound model in rats. On&#xD;
day 11, animals treated with the ethanolic leaf extract exhibited 86.33 %&#xD;
reduction in the wound area, compared to petroleum jelly treated control&#xD;
(69.36%) and the mupirocin treated standard (85.49%). The hydroxyproline content&#xD;
of extract treated animals was higher, as compared to control and the standard&#xD;
groups. Histological analysis was also consistent with the proposal that &lt;i style=""&gt;K. pinnata &lt;/i&gt;leaf extract exhibits&#xD;
significant wound healing potential. The increased rate of wound contraction&#xD;
and hydroxyproline content in the extract treated animals supports the claims&#xD;
made by traditional healers of the benefits obtained from the medicinal use of &lt;i style=""&gt;K. pinnata&lt;/i&gt;.
Page(s): 572-576</summary>
    <dc:date>2010-06-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Galanin regulation of LH release in male rats</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/9082" />
    <author>
      <name>Pandit, Manisha Arora</name>
    </author>
    <author>
      <name>Saxena, R N</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/9082</id>
    <updated>2010-05-30T16:30:33Z</updated>
    <published>2010-06-01T00:00:00Z</published>
    <summary type="text">Title: Galanin regulation of LH release in male rats
Authors: Pandit, Manisha Arora; Saxena, R N
Abstract: The present study examines the role of&#xD;
cerebroventricular administered (III&lt;sup&gt;rd&lt;/sup&gt; ventricle) galanin on LHRH&#xD;
and LH release in adult and immature male rats. In both age groups, galanin&#xD;
stimulated LHRH synthesis and release from the hypothalamus, leading to a&#xD;
higher release of pituitary LH which in turn increased plasma LH levels.&#xD;
Galantide, a galanin receptor blocker, on the other hand, drastically reduced&#xD;
hypothalamic LHRH and plasma LH while increasing pituitary LH. &lt;i style=""&gt;In vitro &lt;/i&gt;incubation of anterior&#xD;
pituitary cells with galanin followed by LHRH resulted in increased release of&#xD;
pituitary LH but not by galanin alone. Galantide exhibited no such effect&#xD;
either alone or with LHRH. These results indicate that galanin is an important&#xD;
regulator for both hypothalamic LHRH and hypophysial LH and its role is&#xD;
independent of age in the case of male rats.
Page(s): 544-548</summary>
    <dc:date>2010-06-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Evaluation of genotoxic effects in male Wistar rats following microwave exposure</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/9081" />
    <author>
      <name>Kumar, Sanjay</name>
    </author>
    <author>
      <name>Kesari, Kavindra Kumar</name>
    </author>
    <author>
      <name>Behari, Jitendra</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/9081</id>
    <updated>2010-05-30T16:30:34Z</updated>
    <published>2010-06-01T00:00:00Z</published>
    <summary type="text">Title: Evaluation of genotoxic effects in male Wistar rats following microwave exposure
Authors: Kumar, Sanjay; Kesari, Kavindra Kumar; Behari, Jitendra
Abstract: Wistar rats (70 days&#xD;
old) were exposed for 2 h a day for 45 days continuously at 10 GHz [power&#xD;
density 0.214 mW/cm&lt;sup&gt;2&lt;/sup&gt;, specific absorption rate (SAR) 0.014 W/kg] and 50 GHz (power density 0.86 μW/cm&lt;sup&gt;2&lt;/sup&gt;,&#xD;
SAR 8.0 ×10&lt;sup&gt;-4&lt;/sup&gt; W/kg). Micronuclei (MN), reactive oxygen species&#xD;
(ROS), and antioxidant enzymes activity were estimated in the blood cells and&#xD;
serum. These radiations induce micronuclei formation and significant increase&#xD;
in ROS production. Significant changes in the level of serum glutathione&#xD;
peroxidase, superoxide dismutase and catalase were observed in exposed group as&#xD;
compared with control group. It is concluded that microwave exposure can be&#xD;
affective at genetic level. This may be an indication of tumor promotion, which&#xD;
comes through the overproduction of reactive oxygen species.
Page(s): 586-592</summary>
    <dc:date>2010-06-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Small-sized neurons of trigeminal ganglia express multiple voltage-sensitive calcium channels: A qualitative immunohistochemical study</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/9080" />
    <author>
      <name>Ray, Subrata Basu</name>
    </author>
    <author>
      <name>Singh, Sagolshem S</name>
    </author>
    <author>
      <name>Mehra, R D</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/9080</id>
    <updated>2010-05-30T16:30:28Z</updated>
    <published>2010-06-01T00:00:00Z</published>
    <summary type="text">Title: Small-sized neurons of trigeminal ganglia express multiple voltage-sensitive calcium channels: A qualitative immunohistochemical study
Authors: Ray, Subrata Basu; Singh, Sagolshem S; Mehra, R D
Abstract: The cell bodies of pseudounipolar neurons of&#xD;
the trigeminal ganglia have been presumed to play a supportive role to&#xD;
neurites, which transmit various sensations like pain from the periphery to the&#xD;
brain stem. However, several studies have recently shown that these neuronal&#xD;
cell bodies could modulate the afferent stimuli by up-regulating various ion&#xD;
channels and also by increasing the synthesis of neuropeptides like calcitonin&#xD;
gene-related peptide (CGRP). Since voltage-sensitive calcium ion channels&#xD;
(VSCCs) determine neuropeptides/ neurotransmitters released by neurons, the aim&#xD;
of the present &#xD;
study was to localize the various VSCCs (N-, P/Q-, L-, T- and R-types) in the&#xD;
trigeminal ganglia neurons by immunohistochemistry. The results showed that all&#xD;
the VSCCs are expressed by the cell bodies of neurons though the small-sized&#xD;
neurons showed higher expression of these channels. The small-sized neurons&#xD;
were identified by immunohistochemical localization of CGRP, the most common&#xD;
neuropeptide for pain transmission in the trigeminal ganglia neurons. Some of&#xD;
these channels (N, P/Q and T types) were also expressed on the cell surface&#xD;
though previous electrophysiological studies have shown the expression of all&#xD;
the channels on the cell surface. It is suggested that the cell bodies could&#xD;
play a more active role than hereto ascribed to these, in the modulation of&#xD;
sensory stimuli.
Page(s): 538-543</summary>
    <dc:date>2010-06-01T00:00:00Z</dc:date>
  </entry>
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