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  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/23020" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/23020</id>
  <updated>2026-10-13T04:05:27Z</updated>
  <dc:date>2026-10-13T04:05:27Z</dc:date>
  <entry>
    <title>Effect of nifedipine and amlodipine on dead space wound healing in rats</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/23095" />
    <author>
      <name>Bhaskar, H N</name>
    </author>
    <author>
      <name>Udupa, Saraswathi L</name>
    </author>
    <author>
      <name>Udupa, A L</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/23095</id>
    <updated>2013-11-09T16:36:10Z</updated>
    <published>2005-03-01T00:00:00Z</published>
    <summary type="text">Title: Effect of nifedipine and amlodipine on dead space wound healing in rats
Authors: Bhaskar, H N; Udupa, Saraswathi L; Udupa, A L
Abstract: Effect of two calcium channel blockers (CCBs)&#xD;
nifedipine and amlodipine, was studied on normal and steroid depressed wound healing&#xD;
in albino rats, using the dead space wound model. The drugs enhanced normal healing&#xD;
as evidenced by increase in tensile strength of 10 days old granulation tissue.&#xD;
There was neither a significant change in the hydroxyproline level (or collagen)&#xD;
nor a change in the glycosaminoglycan content in granulation tissue. However,&#xD;
lysyloxiclase level was increased significantly. The increase in tensile strength&#xD;
could thus be attributed to better cross-linking and maturation of collagen&#xD;
rather than collagen synthesis &lt;i&gt;per se. &lt;/i&gt;The drugs were also able to overcome&#xD;
steroid depressed wound healing. It is likely that the prohealing effects may be&#xD;
related to the improved antioxidant&#xD;
&#xD;
status too, since superoxide dismutase levels&#xD;
were observed to be higher in the CCB-treated animals.
Page(s): 294-296</summary>
    <dc:date>2005-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;i&gt;In vivo &lt;/i&gt;induction of sister chromatid exchanges (SCEs) and chromosomal aberrations (CAs) by lynestrenol</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/23093" />
    <author>
      <name>Siddique, Yasir Hasan</name>
    </author>
    <author>
      <name>Afzal, Mohammad</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/23093</id>
    <updated>2013-11-10T16:35:42Z</updated>
    <published>2005-03-01T00:00:00Z</published>
    <summary type="text">Title: &lt;i&gt;In vivo &lt;/i&gt;induction of sister chromatid exchanges (SCEs) and chromosomal aberrations (CAs) by lynestrenol
Authors: Siddique, Yasir Hasan; Afzal, Mohammad
Abstract: Genotoxicity study of synthetic progestin&#xD;
lynestrenol, was carried out on mouse bone marrow cells using sister chromatid exchanges&#xD;
(SCEs) and chromosomal aberrations (CAs) as parameters. Lynestrenol was studied&#xD;
at three different doses (6.87, 13.75 and 27.50 mg/kg body wt.). SCE and CA increased&#xD;
significantly as compared to normal control when treated with lynestrenol at 13.75&#xD;
and 27.50 mg/kg body wt. The present results suggest that lynestrenol has both a&#xD;
genotoxic and cytotoxic effects in mouse bone marrow cells.
Page(s): 291-293</summary>
    <dc:date>2005-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Inter-specific hybridization between freshwater catfish &lt;i&gt;Mystus cavasius &lt;/i&gt;(Ham &amp; Buch) and &lt;i&gt;M. seenghala &lt;/i&gt;(Sykes) by artificial fertilization</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/23092" />
    <author>
      <name>Raj, A Jesu Arockia</name>
    </author>
    <author>
      <name>Haniffa, M A</name>
    </author>
    <author>
      <name>Seetharaman, S</name>
    </author>
    <author>
      <name>Benziger, P S Allen</name>
    </author>
    <author>
      <name>Jacob, Shybu</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/23092</id>
    <updated>2013-11-10T16:35:24Z</updated>
    <published>2005-03-01T00:00:00Z</published>
    <summary type="text">Title: Inter-specific hybridization between freshwater catfish &lt;i&gt;Mystus cavasius &lt;/i&gt;(Ham &amp; Buch) and &lt;i&gt;M. seenghala &lt;/i&gt;(Sykes) by artificial fertilization
Authors: Raj, A Jesu Arockia; Haniffa, M A; Seetharaman, S; Benziger, P S Allen; Jacob, Shybu
Abstract: By employing the technique of induced ovulation&#xD;
for artificial fertilization, inter-specific hybrids between the threatened catfish&#xD;
species (&lt;i&gt;Mystus cavasius &lt;/i&gt;× &lt;i&gt;M. seenghala&lt;/i&gt;) were produced. Fertilization,&#xD;
hatching and survival were significantly different between control and hybrids.&#xD;
The hatching time of the hybrid was significantly lower than that of the control.&#xD;
The average performance &lt;i&gt;viz., &lt;/i&gt;hatching time and viability of larvae of the&#xD;
control fish, was significantly better than that of the hybrids. In the hybrid cross,&#xD;
hatchlings were mostly deformed and abnormal and after yolk absorption ultimately&#xD;
succumbed.
Page(s): 286-290</summary>
    <dc:date>2005-03-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;i&gt;In vitro &lt;/i&gt;propagation of &lt;i&gt;Dendrobium &lt;/i&gt;hybrids using flower stalk node explants</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/23091" />
    <author>
      <name>Martin, K P</name>
    </author>
    <author>
      <name>Geevarghese, Julie</name>
    </author>
    <author>
      <name>Joseph, Dominic</name>
    </author>
    <author>
      <name>Madassery, Joseph</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/23091</id>
    <updated>2013-11-07T16:36:54Z</updated>
    <published>2005-03-01T00:00:00Z</published>
    <summary type="text">Title: &lt;i&gt;In vitro &lt;/i&gt;propagation of &lt;i&gt;Dendrobium &lt;/i&gt;hybrids using flower stalk node explants
Authors: Martin, K P; Geevarghese, Julie; Joseph, Dominic; Madassery, Joseph
Abstract: Large-scale &lt;i&gt;in vitro &lt;/i&gt;propagation protocol&#xD;
for &lt;i&gt;Dendrobium &lt;/i&gt;hybrids Sonia 17 and 28, two highly prized commercial cut&#xD;
flower cultivars through shoot multiplication using flower stalk node explants and&#xD;
protocorm-like bodies (PLBs) formation was accomplished. Both hybrids did not exhibit&#xD;
significant differences in initiation, multiplication, rooting, and field&#xD;
&#xD;
establishment. Flower stalk nodes cultured&#xD;
on half strength Murashige and Skoog (MS) medium supplemented with 6.97 μ&lt;i&gt;M &lt;/i&gt;kinetin&#xD;
(Kn), or 15% coconut water (CW) or 13.3 μ&lt;i&gt;M &lt;/i&gt;of N&lt;sup&gt;6&lt;/sup&gt;-benzyladenine&#xD;
(BA) evoked bud break. Kn showed better growth of the initiated bud. Excision&#xD;
and culture of the initiated shoots on medium having same amount of Kn&#xD;
developed&#xD;
&#xD;
more than 5 shoots per shoot directly from&#xD;
the base. Subsequent culture enhanced the rate of shoot induction. Transfer of isolated&#xD;
shoots onto 44.4μ&lt;i&gt;M &lt;/i&gt;of BA enriched medium displayed induction of more than&#xD;
6 PLBs from the base within 60 days. PLBs underwent rapid multiplication upon&#xD;
transferral to medium having the same concentration of BA (44.4 μ&lt;i&gt;M&lt;/i&gt;).&#xD;
&#xD;
Subsequent culture increased the proliferation&#xD;
of PLBs. No decline was observed in the proliferation of shoots as well as PLBs&#xD;
up to 15&lt;sup&gt;th&lt;/sup&gt; subculture. PLBs transferred onto half strength MS medium&#xD;
with 6.97 μ&lt;i&gt;M &lt;/i&gt;of Kn underwent conversion of more than 90% PLBs to shoots.&#xD;
The shoots were rooted at the best on half strength MS medium with 2 g 1&lt;sup&gt;-1&lt;/sup&gt;&#xD;
activated charcoal. Survival rate of the plantlets of the two hybrid cultivars after&#xD;
acclimatization was more than 80%.
Page(s): 280-285</summary>
    <dc:date>2005-03-01T00:00:00Z</dc:date>
  </entry>
</feed>

