<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>NOPR Collection:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/29260" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/29260</id>
  <updated>2026-10-12T22:32:59Z</updated>
  <dc:date>2026-10-12T22:32:59Z</dc:date>
  <entry>
    <title>Antiangiogenic and antiproliferative assessment of cyanobacteria</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/29303" />
    <author>
      <name>Kyadari, Mahender</name>
    </author>
    <author>
      <name>Fatma, Tasneem</name>
    </author>
    <author>
      <name>Velpandian, Thirumurthy</name>
    </author>
    <author>
      <name>Malliga, P</name>
    </author>
    <author>
      <name>Bharat, Naveen</name>
    </author>
    <author>
      <name>Bano, Fareha</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/29303</id>
    <updated>2016-07-20T05:09:53Z</updated>
    <published>2014-08-01T00:00:00Z</published>
    <summary type="text">Title: Antiangiogenic and antiproliferative assessment of cyanobacteria
Authors: Kyadari, Mahender; Fatma, Tasneem; Velpandian, Thirumurthy; Malliga, P; Bharat, Naveen; Bano, Fareha
Abstract: Biologically&#xD;
active compounds with different modes of action, such as antiproliferative,&#xD;
antioxidant, antimicrotubule, have been isolated from algae and cyanobacteria. The&#xD;
present study was designed to evaluate antiangiogenic and antiproliferative potential of&#xD;
dichloromethane and methanol (2:1) extracts of different cyanobacteria. Further&#xD;
fingerprinting of the activity possessing extracts were carried out using ESI-LC-MS/MS. Extracts (25, 50 and 100 µg) were&#xD;
screened in the vascular endothelial growth factor (VEGF) induced angiogenesis&#xD;
in &lt;i style="mso-bidi-font-style:normal"&gt;inovo&lt;/i&gt; chick chorioallontoic membrane&#xD;
assay (CAM) at various&#xD;
concentrations using thalidomide and normal saline as positive and untreated&#xD;
control groups respectively. The extracts were also evaluated for their&#xD;
antiproliferative activity by MTT assay using HeLa cancer cell line. The results&#xD;
obtained from the various algal extracts did not show any significant&#xD;
antiangiogenic activity as compared to VEGF control. &lt;i&gt;&lt;span style="letter-spacing:-.1pt;mso-ansi-language:EN-IN"&gt;Oscillatoria sp. &lt;/span&gt;&lt;/i&gt;&lt;span style="letter-spacing:-.1pt;mso-ansi-language:EN-IN;mso-bidi-font-style:italic"&gt;and&lt;i&gt;&#xD;
&lt;/i&gt;&lt;i&gt;Lyngbya officinalis&lt;/i&gt; exhibited significant&#xD;
anti-proliferative&lt;span style="mso-bidi-font-style:italic"&gt; activity at&#xD;
IC&lt;sub&gt;50&lt;/sub&gt; values of &lt;span style="mso-bidi-font-weight:bold"&gt;220 and 260&#xD;
µg/mL respectively. ESI-LC-MS/MS&#xD;
of&lt;i&gt; L. officinalis&lt;/i&gt;&lt;i style="mso-bidi-font-style:normal"&gt;&lt;span style="mso-bidi-font-weight:bold"&gt;&lt;/span&gt;&lt;/i&gt;&lt;span style="mso-bidi-font-weight:&#xD;
bold"&gt; showed the presence of lyngbyatoxin-A and&lt;span style="letter-spacing:-.1pt;mso-ansi-language:EN-IN;mso-bidi-font-style:italic"&gt;&#xD;
that of &lt;i&gt;Oscillatoria sp.&lt;/i&gt; reveals&lt;span style="letter-spacing:-.1pt;mso-bidi-font-weight:bold" lang="EN-GB"&gt; the presence of malyngamide-J suggesting the possibility&#xD;
of antiproliferative activity.&#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 835-842</summary>
    <dc:date>2014-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;i&gt;In vitro &lt;/i&gt;flowering – A system for tracking floral organ development in &lt;i&gt;Dendrocalamus hamiltonii&lt;/i&gt;&lt;span style="mso-bidi-font-style:italic"&gt; Nees et Arn. ex Munro&lt;sup&gt;†&lt;/sup&gt; &lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/29302" />
    <author>
      <name>Kaur, Devinder</name>
    </author>
    <author>
      <name>Thapa, Pooja</name>
    </author>
    <author>
      <name>Sharma, Madhu</name>
    </author>
    <author>
      <name>Bhattacharya, Amita</name>
    </author>
    <author>
      <name>Sood, Anil</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/29302</id>
    <updated>2016-07-20T05:09:00Z</updated>
    <published>2014-08-01T00:00:00Z</published>
    <summary type="text">Title: &lt;i&gt;In vitro &lt;/i&gt;flowering – A system for tracking floral organ development in &lt;i&gt;Dendrocalamus hamiltonii&lt;/i&gt;&lt;span style="mso-bidi-font-style:italic"&gt; Nees et Arn. ex Munro&lt;sup&gt;†&lt;/sup&gt; &lt;/span&gt;
Authors: Kaur, Devinder; Thapa, Pooja; Sharma, Madhu; Bhattacharya, Amita; Sood, Anil
Abstract: &lt;i&gt;Dendrocalamus hamiltonii &lt;/i&gt;plants are slender and tall (15-25 m) thereby, rendering tagging,&#xD;
sampling and tracking the development of flowers difficult. Therefore, a&lt;span style="mso-ansi-language:EN-US" lang="EN-US"&gt; reproducible system &lt;span style="mso-bidi-font-style:italic" lang="EN-GB"&gt;of &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;in vitro &lt;/i&gt;&lt;span style="mso-bidi-font-style:&#xD;
italic" lang="EN-GB"&gt;flowering was established for tracking the&#xD;
stages of flower development. MS medium supplemented with 2.22 µM&lt;sup&gt; &lt;/sup&gt;6-benzylaminopurine,&#xD;
1.23 µM&lt;sup&gt; &lt;/sup&gt;indole-3-butyric acid and 2% sucrose&lt;i style="mso-bidi-font-style:&#xD;
normal"&gt; &lt;/i&gt;&lt;span style="mso-bidi-font-style:italic"&gt;was optimized as the&#xD;
flower induction medium (FIM) wherein 28&#xD;
and 42 days were required for the development of gynoecium and androecium,&#xD;
respectively. Six distinct stages of &lt;i&gt;in vitro &lt;/i&gt;flower development were&#xD;
identified, and the flowers were comparable with that of &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;in planta&lt;/i&gt; sporadic flowers. Pollen viability of the &lt;i style="mso-bidi-font-style:normal"&gt;in vitro&lt;/i&gt; flowers was higher than those&#xD;
of &lt;i style="mso-bidi-font-style:normal"&gt;in planta&lt;/i&gt; ones. The &lt;i&gt;in vitro&lt;/i&gt;&#xD;
system developed in the present study facilitates easy tracking of different&#xD;
stages of flower development under controlled environmental conditions. It can&#xD;
also be used for medium- or long-term storage of pollens and manipulation of &lt;i style="mso-bidi-font-style:normal"&gt;in vitro &lt;/i&gt;fertilization. &#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 825-834</summary>
    <dc:date>2014-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;span style="font-size:15.0pt;mso-bidi-font-size:12.0pt;mso-bidi-font-family:"Times New Roman"" lang="EN-GB"&gt;A simple technique for tracking individual spore and gametophyte development in &lt;i&gt;Adiantum lunulatum &lt;/i&gt;Burm. f. using modified extra thin alginate film technique&lt;sup&gt;†&lt;/sup&gt; &lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/29301" />
    <author>
      <name>Sareen, Bhuvnesh</name>
    </author>
    <author>
      <name>Bhattacharya, Amita</name>
    </author>
    <author>
      <name>Sharma, Madhu</name>
    </author>
    <author>
      <name>Sood, Anil</name>
    </author>
    <author>
      <name>Ahuja, Paramvir Singh</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/29301</id>
    <updated>2016-07-20T05:07:59Z</updated>
    <published>2014-08-01T00:00:00Z</published>
    <summary type="text">Title: &lt;span style="font-size:15.0pt;mso-bidi-font-size:12.0pt;mso-bidi-font-family:"Times New Roman"" lang="EN-GB"&gt;A simple technique for tracking individual spore and gametophyte development in &lt;i&gt;Adiantum lunulatum &lt;/i&gt;Burm. f. using modified extra thin alginate film technique&lt;sup&gt;†&lt;/sup&gt; &lt;/span&gt;
Authors: Sareen, Bhuvnesh; Bhattacharya, Amita; Sharma, Madhu; Sood, Anil; Ahuja, Paramvir Singh
Abstract: &lt;span style="font-size:9.0pt;mso-bidi-font-size:12.0pt;mso-bidi-font-family:" times="" new="" roman""="" lang="EN-GB"&gt;A&#xD;
new&lt;span style="mso-bidi-font-weight:bold"&gt; technique was developed for &lt;span style="mso-bidi-font-weight:bold"&gt;accurate calculation of percent germination&#xD;
and tracking of individual spores from germination to gametophyte development&#xD;
in &lt;i style="mso-bidi-font-style:normal"&gt;Adiantum lunulatum&lt;/i&gt;&lt;span style="mso-bidi-font-weight:bold"&gt;. High percentage of ETAF immobilized&#xD;
spore germination (72.4%) was followed by development of gametophytic clumps.&#xD;
The ETAF immobilized&lt;span style="mso-bidi-font-weight:bold"&gt; clumps were cut&#xD;
into pieces and multiplied &lt;i&gt;en masse&lt;/i&gt;. Apomictic sporophytes developed&#xD;
from the gametophytes. This indicated the potential of ETAF for mass&#xD;
propagation of &lt;i style="mso-bidi-font-style:normal"&gt;A. lunulatum&lt;/i&gt; without&#xD;
the need to start from spores. Since individual spores can be tracked from&#xD;
germination to gametophyte development,&lt;span style="mso-bidi-font-style:italic"&gt;&#xD;
the ETAF technique has the potential to be used for (i) harvesting&#xD;
uniformly developed plants of similar age for extensive experimentations and&#xD;
commercial utilization and (ii) detailed study on developmental and&#xD;
reproductive biology of different ferns and fern allies. &#xD;
&#xD;
&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;
Page(s): 820-824</summary>
    <dc:date>2014-08-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Effect of acute exposure of triazophos on oxidative stress and histopathological alterations in liver, kidney and brain of Wistar rats</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/29300" />
    <author>
      <name>Mohineesh</name>
    </author>
    <author>
      <name>Raj, Jaya</name>
    </author>
    <author>
      <name>Rajvanshi, A C</name>
    </author>
    <author>
      <name>Dogra, T D</name>
    </author>
    <author>
      <name>Raina, Anupuma</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/29300</id>
    <updated>2016-07-20T05:06:58Z</updated>
    <published>2014-08-01T00:00:00Z</published>
    <summary type="text">Title: Effect of acute exposure of triazophos on oxidative stress and histopathological alterations in liver, kidney and brain of Wistar rats
Authors: Mohineesh; Raj, Jaya; Rajvanshi, A C; Dogra, T D; Raina, Anupuma
Abstract: Acute dose of organophosphorus pesticide Triazophos (&lt;i&gt;O,O&lt;/i&gt;-diethyl&#xD;
&lt;i&gt;O&lt;/i&gt;-1-phenyl-1&lt;i&gt;H&lt;/i&gt;-1,2,4-triazol-3-yl phosphorothioate; Tz) administered orally affects oxidative stress&#xD;
parameters and the histo-architecture of liver, kidney and brain tissues. The&#xD;
results indicate a dose dependent induction of oxidative stress as evident by&#xD;
increased malondialdehyde level and decreased antioxidant defense including&#xD;
glutathione and superoxide dismutase activity in rat liver, kidney and brain. AChE&#xD;
activity was found significantly decreased in the Tz treated groups as compared&#xD;
to the vehicle control (DMSO) group. Histopathological examination of liver, kidney&#xD;
and brain in Tz treated rats revealed medullary congestion and hydropic&#xD;
degeneration of hepatocytes in liver and medullary congestion in kidney. However,&#xD;
no significant histopathological changes were observed in brain tissues.
Page(s): 814-819</summary>
    <dc:date>2014-08-01T00:00:00Z</dc:date>
  </entry>
</feed>

