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  <title>NOPR Collection: &lt;b&gt;Pages 245-312&lt;/b&gt;</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31429" />
  <subtitle>&lt;b&gt;Pages 245-312&lt;/b&gt;</subtitle>
  <id>http://nopr.niscpr.res.in/handle/123456789/31429</id>
  <updated>2026-10-11T23:02:05Z</updated>
  <dc:date>2026-10-11T23:02:05Z</dc:date>
  <entry>
    <title>Conserved expression of ubiquitin carboxyl-terminal esterase L1 (UCHL1) in  mammalian testes</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31442" />
    <author>
      <name>Devi, Lalitha</name>
    </author>
    <author>
      <name>Pawar, Rahul Mohanchandra</name>
    </author>
    <author>
      <name>Makala, Himesh</name>
    </author>
    <author>
      <name>Goel, Sandeep</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/31442</id>
    <updated>2016-07-20T05:54:15Z</updated>
    <published>2015-05-01T00:00:00Z</published>
    <summary type="text">Title: Conserved expression of ubiquitin carboxyl-terminal esterase L1 (UCHL1) in  mammalian testes
Authors: Devi, Lalitha; Pawar, Rahul Mohanchandra; Makala, Himesh; Goel, Sandeep
Abstract: Spermatogonia, the adult germ cells that initiate&#xD;
spermatogenesis in mammalian testis, are capable of&#xD;
dividing both mitotically and meiotically. Isolation and preservation of&#xD;
spermatogonia helps in preserving genetic pool of endangered animals. In this&#xD;
context, identification of marker(s) that can distinguish spermatogonia from&#xD;
other cells in testis gains significance. Here, we examined the expression of&#xD;
ubiquitin carboxyl-terminal esterase L1 (UCHL1) gene and protein in the testes&#xD;
of several mammals, including highly endangered species. Semi-quantitative-reverse transcriptase-polymerase&#xD;
chain reaction (RT-PCR) analysis showed presence of &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;UCHL1&lt;/i&gt; amplicon of 442 bp in all the 18 mammals studied.&#xD;
Nucleotide sequence analysis of these amplicons and their predicted protein&#xD;
sequences revealed 88-99% and 95-100% homology with available human UCHL1 and&#xD;
UCHL1 sequences of other available species in the GenBank, respectively.&#xD;
Western blot analysis showed that UCHL1 protein size was unique in all wild&#xD;
mammals. Immunohistology results confirmed UCHL1 expression in the&#xD;
spermatogonia/gonocytes in testes of several mammals belonging to eight&#xD;
distinct families including highly endangered Felidae, Canidae and&#xD;
Cercopithecoidae. These findings suggest that UCHL1 expression is conserved in&#xD;
the mammalian testis, and could be used as a specific marker for&#xD;
gonocytes/spermatogonia for developing male germ-cell based conservation&#xD;
techniques.
Page(s): 305-312</summary>
    <dc:date>2015-05-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Production of 4-Ipomeanol, an anticancer agent from the root tubers and rhizogenic callus of &lt;i style="mso-bidi-font-style: normal"&gt;Ipomoea batatas&lt;/i&gt; Lam.: A Comparative study</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31441" />
    <author>
      <name>Mohanraj, Remya</name>
    </author>
    <author>
      <name>Subha, S</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/31441</id>
    <updated>2016-07-20T05:53:22Z</updated>
    <published>2015-05-01T00:00:00Z</published>
    <summary type="text">Title: Production of 4-Ipomeanol, an anticancer agent from the root tubers and rhizogenic callus of &lt;i style="mso-bidi-font-style: normal"&gt;Ipomoea batatas&lt;/i&gt; Lam.: A Comparative study
Authors: Mohanraj, Remya; Subha, S
Abstract: A comparative study was done on the&#xD;
production of 4-ipomeanol from root tubers of &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;Ipomoea batatas&lt;/i&gt;&lt;span style="mso-bidi-font-style:italic"&gt; and&#xD;
its rhizogenic callus. Best callusing response was obtained on MS medium&#xD;
supplemented with 11 µM NAA (α-Naphthaleneacetic acid) and 1 µM KIN (Kinetin).&#xD;
Effect of various elicitors (&lt;i&gt;Fusarium solani&lt;/i&gt;, chitin and chitosan) on&#xD;
the production of 4-ipomeanol was studied. Methanol extract of the samples were&#xD;
purified by column chromatography and detected using TLC. Identification of 4-ipomeanol&#xD;
was confirmed using HPLC and quantified spectrophotometrically. A mass spectrum&#xD;
was recorded to confirm the presence of 4-ipomeanol. The calli grown under&#xD;
chitin produced highest (6.61mg g&lt;sup&gt;-1&lt;/sup&gt;) amount of &#xD;
4-ipomeanol. This is the first report on &lt;i&gt;in vitro&lt;/i&gt; production of 4-ipomeanol&#xD;
from &lt;i&gt;I.&lt;/i&gt;&lt;i&gt; batatas&lt;/i&gt;. Since 4-ipomeanol&#xD;
is reported to be present only in &lt;i&gt;I.&lt;/i&gt;&lt;i&gt;&#xD;
batatas&lt;/i&gt;, this study would help in standardizing protocols for large scale&#xD;
production without affecting its natural flora.&#xD;
&#xD;
&lt;/span&gt;
Page(s): 297-304</summary>
    <dc:date>2015-05-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Effect of ethanolic extract of &lt;i style="mso-bidi-font-style:normal"&gt;Coriandrum sativum&lt;/i&gt; L. on tacrine induced orofacial dyskinesia</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31440" />
    <author>
      <name>Mohan, Mahalaxmi</name>
    </author>
    <author>
      <name>Yarlagadda, Sanjyothi</name>
    </author>
    <author>
      <name>Chintala, Saritha</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/31440</id>
    <updated>2016-07-20T05:51:57Z</updated>
    <published>2015-05-01T00:00:00Z</published>
    <summary type="text">Title: Effect of ethanolic extract of &lt;i style="mso-bidi-font-style:normal"&gt;Coriandrum sativum&lt;/i&gt; L. on tacrine induced orofacial dyskinesia
Authors: Mohan, Mahalaxmi; Yarlagadda, Sanjyothi; Chintala, Saritha
Abstract: The effect of ethanolic extract of &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;Coriandrum sativum&lt;/i&gt; L. seeds (100, 200 mg/kg) was studied on tacrine&#xD;
induced orofacial dyskinesia. Tacrine (2.5 mg/kg, i.p.) treated animals were&#xD;
observed for vacuous chewing movements (VCM), tongue protrusions (TP) and&#xD;
orofacial bursts (OB) for 1 h followed by observations for locomotor changes&#xD;
and cognitive dysfunction. Sub-chronic administration of &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;Coriandrum sativum&lt;/i&gt; L. seed extract (E-CS) (100, 200 mg/kg, p.o., for&#xD;
15 days significantly (&lt;i style="mso-bidi-font-style:normal"&gt;P&lt;/i&gt; &lt;0.05)&#xD;
decreased the tacrine induced VCM, TP and OB;&#xD;
and also significantly (&lt;i style="mso-bidi-font-style:normal"&gt;P&lt;/i&gt; &lt;0.05),&#xD;
increased locomotion and cognition compared to the tacrine treated group. Biochemical&#xD;
analysis revealed that tacrine administration significantly (&lt;i style="mso-bidi-font-style:normal"&gt;P&lt;/i&gt; &lt;0.05) decreased the levels of&#xD;
superoxide dismutase (SOD), Catalase (CAT), glutathione reductase (GSH) levels&#xD;
and also significantly (&lt;i style="mso-bidi-font-style:normal"&gt;P&lt;/i&gt; &lt;0.05)&#xD;
increased lipid peroxidation (LPO) as an index of oxidative stress, whereas&#xD;
sub-chronic administration of E-CS significantly (&lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;P&lt;/i&gt; &lt;0.05) improved the antioxidant enzyme (i.e. SOD, CAT, and&#xD;
GSH) levels and also significantly (&lt;i style="mso-bidi-font-style:normal"&gt;P&lt;/i&gt;&#xD;
&lt;0.05) decreased lipid peroxidation (LPO). The results have demonstrated the&#xD;
protective role of ethanolic extract of &lt;i style="mso-bidi-font-style:normal"&gt;Coriandrum&#xD;
sativum&lt;/i&gt;. L against tacrine induced orofacial dyskinesia.
Page(s): 292-296</summary>
    <dc:date>2015-05-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>&lt;span style="font-size:15.0pt;mso-bidi-font-weight:bold" lang="EN-GB"&gt;Protective effect of &lt;i style="mso-bidi-font-style:normal"&gt;Clerodendrum colebrookianum&lt;/i&gt; leaves against iron-induced oxidative stress and hepatotoxicity in Swiss albino mice &lt;/span&gt;</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/31439" />
    <author>
      <name>Das, Abhishek</name>
    </author>
    <author>
      <name>Chaudhuri, Dipankar</name>
    </author>
    <author>
      <name>Ghate, Nikhil Baban</name>
    </author>
    <author>
      <name>Panja, Sourav</name>
    </author>
    <author>
      <name>Chatterjee, Anupam</name>
    </author>
    <author>
      <name>Mandal, Nripendranath</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/31439</id>
    <updated>2016-07-20T05:51:11Z</updated>
    <published>2015-05-01T00:00:00Z</published>
    <summary type="text">Title: &lt;span style="font-size:15.0pt;mso-bidi-font-weight:bold" lang="EN-GB"&gt;Protective effect of &lt;i style="mso-bidi-font-style:normal"&gt;Clerodendrum colebrookianum&lt;/i&gt; leaves against iron-induced oxidative stress and hepatotoxicity in Swiss albino mice &lt;/span&gt;
Authors: Das, Abhishek; Chaudhuri, Dipankar; Ghate, Nikhil Baban; Panja, Sourav; Chatterjee, Anupam; Mandal, Nripendranath
Abstract: Liver&#xD;
toxicity due to iron overload leads to oxidative damage of proteins, lipids and&#xD;
nucleic acids which in turn manifests several human diseases. Here, we&#xD;
evaluated the improving effect of &lt;i style="mso-bidi-font-style:normal"&gt;Clerodendrum&#xD;
colebrookianum &lt;/i&gt;leaf on iron overload induced liver injury along with &lt;i style="mso-bidi-font-style:normal"&gt;in vitro&lt;/i&gt; iron chelation and the&#xD;
protection of Fenton reaction induced DNA damage was conducted. Iron overload&#xD;
was induced by intraperitoneal administration of iron-dextran into mice. Post&#xD;
oral administration of different doses of the extract (50, 100 and 200 mg/kg&#xD;
body weight) showed significant decrease in different biochemical markers such&#xD;
as liver iron, serum ferritin and serum enzyme levels, along with decreased&#xD;
lipid peroxidation, protein oxidation and collagen content. In addition, the&#xD;
extract effectively enhanced the antioxidant enzyme levels and also exhibited&#xD;
the potential activity of the reductive release of ferritin iron. The&#xD;
protective effect of &lt;i style="mso-bidi-font-style:normal"&gt;C.&lt;/i&gt; &lt;i style="mso-bidi-font-style:normal"&gt;colebrookianum &lt;/i&gt;extract on injured liver&#xD;
was furthermore supported by the histopathological studies that showed&#xD;
improvement histologically. In conclusion, the present results demonstrated the&#xD;
hepatoprotective efficiency of &lt;i style="mso-bidi-font-style:normal"&gt;C.&lt;/i&gt; &lt;i style="mso-bidi-font-style:normal"&gt;colebrookianum &lt;/i&gt;leaf in iron overloaded&#xD;
mice, and hence, a potential iron chelating drug for iron overload diseases.
Page(s): 281-291</summary>
    <dc:date>2015-05-01T00:00:00Z</dc:date>
  </entry>
</feed>

