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    <title>NISCAIR Online Periodicals Repository Collection: IJEB Vol.44(05) [May 2006]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/6315</link>
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      <title>Secretory factors of human neuroblastoma (IMR-32) and human glioblastoma (U87MG) cell lines induce neurite outgrowths in PC12 cells</title>
      <link>http://nopr.niscair.res.in/handle/123456789/6503</link>
      <description>Title: Secretory factors of human neuroblastoma (IMR-32) and human glioblastoma (U87MG) cell lines induce neurite outgrowths in PC12 cells
&lt;br/&gt;
&lt;br/&gt;Authors: Satpute, Ravindra M; Kashyap, Rajpal S; Kainthla, Rani Poonam; Purohit, Hemant J; Taori, Girdhar M; Daginawala, Hatim F
&lt;br/&gt;
&lt;br/&gt;Abstract: Neurite outgrowth is&#xD;
essential for the communication of the nervous system. The rat Pheochromocytoma&#xD;
(PC12) cells are commonly used in the neuronal cell study. It is well known&#xD;
that exogenous stimuli such as Nerve Growth Factor (NGF) induce neurite&#xD;
outgrowth. In the present study it has been investigated whether or not the&#xD;
conditioned medium from human neuroblastoma cell line (IMR-32) and human&#xD;
glioblastoma cell line (U87MG) may augment neurite outgrowth in PC12 cells.&#xD;
PC12 were cultured with and without conditioned media of IMR-32 and U87MG. The&#xD;
result showed that both the conditioned media induce neurite outgrowth within&#xD;
48 hr and stops further proliferation of PC12 cells. However no outgrowth was&#xD;
noted in PC12 cells incubated without conditioned medium. In conclusion, it is&#xD;
shown that both the conditioned media (IMR-32 and U87MG) have the potential to&#xD;
induce the neurite outgrowth in the PC12 cells.
&lt;br/&gt;
&lt;br/&gt;Page(s): 367-370</description>
      <pubDate>Fri, 28 Apr 2006 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Nanotechnology based drug delivery system(s) for the management of tuberculosis</title>
      <link>http://nopr.niscair.res.in/handle/123456789/6502</link>
      <description>Title: Nanotechnology based drug delivery system(s) for the management of tuberculosis
&lt;br/&gt;
&lt;br/&gt;Authors: Pandey, Rajesh; Khuller, G K
&lt;br/&gt;
&lt;br/&gt;Abstract: The era of nanotechnology has allowed new research strategies&#xD;
to flourish in the field of drug delivery. Nanoparticle-based drug delivery&#xD;
systems are suitable for targeting chronic intracellular infections such as&#xD;
tuberculosis. Polymeric nanoparticles employing poly lactide-co-glycolide have shown&#xD;
promise as far as intermittent chemotherapy in experimental tuberculosis is&#xD;
concerned. It has distinct advantages over the more traditional drug carriers,&#xD;
i.e. liposomes and microparticles. Although the experience with natural&#xD;
carriers, e.g. solid lipid nanoparticles and alginate nanoparticles is in its&#xD;
infancy, future research may rely heavily on these carrier systems. Given the&#xD;
options for oral as well as parenteral therapy, the very nature of the disease&#xD;
and its complex treatment urges one to emphasize on the oral route for&#xD;
controlled drug delivery. Pending the discovery of more potent antitubercular&#xD;
drugs, nanotechnology-based intermittent chemotherapy provides a novel and&#xD;
sound platform for an onslaught against tuberculosis.
&lt;br/&gt;
&lt;br/&gt;Page(s): 357-366</description>
      <pubDate>Fri, 28 Apr 2006 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Analgesic activity of leaf extracts of &lt;i style=""&gt;Culcasia scandens&lt;/i&gt; P. Beauv</title>
      <link>http://nopr.niscair.res.in/handle/123456789/6501</link>
      <description>Title: Analgesic activity of leaf extracts of &lt;i style=""&gt;Culcasia scandens&lt;/i&gt; P. Beauv
&lt;br/&gt;
&lt;br/&gt;Authors: Okoli, C O; Akah, P A; Egbuniwe, O N
&lt;br/&gt;
&lt;br/&gt;Abstract: Analgesic activity of methanol leaf extract&#xD;
of &lt;i style=""&gt;C. scandens&lt;/i&gt; obtained by column&#xD;
chromatography and its graded solvent fractions, was evaluated in mice using&#xD;
acetic acid-induced abdominal writhing and formalin-induced paw licking. The&#xD;
extract and fractions significantly inhibited abdominal writhing and two phases&#xD;
of formalin-induced paw licking in mice, indicating that antinociceptive&#xD;
activity may involve inhibition of pain by peripheral and central mechanisms.
&lt;br/&gt;
&lt;br/&gt;Page(s): 422-424</description>
      <pubDate>Fri, 28 Apr 2006 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Modification of biochemical parameters of gentamicin nephrotoxicity by Coenzyme Q10 and green tea in rats</title>
      <link>http://nopr.niscair.res.in/handle/123456789/6500</link>
      <description>Title: Modification of biochemical parameters of gentamicin nephrotoxicity by Coenzyme Q10 and green tea in rats
&lt;br/&gt;
&lt;br/&gt;Authors: Upaganlawar, Aman; Farswan, Mamta; Rathod, Shivkumar; Balaraman, R
&lt;br/&gt;
&lt;br/&gt;Abstract: The present study was designed to investigate&#xD;
the possible potential protective role of coenzymeQ10 (CoQ10; 10mg/kg/day, ip)&#xD;
and/or green tea (GT; 25mg/kg/day, po) against gentamicin (GM) nephrotoxicity.&#xD;
Marked increase in the level of serum urea, creatinine and lipid peroxidation&#xD;
(LPO) content was found after administration of gentamicin (80mg/kg/day, ip)&#xD;
for eight days along with significant decrease in the antioxidant enzymes,&#xD;
superoxide dismutase (SOD), reduced glutathione (GSH), catalase (CAT) as well&#xD;
as brush border enzymes (Na&lt;sup&gt;+&lt;/sup&gt;/K&lt;sup&gt;+ &lt;/sup&gt;ATPase, Mg&lt;sup&gt;+2&lt;/sup&gt;ATPase&#xD;
and Ca&lt;sup&gt;2+&lt;/sup&gt; ATPase).Treatment with CoQ10 or green tea alone with GM&#xD;
showed significant decrease in serum urea, creatinine and tissue LPO content&#xD;
and significant increase in antioxidant and membrane bound enzymes. Combined&#xD;
treatment with CoQ10 and green tea was more effective in mitigating adverse&#xD;
effect of GM nephrotoxicity. The present work indicated that CoQ10 and green&#xD;
tea due to their antioxidant activity modified the biochemical changes occurred&#xD;
during gentamicin nephrotoxicity and thus had a potential protective effect.
&lt;br/&gt;
&lt;br/&gt;Page(s): 416-418</description>
      <pubDate>Fri, 28 Apr 2006 22:58:59 GMT</pubDate>
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