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  <title>NOPR Community:</title>
  <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/15070" />
  <subtitle />
  <id>http://nopr.niscpr.res.in/handle/123456789/15070</id>
  <updated>2026-10-08T12:18:09Z</updated>
  <dc:date>2026-10-08T12:18:09Z</dc:date>
  <entry>
    <title>Ornithine α-ketoglutarate modulates the levels of antioxidants and lipid peroxidation products in ammonium acetate treated rats</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19789" />
    <author>
      <name>Dakshayani, K B</name>
    </author>
    <author>
      <name>Velvizhi, S</name>
    </author>
    <author>
      <name>Subramanian, P</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19789</id>
    <updated>2013-07-15T16:34:47Z</updated>
    <published>2002-12-01T00:00:00Z</published>
    <summary type="text">Title: Ornithine α-ketoglutarate modulates the levels of antioxidants and lipid peroxidation products in ammonium acetate treated rats
Authors: Dakshayani, K B; Velvizhi, S; Subramanian, P
Abstract: The effects of ornithine α-ketoglutarate (OKG)&#xD;
on ammonium acetate induced hepatotoxicity were studied in experimental rats. The&#xD;
levels of urea, non-protein nitrogen and thiobarbituric acid reactive substances&#xD;
were significantly increased in ammonium acetate treated rats ; but these levels&#xD;
were significantly decreased in ammonium acetate-OKG treated rats. Similar patterns&#xD;
were observed in the levels of free fatty acids, triglycerides and phospholipids.&#xD;
Furthermore, non-enzymatic (reduced glutathione) and enzymatic (glutathione peroxidise,&#xD;
superoxide dismutase and catalase) antioxidants were significantly decreased in&#xD;
ammonium acetate treated rats. When compared with control and were significantly&#xD;
increased in ammonium acetate-OKG treated rats compared to ammonium acetate treatment&#xD;
alone.
Page(s): 422-424</summary>
    <dc:date>2002-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Dietary regulation of adenosine deaminase activity in stomach, small intestine and spleen of mice</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19788" />
    <author>
      <name>Ray, Indrani</name>
    </author>
    <author>
      <name>Sharma, Ramesh</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19788</id>
    <updated>2013-07-16T16:33:21Z</updated>
    <published>2002-12-01T00:00:00Z</published>
    <summary type="text">Title: Dietary regulation of adenosine deaminase activity in stomach, small intestine and spleen of mice
Authors: Ray, Indrani; Sharma, Ramesh
Abstract: Activity of adenosine deaminase (ADA) and its regulation by&#xD;
dietary restriction were studied in the stomach, small intestine and spleen of mice.&#xD;
ADA activity (U/mg&#xD;
protein) was highest in the stomach, followed by small intestine and spleen of mice&#xD;
on normal diet. The activity decreased significantly in the stomach (41%)&lt;i&gt; &lt;/i&gt;and&#xD;
small intestine (45%) of 24 hr fasted mice, when compared to mice fed &lt;i&gt;ad-libitum.&#xD;
&lt;/i&gt;However, ADA&#xD;
activity in spleen did not show any change by dietary intervention. Refeeding of&#xD;
fasted mice for 24 hr restored the activity of ADA in tissues. In addition, dietary restriction&#xD;
(alternate days of feeding for three months) had a cumulative effect, whereby ADA&#xD;
activity decreased significantly in the stomach (53% on the day of feeding and 60%&#xD;
on the day of fasting) and small intestine (50% and 54% on the day of feeding and&#xD;
fasting, respectively) without any change in activity in spleen. These findings&#xD;
indicate that dietary restriction reduces ADA&#xD;
activity in a tissue-specific manner. Long-term dietary restriction leads to a&#xD;
cumulative adaptation in lowering the ADA&#xD;
activity of GIT, but not in spleen.
Page(s): 419-421</summary>
    <dc:date>2002-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Synthesis, conformation and vibrational dynamics of the peptide -Ser-Cys-Lys-Leu- Asp- Phe-, a fragment of apolipoprotein B</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19787" />
    <author>
      <name>Srivastava, Shinoo</name>
    </author>
    <author>
      <name>Srivastava, Seema</name>
    </author>
    <author>
      <name>Melkani, Girish Chandra</name>
    </author>
    <author>
      <name>Singh, Shyam</name>
    </author>
    <author>
      <name>Gupta, Vishwambhar Dayal</name>
    </author>
    <author>
      <name>Gupta, Vijai Prakash</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19787</id>
    <updated>2013-07-20T16:34:03Z</updated>
    <published>2002-12-01T00:00:00Z</published>
    <summary type="text">Title: Synthesis, conformation and vibrational dynamics of the peptide -Ser-Cys-Lys-Leu- Asp- Phe-, a fragment of apolipoprotein B
Authors: Srivastava, Shinoo; Srivastava, Seema; Melkani, Girish Chandra; Singh, Shyam; Gupta, Vishwambhar Dayal; Gupta, Vijai Prakash
Abstract: The collective normal modes of the hexapeptide&#xD;
-Ser-Cys-Lys-Leu-Asp-Phe-, a fragment of apolipoprotein B (apo B), have been obtained.&#xD;
They reflect the dynamic nature and are atleast partly responsible for energy&#xD;
input in autolytic activity. Further, on energetic considerations based on the measurements&#xD;
reported by Sim &amp; Sim, it has been shown that of the two such fragments only&#xD;
one induces autolysis, while the other remains anchored to the coated pit.
Page(s): 410-418</summary>
    <dc:date>2002-12-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Transport through liquid membranes containing omeprazole and lansoprazole</title>
    <link rel="alternate" href="http://nopr.niscpr.res.in/handle/123456789/19786" />
    <author>
      <name>Nagappa, A N</name>
    </author>
    <author>
      <name>Pandi, P V</name>
    </author>
    <author>
      <name>Mishra, P K</name>
    </author>
    <author>
      <name>Girish, Rahul K</name>
    </author>
    <author>
      <name>Shanmukh, I</name>
    </author>
    <id>http://nopr.niscpr.res.in/handle/123456789/19786</id>
    <updated>2013-07-15T16:34:34Z</updated>
    <published>2002-12-01T00:00:00Z</published>
    <summary type="text">Title: Transport through liquid membranes containing omeprazole and lansoprazole
Authors: Nagappa, A N; Pandi, P V; Mishra, P K; Girish, Rahul K; Shanmukh, I
Abstract: Omeprazole and lansoprazole, the therapeutically&#xD;
important drugs belonging to proton pump inhibitor category are extensively used in&#xD;
the treatment of gastric ulcers. Transport through liquid membranes generated by&#xD;
these drugs in lecithincholeste mixture in series with a supporting membrane has&#xD;
been studied. The data obtained show the formation of liquid&#xD;
&#xD;
membrane in series with the supporting membrane.&#xD;
Transport of cations, chloride and bicarbonate ions in the presence liquid membranes&#xD;
generated by omeprazole and lanzoprazole indicate the modification in the permeability&#xD;
or various permeants.
Page(s): 406-409</summary>
    <dc:date>2002-12-01T00:00:00Z</dc:date>
  </entry>
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