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    <title>NISCAIR Online Periodicals Repository Community: IJBB Vol.49 [2012]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/13584</link>
    <description />
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      <title>&lt;span style="font-size:11.0pt;mso-bidi-font-size: 10.0pt;font-family:"Times New Roman";mso-fareast-font-family:"Times New Roman"; mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB"&gt;Anti-inflammatory and antipyretic activities of the ethanolic extract of &lt;i style="mso-bidi-font-style:normal"&gt;Shorea robusta&lt;/i&gt; Gaertn. f. resin&lt;/span&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/15245</link>
      <description>Title: &lt;span style="font-size:11.0pt;mso-bidi-font-size: 10.0pt;font-family:"Times New Roman";mso-fareast-font-family:"Times New Roman"; mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-GB"&gt;Anti-inflammatory and antipyretic activities of the ethanolic extract of &lt;i style="mso-bidi-font-style:normal"&gt;Shorea robusta&lt;/i&gt; Gaertn. f. resin&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Wani, T A; Chandrashekara, H H; Kumar, D; Prasad, R; Sardar, K K; Kumar, D; Tandan, S K
&lt;br/&gt;
&lt;br/&gt;Abstract: &lt;i style="mso-bidi-font-style:normal"&gt;Shorea&#xD;
robusta&lt;/i&gt; &lt;span style="mso-bidi-font-weight:bold"&gt;Gaertn.&#xD;
f. (Sal) is one of the most important traditional Indian medicinal&#xD;
plants. The resin of the plant has been used in the treatment of inflammation&#xD;
in folklore medicine. In the present study, ethanolic extract (70%) of &#xD;
&lt;i style="mso-bidi-font-style:normal"&gt;S. robusta&lt;/i&gt; resin (SRE) was&#xD;
investigated for its anti-inflammatory and antipyretic activities. Acute&#xD;
inflammation was produced by carrageenan-induced hind paw edema and sub-acute&#xD;
by cotton pellet-induced granuloma in male Wistar rats. The antipyretic&#xD;
activity of SRE was studied using Brewer’s yeast-induced pyrexia in rats. The&#xD;
rats were divided into&lt;sup&gt; &lt;/sup&gt;five groups with five animals in each group.&#xD;
Group I was treated with vehicle i.e. 1% v/v Tween-80 and served as control.&#xD;
Groups II to IV were treated with three different doses of SRE (30, 100 and 300&#xD;
mg/kg orally). Group V was treated with standard drug etoricoxib (10 mg/kg&#xD;
orally). The anti-inflammatory activity of SRE was assessed by per cent&#xD;
reduction &#xD;
in edema volume of carrageenan-induced hind paw edema and by per cent decrease&#xD;
in granuloma formation in cotton &#xD;
pellet-induced granuloma test. SRE (100 and 300 mg/kg) produced a significant&#xD;
reduction in edema volume and decrease in granulation tissue formation in rats.&#xD;
Significant reduction in pyrexia was observed at all the dose levels of SRE&#xD;
i.e. 30, 100 and 300 mg/kg. The results of the present study demonstrated&#xD;
anti-inflammatory and antipyretic activities of &lt;i style="mso-bidi-font-style:&#xD;
normal"&gt;S. robusta&lt;/i&gt; resin and supported its traditional therapeutic use in&#xD;
painful inflammatory conditions and fever.&#xD;
&#xD;
&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 463-467</description>
      <pubDate>Wed, 28 Nov 2012 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Homocysteine in occlusive vascular disease: A risk marker or risk factor</title>
      <link>http://nopr.niscair.res.in/handle/123456789/15244</link>
      <description>Title: Homocysteine in occlusive vascular disease: A risk marker or risk factor
&lt;br/&gt;
&lt;br/&gt;Authors: Bhargava, Seema; Ali, Arif; Manocha, Anjali; Kankra, Mamta; Das, Sabari; Srivastava, Lalit Mohan
&lt;br/&gt;
&lt;br/&gt;Abstract: whether it is&#xD;
just an association (risk marker) or actually a causative factor (risk factor).&#xD;
To elucidate this, a retrospective statistical analysis was done of data&#xD;
generated in the course of our study on homocysteine and vascular disease.&#xD;
Homocysteine, lipid profile components and lipoprotein(a) were estimated in&#xD;
fasting blood samples drawn from 252 controls and 536 patients of occlusive&#xD;
vascular disease. The data were analyzed by SPSS version 17. Mean homocysteine&#xD;
levels were significantly higher (p&lt;0.001) in all patients categories, as&#xD;
compared to controls. In fact, homocysteine level was the most significant&#xD;
biochemical risk factor for vascular disease. The odds ratios due to&#xD;
hyperhomocysteinemia varied from 3.170-4.153. When the cut-off was increased by&#xD;
5 µmol/L, the odds ratio became almost three-fold. The prevalence of&#xD;
hyperhomocysteinemia increased by &lt;span style="font-family:&#xD;
Symbol;mso-ascii-font-family:" times="" new="" roman";mso-hansi-font-family:"times="" roman";="" letter-spacing:-.1pt;mso-char-type:symbol;mso-symbol-font-family:symbol"="" lang="EN-GB"&gt;@20%, when the cut-off was reduced by 5&#xD;
µmol/L. Statistical analysis of our data revealed that homocysteine conformed&#xD;
to Hill’s criteria of causation. Moreover, hyperhomocysteinemia was treatable&#xD;
by the administration of B-vitamins, even if the cause was genetic. Hence&#xD;
morbidity due to vascular disease could be reduced by identification and&#xD;
treatment of hyperhomocysteinemia. &#xD;
&#xD;
&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 414-420</description>
      <pubDate>Wed, 28 Nov 2012 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Docking studies on novel alkaloid tryptanthrin and its analogues against enoyl-acyl carrier protein reductase (InhA) of &lt;i&gt;Mycobacterium tuberculosis&lt;/i&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/15243</link>
      <description>Title: Docking studies on novel alkaloid tryptanthrin and its analogues against enoyl-acyl carrier protein reductase (InhA) of &lt;i&gt;Mycobacterium tuberculosis&lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Tripathi, Ankit; Wadia, Nupur; Bindal, Deepak; Jana, Tarakanta
&lt;br/&gt;
&lt;br/&gt;Abstract: Isoniazid resistance is a serious threat in the battle&#xD;
against the treatment of multi-drug resistant tuberculosis (MDR-TB) and&#xD;
extremely drug-resistant tuberculosis (XDR-TB). Isoniazid is an inhibitor of&#xD;
enoyl-acyl carrier protein reductase (InhA) of &lt;i&gt;Mycobacterium tuberculosis, &lt;/i&gt;which&#xD;
is an important and functional enzyme of the type II fatty acid synthesis&#xD;
system and important therapeutic target. Natural alkaloid tryptanthrin and its&#xD;
analogues have shown anti-tubercular activity against &#xD;
MDR-TB, but their cellular target is unknown. In this work, &lt;i&gt;in silico&lt;/i&gt;&#xD;
molecular docking was performed using docking server in order to see the&#xD;
interaction of tryptanthrin and its 15 analogues with InhA of &lt;i&gt;M.&#xD;
tuberculosis&lt;/i&gt;. Results showed that among tryptanthrin and its 15 analogues,&#xD;
tryptanthrin and its two analogues exhibited good affinity to the binding site&#xD;
of InhA with free binding energy of -7.94 kcal/mol and inhibition constant (&lt;i&gt;K&lt;/i&gt;i)&#xD;
of 1.50 µm. Active site residues of InhA&#xD;
interacting with tryptanthrin were Ser13, Thr39, Phe41, Leu63, Asp64, Val65,&#xD;
Ile95, Phe97 and Ile122. In binding mode, polar bond were found between O1 (1)&#xD;
with Asp64 of bond length (3.34 Å) and hydrophobic bonds were found between&#xD;
Leu63 with C15 and C12, Val65 with C7, Val65 with C12 and C4, Ile95 with C6 and&#xD;
C7, Ile95 with C10, C12 and C14. Important pi-pi bonds were found between Phe41&#xD;
with C2, C5, C7, C12, C4, C6, C8, C9, C13 and Phe97 with C9. These interactions indicated stability of tryptanthrin&#xD;
in active residue and suggested it as a potential drug candidate. Thus,&#xD;
good affinity of tryptanthrin to binding site of InhA may lead to synthesis of&#xD;
anti-tubercular drug capable of combating MDR strains of&lt;i&gt; M. tuberculosis&lt;/i&gt;.
&lt;br/&gt;
&lt;br/&gt;Page(s): 435-441</description>
      <pubDate>Wed, 28 Nov 2012 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>&lt;span style="font-size:11.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-bidi-font-family: Mangal;mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language: HI" lang="EN-GB"&gt;Nanoactivator mediated modifications in thermostable amylase from&lt;i style="mso-bidi-font-style:normal"&gt; Bacillus licheniformis&lt;/i&gt;&lt;/span&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/15242</link>
      <description>Title: &lt;span style="font-size:11.0pt;font-family: "Times New Roman";mso-fareast-font-family:"Times New Roman";mso-bidi-font-family: Mangal;mso-ansi-language:EN-GB;mso-fareast-language:EN-US;mso-bidi-language: HI" lang="EN-GB"&gt;Nanoactivator mediated modifications in thermostable amylase from&lt;i style="mso-bidi-font-style:normal"&gt; Bacillus licheniformis&lt;/i&gt;&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Khairnar, Rajendra S; Mahabole, Megha P; Pathak, Anupama P
&lt;br/&gt;
&lt;br/&gt;Abstract: Gram-positive rod-shaped thermophilic bacteria were isolated using&#xD;
samples collected from terrestrial natural thermal spring located at Unkeshwar &lt;span style="mso-bidi-font-style:italic"&gt;(Longitude 78.22 degree East to 78.34 degree&#xD;
East, Latitude 19 degree 34' North to 19 degree 40' North)&lt;i&gt;, &lt;/i&gt;District&#xD;
Nanded, Maharashtra State, India. The isolates were &#xD;
then cultivated using selective media and identified using &#xD;
culture-dependent techniques. One prominent isolate (UN1) exhibited high&#xD;
temperature stability and remarkable amylase production and was identified as &lt;i style="mso-bidi-font-style:normal"&gt;Bacillus licheniformis&lt;/i&gt;. Amylase&#xD;
production was carried out in starch media and the enzyme was partially&#xD;
purified and characterized for optimization of pH and temperature. Amylolytic&#xD;
activity of the enzyme was determined. Nanoactivator-mediated modifications&#xD;
were carried out to enhance amylolytic activity of the partially purified&#xD;
amylase. Three-fold increase in catalytic efficiency of amylase was obtained&#xD;
after modification.&#xD;
&#xD;
&lt;/span&gt;
&lt;br/&gt;
&lt;br/&gt;Page(s): 468-471</description>
      <pubDate>Wed, 28 Nov 2012 22:58:59 GMT</pubDate>
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