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    <title>NISCAIR Online Periodicals Repository Collection: IJBB Vol.48(3) [June 2011]</title>
    <link>http://nopr.niscair.res.in/handle/123456789/11957</link>
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      <title>Growth inhibition of struvite crystals by the aqueous root extract of &lt;i&gt;Rotula aquatica &lt;/i&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/11990</link>
      <description>Title: Growth inhibition of struvite crystals by the aqueous root extract of &lt;i&gt;Rotula aquatica &lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Chauhan, C K; Joshi, M J; Vaidya, A D B
&lt;br/&gt;
&lt;br/&gt;Abstract: Formation of urinary stone is a serious and debilitating problem throughout&#xD;
the world. In the present study, the inhibitory effect of aqueous extract of&#xD;
root of Rotula aquatica was investigated against&#xD;
struvite crystals (one of the components of urinary stone) grown &lt;i&gt;in&#xD;
vitro&lt;/i&gt; using single diffusion gel growth technique. For setting the gel,&#xD;
sodium metasilicate solution (specific gravity 1.05) and 0.5 M aqueous solution&#xD;
of ammonium dihydrogen phosphate were mixed, so that the pH of the mixture&#xD;
could be set at 7.0. Equal amounts of supernatant solution of magnesium acetate&#xD;
(1.0 M) prepared with 0.0%, 0.5% and 1% concentrations of the extract were&#xD;
gently poured on the set gels.&amp;nbsp;It was observed that the number, dimension,&#xD;
total mass, total volume, growth rate and depth of growth of struvite crystals&#xD;
decreased with the increasing extract concentrations in the supernatant&#xD;
solutions. The enhancement of dissolution rate and fragmentation of struvite&#xD;
crystals suggested potential application of the extract&lt;i&gt; &lt;/i&gt;for inhibition&#xD;
of struvite type urinary stone
&lt;br/&gt;
&lt;br/&gt;Page(s): 202-207</description>
      <pubDate>Sun, 29 May 2011 22:58:59 GMT</pubDate>
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    <item>
      <title>Neuroprotective potential of ethanolic extract of&lt;i style=""&gt; Pseudarthria viscida &lt;/i&gt;(L) Wight and Arn&lt;i style=""&gt; &lt;/i&gt;against &lt;img src='/image/spc_char/beta.gif' border=0&gt;-amyloid&lt;sub&gt;(25-35)&lt;/sub&gt;-induced amnesia in mice</title>
      <link>http://nopr.niscair.res.in/handle/123456789/11989</link>
      <description>Title: Neuroprotective potential of ethanolic extract of&lt;i style=""&gt; Pseudarthria viscida &lt;/i&gt;(L) Wight and Arn&lt;i style=""&gt; &lt;/i&gt;against &lt;img src='/image/spc_char/beta.gif' border=0&gt;-amyloid&lt;sub&gt;(25-35)&lt;/sub&gt;-induced amnesia in mice
&lt;br/&gt;
&lt;br/&gt;Authors: Singh, J C Hanish; Alagarsamy, V; Parthiban, P; Selvakumar, P; Reddy, Y Narsimha
&lt;br/&gt;
&lt;br/&gt;Abstract: The neuroprotective potential of&#xD;
ethanolic extract of roots of &lt;i style=""&gt;Pseudarthria&#xD;
viscida&lt;/i&gt; (L) Wight and Arn (EEPV) was investigated against &lt;img src='/image/spc_char/beta.gif' border=0&gt;-amyloid&lt;sub&gt;(25-35)&lt;/sub&gt;-induced&#xD;
amnesia in mice which is a suitable animal model for Alzheimer’s disease (AD). The&#xD;
senile plaques of &#xD;
&lt;img src='/image/spc_char/beta.gif' border=0&gt;-amyloid (A&lt;img src='/image/spc_char/beta.gif' border=0&gt;) are major constituents accumulated during the progression of AD as&#xD;
a potent neurotoxicant. In our investigation, intracerebroventricular injection&#xD;
of A&lt;img src='/image/spc_char/beta.gif' border=0&gt;&lt;sub&gt;(25-35)&lt;/sub&gt; in mice induced the neurodegeneration, exhibited the&#xD;
increased time of escape latency in behavioral pattern using water maze and&#xD;
decreased the levels of antioxidants namley superoxide dismutase (SOD),&#xD;
glutathione peroxidase (GPx), catalase (CAT) and vitamin C with elevated level&#xD;
of acetylcholinesterase enzyme (AChE). The neuroprotective potential of EEPV was&#xD;
determined by behavioral pattern using water maze and biochemical parameters&#xD;
such as SOD, CAT and GPx and vitamin C content as well as AChE. Mice were&#xD;
treated with EEPV at 200 and 400 mg/kg doses for 21 days. Except control, all&#xD;
animals received a single injection of neurotoxicant A&lt;img src='/image/spc_char/beta.gif' border=0&gt;&lt;sub&gt;(25-35) &lt;/sub&gt;on 14&lt;sup&gt;th&lt;/sup&gt;&#xD;
day. In behavioural assessment, treatment with ethanolic extract improved the&#xD;
cognitive function in the water maze and attenuated the elevated levels of AChE&#xD;
with increase in antioxidant enzymes, indicating the neuroprotection with&#xD;
increased levels of vitamin C. These findings suggest that ethanolic extract of&#xD;
&lt;i style=""&gt;P. viscida &lt;/i&gt;exerts anti-amnesiac&#xD;
effects and enhances cognitive function.
&lt;br/&gt;
&lt;br/&gt;Page(s): 197-201</description>
      <pubDate>Sun, 29 May 2011 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>&lt;img src='/image/spc_char/alpha.gif' border=0&gt; -Tocopherol ameliorates cypermethrin-induced toxicity and oxidative stress in the nematode &lt;i&gt;Caenorhabdtis elegans&lt;/i&gt;</title>
      <link>http://nopr.niscair.res.in/handle/123456789/11988</link>
      <description>Title: &lt;img src='/image/spc_char/alpha.gif' border=0&gt; -Tocopherol ameliorates cypermethrin-induced toxicity and oxidative stress in the nematode &lt;i&gt;Caenorhabdtis elegans&lt;/i&gt;
&lt;br/&gt;
&lt;br/&gt;Authors: Shashikumar, Shivaiah; Rajini, P S
&lt;br/&gt;
&lt;br/&gt;Abstract: Oxidative stress and&#xD;
other effects induced by cypermethrin (CYP, 15 mM) and their amelioration by &lt;img src='/image/spc_char/alpha.gif' border=0&gt;-tocopherol &#xD;
(400 &lt;img src='/image/spc_char/micro.gif' border=0&gt;M) was studied in the nematode &lt;i&gt;Caenorhabditis&#xD;
elegans&lt;/i&gt;. The worms exposed for 4 h to CYP showed increased  levels of reactive oxygen species (46%), H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&#xD;
&lt;/sub&gt;(37%) and protein carbonyls (29%), accompanied by decreased lifespan and&#xD;
brood size. However,  exposure to both&#xD;
CYP and a-tocopherol resulted in diminution of&#xD;
above alterations with the worms exhibiting relatively lower levels of ROS&#xD;
(30%), H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; (15%), protein carbonyls (14%), altered&#xD;
antioxidant enzyme activities and normal lifespan and brood size. The results&#xD;
suggest that CYP induces oxidative stress in &lt;i&gt;C. elegans&lt;/i&gt; and the strategy&#xD;
of intervention with &lt;img src='/image/spc_char/alpha.gif' border=0&gt;-tocopherol&#xD;
could be exploited to offset this induced oxidative stress.
&lt;br/&gt;
&lt;br/&gt;Page(s): 191-196</description>
      <pubDate>Sun, 29 May 2011 22:58:59 GMT</pubDate>
    </item>
    <item>
      <title>Lindane-induced biochemical perturbations in rat serum and attenuation by omega-3 and &lt;i&gt;Nigella sativa&lt;/i&gt; seed oil</title>
      <link>http://nopr.niscair.res.in/handle/123456789/11987</link>
      <description>Title: Lindane-induced biochemical perturbations in rat serum and attenuation by omega-3 and &lt;i&gt;Nigella sativa&lt;/i&gt; seed oil
&lt;br/&gt;
&lt;br/&gt;Authors: Attia, Ahmed M; El-Banna, Sabah G; Nomeir, Farid R; El-Basser, Mohammed I Abd
&lt;br/&gt;
&lt;br/&gt;Abstract: Lindane (&lt;img src='/image/spc_char/gamma.gif' border=0&gt;-hexachlorocyclohexane,&#xD;
&lt;img src='/image/spc_char/gamma.gif' border=0&gt;-HCH), a highly persistent&#xD;
organochlorine insecticide is neurotoxic at acute doses and has been reported&#xD;
to induce oxidative stress in cells and tissues. In this study, we investigated&#xD;
the antioxidant property of Nigella sativa seed oil (N.O) and&lt;b&gt; &lt;/b&gt;omega-3&#xD;
polyunsaturated fatty acids (&lt;img src='http://www.niscair.res.in/jinfo/omega.gif' border=0&gt;&lt;sub&gt;3&lt;/sub&gt;) against &lt;img src='/image/spc_char/gamma.gif' border=0&gt;-HCH-induced&#xD;
oxidative hepatic and renal damage in male rats serum. Rats were orally given&#xD;
sublethal dose of &lt;img src='/image/spc_char/gamma.gif' border=0&gt;-HCH (12&#xD;
mg/kg, 24 h prior to decapitation), while N.O (0.3 ml/kg) and &lt;img src='http://www.niscair.res.in/jinfo/omega.gif' border=0&gt;&lt;sub&gt;3&lt;/sub&gt;&#xD;
(20 mg/kg) were given every 48 h for 20 days single or together, or also&#xD;
combined with&#xD;
&lt;img src='/image/spc_char/gamma.gif' border=0&gt;-HCH. &lt;img src='/image/spc_char/gamma.gif' border=0&gt;-HCH&#xD;
caused a significant increase in the levels of serum total lipids, cholesterol, and triglycerides by 49, 61 and 30% respectively,&#xD;
while HDL-cholesterol decreased by 45% compared to control group. Pretreatment&#xD;
with &lt;img src='http://www.niscair.res.in/jinfo/omega.gif' border=0&gt;&lt;sub&gt;3&lt;/sub&gt;&#xD;
and N.O prior &lt;img src='/image/spc_char/gamma.gif' border=0&gt;-HCH&#xD;
administration re-established the altered biochemical features and alleviated&#xD;
the harmful effects of g-HCH on lipid&#xD;
profile. The concentration of serum total protein and albumin was significantly&#xD;
decreased by 35 and 45% respectively in rats treated with &lt;img src='/image/spc_char/gamma.gif' border=0&gt;-HCH compared to control. &lt;img src='/image/spc_char/gamma.gif' border=0&gt;-HCH also&#xD;
caused hepatic and renal damage, as observed from the elevated serum levels of&#xD;
urea, creatinine, total bilirubin and&#xD;
uric acid contents and aminotransferases (AST and ALT), phosphatases&#xD;
(ACP and ALP) and lactate dehydrogenase (LDH) activities.&#xD;
Co-administration of &lt;img src='http://www.niscair.res.in/jinfo/omega.gif' border=0&gt;&lt;sub&gt;3&lt;/sub&gt; and N.O reversed the hazardous effects&#xD;
induced by &lt;img src='/image/spc_char/gamma.gif' border=0&gt;-HCH on the liver&#xD;
and kidney and also protected acetylcholinesterase from the inhibitory action&#xD;
of &lt;img src='/image/spc_char/gamma.gif' border=0&gt;-HCH as well as suppressed the&#xD;
lipid peroxidation. Thus, the results show that &lt;img src='http://www.niscair.res.in/jinfo/omega.gif' border=0&gt;&lt;sub&gt;3&lt;/sub&gt; and N.O might&#xD;
prevent oxidative stress and attenuate the changes in the biochemical&#xD;
parameters induced by &lt;img src='/image/spc_char/gamma.gif' border=0&gt;-HCH in male rats.
&lt;br/&gt;
&lt;br/&gt;Page(s): 184-190</description>
      <pubDate>Sun, 29 May 2011 22:58:59 GMT</pubDate>
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