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<title>Faculty</title>
<link>http://dyuthi.cusat.ac.in:80/xmlui/handle/purl/427</link>
<description/>
<pubDate>Thu, 23 May 2013 20:05:28 GMT</pubDate>
<dc:date>2013-05-23T20:05:28Z</dc:date>
<item>
<title>Decreased GABAA Receptors Functional Regulation 3 in the Cerebral Cortex and Brainstem of Hypoxic Neonatal Rats: 4 Effect of Glucose and Oxygen Supplementation</title>
<link>http://dyuthi.cusat.ac.in:80/xmlui/handle/purl/1622</link>
<description>Decreased GABAA Receptors Functional Regulation 3 in the Cerebral Cortex and Brainstem of Hypoxic Neonatal Rats: 4 Effect of Glucose and Oxygen Supplementation
Paulose, C S; Peeyush, K T; Anju, T R
Hypoxia in neonates can lead to biochemical&#13;
 and molecular alterations mediated through changes in&#13;
 neurotransmitters resulting in permanent damage to brain.&#13;
 In this study, we evaluated the changes in the receptor&#13;
 status of GABAA in the cerebral cortex and brainstem of&#13;
 hypoxic neonatal rats and hypoxic rats supplemented with&#13;
 glucose and oxygen using binding assays and gene&#13;
 expression of GABAAa1 and GABAAc5. In the cerebral&#13;
 cortex and brainstem of hypoxic neonatal rats, a significant&#13;
 decrease in GABAA receptors was observed, which&#13;
 accounts for the respiratory inhibition. Hypoxic rats sup-&#13;
 plemented with glucose alone and with glucose and oxygen&#13;
 showed, respectively, a reversal of the GABAA receptors,&#13;
andGABAAa1 and GABAAc5 gene expression to control.&#13;
Glucose acts as an immediate energy source thereby&#13;
 reducing the ATP-depletion-induced increase in GABA&#13;
 and oxygenation, which helps in encountering anoxia.&#13;
 Resuscitation with oxygen alone was less effective in&#13;
 reversing the receptor alterations. Thus, the results of this&#13;
 study suggest that reduction in the GABAA receptors&#13;
 functional regulation during hypoxia plays an important&#13;
 role in mediating the brain damage. Glucose alone and&#13;
 glucose and oxygen supplementation to hypoxic neonatal&#13;
 rats helps in protecting the brain from severe hypoxic&#13;
damage.
</description>
<pubDate>Thu, 01 Jan 2009 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://dyuthi.cusat.ac.in:80/xmlui/handle/purl/1622</guid>
<dc:date>2009-01-01T00:00:00Z</dc:date>
</item>
<item>
<title>Down-regulation of cerebellar 5-HT2C receptors in pilocarpine-induced epilepsy in rats: Therapeutic role of Bacopa monnieri extract</title>
<link>http://dyuthi.cusat.ac.in:80/xmlui/handle/purl/1621</link>
<description>Down-regulation of cerebellar 5-HT2C receptors in pilocarpine-induced epilepsy in rats: Therapeutic role of Bacopa monnieri extract
Paulose,C S; Amee,Krishnakumar; Pretty Mary,Abraham; Jes,Paul
Epilepsy is a syndrome of episodic brain dysfunction characterized by recurrent unpredictable, spontaneous&#13;
seizures. Cerebellar dysfunction is a recognized complication of temporal lobe epilepsy and it is associated&#13;
with seizure generation, motor deficits and memory impairment. Serotonin is known to exert a modulatory&#13;
action on cerebellar function through 5HT2C receptors. 5-HT2C receptors are novel targets for developing anticonvulsant&#13;
drugs. In the present study, we investigated the changes in the 5-HT2C receptors binding and gene&#13;
expression in the cerebellum of control, epileptic and Bacopa monnieri treated epileptic rats. There was a&#13;
significant down regulation of the 5-HT content (pb0.001), 5-HT2C gene expression (pb0.001) and 5-HT2C&#13;
receptor binding (pb0.001) with an increased affinity (pb0.001). Carbamazepine and B. monnieri treatments&#13;
to epileptic rats reversed the down regulated 5-HT content (pb0.01), 5-HT2C receptor binding (pb0.001) and&#13;
gene expression (pb0.01) to near control level. Also, the Rotarod test confirms the motor dysfunction and&#13;
recovery by B. monnieri treatment. These data suggest the neuroprotective role of B. monnieri through the&#13;
upregulation of 5-HT2C receptor in epileptic rats. This has clinical significance in the management of epilepsy
</description>
<pubDate>Thu, 01 Jan 2009 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://dyuthi.cusat.ac.in:80/xmlui/handle/purl/1621</guid>
<dc:date>2009-01-01T00:00:00Z</dc:date>
</item>
<item>
<title>Superoxide dismutase functional regulation in neonatal hypoxia</title>
<link>http://dyuthi.cusat.ac.in:80/xmlui/handle/purl/1620</link>
<description>Superoxide dismutase functional regulation in neonatal hypoxia
Paulose, C S; Athira, Babu; Anju, T R
Hypoxia is one of the major causes of damage to the fetal and neonatal brain and cardiac functions. in earlier studies we have reported the brain damage caused by hypoxia and resusciation with oxygen and epinephrine and have found that glucose treatment to hypoxic rats and hypoxic rats treated with oxygen shows a reversal of brain damage. during this study the findings may have clinical significance in the proper management of heart and brain functions.
</description>
<pubDate>Wed, 01 Apr 2009 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://dyuthi.cusat.ac.in:80/xmlui/handle/purl/1620</guid>
<dc:date>2009-04-01T00:00:00Z</dc:date>
</item>
<item>
<title>Enhanced dopamine D2 receptor function in hypothalamus and corpus striatum: their role in liver, plasma and in vitro hepatocyte ALDH regulation in ethahol treated rats</title>
<link>http://dyuthi.cusat.ac.in:80/xmlui/handle/purl/1619</link>
<description>Enhanced dopamine D2 receptor function in hypothalamus and corpus striatum: their role in liver, plasma and in vitro hepatocyte ALDH regulation in ethahol treated rats
Paulose, C S; Akash, K George; Anju, T R; Peeyush, K T
Dopamine D2 receptors are involved in ethanol&#13;
self- administration behavior and also suggested to mediate&#13;
the onset and offset of ethanol drinking. In the present&#13;
study, we investigated dopamine (DA) content and Dopamine&#13;
D2 (DA D2) receptors in the hypothalamus and corpus&#13;
striatum of ethanol treated rats and aldehyde dehydrogenase&#13;
(ALDH) activity in the liver and plasma of ethanol&#13;
treated rats and in vitro hepatocyte cultures. Hypothalamic&#13;
and corpus striatal DA content decreased significantly&#13;
(P\0.05, P\0.001 respectively) and homovanillic acid/&#13;
dopamine (HVA/DA) ratio increased significantly&#13;
(P\0.001) in ethanol treated rats when compared to&#13;
control. Scatchard analysis of [3H] YM-09151-2 binding to&#13;
DA D2 receptors in hypothalamus showed a significant&#13;
increase (P\0.001) in Bmax without any change in Kd in&#13;
ethanol treated rats compared to control. The Kd of DA D2&#13;
receptors significantly decreased (P\0.05) in the corpus&#13;
striatum of ethanol treated rats when compared to control.&#13;
DA D2 receptor affinity in the hypothalamus and corpus&#13;
striatum of control and ethanol treated rats fitted to a single&#13;
site model with unity as Hill slope value. The in vitro&#13;
studies on hepatocyte cultures showed that 10-5 M and&#13;
10-7 M DA can reverse the increased ALDH activity in&#13;
10% ethanol treated cells to near control level. Sulpiride,&#13;
an antagonist of DA D2, reversed the effect of dopamine on&#13;
10% ethanol induced ALDH activity in hepatocytes. Our&#13;
results showed a decreased dopamine concentration with&#13;
enhanced DA D2 receptors in the hypothalamus and corpus&#13;
striatum of ethanol treated rats. Also, increased ALDH was observed in the plasma and liver of ethanol treated rats and&#13;
in vitro hepatocyte cultures with 10% ethanol as a compensatory&#13;
mechanism for increased aldehyde production&#13;
due to increased dopamine metabolism. A decrease in&#13;
dopamine concentration in major brain regions is coupled&#13;
with an increase in ALDH activity in liver and plasma,&#13;
which contributes to the tendency for alcoholism. Since the&#13;
administration of 10-5 M and 10-7 M DA can reverse the&#13;
increased ALDH activity in ethanol treated cells to near&#13;
control level, this has therapeutic application to correct&#13;
ethanol addicts from addiction due to allergic reaction&#13;
observed in aldehyde accumulation.
</description>
<pubDate>Sat, 07 Jun 2008 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://dyuthi.cusat.ac.in:80/xmlui/handle/purl/1619</guid>
<dc:date>2008-06-07T00:00:00Z</dc:date>
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