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<dc:title>role of pentazocine in an in vitro model of hypoxia/reoxygenation</dc:title>
<dc:creator>HEISS, KATHRIN</dc:creator>
<dc:contributor>Heiss, Kathrin</dc:contributor>
<dc:contributor>LI VOLTI, Giovanni</dc:contributor>
<dc:contributor>SALOMONE, Salvatore</dc:contributor>
<dc:subject>microglia pentazocina hypoxia</dc:subject>
<dc:description>Experimental research is making considerable efforts to understand the rules that regulate &#xd;
the balance between toxic and protective brain innate immunity. Sigma-1 receptor is &#xd;
expressed in both neurons and glia is a unique class of intracellular proteins and is &#xd;
involved in neurodegeneration. Our aim was to evaluate the biological effects of sigma-1 selective ligands, and bifunctional sigma-1 selective ligands conjugated with lipoil &#xd;
function in microglia following hypoxia/reoxygenation condition. BV2 cells were exposed &#xd;
to 3 hours of hypoxia and 24h of reoxygenation. Cells were treated with sigma-1 agonist &#xd;
(+)-Pentazocine, various bifunctional sigma-1 agonists conjugated with lipoil function and &#xd;
with lipoic acid alone. We assessed cell viability, apoptosis, reactive oxygen species (ROS) &#xd;
formation, mitochondria membrane potential, and total thiol groups content (GSH). Our &#xd;
results showed that 24h of reoxygenation resulted in a significant decrease of cell viability &#xd;
and increase in apoptosis when compared to control. No significant effect of (+)Pentazocine and tested compounds was observed on cell viability following 24h of &#xd;
reoxygenation. Furthermore, all treatments resulted in a significant decrease of ROS &#xd;
formation when compared to untreated cells. Finally, pharmacological treatments restored &#xd;
mitochondrial membrane potential when compared to the untreated group. Consistently &#xd;
with these results we also showed that GSH content was restored following &#xd;
pharmacological treatments. Our results showed that newly synthetized bifunctional &#xd;
sigma-1 compounds exhibited significant antioxidant activity and induce apoptosis in &#xd;
activated microglia thus providing a new tool for effective manipulation of brain &#xd;
inflammation, with the specific aim of favoring its protective arm and boosting innate &#xd;
neuroprotective mechanisms &#xd;
 &#xd;
 &#xd;
	6	&#xd;
 &#xd;
GENERAL INTRODUCTION MICROGLIA  &#xd;
The concept of microglia was introduced by Pio del Rio-Hortega as a defined cellular &#xd;
element</dc:description>
<dc:date>2017-01-25</dc:date>
<dc:type>info:eu-repo/semantics/doctoralThesis</dc:type>
<dc:identifier>https://hdl.handle.net/20.500.11769/582738</dc:identifier>
<dc:language>eng</dc:language>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>Università degli studi di Catania</dc:publisher>
<dc:publisher>place:Catania</dc:publisher>
<dc:rights>license:PUBBLICO - Pubblico con Copyright</dc:rights>
<dc:rights>license uri:iris.PUB02</dc:rights>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>