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<title>DFIFA. Ponencias / Actas del Departamento de Fisiología y Farmacología</title>
<link>http://hdl.handle.net/10366/3998</link>
<description/>
<pubDate>Thu, 23 Apr 2026 17:32:27 GMT</pubDate>
<dc:date>2026-04-23T17:32:27Z</dc:date>
<item>
<title>In situ detection and measurement of intracellular ROS and nitric oxide generation in isolated mature skeletal muscle fibres by real-time fluorescence microscopy</title>
<link>http://hdl.handle.net/10366/154099</link>
<description>[EN] Reactive oxygen species (ROS) produced by skeletal muscle stimulate adaptive responses to activity and mediate some degenerative processes. ROS activity is usually studied by measuring indirect end-points of their&#13;
reactions with various biomolecules. In order to develop a method to measure the intracellular ROS generation in real-time in mature skeletal muscle fibers, these were isolated from the flexor digitorum brevis (FDB)&#13;
muscle of mice and cultured on collagen-coated plates. Fibers were loaded with 5- (and 6-) chloromethyl-2,7-&#13;
dichlorodihydrofluorescein diacetate (CM-DCFH DA) and measurements of 5- (and 6-) chloromethyl-2,7-&#13;
dichlorofluorescin (CM-DCF) fluorescence from individual fibers obtained by microscopy over 45 min. The&#13;
sensitivity of this approach was demonstrated by addition of 1 M H2O2 to the extracellular medium. Contractions of isolated fibers induced by field electrical stimulation caused a significant increase in CM-DCF&#13;
fluorescence that was abolished by pre-treatment of fibers with glutathione ethyl ester. Thus, CM-DCF fluorescence microscopy can detect physiologically relevant changes in intracellular ROS activity in single isolated mature skeletal muscle fibers in real-time, and contractions generated a net increase that was abolished&#13;
when the intracellular glutathione content was enhanced. This technique has advantages over previous approaches because of the maturity of the fibers and the analysis of single cells, which prevent contributions&#13;
from nonmuscle cells.
</description>
<pubDate>Sun, 01 Jan 2006 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10366/154099</guid>
<dc:date>2006-01-01T00:00:00Z</dc:date>
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<item>
<title>Biosensor HyPer2 to monitor intracellular hydrogen peroxide induced by insulin and interleukin 1 beta stimulation in isolated skeletal muscle fibres</title>
<link>http://hdl.handle.net/10366/154082</link>
<pubDate>Tue, 01 Jan 2019 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10366/154082</guid>
<dc:date>2019-01-01T00:00:00Z</dc:date>
</item>
<item>
<title>The long-term control of nitric oxide on aortic structure and  function in uninephrectomized spontaneously hypertensive rats</title>
<link>http://hdl.handle.net/10366/19325</link>
<description>Higher blood pressure and organ damage were always observed in chronic hypertension. Here, we have investigated in female uninephrectomized spontaneously hypertensive rats (UNX-SHRs) the role of NO on changes in blood pressure, renal function, thoracic aortic relaxations and structure.
</description>
<pubDate>Wed, 01 Jan 2003 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/10366/19325</guid>
<dc:date>2003-01-01T00:00:00Z</dc:date>
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