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<title>DFIFA. Ponencias / Actas del Departamento de Fisiología y Farmacología</title>
<link href="http://hdl.handle.net/10366/3998" rel="alternate"/>
<subtitle/>
<id>http://hdl.handle.net/10366/3998</id>
<updated>2026-04-24T14:59:49Z</updated>
<dc:date>2026-04-24T14:59:49Z</dc:date>
<entry>
<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 href="http://hdl.handle.net/10366/154099" rel="alternate"/>
<author>
<name>Palomero Labajos, Jesús</name>
</author>
<author>
<name>Pye, Deborah</name>
</author>
<author>
<name>Kabayo, Tabitha</name>
</author>
<author>
<name>Jackson, Malcolm J.</name>
</author>
<id>http://hdl.handle.net/10366/154099</id>
<updated>2025-04-30T19:34:04Z</updated>
<published>2006-01-01T00:00:00Z</published>
<summary type="text">[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.
</summary>
<dc:date>2006-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Biosensor HyPer2 to monitor intracellular hydrogen peroxide induced by insulin and interleukin 1 beta stimulation in isolated skeletal muscle fibres</title>
<link href="http://hdl.handle.net/10366/154082" rel="alternate"/>
<author>
<name>Fernández Puente, Escarlata</name>
</author>
<author>
<name>Llanos, Paola</name>
</author>
<author>
<name>Palomero Labajos, Jesús</name>
</author>
<id>http://hdl.handle.net/10366/154082</id>
<updated>2025-11-03T09:22:41Z</updated>
<published>2019-01-01T00:00:00Z</published>
<dc:date>2019-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>The long-term control of nitric oxide on aortic structure and  function in uninephrectomized spontaneously hypertensive rats</title>
<link href="http://hdl.handle.net/10366/19325" rel="alternate"/>
<author>
<name>López Hernández, Francisco José</name>
</author>
<author>
<name>Carrón de la Calle, Rosalía</name>
</author>
<author>
<name>Montero Gómez, María Josefa</name>
</author>
<author>
<name>Reverte Bernal, María Perpetuo Socorro</name>
</author>
<id>http://hdl.handle.net/10366/19325</id>
<updated>2025-06-05T12:40:28Z</updated>
<published>2003-01-01T00:00:00Z</published>
<summary type="text">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.
</summary>
<dc:date>2003-01-01T00:00:00Z</dc:date>
</entry>
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