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INTRODUCCIÓN: REVISIÓN CRITICA DEL PROBLEMA

INTRODUCCIÓN: REVISIÓN CRITICA DEL PROBLEMA

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CAPÍTULO IX<br />

e) Effects of NOS activity on ROS production induced by gHSA.<br />

As we have commented above, eNOS can be a source of superoxide anion when<br />

it is uncoupled 7 . Therefore, eNOS down-regulation by SP600125 would decrease<br />

ROS production if eNOS was uncoupled. On the contrary, down-regulation of<br />

wellfunctioning eNOS will cause an increase in superoxide anion biodisponibility<br />

(enhanced ROS production).<br />

In order to determine the possible eNOS uncoupling in HUVEC, we measured the<br />

extracelular ROS production after treatment with HSA or gHSA (25 μg/mL) during<br />

4 hours in the presence of the eNOS inhibitor L-NAME (100 μM). L-NAME<br />

(100μM), in the presence of HSA (25 μg/mL), induced a significant increment in<br />

ROS production (enhanced cytochrome c reduction), similar to that observed with<br />

gHSA (25 μg/mL) alone (1.06 ± 0.02 for HSA+L-NAME, p0.05, n > 7; Figure 5).<br />

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