
2009/07/22
Researchers from CIC bioGUNE find a way to treat ischemic pathologies
A team of researchers from CIC bioGUNE, led by Dr Edurne Berra from the Cellular Biology and Stem Cell Unit, alongside a team from Paris' Cardiovascular Research Centre (INSERM U970), led by Dr Jean Sebastién Silvestre, have developed a new area of research which looks extremely promising as regards the development of new therapeutic responses to ischemic pathologies and cardiovascular diseases in general.
The results of this research project, which was initiated in 2005 and is supported by Bizkaia:Xede and the Basque Government's Etortek programme, were published in the prestigious scientific journal Circulation on 7th of July.
By activating a protein called HIF, the strategy is to stimulate revascularisation and the repair of the damaged organ following ischemia caused by the obstruction of a blood vessel preventing normal blood flow. These obstructions occur, for example, in the event of thrombosis in a limb, myocardial infarction or a stroke. It is important to highlight the fact that cardiovascular diseases are the principal cause of death throughout the world (in the European Union, they account for 40% of all deaths, a figure equivalent to 2 million deaths per year).
In general, cells tend to respond to the lack of oxygen caused by poor blood flow by activating HIF. However, in the case of an ischemic pathology, HIF is not sufficiently activated. "We decided to over-produce HIF following ischemia as an attractive therapeutic alternative. For our research purposes, we used an ischemic model provoked in a mouse leg through ligation of the femoral artery. In other words, we closed off the femoral artery and stopped the blood flow to the limb. When this happens, the leg develops necrosis and after a time, the mouse dies," stated Dr Berra. The aim was to artificially help stimulate the production of HIF after the femoral artery had been closed off. "And what we saw was that when we did this, the mouse's leg revascularised and no longer entered into a degenerative process," added Dr Berra. How is this high level of HIF production achieved? HIF is a protein which, when not required, degrades constitutively and this degradation is regulated by enzymes called PHDs.
"These enzymes hydroxylate HIF and, as a result of this hydroxylation, the protein degrades. Therefore, when these enzymes are inhibited, HIF cannot degrade and so accumulates. To inhibit PHDs, we use siRNAs," concluded Dr Berra.
See a large version of the first picture

See a large version of the second picture