Study identifies potential new approach for treating diabetes complications

A potential new treatment approach for complications relating to diabetes has been described today in the open-access eLife journal.

Diabetes is a serious condition that causes the blood sugar level to become too high. In patients with diabetes, the overproduction of cellular reactive oxygen species (ROS) – highly reactive chemicals formed from oxygen – can lead to severe tissue damage. The new study suggests that the repression of a protein complex called hypoxia-inducible factor-1 (HIF-1) contributes to this overproduction of ROS, and is therefore an attractive therapeutic target.

“Hypoxia, a condition where oxygen levels drop in our tissues, has also recently been identified as a harmful player in diabetes,” explains Xiao-Wei Zheng, Senior Lab Manager at Karolinska Institutet, Stockholm, Sweden, and a co-first author of the study alongside Sampath Narayanan and Cheng Xu, also from Karolinska Institutet. “In our study, we wanted to find out if the overproduction of cellular ROS in diabetes is caused by impaired responses to hypoxia due to the inhibition of HIF-1 by high blood sugar levels.”

To answer this question, Zheng, Narayanan, Xu and colleagues recruited 13 non-smoking volunteers with type 1 diabetes and 11 healthy volunteers. They exposed the participants to mild and intermittent hypoxia five times in total for one hour. They took blood samples from the participants before and immediately after exposure to hypoxia, and analysed the changes in their ROS levels. The results showed that hypoxia led to increased ROS levels in the volunteers with diabetes, while those without the condition were unaffected.

As hypoxia increases cellular ROS levels in diabetes, and HIF-1 helps cells to respond to hypoxia, the team hypothesised that repressing HIF-1 would contribute to the overproduction of ROS. To test this, they analysed the relation between HIF-1, glucose levels, and ROS production and its functional consequences, in cells taken from mouse kidneys and directly in the kidneys of mouse models of diabetes. They found that high glucose levels repressed HIF-1 both in hypoxic cells and in the mouse kidneys through a mechanism that relied on enzymes called HIF prolyl-hydroxylases (PHDs). This repression of HIF-1 contributed in turn to the excess production of ROS.

Finally, the team demonstrated that restoring HIF-1 function in the mice reduced the overproduction of ROS in their tissue cells and protected the animals’ kidneys against cell death and injury.

“We’ve shown that the repression of HIF-1 plays a central role in ROS overproduction and tissue damage in diabetes, and is therefore a potential treatment target for these complications,” concludes Sergiu Catrina, Lecturer/Senior Physician at Karolinska Institutet, and a co-senior author of the study alongside Fredrik Palm, from Uppsala University, Sweden. “These results are timely, since the first PHD inhibitor that can activate HIF-1 has recently been approved for clinical use in patients with chronic kidney diseases. If our findings are verified by future studies, then similar inhibitors could be tested as potential new therapies for diabetes.”

##

Media contacts

Emily Packer, Media Relations Manager

eLife

e.packer@elifesciences.org

+44 (0)1223 855373

Press Office

Karolinska Institutet

pressinfo@ki.se

+46 (0)8 524 860 77

About eLife

eLife is a non-profit organisation created by funders and led by researchers. Our mission is to accelerate discovery by operating a platform for research communication that encourages and recognises the most responsible behaviours. We review selected preprints in all areas of biology and medicine, including Cell Biology and Medicine, while exploring creative new ways to improve how research is assessed and published. eLife receives financial support and strategic guidance from the Howard Hughes Medical Institute, the Knut and Alice Wallenberg Foundation, the Max Planck Society and Wellcome. Learn more at https://elifesciences.org/about.

To read the latest Cell Biology research published in eLife, visit https://elifesciences.org/subjects/cell-biology.

And for the latest in Medicine, see https://elifesciences.org/subjects/medicine.