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Home NEWS Science News Biology

New theory may explain cause of depression and improve treatments

Bioengineer by Bioengineer
August 9, 2018
in Biology
Reading Time: 3 mins read
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A new area in depression research suggests dysfunction in mitochondria — the main source of energy for cells — could lead to major depression. Published in Frontiers in Neuroscience, this new insight to long-held theories on the causes of depression could lead to the development of novel and more effective antidepressant drugs.

Depression is a highly prevalent disorder affecting up to 20% of the population. It is commonly thought to be caused by a chemical imbalance in the brain, yet the specific biological mechanisms which lead to depression are not fully understood.

"Until now, most theories about the biological causes of depression have focused on the idea that depression is caused by an imbalance in neurotransmitters like serotonin," says Dr Lisa E. Kalynchuk, co-author of the review from the University of Victoria, Canada.

"However, antidepressants can increase serotonin levels almost immediately, yet take weeks to have a therapeutic effect on the symptoms of depression. This suggests serotonin is unlikely to be the root cause of depression."

Most antidepressant drugs used today are the same as those developed more than 50 years ago. In addition to the delayed onset of effective symptom relief, antidepressants only work in around half of patients — and often have adverse side effects.

The team recognized the necessity for new and more effective treatments for depression. However, before new drugs can be developed, it is necessary to first understand the cellular causes of depression.

"Despite extensive research efforts, there is still a fundamental lack of understanding about the specific biological changes that give rise to depressive symptoms," explains Kalynchuk.

To better understand how depression arises, the researchers looked for specific causes within the brain cells. This led them to a small organelle found within brain cells called mitochondria. Mitochondria are the main source of energy for cells, but they also help to regulate brain function.

"Animal models showed that depression is associated with the decreased generation of new cells in the hippocampus — a region of the adult brain known to regulate emotion, mood, cognition and stress," says Kalynchuk.

"As these are all implicated in depression, this originally led us to think that depression was caused by the deficiency in new cell generation. However, this theory does not explain all the research findings because depressive symptoms can occur in the absence of this deficiency.

"What we do know that this process is metabolically demanding and requires a lot of energy. This led us to suspect mitochondria as the root cause of depression, as they provide energy for cells."

The researchers believe the dysfunction of mitochondria can lead to a cascade of effects which result in depression. This idea offers new opportunity for the development of new antidepressant drugs which can normalize mitochondria function.

"This would be a completely novel approach that has little to do with what current anti-depressants are doing," says Kalynchuk. "It will take time to fully explore these ideas, but we hope it will open doors to new areas of research in the depression field and lead to the development of more effective antidepressant medication."

###

The research is part of a special article collection on mitochondrial dysfunction and neurodegeneration.

Please include a link to the original research article in your reporting: https://www.frontiersin.org/articles/10.3389/fnins.2018.00386/full

Frontiers is an award-winning Open Science platform and leading open-access scholarly publisher. Our mission is to make high-quality, peer-reviewed research articles rapidly and freely available to everybody in the world, thereby accelerating scientific and technological innovation, societal progress and economic growth. For more information, visit http://www.frontiersin.org and follow @Frontiersin on Twitter.

Media Contact

Emma Duncan
[email protected]
@frontiersin

http://www.frontiersin.org

http://dx.doi.org/10.3389/fnins.2018.00386

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