Alzheimer’s Breakthrough – New Therapeutic Target Discovered

Neuron Brain Neuroscience Concept

Scientists discovered that restoring KCC2, a neuron-regulating mechanism reduced in Alzheimer’s disease, can potentially reverse some of the disease’s cognitive manifestations in mice. The molecule used for this, CLP290, showed positive results in mice but isn’t suitable for human use, prompting the search for other KCC2-activating molecules.

Researchers from Laval University and the University of Lethbridge have successfully reversed certain cognitive manifestations linked to Alzheimer’s disease in an animal model. Their findings were recently published in the journal Brain.

Previous studies have shown that even before Alzheimer’s symptoms appear, brain activity is disrupted in people who go on to develop the disease. “There is neuronal hyperactivity and signal disorganization in the brain. Our hypothesis is that a mechanism that regulates neuronal activity, more specifically the one responsible for inhibiting neuronal signals, is disrupted,” explains the researcher.

“A loss of KCC2 in the cell membrane can lead to neuronal hyperactivity. One study has already shown that KCC2 levels were reduced in the brains of deceased Alzheimer’s patients. This gave us the idea of examining the role of KCC2 in an animal model of Alzheimer’s disease,” adds the researcher.

Promising Results in Mice

To do this, scientists used mouse lines expressing a manifestation of Alzheimer’s disease. The researchers found that when these mice reached the age of four months, KCC2 levels decreased in two regions of their brains: the hippocampus and the prefrontal cortex. These two regions are also affected in people suffering from Alzheimer’s disease.

In light of these results, the researchers turned to a molecule developed in their laboratory, CLP290, a KCC2 activator that prevents its depletion. In the short term, the administration of this molecule to mice that already had reduced KCC2 levels improved their spatial memory and social behavior. In the long term, CLP290 protected them against cognitive decline and neuronal hyperactivity.

“Our results do not imply that the loss of KCC2 causes Alzheimer’s disease,” insists Prof. De Koninck. “On the other hand, it does appear to cause an ionic imbalance leading to neuronal hyperactivity that can lead to neuronal death. This suggests that by preventing the loss of KCC2, we could slow down and perhaps even reverse certain manifestations of the disease.”

For various reasons, CLP290 cannot be used in humans. Professor De Koninck’s team is searching for other KCC2-activating molecules that would be well tolerated by Alzheimer’s sufferers.

“We have developed new molecules which are currently being evaluated in our laboratory. In parallel with this research, we are testing drugs that are used for purposes other than Alzheimer’s in humans, in order to assess their effects on KCC2. Repositioning an existing drug would accelerate work on this new therapeutic avenue,” emphasizes the researcher.

Reference: “Restoring neuronal chloride extrusion reverses cognitive decline linked to Alzheimer’s disease mutations” by Iason Keramidis, Brendan B McAllister, Julien Bourbonnais, Feng Wang, Dominique Isabel, Edris Rezaei, Romain Sansonetti, Phil Degagne, Justin P Hamel, Mojtaba Nazari, Samsoon Inayat, Jordan C Dudley, Annie Barbeau, Lionel Froux, Antoine G Godin, Majid H Mohajerani and Yves De Koninck, 8 August 2023, Brain.
DOI: 10.1093/brain/awad250

The other signatories of the study published in Brain are Iason Keramidis, Julien Bourbonnais, Feng Wang, Dominique Isabel, Marie-Eve Paquet, Romain Sansonetti, Annie Barbeau, Lionel Froux and Antoine Godin, from Laval University, and Brendan McAllister, Edris Rezaei, Phil Degagne, Mojtaba Nazari, Samsoon Inayat, and Majid Mohajerani, from the University of Lethbridge.