The hippocampus, an area of the brain commonly linked with memory and dementia, may also yield important clues about a range of mental health illnesses including addiction, anxiety and depression, new University of Toronto research suggests.
The finding that calls into question our understanding of how exactly this part of the brain works.
“What this shows is that we may need to rethink how the hippocampus processes information,"
Rutsuko Ito, an associate professor in the Department of Psychology, said.
Memory Processing And Spatial Cognition
The hippocampus is a seahorse-shaped structure located deep inside the brain. As part of the limbic system, it plays an important role in memory processing and spatial cognition, including how mammals learn to understand and navigate their environment.
Researchers have long looked at the hippocampus for its role in memory and dementia, especially in relation to Alzheimer’s disease. In Alzheimer’s patients for instance, this region is one of the first areas of the brain to suffer damage.
But there’s been a few studies that suggest the anterior hippocampus, a sub-region located at the front, could play a role in emotional regulation, including anxiety.
For this study, Ito and her team looked at the ventral hippocampus in rats, a sub-region that correlates to the anterior hippocampus in humans. They wanted to see what role two further subareas of the ventral hippocampus - called the CA1 and CA3 - play in terms of approach-avoidance conflict processing.
Approach Or Avoid
Approach-avoidance conflict is a model used in psychology to test how animals deal with regulating fear and anxiety. It basically offers a situation that involves a decision about whether to pursue or avoid something that could have both positive and negative aspects to it.
“One good example is imagine going to a restaurant you love, but the moment you walk in you see someone you can’t stand - do you go in, or avoid going in?"
said Associate Professor Andy Lee, who collaborated on the research.
What they found is that after temporarily inactivating the CA1, it increased avoidance of the conflict. Meanwhile, inactivating the CA3 increased approach behaviour to the conflict.
Ito says this finding is important because the conventional thinking is that these areas, along with another part called the dentate gyrus, form a circuit through which information flow occurs in one direction. Information processed by the dentate gyrus gets passed along to the CA3, and then on to CA1. In other words, the CA1 and CA3 should carry out the same function because they’re both part of the same information processing circuit.
“But that’s not the case, the CA1 and CA3 in the ventral hippocampus seem to do very opposite things in relation to conflict processing. It’s this strange bi-directional or oppositional effect, and that goes against traditional thinking of how information processing takes place in this part of the brain,"
Because of its possible role in basic motivational behaviour, it may also offer important insights into a range of mental illnesses.
Addiction, for example, could be linked to deficits of approach motivation. Anxiety and depression on the other hand could be linked to avoidance behaviours, all of which could manifest itself in this part of the brain.
Ito says the next step is to explore which connections to the CA1, CA3, or other parts of the brain could be responsible for this effect.
Meanwhile, Lee is investigating the role sub-regions of the hippocampus play in conflict processing in humans.
“Some patients have lesions to certain areas of this part of the brain, so hopefully we can assess them to see what particular aspects of approach avoidance behaviour may or may not be impacted,"
The work received funding from the Natural Sciences and Engineering Research Council of Canada, and the Canada Institutes for Health Research.
Anett Schumacher, Franz R. Villaruel, Alicia Ussling, Sadia Riaz, Andy C.H. Lee4, Rutsuko Ito Ventral Hippocampal CA1 and CA3 Differentially Mediate Learned Approach-Avoidance Conflict Processing Current Biology (2018). DOI: 10.1016/j.cub.2018.03.012