A characteristic of depression is a lack of motivation. Cold Spring Harbor Laboratory (CSHL) Professor Bo Li, in collaboration with CSHL Adjunct Professor Z. Josh Huang, discovered a group of neurons in the mouse brain that influences the animal’s motivation to perform tasks for rewards.
Dialling up the activity of these neurons makes a mouse work faster or more vigorously—up to a point. These neurons have a feature that prevents the mouse from becoming addicted to the reward. The findings may point to new therapeutic strategies for treating mental illnesses like depression that affect motivation in humans.
The anterior insular cortex is a region of the brain that plays a critical role in motivation. A set of neurons that activate a gene called Fezf2(Fezf2 neurons) in this area are active when mice are doing both physical and cognitive tasks. Li and his lab hypothesised that these neurons do not affect the mouse’s ability to do the task; rather, the brain cells influence the mouse’s motivational drive.
Mice were trained to lick a water bottle spout to receive a small sugar reward. When researchers dialled up the activity of these Fezf2 neurons, mice would lick more vigorously. If the neuron activity was dialled down, the mice would lick more slowly. The researchers saw a similar result in another experiment in which the mice ran on a wheel to receive a reward. The mice ran faster if the Fezf2 neurons were stimulated. The same effect occurred with other tasks.
Li and his team were surprised to discover a feature that prevents the mice from becoming addicted to the tasks and their rewards. When mice drank their fill of sugar water and were satiated, they would not lick or run faster to get more sugar, even if the researchers dialled up the activity of the Fezf2 neurons.
Finding a way to fine-tune the human equivalent of these neurons might help people struggling with motivation due to mental illnesses like depression. Li says: ‘We want to selectively increase the motivation of the person so that they can do the things that they need to do, but we don’t want to create addictive drugs.’ Findings were published in the journal Cell.