By manipulating the dopamine receptors of monkeys and studying their behavior, scientists reveal how our brain makes us feel motivated
From:
The National Institutes for Quantum and Radiological Science and
Technology
August 6, 2021 -- Our motivation to put
effort for achieving a goal is controlled by a reward system wired in the
brain. However, many neuropathological conditions impair the reward system,
diminishing the will to work. Recently, scientists in Japan experimentally
manipulated the reward system network of monkeys and studied their behavior. They
deciphered a few critical missing pieces of the reward system puzzle that might
help in increasing motivation.
Why do we do things? What persuades us
to put an effort to achieve goals, however mundane? What, for instance, drives
us to search for food? Neurologically, the answer is hidden in the reward
system of the brain -- an evolutionary mechanism that controls our willingness
to work or to take a risk as the cost of achieving our goals and enjoying the
perceived rewards. In people suffering from depression, schizophrenia, or
Parkinson's disease, often the reward system of the brain is impaired, leading
them to a state of diminished motivation for work or chronic fatigue.
To find a way to overcome the
debilitating behavioral blocks, neuroscientists are investigating the
"anatomy" of the reward system and determining how it evaluates the
cost-benefit trade-off while deciding on whether to pursue a task. Recently,
Dr. Yukiko Hori of National Institutes for Quantum and Radiological Science and
Technology, Japan, along with her colleagues have conducted a study that has
answered some of the most critical questions on benefit- and cost-based
motivation of reward systems. The findings of their study have been published
in PLoS Biology.
Discussing what prompted them to
undertake the study, Dr. Hori explains: "Mental responses such as 'feeling
more costly and being too lazy to act,' are often a problem in patients with
mental disorders such as depression, and the solution lies in the better
understanding of what causes such responses. We wanted to look deeper into the
mechanism of motivational disturbances in the brain."
To do so, Dr. Hori and her team focused
on dopamine (DA), the "neurotransmitter" or the signaling molecule
that plays the central role in inducing motivation and regulation of behavior
based on cost-benefit analysis. The effect of DA in the brain transmits via DA
receptors, or molecular anchors that bind the DA molecules and propagate the
signals through the neuronal network of the brain. However, as these receptors
have distinct roles in DA signal transduction, it was imperative to assess
their relative impacts on DA signaling. Therefore, using macaque monkeys as
models, the researchers aimed to decipher the roles of two classes of DA
receptors -- the D1-like receptor (D1R) and the D2-like receptor (D2R) -- in
developing benefit- and cost-based motivation.
In their study, the researchers first
trained the animals to perform "reward size" tasks and
"work/delay tasks." These tasks allowed them to measure how perceived
reward size and required effort influenced the task-performing behavior. Dr.
Takafumi Minamimoto, the corresponding author of the study explains, "We
systematically manipulated the D1R and D2R of these monkeys by injecting them
with specific receptor-binding molecules that dampened their biological
responses to DA signaling. By positron emission tomography-based imaging of the
brains of the animals, the extent of bindings or blockades of the receptors was
measured." Then, under experimental conditions, they offered the monkeys
the chance to perform tasks to achieve rewards and noted whether the monkeys
accepted or refused to perform the tasks and how quickly they responded to the
cues related to the tasks.
Analysis of these data unearthed some
intriguing insights into the neurobiological mechanism of the decision-making
process. The researchers observed that decision-making based on perceived
benefit and cost required the involvement of both D1R and D2R, in both
incentivizing the motivation (the process in which the size of the rewards
inspired the monkeys to perform the tasks) and in increasing delay discounting
(the tendency to prefer immediate, smaller rewards over larger, but delayed
rewards). It also became clear that DA transmission via D1R and D2R regulates
the cost-based motivational process by distinct neurobiological processes for
benefits or "reward availability" and costs or "energy
expenditure associated with the task." However, workload discounting --
the process of discounting the value of the rewards based on the proportion of
the effort needed -- was exclusively related to D2R manipulation.
Prof. Hori emphasizes, "The
complementary roles of two dopamine receptor subtypes that our study revealed,
in the computation of the cost-benefit trade-off to guide action will help us
decipher the pathophysiology of psychiatric disorders." Their research
brings the hope of a future when by manipulating the inbuilt reward system and
enhancing the motivation levels, lives of many can be improved.
https://www.sciencedaily.com/releases/2021/08/210806104359.htm
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