Neuroscientists have just begun studying exercise’s impact within brain cells-at the genes themselves. Even there, in the roots of our biology, they’ve found signs of the body’s influence on the mind.
It turns out that moving our muscles produces proteins that travel through the bloodstream and into the brain, where they play pivotal roles in the mechanisms of our highest thought processes. They bear names such as insulin-like growth factor (IGF-1) and vascular endothelial growth factor (VEGF), and they provide an unprecedented view of the mind-body connection. It’s only in the past few years that neuroscientists have begun to describe these factors and how they work, and each new discovery adds awe-inspiring depth to the picture.
Darwin taught us that learning is the survival mechanism we use to adapt to constantly changing environments. Inside the microenvironment of the brain, that means forging new connections between cells to relay information. When we learn some-thing, whether it’s a French word or a salsa step, cells morph in order to encode that information; the memory physically becomes part of the brain. As a theory, this idea has been around for more than a century, but only recently has it been borne out in the lab.
What we now know is that the brain is flexible, or plastic in the parlance of neuroscientists – more Play-Doh than porcelain. It is an adaptable organ that can be molded by input in much the same way as a muscle can be sculpted by lifting barbells. The more you use it, the stronger and more flexible it becomes.
The concept of plasticity is fundamental to understanding how the brain works and how exercise optimizes brain function by fostering that quality. Everything we do and think and feel is governed by how our brain cells, or neurons, connect to one another. What most people think of as psychological makeup is rooted in the biology of these connections. Likewise, our thoughts and behavior and environment reflect back on our neurons, influencing the pattern of connections. Far from being hardwired, as scientists once envisioned it, the brain is constantly being rewired. I’m here to teach you how to be your own electrician.
About 80 percent of the signaling in the brain is carried out by two neurotransmitters that balance each other’s effect: glutamate stirs up activity to begin the signaling cascade, and gamma-aminobutyric acid (GABA) clamps down on activity. When glutamate delivers a signal between two neurons that haven’t spoken before, the activity primes the pump. The more often the connection is activated, the stronger the attraction becomes, which is what neuroscientists mean when they talk about binding. As the saying goes, neurons that fire together wire together. Which makes glutamate a crucial ingredient in learning.
Glutamate is a workhorse, but psychiatry focuses more on a group of neurotransmitters that act as regulators -of the signaling process and of everything else the brain does. These are serotonin, norepinephrine, and dopamine. And although the neurons that produce them account for only 1 percent of the brain’s hundred billion cells, these neurotransmitters wield powerful influence. They might instruct a neuron to make more glutamate, or they might make the neuron more efficient or alter the sensitivity of its receptors. They can override other signals coming into the synapse, thus lowering the “noise” in the brain, or, conversely, amplify those signals. They can deliver signals directly, like glutamate and GABA, but their primary role is in adjusting the flow of information in order to fine-tune the overall balance of neurochemicals.
As fundamental as the neurotransmitters are, there’s another class of master molecules that over the past fifteen years or so has dramatically changed our understanding of connections in the brain, specifically, how they develop and grow. I’m talking about a family of proteins loosely termed factors, the most prominent of which is brain-derived neurotrophic factor (BDNF). Whereas neurotransmitters carry out signaling, neurotrophins such as BDNF build and maintain the cell circuitry – the infrastructure itself.
Learning requires strengthening the affinity between neurons through a dynamic mechanism called long-term potentiation (LTP). When the brain is called on to take in information, the demand naturally causes activity between neurons. The more activity, the stronger the attraction becomes, and the easier it is for the signal to fire and make the connection. The initial activity marshals existing stores of glutamate in the axon to be sent across the synapse and reconfigures receptors on the receiving side to accept the signal. The voltage on the receiving side of the synapse becomes stronger in its resting state, thereby attracting the glutamate signal like a magnet. If the firing continues, genes inside the neuron’s cell nucleus are turned on to produce more building material for the synapses, and it is this bolstering of the infrastructure that allows the new information to stick as a memory.
BDNF also binds to receptors at the synapse, unleashing the flow of ions to increase the voltage and immediately improve the signal strength. Inside the cell, BDNF activates genes that call for the production of more BDNF as well as serotonin and proteins that build up the synapses. BDNF directs traffic and engineers the roads as well. Overall, it improves the function of neurons, encourages their growth, and strengthens and protects them against the natural process of cell death.
Source : Spark: The Revolutionary New Science of Exercise and the Brain by John J. Ratey, Eric Hagerman
Goodreads : https://www.goodreads.com/book/show/721609.Spark
Read Next Article : https://thinkingbeyondscience.in/2025/02/19/the-brains-evolution-learning-and-memory-explained/








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