Exercise-induced activation of ventromedial hypothalamic steroidogenic factor-1 neurons mediates improvements in endurance 2026 Betley et al

[Andy]

Highlights
• The brain is a key intermediate for physiological improvement following exercise
• Exercise strengthens inputs to and increases the activity of VMH SF1 neurons
• Activation of VMH SF1 neurons following exercise is required to improve endurance
• Exogenous activation of VMH SF1 neurons following exercise enhances endurance gains

Summary
Repeated exercise produces robust physiological benefits and is the leading lifestyle intervention for human health. The benefits from exercise training result from the remodeling of skeletomuscular, cardiovascular, metabolic, and endocrine systems. In mice, we find that activation of the central nervous system following exercise is essential for subsequent endurance performance and metabolism benefits. Ventromedial hypothalamic steroidogenic factor-1 (SF1) neurons are activated following exercise, and repeated training results in increased post-exercise SF1 neuron activation. Exercise training increases the intrinsic excitability and density of excitatory synapses on SF1 neurons, suggesting that exercise history is encoded through hypothalamic plasticity. Inhibition of SF1 neuron output blocks endurance gains and metabolic improvements that result from exercise training. Conversely, stimulation of SF1 neurons following exercise enhances gains in endurance. These results demonstrate that exercise-induced hypothalamic SF1 neuron activity is essential for the coordination of physiological improvements following exercise training.

Open access

 

[Jonathan Edwards]

In mice but intriguing.
Maybe in PEM the neurons are backfiring.

 

[jnmaciuch]

Maybe in PEM the neurons are backfiring.

It might be relevant in exercise intolerance but I don't know how much it would be relevant in PEM specifically. This paper and prior studies on this neuron population all point to them being highly sensitive glucose regulators. VO2 max is normal when these neurons are knocked down--the main difference seems to be how long activity can be sustained, which makes perfect sense if the SF1 neurons are responsible for quickly mobilizing additional glucose after local reserves have run out. The piece on endurance improvement seems to largely be driven by transcriptional changes in the muscle itself, which doesn't happen when the glucose uptick doesn't happen

In PEM the story seems to include impairment right off the bat, so I'm not sure this neuron population would explain much.

 

[Jonathan Edwards]

But they might feed signals to other cells telling them that resources are being stretched and then might send signals saying everything is OK now, after a delay period to make sure it really is, and that might backfire?

We know that neural control systems are hugely complex in terms og knock on effects

 

[jnmaciuch]

Sure, you could theorize that anything in the brain causes any problem if you include enough steps