A team of UVM scientists headed by Mark Nelson, Ph.D., from the Larner College of Medicine at the University of Vermont, has uncovered a novel mechanism that reshapes understanding how blood flow is regulated in the brain. This study, published in The Proceedings of the National Academy of Sciences (PNAS) – a high-impact, peer-reviewed journal of the National Academy of Sciences (NAS) – introduces Electro-Calcium (E-Ca) Coupling. This process integrates electrical and calcium signaling in brain capillaries to deliver precise blood flow to active neurons.
Blood is delivered into the brain from surface arteries through penetrating arterioles (or tiny blood vessels that branch off from arteries) and hundreds of miles of capillaries, which enormously extend the perfusion territory. The brain is a highly metabolically demanding organ that lacks substantial energy reserves. It maintains constant blood flow in the face of blood pressure fluctuations (autoregulation). Still, it depends on an on-demand delivery process in which neuronal activity triggers a local increase in blood flow to distribute oxygen and nutrients selectively to active regions.
Cerebral blood delivery relies on mechanisms such as electrical signaling, propagating through capillary networks to upstream arterioles to deliver blood, and calcium signaling, fine-tuning local blood flow. And for years, these mechanisms were thought to operate independently. However, Nelson’s research reveals that these systems are deeply interconnected through E-Ca coupling, where electrical signals enhance calcium entry into cells, amplifying localized signals and extending their influence to neighboring cells.
The study showed that electrical hyperpolarization in capillary cells spreads rapidly through the activation of capillary endothelial Kir2.1 channels. These specialized proteins in the cell membrane detect changes in potassium levels and amplify electrical signals by passing them from cell to cell. This creates a wave-like electrical signal that travels across the capillary network. At the same time, calcium signals, initiated by IP3 receptors—proteins located in the membranes of intracellular storage sites—release stored calcium in response to specific chemical signals.
This local release of calcium fine-tunes blood flow by triggering vascular responses. E-Ca coupling bridges these two processes, with the electrical waves generated by Kir2.1 channels enhancing calcium activity, creating a synchronized system that adjusts blood flow locally and across wider distances.
The researchers could observe this mechanism in action through advanced imaging and computer models. And they found that electrical signals in capillary cells boosted calcium activity by 76%, significantly increasing its ability to influence blood flow. When the team mimicked brain activity by stimulating these cells, calcium signals increased by 35%, showing how these signals travel through the capillary network. They also discovered that the signals spread evenly throughout the capillary bed, ensuring blood flow is balanced across all areas without favoring one direction.
This discovery emphasizes the vital role of capillaries in managing blood flow within the brain. And by identifying how electrical and calcium signals work together through electro-calcium coupling, the research sheds light on the brain’s ability to efficiently direct blood to areas with the greatest demand for oxygen and nutrients.
This is especially significant because disruptions in blood flow are a hallmark of many neurological conditions, such as stroke, dementia, and Alzheimer’s disease. And understanding the mechanics of E-Ca coupling offers a new framework for exploring treatments for these conditions, potentially leading to therapies that restore or enhance blood flow and protect brain health. This breakthrough also provides a deeper understanding of how the brain maintains energy balance, which is critical for sustaining cognitive and physical function.
KEY QUOTE:
“This use-dependent increase in local blood flow (functional hyperemia), mediated by mechanisms collectively termed neurovascular coupling (NVC), is essential for normal brain function and represents the physiological basis for functional magnetic resonance imaging. Furthermore, deficits in cerebral blood flow (CBF) including functional hyperemia are an early feature of small vessel diseases (SVDs) of the brain and Alzheimer’s long before overt clinical symptoms.”
“Recently, the UVM team also demonstrated that deficits in cerebral blood flow in small vessel disease of the brain and Alzheimer’s could be corrected by an essential co-factor of electrical signaling. The current work indicates that calcium signaling could also be restored. The ‘Holy Grail,’ so to speak, is whether early restoration of cerebral blood flow in brain blood vessel disease slows cognitive decline.”
- Mark Nelson
