4.6 Article

Non-Linear Frequency Dependence of Neurovascular Coupling in the Cerebellar Cortex Implies Vasodilation-Vasoconstriction Competition

期刊

CELLS
卷 11, 期 6, 页码 -

出版社

MDPI
DOI: 10.3390/cells11061047

关键词

cerebellum; neurovascular coupling; granule cells; nitric oxide; NMDA receptor

资金

  1. European Union's Horizon 2020 Framework Programme for Research and Innovation under the Specific Grant [945539, SGA3, 785907, SGA2]
  2. Centro Fermi project Local Neuronal Microcircuits (LNM) [77]
  3. Wings for Life [169111]
  4. BRC [BRC704/CAP/CGW]
  5. UCL Global Challenges Research Fund (GCRF)
  6. MRC [MR/S026088/1]
  7. Ataxia UK
  8. MRC [MR/S026088/1] Funding Source: UKRI
  9. Medical Research Council [MR/S026088/1] Funding Source: researchfish

向作者/读者索取更多资源

This study investigates the relationship between neurovascular coupling (NVC) and neuronal activity (NA) using acute mouse cerebellar slices. The findings suggest that NVC involves a balance between the NMDAR-NO pathway and the mGluRs-20HETE pathway, with the latter playing a role at intermediate frequencies. This has important implications for interpreting fMRI signals.
Neurovascular coupling (NVC) is the process associating local cerebral blood flow (CBF) to neuronal activity (NA). Although NVC provides the basis for the blood oxygen level dependent (BOLD) effect used in functional MRI (fMRI), the relationship between NVC and NA is still unclear. Since recent studies reported cerebellar non-linearities in BOLD signals during motor tasks execution, we investigated the NVC/NA relationship using a range of input frequencies in acute mouse cerebellar slices of vermis and hemisphere. The capillary diameter increased in response to mossy fiber activation in the 6-300 Hz range, with a marked inflection around 50 Hz (vermis) and 100 Hz (hemisphere). The corresponding NA was recorded using high-density multi-electrode arrays and correlated to capillary dynamics through a computational model dissecting the main components of granular layer activity. Here, NVC is known to involve a balance between the NMDAR-NO pathway driving vasodilation and the mGluRs-20HETE pathway driving vasoconstriction. Simulations showed that the NMDAR-mediated component of NA was sufficient to explain the time course of the capillary dilation but not its non-linear frequency dependence, suggesting that the mGluRs-20HETE pathway plays a role at intermediate frequencies. These parallel control pathways imply a vasodilation-vasoconstriction competition hypothesis that could adapt local hemodynamics at the microscale bearing implications for fMRI signals interpretation.

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