Differential contribution of excitatory and inhibitory neurons in shaping neurovascular coupling in different epileptic neural states.


Journal

Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism
ISSN: 1559-7016
Titre abrégé: J Cereb Blood Flow Metab
Pays: United States
ID NLM: 8112566

Informations de publication

Date de publication:
05 2021
Historique:
pubmed: 17 7 2020
medline: 30 7 2021
entrez: 17 7 2020
Statut: ppublish

Résumé

Understanding the neurovascular coupling (NVC) underlying hemodynamic changes in epilepsy is crucial to properly interpreting functional brain imaging signals associated with epileptic events. However, how excitatory and inhibitory neurons affect vascular responses in different epileptic states remains unknown. We conducted real-time in vivo measurements of cerebral blood flow (CBF), vessel diameter, and excitatory and inhibitory neuronal calcium signals during recurrent focal seizures. During preictal states, decreases in CBF and arteriole diameter were closely related to decreased γ-band local field potential (LFP) power, which was linked to relatively elevated excitatory and reduced inhibitory neuronal activity levels. Notably, this preictal condition was followed by a strengthened ictal event. In particular, the preictal inhibitory activity level was positively correlated with coherent oscillating activity specific to inhibitory neurons. In contrast, ictal states were characterized by elevated synchrony in excitatory neurons. Given these findings, we suggest that excitatory and inhibitory neurons differentially contribute to shaping the ictal and preictal neural states, respectively. Moreover, the preictal vascular activity, alongside with the γ-band, may reflect the relative levels of excitatory and inhibitory neuronal activity, and upcoming ictal activity. Our findings provide useful insights into how perfusion signals of different epileptic states are related in terms of NVC.

Identifiants

pubmed: 32669018
doi: 10.1177/0271678X20934071
pmc: PMC8054729
doi:

Substances chimiques

Calcium SY7Q814VUP

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1145-1161

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Auteurs

Hyun-Kyoung Lim (HK)

Center for Neuroscience Imaging Research (CNIR), Institute for Basic Science (IBS), Suwon, South Korea.
Department of Biological Sciences, Sungkyunkwan University, Suwon, South Korea.

Nayeon You (N)

Center for Neuroscience Imaging Research (CNIR), Institute for Basic Science (IBS), Suwon, South Korea.
Department of Biomedical Engineering, Sungkyunkwan University, Suwon, South Korea.

Sungjun Bae (S)

Center for Neuroscience Imaging Research (CNIR), Institute for Basic Science (IBS), Suwon, South Korea.
Department of Biomedical Engineering, Sungkyunkwan University, Suwon, South Korea.

Bok-Man Kang (BM)

Center for Neuroscience Imaging Research (CNIR), Institute for Basic Science (IBS), Suwon, South Korea.
Department of Biomedical Engineering, Sungkyunkwan University, Suwon, South Korea.

Young-Min Shon (YM)

Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.

Seong-Gi Kim (SG)

Center for Neuroscience Imaging Research (CNIR), Institute for Basic Science (IBS), Suwon, South Korea.
Department of Biomedical Engineering, Sungkyunkwan University, Suwon, South Korea.

Minah Suh (M)

Center for Neuroscience Imaging Research (CNIR), Institute for Basic Science (IBS), Suwon, South Korea.
Department of Biomedical Engineering, Sungkyunkwan University, Suwon, South Korea.
Biomedical Institute for Convergence at SKKU (BICS), Sungkyunkwan University, Suwon, South Korea.
Samsung Advanced Institute for Health Sciences & Technology (SAIHST), Sungkyunkwan University, Suwon, South Korea.

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