TY - JOUR
T1 - A Postictal Traffic Jam
AU - Eyal, Sara
N1 - Publisher Copyright:
© The Author(s) 2023.
PY - 2023/9/1
Y1 - 2023/9/1
N2 - Seizure-Induced Neutrophil Adhesion in Brain Capillaries Leads to a Decrease in Postictal Cerebral Blood Flow Lim H-K, Bae S, Han K, Kang B-M, Jeong Y, Kim S-G, Suh M. iScience. 2023;26(5):106655. doi:10.1016/j.isci.2023.106655 Cerebral hypoperfusion has been proposed as a potential cause of postictal neurological dysfunction in epilepsy, but its underlying mechanism is still unclear. We show that a 30% reduction in postictal cerebral blood flow (CBF) has two contributing factors: the early hypoperfusion up to ∼30 min post-seizure was mainly induced by arteriolar constriction, while the hypoperfusion that persisted for over an hour was due to increased capillary stalling induced by neutrophil adhesion to brain capillaries, decreased red blood cell (RBC) flow accompanied by constriction of capillaries and venules, and elevated intercellular adhesion molecule-1 (ICAM-1) expression. Administration of antibodies against the neutrophil marker Ly6G and against LFA-1, which mediates adhesive interactions with ICAM-1, prevented neutrophil adhesion and recovered the prolonged CBF reductions to control levels. Our findings provide evidence that seizure-induced neutrophil adhesion to cerebral microvessels via ICAM-1 leads to prolonged postictal hypoperfusion, which may underlie neurological dysfunction in epilepsy.
AB - Seizure-Induced Neutrophil Adhesion in Brain Capillaries Leads to a Decrease in Postictal Cerebral Blood Flow Lim H-K, Bae S, Han K, Kang B-M, Jeong Y, Kim S-G, Suh M. iScience. 2023;26(5):106655. doi:10.1016/j.isci.2023.106655 Cerebral hypoperfusion has been proposed as a potential cause of postictal neurological dysfunction in epilepsy, but its underlying mechanism is still unclear. We show that a 30% reduction in postictal cerebral blood flow (CBF) has two contributing factors: the early hypoperfusion up to ∼30 min post-seizure was mainly induced by arteriolar constriction, while the hypoperfusion that persisted for over an hour was due to increased capillary stalling induced by neutrophil adhesion to brain capillaries, decreased red blood cell (RBC) flow accompanied by constriction of capillaries and venules, and elevated intercellular adhesion molecule-1 (ICAM-1) expression. Administration of antibodies against the neutrophil marker Ly6G and against LFA-1, which mediates adhesive interactions with ICAM-1, prevented neutrophil adhesion and recovered the prolonged CBF reductions to control levels. Our findings provide evidence that seizure-induced neutrophil adhesion to cerebral microvessels via ICAM-1 leads to prolonged postictal hypoperfusion, which may underlie neurological dysfunction in epilepsy.
UR - http://www.scopus.com/inward/record.url?scp=85165298436&partnerID=8YFLogxK
U2 - 10.1177/15357597231185197
DO - 10.1177/15357597231185197
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C2 - 37901775
AN - SCOPUS:85165298436
SN - 1535-7597
VL - 23
SP - 306
EP - 308
JO - Epilepsy Currents
JF - Epilepsy Currents
IS - 5
ER -