TY - JOUR
T1 - Switching Off Vascular MAPK Signaling
T2 - A Novel Strategy to Prevent Delayed Cerebral Ischemia Following Subarachnoid Hemorrhage
AU - Edvinsson, Lars
AU - Krause, Diana N
N1 - © 2024. The Author(s).
PY - 2025/6
Y1 - 2025/6
N2 - Patients who initially survive the rupture and repair of a brain aneurysm often take a devastating turn for the worse some days later and die or suffer permanent neurologic deficits. This catastrophic sequela is attributed to a delayed phase of global cerebral ischemia (DCI) following aneurysmal subarachnoid hemorrhage (aSAH), but we lack effective treatment. Here we present our view, based on 20 years of research, that the initial drop in blood flow at the time of rupture triggers genomic responses throughout the brain vasculature that manifest days later as increased vasoconstriction and decreased cerebral blood flow. We propose a novel treatment strategy to prevent DCI by early inhibition of the vascular mitogen-activated protein kinase (MAPK) pathway that triggers expression of vasoconstrictor and inflammatory mediators. We summarize evidence from experimental SAH models showing early treatment with MAPK inhibitors "switches off" these detrimental responses, maintains flow, and improves neurological outcome. This promising therapy is currently being evaluated in clinical trials.
AB - Patients who initially survive the rupture and repair of a brain aneurysm often take a devastating turn for the worse some days later and die or suffer permanent neurologic deficits. This catastrophic sequela is attributed to a delayed phase of global cerebral ischemia (DCI) following aneurysmal subarachnoid hemorrhage (aSAH), but we lack effective treatment. Here we present our view, based on 20 years of research, that the initial drop in blood flow at the time of rupture triggers genomic responses throughout the brain vasculature that manifest days later as increased vasoconstriction and decreased cerebral blood flow. We propose a novel treatment strategy to prevent DCI by early inhibition of the vascular mitogen-activated protein kinase (MAPK) pathway that triggers expression of vasoconstrictor and inflammatory mediators. We summarize evidence from experimental SAH models showing early treatment with MAPK inhibitors "switches off" these detrimental responses, maintains flow, and improves neurological outcome. This promising therapy is currently being evaluated in clinical trials.
KW - Cerebral vasculature
KW - Delayed cerebral ischemia
KW - MAPK kinase inhibitor
KW - Subarachnoid hemorrhage
KW - Vasoconstriction
KW - Subarachnoid Hemorrhage/complications
KW - Animals
KW - Humans
KW - MAP Kinase Signaling System/physiology
KW - Cerebrovascular Circulation/physiology
KW - Brain Ischemia/prevention & control
UR - http://www.scopus.com/inward/record.url?scp=85184507967&partnerID=8YFLogxK
U2 - 10.1007/s12975-024-01234-z
DO - 10.1007/s12975-024-01234-z
M3 - Review
C2 - 38334872
SN - 1868-4483
VL - 16
SP - 952
EP - 961
JO - Translational Stroke Research
JF - Translational Stroke Research
IS - 3
ER -