🧬 BDNF Extraction Viewer

Извлечено: 997 / 997 (100.0%) Средняя confidence: 0.13
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Temporal association between NRF2/HO-1 activation, endogenous BDNF up-regulation, and motor recovery in a male mouse MCAO model.

PMID: 41876036 · DOI: 10.1016/j.jstrokecerebrovasdis.2026.108616 · Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 2026 · Junghee Park, Hyoin Hwang, Hyekyoung Shin, Yoonyoung Chung, Dongjoon Kim, Yonghyun Jun
📄 Abstract

Stroke induces severe neurological impairment, however, there is limited understanding of the mechanisms underlying post-stroke recovery. Nuclear factor erythroid 2-related factor 2 (NRF2) and brain-derived neurotrophic factor (BDNF) have been implicated in tissue responses to ischemic injury; however, their temporal interactions in middle cerebral artery occlusion (MCAO) models are not fully understood. Male C57BL/6 mice (7-8 weeks) were subjected to transient MCAO (tMCAO). Motor behavior, cerebral blood flow, and temporal changes in NRF2, heme oxygenase-1 (HO-1), and BDNF expression were assessed over 14 days. Cerebral blood flow in the ischemic cortex remained significantly reduced for up to 14 days after MCAO. Motor deficits were most severe on day 3 and showed gradual recovery by day 7. NRF2 expression peaked on day 3, whereas HO-1 and BDNF expression increased on days 7 and 14, coinciding with improved motor performance and increased neuronal preservation. These findings indicate that activation of the NRF2/HO-1 pathway is temporally associated with increased expression of endogenous BDNF and recovery of motor function following ischemic injury in male mice.

Confidence: 0.18 · 9 полей извлечено
Идентификация (6 полей)
Target
NRF2
0.95
Alt. target
Nuclear factor erythroid 2-related factor 2
0.95
Protein family
Basic leucine zipper (bZIP) transcription factor
0.70
Functional class
Transcription factor
0.90
Subcellular loc.
Nucleus and cytoplasm
0.80
Isoforms (metab/obesity)
0.00
Механизм действия (21 полей)
Mechanism
0.00
Mutations (obesity/lean)
0.00
Activity (obesity)
0.00
Activity temporal
0.00
Energy balance
0.00
Appetite
0.00
Fat metabolism
0.00
Lipolysis
0.00
Thermogenesis
0.00
Muscle metabolism
0.00
Inflammation
0.00
Glucose metabolism
0.00
AA metabolism
0.00
Hormonal pathways
0.00
Cell death
0.00
Adipocyte fibrosis
0.00
Upstream (biochem)
0.00
Upstream (physiol)
0.00
Downstream (biochem)
0.00
Downstream (physiol)
0.00
PTMs
0.00
Экспрессия (8 полей)
Tissue expression
NRF2 expression peaked on day 3 in ischemic cortex; HO-1 and BDNF expression increased on days 7 and 14 in ischemic cortex
0.90
In vitro
0.00
In vivo
Male C57BL/6 mice (7-8 weeks) subjected to transient MCAO; motor behavior, cerebral blood flow, and temporal changes in NRF2, HO-1, and BDNF expression assessed over 14 days
0.95
In silico
0.00
Genetic association
0.00
Ex vivo
0.00
Animal model
Male C57BL/6 mice (7-8 weeks) subjected to transient middle cerebral artery occlusion (tMCAO)
0.95
Diet/model
Transient middle cerebral artery occlusion (tMCAO) model
0.95
Клиника (11 полей)
Drug
0.00
Indication
0.00
Patient subgroups
0.00
Safety concerns
0.00
Off-target
0.00
Trial stage
0.00
Pharma competitors
0.00
AE severity
0.00
MOA weight loss
0.00
Endpoints
0.00
Approved
0.00