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Nrf2 activation in the human brain after stroke due to supratentorial intracerebral haemorrhage: a case-control study.
Christopher, Edward; Loan, James J M; Samarasekera, Neshika; McDade, Karina; Rose, Jamie; Barrington, Jack; Hughes, Jeremy; Smith, Colin; Al-Shahi Salman, Rustam.
Afiliação
  • Christopher E; The University of Edinburgh College of Medicine and Veterinary Medicine, Edinburgh, UK.
  • Loan JJM; Division of Clinical Neurosciences, NHS Lothian, Edinburgh, UK.
  • Samarasekera N; Centre for Clinical Brain Sciences, The University of Edinburgh, Edinburgh, UK.
  • McDade K; Division of Clinical Neurosciences, NHS Lothian, Edinburgh, UK.
  • Rose J; Centre for Clinical Brain Sciences, The University of Edinburgh, Edinburgh, UK.
  • Barrington J; Academic Neuropathology, The University of Edinburgh, Edinburgh, UK.
  • Hughes J; Academic Neuropathology, The University of Edinburgh, Edinburgh, UK.
  • Smith C; UK Dementia Research Institute, The University of Edinburgh, Edinburgh, UK.
  • Al-Shahi Salman R; Centre for Clinical Brain Sciences, The University of Edinburgh, Edinburgh, UK.
BMJ Neurol Open ; 4(1): e000238, 2022.
Article em En | MEDLINE | ID: mdl-35265844
ABSTRACT

Aims:

Pharmacological activation of the antioxidative transcription factor nuclear factor erythroid 2-related factor 2 (Nrf2) improves outcomes in experimental models of intracerebral haemorrhage (ICH). However, the Nrf2 pathway has not been previously studied in humans after ICH. Our study aims to address this gap.

Methods:

We selected cases with fatal ICH from a prospective community-based inception cohort study and age-matched and sex-matched controls who died suddenly of non-neurological disease. We used immunohistochemistry to quantify Nrf2 (% total area stained overall and % of nuclei stained) and CD68 expression in controls and perihaematomal, ipsilateral and contralateral brain tissue from cases. We measured downstream haem oxygenase-1 (HMOX1) and NAD(P)H dehydrogenase quinone 1 [NQO1] expression using RNA in situ hybridisation.

Results:

26 ICH cases (median age 82 (IQR 76-86); 13 (50%) male) and eight controls (median age 79 (IQR 77-80); 3 (37.5%) male) were included. We found no significant differences in overall % of Nrf2 staining between ICH cases and controls. However, the mean % of nuclei staining for Nrf2 seemed higher in perihaematomal compared with contralateral regions, although this was only statistically significant >60 days after ICH (25% (95% CI 17% to 33%) vs 14% (95% CI 11% to 17%), p=0.029). The percentage of perihaematomal tissue staining for CD68 was higher >60 days after ICH (6.75%, 95% CI 2.78% to 10.73%) compared with contralateral tissue (1.45%, 95% CI 0.93% to 1.96%, p=0.027) and controls (1.08%, 95% CI 0.20% to 1.97%, p=0.0008). RNA in situ hybridisation suggested increased abundance of HMOX1 and NQO1 transcripts in perihaematomal versus distant ipsilateral brain tissue obtained <7 days from onset of ICH.

Conclusions:

We found evidence of Nrf2 activation in human brain tissue after ICH. Pharmacological augmentation of Nrf2 activation after ICH might be a promising therapeutic approach.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies Idioma: En Revista: BMJ Neurol Open Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies Idioma: En Revista: BMJ Neurol Open Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido