Resveratrol Prevents GLUT3 Up-Regulation Induced by Middle Cerebral Artery Occlusion.
Germán Fernando Gutiérrez AguilarIván Alquisiras-BurgosJavier Franco-PérezNarayana Pineda-RamírezAlma Ortiz-PlataIsmael TorresPedraza-Chaverri JoséPenélope AguileraPublished in: Brain sciences (2020)
Glucose transporter (GLUT)3 up-regulation is an adaptive response activated to prevent cellular damage when brain metabolic energy is reduced. Resveratrol is a natural polyphenol with anti-oxidant and anti-inflammatory features that protects neurons against damage induced in cerebral ischemia. Since transcription factors sensitive to oxidative stress and inflammation modulate GLUT3 expression, the purpose of this work was to assess the effect of resveratrol on GLUT3 expression levels after ischemia. Male Wistar rats were subjected to 2 h of middle cerebral artery occlusion (MCAO) followed by different times of reperfusion. Resveratrol (1.9 mg/kg; i. p.) was administered at the onset of the restoration of the blood flow. Quantitative-PCR and Western blot showed that MCAO provoked a substantial increase in GLUT3 expression in the ipsilateral side to the lesion of the cerebral cortex. Immunofluorescence assays indicated that GLUT3 levels were upregulated in astrocytes. Additionally, an important increase in GLUT3 occurred in other cellular types (e.g., damaged neurons, microglia, or infiltrated macrophages). Immunodetection of the microtubule-associated protein 2 (MAP2) showed that MCAO induced severe damage to the neuronal population. However, the administration of resveratrol at the time of reperfusion resulted in injury reduction. Resveratrol also prevented the MCAO-induced increase of GLUT3 expression. In conclusion, resveratrol protects neurons from damage induced by ischemia and prevents GLUT3 upregulation in the damaged brain that might depend on AMPK activation.
Keyphrases
- cerebral ischemia
- oxidative stress
- middle cerebral artery
- poor prognosis
- diabetic rats
- subarachnoid hemorrhage
- high glucose
- brain injury
- blood flow
- blood brain barrier
- internal carotid artery
- spinal cord
- drug induced
- acute myocardial infarction
- binding protein
- transcription factor
- type diabetes
- resting state
- dna damage
- functional connectivity
- high resolution
- adipose tissue
- coronary artery disease
- skeletal muscle
- endothelial cells
- heart failure
- induced apoptosis
- ischemia reperfusion injury
- metabolic syndrome
- signaling pathway
- multiple sclerosis
- high density