Effects of hyperglycemia on neuronal network function in an in vitro model of the ischemic penumbra

•Hyperglycemia is common in acute ischemic stroke patients, and associated with unfavorable functional outcome.•Active glucose lowering in patients with acute ischemic stroke had no effect on infarct size nor on functional outcome. A factor hampering the design and interpretation of intervention stu...

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Veröffentlicht in:Brain research 2025-02, Vol.1849, p.149370, Article 149370
Hauptverfasser: Kersten, C.J.B.A., Vrielink, T.H., den Hertog, H.M., Hofmeijer, J., le Feber, J.
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container_title Brain research
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Vrielink, T.H.
den Hertog, H.M.
Hofmeijer, J.
le Feber, J.
description •Hyperglycemia is common in acute ischemic stroke patients, and associated with unfavorable functional outcome.•Active glucose lowering in patients with acute ischemic stroke had no effect on infarct size nor on functional outcome. A factor hampering the design and interpretation of intervention studies is that the effects of glucose concentration on the cellular level are unclear.•We observed that hyperglycemia was associated with a more rapid decline of neuronal network activity during hypoxia and more apoptosis at the cellular level.•These results provide a starting point for further studies into neurophysiological and cellular effects of hyperglycemia to mechanistically assess the role of hyperglycemia in acute ischemic stroke. Hyperglycemia is common in acute ischemic stroke, and associated with unfavorable outcome. However, the optimal glucose level is not known and cellular effects of hyperglycemia under hypoxia are largely unclear. We assessed how the extracellular glucose concentration affects cultured neuronal networks under experimental in vitro conditions, to provide a starting point for assessment of mechanisms at the neuronal network and cellular levels. We used in vitro cultured rat neuronal networks on micro-electrode arrays (MEAs) and glass coverslips. Twenty-four hours of controlled hypoxia was induced. We measured neuronal network activity during baseline (normoxia, 6 h), 24 h of hypoxia, and 6 h after reoxygenation, defined as the summed number of action potentials in 1 h bins. Apoptosis was determined intermittently with caspase 3/7 staining and microscopy. We compared groups of networks under glucose concentrations of 5.0 mmol/L, 7.0 mmol/L, 9.0 mmol/L, and 12.0 mmol/L. Overall, during hypoxia, a gradual decrease in neuronal network activity and increase in apoptosis was found. There were faster decrease in activity (p 
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A factor hampering the design and interpretation of intervention studies is that the effects of glucose concentration on the cellular level are unclear.•We observed that hyperglycemia was associated with a more rapid decline of neuronal network activity during hypoxia and more apoptosis at the cellular level.•These results provide a starting point for further studies into neurophysiological and cellular effects of hyperglycemia to mechanistically assess the role of hyperglycemia in acute ischemic stroke. Hyperglycemia is common in acute ischemic stroke, and associated with unfavorable outcome. However, the optimal glucose level is not known and cellular effects of hyperglycemia under hypoxia are largely unclear. We assessed how the extracellular glucose concentration affects cultured neuronal networks under experimental in vitro conditions, to provide a starting point for assessment of mechanisms at the neuronal network and cellular levels. We used in vitro cultured rat neuronal networks on micro-electrode arrays (MEAs) and glass coverslips. Twenty-four hours of controlled hypoxia was induced. We measured neuronal network activity during baseline (normoxia, 6 h), 24 h of hypoxia, and 6 h after reoxygenation, defined as the summed number of action potentials in 1 h bins. Apoptosis was determined intermittently with caspase 3/7 staining and microscopy. We compared groups of networks under glucose concentrations of 5.0 mmol/L, 7.0 mmol/L, 9.0 mmol/L, and 12.0 mmol/L. Overall, during hypoxia, a gradual decrease in neuronal network activity and increase in apoptosis was found. There were faster decrease in activity (p &lt; 0.01) and more apoptosis after 24 h of hypoxia under glucose levels of 12 mmol/L in a single-well MEA set-up (p &lt; 0.05), and more apoptosis in glass coverslips with glucose levels of 12.0 mmol/L in comparison with 5 mmol/L (p = 0.03). These differences were not observed in multi-well MEAs, in which effects of hypoxia were much smaller than in single-well MEAs. Hyperglycemia was associated with a more rapid decrease of neuronal network activity during and more apoptosis after 24 h of hypoxia in cultured neuronal networks. Loss of neuronal activity and apoptosis probably play a role in poorer outcomes of stroke patients under hyperglycemia. 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We used in vitro cultured rat neuronal networks on micro-electrode arrays (MEAs) and glass coverslips. Twenty-four hours of controlled hypoxia was induced. We measured neuronal network activity during baseline (normoxia, 6 h), 24 h of hypoxia, and 6 h after reoxygenation, defined as the summed number of action potentials in 1 h bins. Apoptosis was determined intermittently with caspase 3/7 staining and microscopy. We compared groups of networks under glucose concentrations of 5.0 mmol/L, 7.0 mmol/L, 9.0 mmol/L, and 12.0 mmol/L. Overall, during hypoxia, a gradual decrease in neuronal network activity and increase in apoptosis was found. There were faster decrease in activity (p &lt; 0.01) and more apoptosis after 24 h of hypoxia under glucose levels of 12 mmol/L in a single-well MEA set-up (p &lt; 0.05), and more apoptosis in glass coverslips with glucose levels of 12.0 mmol/L in comparison with 5 mmol/L (p = 0.03). These differences were not observed in multi-well MEAs, in which effects of hypoxia were much smaller than in single-well MEAs. Hyperglycemia was associated with a more rapid decrease of neuronal network activity during and more apoptosis after 24 h of hypoxia in cultured neuronal networks. Loss of neuronal activity and apoptosis probably play a role in poorer outcomes of stroke patients under hyperglycemia. 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A factor hampering the design and interpretation of intervention studies is that the effects of glucose concentration on the cellular level are unclear.•We observed that hyperglycemia was associated with a more rapid decline of neuronal network activity during hypoxia and more apoptosis at the cellular level.•These results provide a starting point for further studies into neurophysiological and cellular effects of hyperglycemia to mechanistically assess the role of hyperglycemia in acute ischemic stroke. Hyperglycemia is common in acute ischemic stroke, and associated with unfavorable outcome. However, the optimal glucose level is not known and cellular effects of hyperglycemia under hypoxia are largely unclear. We assessed how the extracellular glucose concentration affects cultured neuronal networks under experimental in vitro conditions, to provide a starting point for assessment of mechanisms at the neuronal network and cellular levels. 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These differences were not observed in multi-well MEAs, in which effects of hypoxia were much smaller than in single-well MEAs. Hyperglycemia was associated with a more rapid decrease of neuronal network activity during and more apoptosis after 24 h of hypoxia in cultured neuronal networks. Loss of neuronal activity and apoptosis probably play a role in poorer outcomes of stroke patients under hyperglycemia. Our model provides a starting point for further assessment of pathomechanisms.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>39622484</pmid><doi>10.1016/j.brainres.2024.149370</doi></addata></record>
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subjects Action Potentials - physiology
Animals
Apoptosis - physiology
Brain Ischemia - metabolism
Brain Ischemia - pathology
Brain Ischemia - physiopathology
Cell Hypoxia - physiology
Cells, Cultured
Glucose - metabolism
Hyperglycemia
Hyperglycemia - metabolism
Hyperglycemia - physiopathology
Ischemic stroke
Nerve Net - metabolism
Nerve Net - physiopathology
Neuronal networks
Neurons - metabolism
Rats
Rats, Wistar
title Effects of hyperglycemia on neuronal network function in an in vitro model of the ischemic penumbra
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