Title : Midazolam contributes to neuroprotection against hypoxia/reoxygenation-induced brain injury in neonatal rats via regulation of EAAT2.

Pub. Date : 2020 Aug

PMID : 32433937






6 Functional Relationships(s)
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1 Midazolam contributes to neuroprotection against hypoxia/reoxygenation-induced brain injury in neonatal rats via regulation of EAAT2. Midazolam solute carrier family 1 member 2 Rattus norvegicus
2 The present study aimed to detect the role of EAAT2 in the neuroprotective effect of midazolam in neonatal rat brain subjected to H/R. Midazolam solute carrier family 1 member 2 Rattus norvegicus
3 Pretreatment with midazolam reversed H/R-induced apoptosis and downregulation of EAAT2 mRNA and protein expression in the hippocampus. Midazolam solute carrier family 1 member 2 Rattus norvegicus
4 Pretreatment with dihydrokainic acid (a selective inhibitor of EAAT2) exacerbated apoptosis, and thus inhibited the neuroprotective effect of midazolam against H/R injury. Midazolam solute carrier family 1 member 2 Rattus norvegicus
5 We demonstrated for the first time that dysregulation of EAAT2 expression may be related to the neural injury induced by H/R in rat pups, and pretreatment with midazolam attenuated apoptosis and improved learning and memory partly due to regulating EAAT2 expression. Midazolam solute carrier family 1 member 2 Rattus norvegicus
6 We demonstrated for the first time that dysregulation of EAAT2 expression may be related to the neural injury induced by H/R in rat pups, and pretreatment with midazolam attenuated apoptosis and improved learning and memory partly due to regulating EAAT2 expression. Midazolam solute carrier family 1 member 2 Rattus norvegicus