Abstract
Glutamate-excitotoxicity is a primary contributor of ischemic neuronal death. Several strategies have been developed against glutamate-excitotoxicity, however any of them have not showed positive results in the clinical practice so far. Nowadays, the concept of blood/brain glutamate grabbing is well recognized as a novel and attractive protective strategy to reduce the excitotoxic effect of excess extracellular glutamate that accumulates in the brain following an ischemic stroke. The main advantage of this novel therapeutic strategy is that occurs in the blood circulation and therefore does not affect the normal brain neurophysiology, as it has been described for other drug treatments used against glutamate excitotoxicity. In this work, we summarize all experimental data about the potential application of this therapy against stroke pathology. Ischemic stroke, caused by interruption of the blood supply to the brain, is one of the most important causes of morbidity and mortality worldwide. Currently, the control of systemic parameters, such as body temperature, blood pressure, and glycemia, has considerably improved the outcome of stroke patients. In the absence of protective therapy, an early artery reperfusion, i.e. mechanical or enzymatic thrombolysis, remains the primary goal of treatment for acute ischemic stroke. However, because of the progressive increase in stroke incidence, the high morbidity and the limited therapeutic tools against stroke, seeking new alternatives that can be applied more universally and with less technological requirements is in high demand1, 2.
Highlights
More than 15 years ago, we reported, in clinical studies, that glutamate is critical for neuronal damage after ischemic stroke[8,9,10]
Ischemic patients presented higher blood and Cerebrospinal fluid (CSF) glutamate levels than control subjects at admission[8, 9], suggesting that glutamate concentrations above 200 μM in plasma acted as an important predictor of neuronal damage at 48 hours, with a sensitivity of 85% and a specificity of 97%11
High levels of glutamate in the plasma for at least 24 hours was associated with early neurological deterioration, whereas in patients with stable ischemic stroke, glutamate levels dropped to normal values less than 6 hours from onset[11]
Summary
Beyond Glutamate Antagonists for Treatment of Ischemic Stroke: Blood Glutamate Grabbing. José Castillo[1], María Isabel Loza[2,3], David Mirelman[4], Tomás Sobrino[1], Francisco Campos[1]
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