Revisiting Excitotoxicity in Traumatic Brain Injury: From Bench to Bedside.
Daniela Baracaldo-SantamaríaDaniel Felipe Ariza-SalamancaMaría Gabriela Corrales-HernándezMaria José Pachón-LondoñoIsabella Hernandez-DuarteCarlos-Alberto Calderon-OspinaPublished in: Pharmaceutics (2022)
Traumatic brain injury (TBI) is one of the leading causes of morbidity and mortality. Consequences vary from mild cognitive impairment to death and, no matter the severity of subsequent sequelae, it represents a high burden for affected patients and for the health care system. Brain trauma can cause neuronal death through mechanical forces that disrupt cell architecture, and other secondary consequences through mechanisms such as inflammation, oxidative stress, programmed cell death, and, most importantly, excitotoxicity. This review aims to provide a comprehensive understanding of the many classical and novel pathways implicated in tissue damage following TBI. We summarize the preclinical evidence of potential therapeutic interventions and describe the available clinical evaluation of novel drug targets such as vitamin B12 and ifenprodil, among others.
Keyphrases
- traumatic brain injury
- oxidative stress
- mild cognitive impairment
- cognitive decline
- end stage renal disease
- severe traumatic brain injury
- cell therapy
- newly diagnosed
- chronic kidney disease
- ejection fraction
- physical activity
- dna damage
- peritoneal dialysis
- prognostic factors
- emergency department
- single cell
- cerebral ischemia
- white matter
- risk factors
- mesenchymal stem cells
- signaling pathway
- blood brain barrier
- induced apoptosis
- patient reported outcomes
- adverse drug
- heat stress