Khiany Mathias

ORCID: 0000-0002-0067-3227
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About
Contact & Profiles
Research Areas
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Intensive Care Unit Cognitive Disorders
  • Tryptophan and brain disorders
  • Stress Responses and Cortisol
  • Traumatic Brain Injury and Neurovascular Disturbances
  • Anesthesia and Neurotoxicity Research
  • Mitochondrial Function and Pathology
  • Respiratory Support and Mechanisms
  • Acute Ischemic Stroke Management
  • Neonatal and fetal brain pathology
  • Cannabis and Cannabinoid Research
  • Neurological Disease Mechanisms and Treatments
  • Sepsis Diagnosis and Treatment
  • Fatty Acid Research and Health
  • Neuroscience and Neuropharmacology Research
  • Heme Oxygenase-1 and Carbon Monoxide
  • Neonatal Respiratory Health Research
  • Psychedelics and Drug Studies
  • Exercise and Physiological Responses
  • IL-33, ST2, and ILC Pathways
  • Barrier Structure and Function Studies
  • Treatment of Major Depression
  • Studies on Chitinases and Chitosanases
  • Immune responses and vaccinations
  • Bipolar Disorder and Treatment

Universidade do Sul de Santa Catarina
2017-2025

Centro Universitário do Espírito Santo
2025

Universidade do Extremo Sul Catarinense
2025

Oxidative stress has been reported to be an important mechanism for brain damage following ischemic stroke. Recently, the involvement of cytosolic receptors capable forming protein complexes called inflammasomes demonstrated perpetuate oxidative stress. Herein, we report effect NLRP3 inhibition with MCC950 on in animal model transient global cerebral ischemia.

10.1080/00207454.2021.1922402 article EN International Journal of Neuroscience 2021-04-27
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