L-2-Hydroxyglutaric Acid Administration to Neonatal Rats Elicits Marked Neurochemical Alterations and Long-Term Neurobehavioral Disabilities Mediated by Oxidative Stress.
Rafael Teixeira RibeiroAndrey Vinícios Soares CarvalhoRafael PalavroLuz Elena Durán-CarabaliÂngela Beatris ZemniaçakAlexandre Umpierrez AmaralCarlos Alexandre NettoMoacir WajnerPublished in: Neurotoxicity research (2022)
L-2-Hydroxyglutaric aciduria (L-2-HGA) is an inherited neurometabolic disorder caused by deficient activity of L-2-hydroxyglutarate dehydrogenase. L-2-Hydroxyglutaric acid (L-2-HG) accumulation in the brain and biological fluids is the biochemical hallmark of this disease. Patients present exclusively neurological symptoms and brain abnormalities, particularly in the cerebral cortex, basal ganglia, and cerebellum. Since the pathogenesis of this disorder is still poorly established, we investigated the short-lived effects of an intracerebroventricular injection of L-2-HG to neonatal rats on redox homeostasis in the cerebellum, which is mostly affected in this disorder. We also determined immunohistochemical landmarks of neuronal viability (NeuN), astrogliosis (S100B and GFAP), microglia activation (Iba1), and myelination (MBP and CNPase) in the cerebral cortex and striatum following L-2-HG administration. Finally, the neuromotor development and cognitive abilities were examined. L-2-HG elicited oxidative stress in the cerebellum 6 h after its injection, which was verified by increased reactive oxygen species production, lipid oxidative damage, and altered antioxidant defenses (decreased concentrations of reduced glutathione and increased glutathione peroxidase and superoxide dismutase activities). L-2-HG also decreased the content of NeuN, MBP, and CNPase, and increased S100B, GFAP, and Iba1 in the cerebral cortex and striatum at postnatal days 15 and 75, implying long-standing neuronal loss, demyelination, astrocyte reactivity, and increased inflammatory response, respectively. Finally, L-2-HG administration caused a delay in neuromotor development and a deficit of cognition in adult animals. Importantly, the antioxidant melatonin prevented L-2-HG-induced deleterious neurochemical, immunohistochemical, and behavioral effects, indicating that oxidative stress may be central to the pathogenesis of brain damage in L-2-HGA.
Keyphrases
- oxidative stress
- cerebral ischemia
- fluorescent probe
- diabetic rats
- inflammatory response
- resting state
- functional connectivity
- aqueous solution
- subarachnoid hemorrhage
- white matter
- living cells
- dna damage
- induced apoptosis
- end stage renal disease
- ischemia reperfusion injury
- reactive oxygen species
- brain injury
- newly diagnosed
- ejection fraction
- lipopolysaccharide induced
- chronic kidney disease
- preterm infants
- blood brain barrier
- depressive symptoms
- single molecule
- ultrasound guided
- prognostic factors
- young adults
- hydrogen peroxide
- mild cognitive impairment
- anti inflammatory
- toll like receptor
- spinal cord
- heat shock
- neuropathic pain
- drug induced
- heat shock protein
- fatty acid
- prefrontal cortex
- patient reported