alpha-Ketoadipic Acid and alpha-Aminoadipic Acid Cause Disturbance of Glutamatergic Neurotransmission and Induction of Oxidative Stress In Vitro in Brain of Adolescent Rats

作者：da Silva Janaina Camacho; Amaral Alexandre Umpierrez; Cecatto Cristiane; Wajner Alessandro; Godoy Kalita dos Santos; Ribeiro Rafael Teixeira; Goncalves Aline de Mello; Zanatta Angela; da Rosa Mateus Struecker; Loureiro Samanta Oliveira; Vargas Carmen Regla; Leipnitz Guilhian; Gomes de Souza Diogo Onofre; Wajner Moacir

来源：Neurotoxicity Research, 2017, 32(2): 276-290.

DOI：10.1007/s12640-017-9735-8

• alpha-Ketoadipic aciduria
• alpha-Ketoadipic acid
• alpha-Aminoadipic acid
• Glutamatergic neurotransmission
• Redox homeostasis
• Bioenergetics

Tissue accumulation of alpha-ketoadipic (KAA) and alpha-aminoadipic (AAA) acids is the biochemical hallmark of alpha-ketoadipic aciduria. This inborn error of metabolism is currently considered a biochemical phenotype with uncertain clinical significance. Considering that KAA and AAA are structurally similar to alpha-ketoglutarate and glutamate, respectively, we investigated the in vitro effects of these compounds on glutamatergic neurotransmission in the brain of adolescent rats. Bioenergetics and redox homeostasis were also investigated because they represent fundamental systems for brain development and functioning. We first observed that AAA significantly decreased glutamate uptake, whereas glutamate dehydrogenase activity was markedly inhibited by KAA in a competitive fashion. In addition, AAA and more markedly KAA induced generation of reactive oxygen and nitrogen species (increase of 2',7'-dichloroflurescein (DCFH) oxidation and nitrite/nitrate levels), lipid peroxidation (increase of malondialdehyde concentrations), and protein oxidation (increase of carbonyl formation and decrease of sulfhydryl content), besides decreasing the antioxidant defenses (reduced glutathione (GSH)) and aconitase activity. Furthermore, KAA-induced lipid peroxidation and GSH decrease were prevented by the antioxidants alpha-tocopherol, melatonin, and resveratrol, suggesting the involvement of reactive species in these effects. Noteworthy, the classical inhibitor of NMDA glutamate receptors MK-801 was not able to prevent KAA-induced and AAA-induced oxidative stress, determined by DCFH oxidation and GSH levels, making unlikely a secondary induction of oxidative stress through overstimulation of glutamate receptors. In contrast, KAA and AAA did not significantly change brain bioenergetic parameters. We speculate that disturbance of glutamatergic neurotransmission and redox homeostasis by KAA and AAA may play a role in those cases of alpha-ketoadipic aciduria that display neurological symptoms.

• 出版日期2017-8