Lidocaine protects neurons of the spinal cord in an excitotoxicity model

NISHIDA, FABIÁN; CANTET, RODOLFO J.C.; NISHIDA, FABIÁN; CANTET, RODOLFO J.C.; ZANUZZI, CAROLINA N.; PORTIANSKY, ENRIQUE L.; ZANUZZI, CAROLINA N.; PORTIANSKY, ENRIQUE L.; SISTI, MARÍA S.; LAURELLA, SERGIO L.; SISTI, MARÍA S.; LAURELLA, SERGIO L.

NEUROSCIENCE LETTERS

ELSEVIER IRELAND LTD

Año: 2019 vol. 698 p. 105 - 112

0304-3940

Motor Neuron Disease disorders, described in domestic animals, are characterized by neuronal degeneration at the spinal cord. Excitotoxicity is a crucial factor for the selective loss of these neurons, being the fundamental processes involved in lesion progression after spinal cord injury, where glutamate is one of the main neurotransmitters involved. Kainic acid (KA) resembles the effects induced by the pathological release of glutamate. Lidocaine administered by different routes exerts some neuroprotective effects in the CNS. The aim of the present work was to determine whether lidocaine simultaneously injected with KA into the spinal cord could prevent the excitotoxic effects of the latter. Sprague-Dawley rats were injected by intraparenchymal route with KA or with KA plus 0.5% lidocaine into the C5 segment. Sham rats were injected with saline. Animals were motor and sensory tested at 0, 1, 2, 3, 7 and 14 post-injection days and then euthanized. Sections of the C5 segment were used for histological and immunohistochemical analysis. No KA-induced motor and sensitive impairments were observed when lidocaine was simultaneously injected with KA. Moreover, neuronal counting was statistically higher when compared with KA-injected animals. Thus, lidocaine could be considered as a neuroprotective drug in diseases and models involving excitotoxicity.