Affiliation:
1. Dipartimento di Scienze Farmaceutiche, Università di Salerno, Via Ponte Don Melillo, (84084) Fisciano, Salerno, Italia
2. Istituto Superiore di Sanità, viale Regina Elena 299, (00161) Roma, Italia
Abstract
Abstract
This study investigated the possible role of nitric oxide (NO) in the development of neocortical spike-and-wave spindling episodes (S&W) of DBA/2J mice. The administration of distilled water did not modify either the number or duration of S&W in DBA/2J mice during the whole recording period (240min). l-NG-nitro arginine methyl ester (L-NAME) (3–300 μg/mouse, i.c.v.) dose-dependently reduced the S&W of DBA/2J mice. This effect appeared 30 min after drug administration and lasted for the duration of the recording period (240min). In addition, L-NAME treatment did not induce significant alterations of stereotyped behaviour such as licking, sniffing, chewing or tremors of the head and body and behavioural excitability, whereas the electroencephalogram desynchronized pattern was also significantly reduced. By contrast d-NG-nitro arginine methyl ester at the same doses did not affect S&W of mice. The inhibitory effect of L-NAME on S&W of mice was dose-dependently reversed by l-arginine (L-ARG, 3–300 μg/mouse, i.c.v.) but not by d-arginine. Finally, glyceryl trinitrate on its own (3–300 μg/mouse, i.c.v.) significantly increased the S&W of mice and it was also able to reverse the inhibition on S&W of mice operated by L-NAME. These results provide evidence that NO may play a significant role in the development of brain excitability.
Publisher
Oxford University Press (OUP)
Subject
Pharmaceutical Science,Pharmacology
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