Acute and repeated exposure with the nitric oxide (NO) donor sodium nitroprusside (SNP) differentially modulate responses in a rat model of anxiety

• Published in: Nitric oxide Vol. 69; pp. 56 - 60
• Main Authors: Orfanidou, Martha A., Lafioniatis, Anastasios, Trevlopoulou, Aikaterini, Touzlatzi, Ntilara, Pitsikas, Nikolaos
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 30.09.2017
• Subjects: Animals; Anxiety; Anxiety - drug therapy; Light/dark test; Locomotion - drug effects; Male; Nitric oxide; Nitric Oxide Donors - administration & dosage; Nitric Oxide Donors - therapeutic use; Nitroprusside - administration & dosage; Nitroprusside - therapeutic use; Rat; Rats, Wistar; Sodium nitroprusside; Time and Motion Studies; Sodium nitroprusside; Anxiety; Rat; Light/dark test; Nitric oxide
• DOI: 10.1016/j.niox.2017.05.002
• ISSN: 1089-8603

The nitric oxide (NO) donor sodium nitroprusside (SNP) actually is under investigation for the treatment of schizophrenia. That anxiety disorders are noted to occur commonly in schizophrenia patients is known. Contradictory results were reported however, concerning the effects of SNP in animal models of anxiety disorders. The present study investigated the effects of acute and repeated administration of SNP on anxiety-like behaviour in rats assessed in the light/dark test. The effects of SNP on motility in a locomotor activity chamber were also investigated in rats. Acute administration of 1 mg/kg SNP 30 but not 60 min before testing induced anxiolytic-like behaviour which cannot be attributed to changes in locomotor activity. Conversely, a single injection of 3 mg/kg SNP at 30 min before testing depressed rats' general activity, while at 60 min this dose did not influence performance of animals either in the light/dark or in the motor activity test. Repeated application of SNP (1 and 3 mg/kg, for 5 consecutive days) did not alter rodents' performance in the above described behavioural paradigms. The present results suggest that the effects exerted by SNP in the light/dark test in rats are dose, time and treatment schedule-dependent. The current findings propose also a narrow therapeutic window for SNP in this animal model of anxiety. •The effects of the nitric oxide donor SNP on anxiety were studied.•Acute exposure to SNP induced anxiolysis in rats.•These effects seem to be time and dose dependent.•Repeated exposure to SNP did not alter anxiety in rats.