NKP608, an NK1 receptor antagonist, has an anxiolytic action in the social interaction test in rats

• Published in: Psychopharmacologia Vol. 152; no. 1; pp. 105 - 109
• Main Author: FILE, Sandra E
• Format: Journal Article
• Language: English
• Published: Berlin Springer 01.09.2000
• Subjects: Aggression - drug effects; Animals; Anti-Anxiety Agents - adverse effects; Anti-Anxiety Agents - pharmacology; Biological and medical sciences; Interpersonal Relations; Male; Medical sciences; Motor Activity - drug effects; Neurokinin-1 Receptor Antagonists; Neuropharmacology; Pharmacology. Drug treatments; Piperidines - adverse effects; Piperidines - pharmacology; Psycholeptics: tranquillizer, neuroleptic; Psychology. Psychoanalysis. Psychiatry; Psychopharmacology; Quinolines - adverse effects; Quinolines - pharmacology; Rats; Substance Withdrawal Syndrome - psychology; Mood disorder; NK1 Tachykinin receptor; Psychotropic; Substance P; Toxicity; Detoxification; Oral administration; Long term; Biological activity; Locomotion; Chemotherapy; Treatment; Tranquillizer; Social interaction; Anxiety; Antagonist; Withdrawal syndrome
• ISSN: 0033-3158; 1432-2072
• DOI: 10.1007/s002130000513

Evidence is starting to accumulate that NK1 receptor antagonists might have anxiolytic effects in animal tests and in patients. To examine the effects of NKP608, a substance P antagonist acting at NK1 receptors, in various conditions of the social interaction test of anxiety and to determine its effects after 3 and 6 weeks of treatment. Rats were tested after vehicle, 0.01 or 0.1 mg/kg PO in three conditions of the social interaction test that varied in the level of anxiety generated. Thus pairs of rats were tested in an arena with which they were unfamiliar that was lit by high (HU) or low (LU) light and in the condition that generated the lowest level of anxiety, i.e. an arena with which they were familiar, lit by low light (LF). They were also tested after 3 and 6 weeks of treatment with 0.03 mg/kg and after 24 h withdrawal from these chronic treatments. NKP608 had significant anxiolytic effects at 0.01, 0.03 and 0.1 mg/kg PO in the HU and LU test conditions, but was without effect in the LF condition, except for an increased incidence of bite attacks at 0.1 mg/kg. The anxiolytic effect of 0.03 mg/kg remained after 3 weeks of chronic treatment and there was no anxiogenic effect after 24 h of drug withdrawal. Following 6 weeks of chronic treatment (0.03 mg/kg per day), tolerance had developed, but no anxiogenic withdrawal effect was seen 24 h after the last dose. These results provide further evidence that substance P may play a role in mediating states of anxiety and suggest that the selective NK1 receptor antagonist NKP608 may prove a useful anxiolytic compound.