Similar behavioural effects of sigma agonists and PCP-like non-competitive NMDA antagonists in guinea-pigs.
P J Brent
Psychopharmacology 1991 DOI: 10.1007/bf02244439 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Experimental animal study Peer reviewed |
|---|---|
| Population | Guinea-pigs |
| Interventions | (+)NANM (-)NANM pentazocine ketamine (+)dizocilpine DTG naloxone hydrochloride haloperidol quinpirole |
| Dose | (+)NANM 1 and 10 mg/kg SC; (-)NANM 1 and 10 mg/kg SC; pentazocine (dose not stated); ketamine 20 mg/kg SC; (+)dizocilpine 0.025, 0.1 and 1 mg/kg SC; DTG 1 and 10 mg/kg SC; naloxone hydrochloride 15 mg/kg SC; haloperidol 1 and 10 mg/kg SC; quinpirole 3 mg/kg IP |
| Key findings | Sigma agonists and PCP-like NMDA antagonists produced sedation, exophthalmos, locomotor depression, flattened posture and flaccidity in guinea-pigs, effects reversed by the dopamine D-2 agonist quinpirole but not by naloxone, haloperidol or DTG. The authors propose these behaviours may be mediated by non-competitive antagonism of the NMDA subtype of glutamate receptors, and note the depressant response contrasts with stimulatory effects of similar doses in other rodent species. |
Abstract
The present study examined the behavioural effects of sigma agonists and PCP-like non-competitive N-methyl-D-aspartate (NMDA) antagonists in guinea-pigs. Subcutaneous (SC) injection of the putative sigma agonist (+)NANM (1 and 10 mg/kg SC) and (-)NANM (1 and 10 mg/kg SC) produced a behavioural response in guinea-pigs which was characterized by sedation and exophthalmos, with locomotor depression, flattened posture and flaccidity, whereas the sigma ligand pentazocine induced sedation but no flattened posture. Ketamine (20 mg/kg SC) and (+)dizocilpine (0.025, 0.1 and 1 mg/kg SC) produced similar effects to those of (+) and (-)NANM. However, the putative sigma receptor ligand DTG (1 and 10 mg/kg SC) had no observable effect on behaviours in guinea-pigs, similar to results for other species. The behavioural effects produced by (+) and (-)NANM were not reversed by injection 1 h later of naloxone hydrochloride (15 mg/kg SC), haloperidol (10 mg/kg SC) or DTG (10 and 30 mg/kg SC), but the effects of all drugs were reversed by the selective dopamine D-2 agonist quinpirole (3 mg/kg IP). Moreover, injection of naloxone (15 mg/kg SC), DTG (10 and 30 mg/kg SC) or haloperidol (1 and 10 mg/kg SC) 10 min before, did not reverse the behaviour induced by (+)NANM (10 mg/kg SC). These data indicate that sigma and PCP-like drugs have a similar gross behavioural effect in guinea-pigs, possibly mediated by non-competitive antagonism of the NMDA subtype of glutamate receptors. The results demonstrating behavioural depression were in contrast to the stimulatory effects of these drugs at similar doses in other rodent species.(ABSTRACT TRUNCATED AT 250 WORDS)
Citations in the library
Cites 4
- Sigma binding states in the brain; An emerging concept for multiple sites and their relevance for psychiatric disorders Life Sciences 1990
- Specificity of phencyclidine-like drugs and benzomorphan opiates for two high affinity phencyclidine binding sites in guinea pig brain. Neuropharmacology September 1, 1990
- MK-801, a proposed noncompetitive antagonist of excitatory amino acid neurotransmission, produces phencyclidine-like behavioral effects in pigeons, rats and rhesus monkeys. Journal of Pharmacology and Experimental Therapeutics June 1, 1988
- Sigma receptors mediated the psychotomimetic effects of N-allylnormetazocine (SKF-10,047), but not its opioid agonistic-antagonistic properties. Neuropharmacology August 1, 1984