Effects of acute or chronic administration of risperidone on motor and sexual behavior of male rats
- PMID: 9149311
- DOI: 10.1006/phrs.1996.0101
Effects of acute or chronic administration of risperidone on motor and sexual behavior of male rats
Abstract
A number of experiments were carried out to explore the behavioral profile of a novel antipsychotic, risperidone, after acute or chronic administration, in a dose range of 0.1-10 mg kg-1. This drug did not affect the acquisition and retention of avoidance behaviors in a dose of 0.1 mg kg-1, either after acute or chronic administration. Higher doses induced a inhibited acquisition and a facilitated extinction (only after chronic treatment) of active avoidance behavior, but no significant effect on the retention of passive avoidance responses. In contrast, haloperidol inhibited the acquisition and facilitated the extinction of active avoidance behavior, and reduced the retention of passive avoidance reaction at the dose of 0.1 mg kg-1 injected either acutely or chronically. Ambulation and rearing of rats rated in an open field was increased by risperidone injected acutely at the dose of 1 mg kg-1. Under the same experimental conditions, grooming appeared to be reduced. In the same test, acute or chronic haloperidol 1 or 10 mg kg-1 inhibited all behavioral items. Furthermore, in contrast to haloperidol, the acute or chronic administration of risperidone in a dose range of 0.1-10 mg kg-1 did not substantially induce catalepsy and did not affect apomorphine-induced stereotypies. Also, the dose of 0.1 mg kg-1 induced a facilitation of male sexual behavior by increasing the frequency and reducing the latency of mountings, intromissions and ejaculations, while haloperidol 1 or 10 mg kg-1 inhibited this behavior. These findings suggest that the pharmacological profile of risperidone differs from that of classical neuroleptics, like haloperidol, probably due to different mechanism or site of action.
Similar articles
-
The dose-dependent effect of chronic administration of haloperidol, risperidone, and quetiapine on sexual behavior in the male rat.J Sex Med. 2011 Dec;8(12):3345-53. doi: 10.1111/j.1743-6109.2010.01740.x. Epub 2010 Mar 8. J Sex Med. 2011. PMID: 20233290
-
Behavioral effects of deprenyl in aged rats.Funct Neurol. 1986 Apr-Jun;1(2):165-74. Funct Neurol. 1986. PMID: 3111946
-
Role of neuroactive steroid allopregnanolone in antipsychotic-like action of olanzapine in rodents.Neuropsychopharmacology. 2004 Sep;29(9):1597-609. doi: 10.1038/sj.npp.1300460. Neuropsychopharmacology. 2004. PMID: 15100702
-
Pharmacological profile of the new potent neuroleptic ocaperidone (R 79,598).J Pharmacol Exp Ther. 1992 Jan;260(1):146-59. J Pharmacol Exp Ther. 1992. PMID: 1370538
-
Sex differences in the effects of neuroleptics on escape-avoidance behavior in mice: a review.Pharmacol Biochem Behav. 1999 Dec;64(4):813-20. doi: 10.1016/s0091-3057(99)00144-6. Pharmacol Biochem Behav. 1999. PMID: 10593205 Review.
Cited by
-
Gender dimorphic effect of dopamine D2 and muscarinic cholinergic receptors on memory retrieval.Psychopharmacology (Berl). 2021 Aug;238(8):2225-2234. doi: 10.1007/s00213-021-05847-2. Epub 2021 Apr 23. Psychopharmacology (Berl). 2021. PMID: 33891128
-
Management Strategies for Antipsychotic-Related Sexual Dysfunction: A Clinical Approach.J Clin Med. 2021 Jan 15;10(2):308. doi: 10.3390/jcm10020308. J Clin Med. 2021. PMID: 33467621 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources