Abstract
In agreement with previous results from this laboratory, the ergot derivative lisuride (0.4 mg/kg IP) and the ergot congener 8-OH-DPAT (0.25 mg/kg IP) produced a marked facilitation of male rat sexual behavior. Furthermore, another ergot compound, the dopamine-2 selective agonist LY-141865 (2.5–20 mg/kg IP), was shown to facilitate male rat sexual behavior to the same degree. Neither the effects produced by LY-141865, nor the effects produced by lisuride or 8-OH-DPAT, were antagonized by pretreatment with the dopamine receptor blocking agent haloperidol, 0.16 mg/kg IP. A higher dose of haloperidol (0.32 mg IP), which produced clear extrapyramidal symptoms, was also ineffective in antagonizing the lisuride- or 8-OH-DPAT-induced facilitation of male rat sexual behavior. It is concluded that the stimulation of male rat sexual behavior produced by ergot and ergot-like drugs is mediated via a non-dopaminergic mechanism.
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Ahlenius, S., Larsson, K. Lisuride, LY-141865, and 8-OH-DPAT facilitate male rat sexual behavior via a non-dopaminergic mechanism. Psychopharmacology 83, 330–334 (1984). https://doi.org/10.1007/BF00428540
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DOI: https://doi.org/10.1007/BF00428540