Henning Sommermeyer

Effects of prazosin on the dopaminergic neurotransmission in rat brain.

Effects of systemic and local administration of prazosin, an alpha 1-adrenoceptor antagonist, on dopaminergic neurotransmission in the caudate putamen and nucleus accumbens were characterized in microdialysis experiments. Prazosin (10 mg/kg s.c.) resulted in blood pressure reduction, however, did not alter dopamine release in the two examined brain areas. In contrast, local administration of prazosin (10 microM) via the microdialysis probe resulted in a clear attenuation of dopamine output, indicating that tonically activated alpha 1-adrenoceptors stimulate dopamine release in the caudate putamen as well as in the nucleus accumbens. The relevance of this finding for antipsychotics exhibiting antagonism at alpha 1-adrenoceptors is discussed.

Anxiolytic effects of the 5-HT1A receptor agonist ipsapirone in the rat: neurobiological correlates

Ipsapirone, a 5-HT1A receptor agonist, is a psychoactive compound with anxiolytic and antidepressive properties. Concerning the mechanism of action of ipsapirone, most studies point towards an interaction with the central serotonergic system. For characterization of the anxiolytic properties of ipsapirone, the ultrasonic vocalization test, a rat model based on conditioned anxiety, was used. In this test ipsapirone time and dose dependently inhibited the shock induced ultrasonic vocalization of rats after systemic application of ipsapirone, indicating its potent anxiolytic properties. To gain further insight into the mechanism underlying the anxiolytic activity of ipsapirone, the effects of this compound on the central serotonergic system of rats were characterized. Extracellular single unit recordings, measuring the firing rate of serotonergic dorsal raphe neurons in anaesthetized rats, showed that ipsapirone dose and time dependently suppressed neuronal firing. In the hippocampus, one of the projection areas of the serotonergic dorsal raphe neurons, systemic application of ipsapirone resulted in a dose- and time-dependent reduction in serotonergic neurotransmission, measured as a reduced serotonin output in microdialysis experiments with freely moving rats. The time- and dose-effect curves reflecting the anxiolytic, electrophysiological, and biochemical effects correlated well with each other for different doses of ipsapirone. It is concluded that ipsapirone exhibits its anxiolytic effects, at least partially, by stimulating presynaptic somatodendritic 5-HT1A receptors in the brain stem raphe nuclei (i.e., the dorsal raphe), resulting in attenuation of presynaptic cell firing and subsequent inhibition of serotonergic neurotransmission in the limbic system (i.e., the hippocampus).