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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 107 (2000), S. 903-917 
    ISSN: 1435-1463
    Keywords: Keywords: Serotonin receptors ; β-adrenoceptors ; DOI ; pindolol ; locomotor activity ; rat.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary. [1] We have previously shown that the β-adrenergic/5-HT1 receptor partial agonist (−)-pindolol (2.0–32.0 μmol kg−1) enhances the increase in forward locomotion in rats produced by the 5-HT2 receptor agonist DOI (0.7 μmol kg−1) via net activation of post-synaptic 5-HT2 receptors. [2] It was found that neither the 5-HT1A receptor agonist and partial agonist, (±) 8-OH-DPAT (0.2–2.4 μmol kg−1) and (S)-(−)-UH-301, respectively, nor the 5-HT1A receptor antagonist WAY-100635 (0.09–1.5 μmol kg−1), substituted for (−)-pindolol in this in vivo behavioral model. [3] This also applies to the 5-HT1B receptor agonist and antagonist anpirtoline (0.3–4.0 μmol kg−1) and isamoltane (1.0–64.0 μmol kg−1), respectively. Neither of these compounds mimicked (−)-pindolol in its interactions with DOI. [4] The (−)-pindolol/DOI-induced increase in forward locomotion could be antagonized by the β1 adrenoceptor antagonist betaxolol (24 μmol kg−1). [5] It is suggested that the intrinsic efficacy of (−)-pindolol at β-adrenoceptors is an important aspect of its in vivo pharmacodynamic profile.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 104 (1997), S. 605-614 
    ISSN: 1435-1463
    Keywords: Serotonin receptors ; autoreceptors ; DOI ; pindolol ; locomotor activity ; rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The present experiments were undertaken in order to examine mechanisms of action for reported interactions between the β-blocker (−)-pindolol and serotonergic agents. It was found that pretreatment with (−)-pindolol (2mg kg−1 s.c.) potentiated the stereotyped forward locomotion induced by the 5-HT2a/c receptor agonist DOI (0.125–1.0mg kg−1 s.c.) in rats observed in an open-field arena. This (−)-pindolol/DOI-induced stereotyped forward locomotion was fully antagonized by the 5-HT2a/c receptor antagonist ritanserin (2mg kg−1 s.c.), suggesting that (−)-pindolol enhances serotonin release, resulting i.a. in postsynaptic 5-HT2a/c receptor activation. This effect by (−)-pindolol is in all probability indirect since this compound lacks affinity for 5-HT2a/c receptors, and could be explained by reported antagonism of inhibitory serotonergic somato-dendritic 5-HT1a autoreceptors, although other possibilities related to 5-HT1b receptors or β-adrenoceptors can not be excluded at this time. Furthermore, (−)-pindolol treatment also enhanced 5-HTP-induced (12.5–100 mg kg−1 i.p.) effects on spontaneous motor activity. These effects, however, were of smaller magnitude, and less consistent than those seen in combination with DOI.
    Type of Medium: Electronic Resource
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