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  • 1
    ISSN: 1435-1463
    Keywords: Seizures ; hyperbaric oxygen ; dopamine ; autoreceptors ; mice
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In the present report we have investigated the effects of apomorphine, (−)3-PPP,L-DOPA and haloperidol on the elicitation of convulsions induced in mice by exposure to oxygen at high pressure (HBO) (5 ata O2). It was found that the administration of apomorphine (0.025–0.1 mg · kg−1 s. c.), (−)3-PPP (4 mg · kg−1 i. p.)L-DOPA (200–400 mg · kg−1 i. p.) as well as halo-peridol (0.25–2.0 mg · kg−1 i. p.) produced a significant protection against HBO-induced convulsions. Haloperidol was the only drug to produce a dose-dependent decrease in respiration, and this effect does probably explain the anticonvulsant effects observed. The low doses at which apomorphine was effective, and the effects produced by (−)3-PPP, indicate an effect mediated via DA autoreceptors. Alternatively, and more likely taking the effects ofL-DOPA into account, the DA receptors involved are sensitive enough to disclose postsynaptic agonist properties of apomorphine and (−)3-PPP at the doses employed.
    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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