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Showing papers by "Eero Vasar published in 1999"


Journal ArticleDOI
TL;DR: It is concluded that methylene blue inhibits brain NOS activity in vivo and thus interferes with NO-cGMP cascade in different levels.

62 citations


Journal ArticleDOI
TL;DR: Morphine induces a potent anxiolytic-like action in the elevated plus-maze and cholecystokinin is acting as an endogenous antagonist of this effect of morphine.

59 citations


Journal ArticleDOI
TL;DR: D1 and D1 receptors are involved in the expression of apomorphine-induced behavioural sensitization and the established changes of stereotyped behaviour did not correlate with the increase of locomotor activity, suggesting at least three different molecular targets are involved.

21 citations


Journal ArticleDOI
TL;DR: It is likely that the anti-exploratory action of a low dose of paroxetine is not related to the increase in anxiety, but rather to the reduction of exploratory drive, and evidence exists that this effect of paroxin is mediated via the activation of CCK-ergic transmission.
Abstract: The administration of paroxetine (0.5–8 mg/kg), a selective 5-HT reuptake inhibitor, induced a dose-dependent reduction of exploratory activity of rats in the motility test. In the elevated plus-maze paroxetine was less effective, only 8 mg/kg of paroxetine decreased the exploratory behaviour of rats. The doses of paroxetine (2–8 mg/kg) reducing the exploratory activity in the motility test increased the density of CCK receptors in the frontal cortex, but not in the hippocampus. The treatment of rats with the CCKB receptor antagonist LY288,513 (0.01–1 mg/kg) did not change the exploratory activity. However, the reduction of exploratory activity induced by the low dose of paroxetine (2 mg/kg), but not by the higher dose (8 mg/kg), was dose-dependently reversed by the administration of LY288,513. Moreover, LY288,513 did not affect the anti-exploratory action of paroxetine (8 mg/kg) in the elevated plus-maze. Diazepam at doses (0.5–1.0 mg/kg) not suppressing the locomotor activity did not change the anti-exploratory action of paroxetine in the motility test. It is likely that the anti-exploratory action of a low dose of paroxetine (2 mg/kg) is not related to the increase in anxiety, but rather to the reduction of exploratory drive. Evidence exists that this effect of paroxetine is mediated via the activation of CCK-ergic transmission.

14 citations


Journal ArticleDOI
TL;DR: The antagonism of CCK agonists against naloxone-precipitated jumping behaviour is apparently mediated via the CCK(A) receptor subtype, which seems to increase the release of endogenous enkephalins.

11 citations