2004
DOI: 10.1016/j.neuropharm.2004.03.014
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Facilitation of cholinergic transmission by combined treatment of ondansetron with flumazenil after cortical cholinergic deafferentation

Abstract: We have studied the effects of concomitant blockade of 5-HT 3 and GABA A receptors on acetylcholine (ACh) release in the frontal cortex of rats with a selective cholinergic lesion. Lesions were performed by microinjection of the cholinergic toxin 192 IgG-saporin into the nucleus basalis magnocellularis. Single treatment with either the 5-HT 3 receptor antagonist ondansetron, 0.1 lg/kg, or the GABA A receptor benzodiazepine site antagonist flumazenil, 10 mg/kg, did not affect ACh release. However, the combined … Show more

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Cited by 16 publications
(11 citation statements)
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“…All the aforementioned groups of animals under study consisted of half number of Sham-operated rats and half number of 192 IgG-saporin-treated rats. To assess the extent and selectivity of the cholinergic lesion, AChE activity in hippocampus as described previously (Gil-Bea et al, 2004) and cholinacetyltransferase (ChAT)-ir cells in MS were measured.…”
Section: Cholinergic Lesion Proceduresmentioning
confidence: 99%
“…All the aforementioned groups of animals under study consisted of half number of Sham-operated rats and half number of 192 IgG-saporin-treated rats. To assess the extent and selectivity of the cholinergic lesion, AChE activity in hippocampus as described previously (Gil-Bea et al, 2004) and cholinacetyltransferase (ChAT)-ir cells in MS were measured.…”
Section: Cholinergic Lesion Proceduresmentioning
confidence: 99%
“…Many studies showed that 5-HT 3 antagonists enhance cognitive functions and alleviate cognitive deficits associated with aging or the drug treatments in various animal models (e.g., Morris water maze test and novel object recognition test) (Table 3) (Arnsten et al, 1997;Barnes et al, 1990;Gil-Bea et al, 2004;Hodges et al, 1996).…”
Section: -Ht 3 Receptorsmentioning
confidence: 99%
“…the 5-HT 1 , 5-HT 1B , α 1 -adrenergic, µ-opioid receptors, and α7 and α4β2 nicotinic receptors [16]. This means that this medication may have anxiolytic, antidepressant, and anti-nociceptive properties [17]; furthermore, it can cause release of acetylcholine [18]. Another postulated mechanism for the anxiolytic and antidepressant activities is that the antagonism at 5-HT 3 receptor increases the synaptic concentration of the neurotransmitter that is made available to bind elsewhere [19].…”
Section: Introductionmentioning
confidence: 99%