Activation of 5-HT3 receptor by 1-phenylbiguanide increases dopamine release in the rat nucleus accumbens
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Alcohol and the dopamine system
2024, International Review of NeurobiologySerotonin/dopamine interaction: Electrophysiological and neurochemical evidence
2021, Progress in Brain ResearchCitation Excerpt :The 5-HT3 receptor has rapidly emerged as a potential target of diseases related to DA neuron dysfunctions including schizophrenia. To illustrate this interest, we can recall that soon after the determination that 5-HT3 receptors were present in the rat brain in 1987 (Kilpatrick et al., 1987), potentially exerting an excitatory control on the release of neurotransmitters, a couple of studies indicated that 5-HT3 receptors exerted an excitatory control on DA release in the striatum, the Nac or the cortex (Blandina et al., 1989; Chen et al., 1991, 1992). It corresponded also to the identification of a 5-HT3 receptor antagonism in the pharmacological profile of the atypical antipsychotic drug clozapine (Deutch et al., 1991) and the ability of 5-HT3 antagonists to behave as atypical antipsychotics in preclinical studies (Costall et al., 1987, 1990).
Manipulation of gut microbiota blunts the ventilatory response to hypercapnia in adult rats
2019, EBioMedicineCitation Excerpt :We conclude that manipulation of the microbiota by ABX and FMT interventions does not alter the cardiorespiratory response to the vagal afferent pulmonary C-fibre stimulation, notwithstanding evidence of significant disruptions in brainstem monoamine concentrations. Whereas PBG can also induce neurotransmitter release centrally in the nucleus accumbens [74] and the nucleus tractus solitarius [75], we confirmed in our study that cardiorespiratory effects were mediated exclusively by vagal afferent feedback since responses were abolished following bilateral cervical vagotomy. Examination of vagal afferent activation from other peripheral sites, notably the gut, was not performed in this study, but would be interesting to determine in future work.
Serotonergic modulation of the activity of mesencephalic dopaminergic systems: Therapeutic implications
2017, Progress in NeurobiologyCitation Excerpt :Local PBG or methyl-chlorophenylbiguanide or systemic administration of the 5-HT3 receptor agonist 2-Me-5-HT increased DA release in the NAc. This effect was blocked by local application of the 5-HT3 receptor antagonists granisetron, zacopride or ondansetron (Campbell and McBride, 1995; Chen et al., 1991; Jiang et al., 1990). A role for VTA 5-HT3 receptors in facilitating somatodendritic DA release in the same area has also been described (Campbell and McBride, 1995).
Pharmacotherapy for alcohol dependence: A stratified approach
2015, Pharmacology and TherapeuticsUnraveling the modulatory actions of serotonin on male rat sexual responses
2015, Neuroscience and Biobehavioral ReviewsCitation Excerpt :Nevertheless, it seems paradoxical that a neurotransmitter that inhibits sexual behavior stimulates the release of neurotransmitters such as Glu, DA or oxytocin (OT) that have clear sexual facilitative actions! Biochemical investigations have shown that 5-HT2A (De Deurwaerdère and Spampinato, 1999) and 5HT3 receptor stimulation increases DA release in the nucleus accumbens (Imperato and Angelucci, 1989; Jiang et al., 1990; Chen et al., 1991; Parsons and Justice, 1993; Mylecharane, 1996), an important brain area in which DA increases during appetitive and consummatory phases of male sexual behavior (Pfaus et al., 1990; Pleim et al., 1990; Damsma et al., 1992; Wenkstern et al., 1993; Fumero et al., 1994; Mas et al., 1995). OT, as DA, has also clear facilitative effects.
Supported by a research grant from the Aaron Diamond Foundation to E.L.G. We thank Dr. A.M. Etgen for helpul comments.