2001
DOI: 10.1016/s0006-8993(01)02656-7
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Acute melatonin and para-chloroamphetamine interactions on pineal, brain and serum serotonin levels as well as stress hormone levels

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Cited by 6 publications
(3 citation statements)
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“…At neuroendocrine level AMPH increased in a dose-dependent manner plasma corticosterone levels but had no effects on circulating catecholamine levels. Effects of chronic AMPH on 5-HT and 5-HIAA contents in the hypothalamus are in agreement to previously reported for methamphetamine (MA) (15,16) or AMPH (13) and several observations suggest that serotonergic neurons are responsible of the corticosterone. Serotonin would stimulate CRF release from hypothalamic neurons producing an increase of plasma ACTH and corticosterone (13).…”
Section: Discussionsupporting
confidence: 91%
“…At neuroendocrine level AMPH increased in a dose-dependent manner plasma corticosterone levels but had no effects on circulating catecholamine levels. Effects of chronic AMPH on 5-HT and 5-HIAA contents in the hypothalamus are in agreement to previously reported for methamphetamine (MA) (15,16) or AMPH (13) and several observations suggest that serotonergic neurons are responsible of the corticosterone. Serotonin would stimulate CRF release from hypothalamic neurons producing an increase of plasma ACTH and corticosterone (13).…”
Section: Discussionsupporting
confidence: 91%
“…Moreover a decrease in 5-HT release from synaptosomes of the preoptic and anterior hypothalamic areas was reported after a single dose of MLT (0.5 mg/kg). However, no effect on 5-HT content after MLT administration at high doses (ranging from 10–50 mg/kg) was found in whole mouse brain or in rat cortex, brain stem, pineal gland, or serum (Manzana et al, 2001; Sugden, 1983), although following administration of an even higher dose (60 mg/kg) a decrease in 5-HT release in the hypothalamus, corpus striatum and nucleus accumbens has been reported (Chuang and Lin, 1994). Based on the above-mentioned studies, a lower dose of MLT induces an accumulation of 5-HT in discrete brain areas, but decreased release in synaptic terminals.…”
Section: Discussionmentioning
confidence: 99%
“…Amphetamine, a psychostimulant drug, has been progressively more commonly abused in recent years; it acts in the central nervous system, causing damage to dopaminergic, adrenergic, and serotonergic nerve terminals in many brain areas [11–13]. Growing evidence has shown that acute AMPH exposure is toxic to the dopaminergic system, causing the release of excess dopamine from vesicles, inhibition of mitochondrial function, and the generation of reactive quinines, reactive oxygen species (ROS), and reactive nitrogen (RNS) species [14].…”
Section: Introductionmentioning
confidence: 99%