2022
DOI: 10.1007/112_2022_72
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Role of Oxytocin in Different Neuropsychiatric, Neurodegenerative, and Neurodevelopmental Disorders

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Cited by 10 publications
(6 citation statements)
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“…The potential clinical usefulness of OT as adjunctive drug therapy in PD patients would be therefore based also on the possibility to reduce the dopaminergic therapy side effects, including the impulsivity disorders mainly in patients with addictive behaviors. As a matter of fact, evidence in animal PD models is provided that OT administration may possess neuroprotective effects on dopaminergic neurons related to anti-inflammatory, antioxidant, and anti-apoptotic activities [103], that dopamine levels increased when OT was administrated [104], that the OT levels were decreased in the models, that OT supplementation rescued locomotor disabilities and anxiety-like behaviors [101], and that after intranasal administration OT concentrates in brain regions including the striatum [105]; nevertheless, studies investigating OT in PD clinical settings are still needed [106]. In fact, critical examinations appear fundamental for enabling the utilization of OT mechanisms as a curative tool in psychiatric disorders, in particular when considering that the understanding of how OT impacts social behavior is still insufficient, life experience can change the OT systems function, and the OT effects appear highly context-dependent [107].…”
Section: Potential Relevance Of Striatal Astrocytic D2-otr Heteromersmentioning
confidence: 99%
“…The potential clinical usefulness of OT as adjunctive drug therapy in PD patients would be therefore based also on the possibility to reduce the dopaminergic therapy side effects, including the impulsivity disorders mainly in patients with addictive behaviors. As a matter of fact, evidence in animal PD models is provided that OT administration may possess neuroprotective effects on dopaminergic neurons related to anti-inflammatory, antioxidant, and anti-apoptotic activities [103], that dopamine levels increased when OT was administrated [104], that the OT levels were decreased in the models, that OT supplementation rescued locomotor disabilities and anxiety-like behaviors [101], and that after intranasal administration OT concentrates in brain regions including the striatum [105]; nevertheless, studies investigating OT in PD clinical settings are still needed [106]. In fact, critical examinations appear fundamental for enabling the utilization of OT mechanisms as a curative tool in psychiatric disorders, in particular when considering that the understanding of how OT impacts social behavior is still insufficient, life experience can change the OT systems function, and the OT effects appear highly context-dependent [107].…”
Section: Potential Relevance Of Striatal Astrocytic D2-otr Heteromersmentioning
confidence: 99%
“…Oxytocin neurons in the SCN, SON, and PVN project to the PP gland and secrete oxytocin into the circulating blood [7]. A previous study reported the presence of -synuclein-positive deposits in the PP glands of the majority of elderly patients with Parkinson's disease and Lewy body dementia; however, -synuclein-positive deposits were also present in the PP glands of elderly patients without these diseases [44].…”
Section: Discussionmentioning
confidence: 94%
“…Oxytocin is a pleiotropic peptide hormone with broad implications in general health, adaptation, development, behavior, and reproduction [6]. The cell bodies of oxytocin neurons are located in the suprachiasmatic nucleus (SCN), supraoptic nucleus (SON), and paraventricular hypothalamic nucleus (PVN), and their fibers project to various brain regions (to secrete oxytocin as neurotransmitter) or to the posterior pituitary (PP) gland (to secrete oxytocin as hormone into the blood) [7]. Oxytocin is a potential therapeutic target for brain diseases such as Alzheimer's disease and Parkinson's disease in the elderly [7].…”
Section: Introductionmentioning
confidence: 99%
“…The halflife of the drug is 1 -6 min, and the effect of oxytocin depends on the number of oxytocin receptors in the body. When the receptor is saturated, increasing the dose does not enhance uterine contraction, but gives rise to various adverse reactions which limit the clinical application of oxytocin [16].…”
Section: Discussionmentioning
confidence: 99%