8 research outputs found

    Physiological and pathological aspects of Aβ in iron homeostasis via 5'UTR in the APP mRNA and the therapeutic use of iron-chelators

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    Many studies have highlighted the pathological involvement of iron accumulation and iron-related oxidative stress (OS) in Alzheimer's disease (AD). Iron was further demonstrated to modulate expression of the Alzheimer's amyloid precursor holo-protein (APP) by a mechanism similar to that of regulation of ferritin-L and -H mRNA translation through an iron-responsive element (IRE) in their 5' untranslated regions (UTRs). Here, we discuss two aspects of the link between iron and AD, in relation to the recently discovered IRE in the 5'UTR of APP mRNA. The first is the physiological aspect: a compensatory neuroprotective response of amyloid-β protein (Aβ) in reducing iron-induced neurotoxicity. Thus, given that Aβ possesses iron chelation sites, it is hypothesized that OS-induced intracellular iron may stimulate APP holo-protein translation (via the APP 5'UTR) and subsequently the generation of its cleavage product, Aβ, as a compensatory response that eventually reduces OS. The second is the pathological aspect: iron chelating compounds target the APP 5'UTR and possess the capacity to reduce APP translation, and subsequently Aβ levels, and thus represent molecules with high potential in the development of drugs for the treatment of AD

    MONOAMINE-OXIDASE INHIBITORS AND PROLACTIN SECRETION

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    SCOPUS: le.jinfo:eu-repo/semantics/publishe

    Anti-depressant potentiation of 5-hydroxytryptophan by L-deprenyl, an MAO "type B" inhibitor

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    SCOPUS: ar.jinfo:eu-repo/semantics/publishe

    A double-blind placebo study of L-deprenyl in affective disorders

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    The degree of platelet MAO inhibition may be useful as a biological peripheral marker to distinguish responders from nonresponders in MAO-B inhibitor therapy. Furthermore, the good tolerance and the absence of 'cheese effect' observed with L-deprenyl is of great interest for the pharmacological treatment of depressive illness.SCOPUS: NotDefined.jinfo:eu-repo/semantics/publishe
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