BACKGROUND: It is now widely established the devastating effects of prenatal alcohol exposure on the embryo and fetus development causing marked cognitive and neurobiological deficits in the newborns. The negative effects of the gestational alcohol use have been well documented and known for some time. However, also the subtle role of alcohol consumption by fathers prior to mating is drawing special attention. OBJECTIVE: Both paternal and maternal alcohol exposure have been shown to affect the neurotrophins' signalling pathways in the brain and in target organs of ethanol intoxication. Neurotrophins, in particular nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF), are molecules playing a pivotal role in the survival, development and function of the peripheral and central nervous systems but also in the pathogenesis of developmental defects caused by alcohol exposure. METHODS: New researches from the available literature and experimental data from our laboratory are presented in this review to offer the most recent findings regarding the effects of maternal and paternal prenatal ethanol exposure especially on the neurotrophins' signalling pathways. RESULTS: NGF and BDNF changes play a subtle role in short- and long-lasting effects of alcohol in ethanol target tissues, including neuronal cell death and severe cognitive and physiological deficits in the newborns. CONCLUSIONS: The review suggests a possible therapeutic intervention based on the use of specific molecules with antioxidant properties in order to induce a potential prevention of the harmful effects of the paternal and/or maternal alcohol exposure.

NGF and BDNF Alterations by Prenatal Alcohol Exposure / Carito, Valentina; Ceccanti, Mauro; Ferraguti, Giampiero; Coccurello, Roberto; Ciafre', Stefania; Tirassa, Paola; Fiore, Marco. - In: CURRENT NEUROPHARMACOLOGY. - ISSN 1570-159X. - ELETTRONICO. - 16:(2017). [10.2174/1570159X15666170825101308]

NGF and BDNF Alterations by Prenatal Alcohol Exposure

CECCANTI MAURO;FERRAGUTI GIAMPIERO;COCCURELLO ROBERTO;
2017

Abstract

BACKGROUND: It is now widely established the devastating effects of prenatal alcohol exposure on the embryo and fetus development causing marked cognitive and neurobiological deficits in the newborns. The negative effects of the gestational alcohol use have been well documented and known for some time. However, also the subtle role of alcohol consumption by fathers prior to mating is drawing special attention. OBJECTIVE: Both paternal and maternal alcohol exposure have been shown to affect the neurotrophins' signalling pathways in the brain and in target organs of ethanol intoxication. Neurotrophins, in particular nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF), are molecules playing a pivotal role in the survival, development and function of the peripheral and central nervous systems but also in the pathogenesis of developmental defects caused by alcohol exposure. METHODS: New researches from the available literature and experimental data from our laboratory are presented in this review to offer the most recent findings regarding the effects of maternal and paternal prenatal ethanol exposure especially on the neurotrophins' signalling pathways. RESULTS: NGF and BDNF changes play a subtle role in short- and long-lasting effects of alcohol in ethanol target tissues, including neuronal cell death and severe cognitive and physiological deficits in the newborns. CONCLUSIONS: The review suggests a possible therapeutic intervention based on the use of specific molecules with antioxidant properties in order to induce a potential prevention of the harmful effects of the paternal and/or maternal alcohol exposure.
2017
NGF, BDNF, NEUROTROPHIC FACTORS, ALCOHOL, ADDICTION
01 Pubblicazione su rivista::01a Articolo in rivista
NGF and BDNF Alterations by Prenatal Alcohol Exposure / Carito, Valentina; Ceccanti, Mauro; Ferraguti, Giampiero; Coccurello, Roberto; Ciafre', Stefania; Tirassa, Paola; Fiore, Marco. - In: CURRENT NEUROPHARMACOLOGY. - ISSN 1570-159X. - ELETTRONICO. - 16:(2017). [10.2174/1570159X15666170825101308]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1122342
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