Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Roberta A. Gillespie"'
Publikováno v:
PLoS ONE, Vol 7, Iss 2, p e32263 (2012)
Alcohol consumption during adolescence has long-term sexually dimorphic effects on anxiety behavior and mood disorders. We have previously shown that repeated binge-pattern alcohol exposure increased the expression of two critical central regulators
Externí odkaz:
https://doaj.org/article/c599aed2153b469aab15a377e155f397
Autor:
Magdalena M Przybycien-Szymanska, Natasha N Mott, Caitlin R Paul, Roberta A Gillespie, Toni R Pak
Publikováno v:
PLoS ONE, Vol 6, Iss 4, p e18350 (2011)
Adolescence is a dynamic and important period of brain development however, little is known about the long-term neurobiological consequences of alcohol consumption during puberty. Our previous studies showed that binge-pattern ethanol (EtOH) treatmen
Externí odkaz:
https://doaj.org/article/1f005883ac9c49b5a2bec370a4cd7de1
Publikováno v:
Brain Research. 1383:13-21
This laboratory showed that ethanol augments apoptosis in fetal rhombencephalic neurons and co-treatment with alpha-lipoic acid (LA) or one of several other antioxidants prevents ethanol-associated apoptosis. Because ethanol increases oxidative stres
Publikováno v:
Developmental Brain Research. 121:133-143
This laboratory previously showed that in utero ethanol exposure severely impairs the development of the cell bodies and projections of serotonin (5-HT) neurons, and that maternal treatment with a 5-HT(1A) agonist prevents many of these abnormalities
Publikováno v:
Alcoholism: Clinical and Experimental Research. 21:1169-1178
In utero ethanol exposure results in a decreased concentration of serotonin (5-HT) in brain regions containing the cell bodies of 5-HT neurons and their cortical projections. The concentration of 5-HT reuptake sites is also reduced in several brain a
Publikováno v:
Alcoholism: Clinical and Experimental Research. 21:452-459
Previously, it was shown that in utero ethanol exposure results in decreased serotonin (5-HT) and altered concentrations of 5-HT reuptake sites and 5-HT 1A receptors in fetal and/or postnatal rats. Because fetal 5-HT is an essential trophic factor, t
Publikováno v:
Alcoholism: Clinical and Experimental Research. 18:47-52
Previous work in this and other laboratories has demonstrated that in utero ethanol exposure adversely affects the development of the serotonergic, dopaminergic, cholinergic, and other neurotransmitter systems. In several of these systems, receptor n
Publikováno v:
Brain research. 1150
Previously, this laboratory demonstrated that ethanol treatment significantly reduces the number of developing serotonin (5-HT) and other fetal rhombencephalic neurons in rats by augmenting apoptosis. Using a 5-HT 1A agonist we were able to attenuate
Publikováno v:
Brain research. 1092(1)
Previously, this laboratory demonstrated that ethanol reduces the number of developing serotonin (5-HT)-containing neurons by increasing apoptosis. We also found that 5-HT(1A) agonists attenuate the proapoptotic effects of ethanol and the ethanol-med
Publikováno v:
Brain research. Developmental brain research. 159(1)
Previously, this laboratory demonstrated that developing serotonin (5-HT) neurons and other fetal rhombencephalic neurons are reduced by in vivo and in vitro exposure to ethanol, effects that are related to ethanol's augmentation of apoptosis. We als