Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Sarah E. Ewin"'
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract The hippocampus, particularly its ventral domain, can promote negative affective states (i.e. stress and anxiety) that play an integral role in the development and persistence of alcohol use disorder (AUD). The ventral hippocampus (vHC) rece
Externí odkaz:
https://doaj.org/article/5bdbf50f124842879e22fae4bd1617a8
Autor:
Eva C. Bach, James W. Morgan, Sarah E. Ewin, Samuel H. Barth, Kimberly F. Raab-Graham, Jeffrey L. Weiner
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Alcohol use disorder (AUD) differentially impacts men and women and a growing body of evidence points to sex-dependent adaptations in a number of brain regions. In a prior study, we explored the effect of a chronic intermittent ethanol exposure (CIE)
Externí odkaz:
https://doaj.org/article/1d7ec75b247746a8bacf13b46d437538
Autor:
Eva C. Bach, Sarah E. Ewin, Chelcie F. Heaney, Hannah N. Carlson, Olivia A. Ortelli, Antoine G. Almonte, Ann M. Chappell, Kimberly F. Raab‐Graham, Jeffrey L. Weiner
Publikováno v:
European Journal of Neuroscience. 57:1241-1259
Autor:
null Eva C. Bach, null Sarah E. Ewin, null Chelcie F. Heaney, null Hannah N. Carlson, null Olivia A. Ortelli, null Antoine G. Almonte, null Ann M. Chappell, null Kimberly F. Raab‐Graham, null Jeffrey L. Weiner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53eeb787490f510c786b12dcae16df4d
https://doi.org/10.1111/ejn.15944/v2/response1
https://doi.org/10.1111/ejn.15944/v2/response1
Autor:
Nathan P McMullen, Antoine G. Almonte, James W. Morgan, Jeff L. Weiner, Kimberly F. Raab-Graham, Samuel H. Barth, Farr Nierre, Sarah E. Ewin
Publikováno v:
Neuroscience. 398:144-157
Many studies have implicated hippocampal dysregulation in the pathophysiology of alcohol use disorder (AUD). However, over the past twenty years, a growing body of evidence has revealed distinct functional roles of the dorsal (dHC) and ventral (vHC)
Autor:
Samuel H. Barth, Kimberly F. Raab-Graham, Eva C. Bach, Sarah E. Ewin, Jeff L. Weiner, James W. Morgan
Publikováno v:
Frontiers in Neuroscience
Frontiers in Neuroscience, Vol 15 (2021)
Frontiers in Neuroscience, Vol 15 (2021)
Alcohol use disorder (AUD) differentially impacts men and women and a growing body of evidence points to sex-dependent adaptations in a number of brain regions. In a prior study, we explored the effect of a chronic intermittent ethanol exposure (CIE)
Autor:
Eva C. Bach, Sarah E. Ewin, Chelcie F. Heaney, Hannah N. Carlson, Antoine G. Almonte, Ann M. Chappell, Kimberly F. Raab-Graham, Jeffrey L. Weiner
Alcohol use disorder (AUD) and anxiety/stressor disorders frequently co-occur and this dual diagnosis represents a major health and economic problem worldwide. The basolateral amygdala (BLA) is a key brain region that is known to contribute to the et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40e56ee1f1394b906e4321eeb76d155e
https://doi.org/10.1101/529719
https://doi.org/10.1101/529719
Publikováno v:
Experimental and Clinical Psychopharmacology. 23:387-394
Environmental enrichment has previously been shown to alter sensitivity to psychostimulants and opiates in various preclinical models. However, little research has been conducted studying the effects of environmental enrichment on the more commonly a
Autor:
Jeff L. Weiner, Sarah E. Ewin, James W. Morgan, Eugenia S. Carter, Antoine G. Almonte, Madelyn I. Mauterer
Publikováno v:
Scientific Reports
Scientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
Scientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
It has long been appreciated that adolescence represents a uniquely vulnerable period when chronic exposure to stressors can precipitate the onset of a broad spectrum of psychiatric disorders and addiction in adulthood. However, the neurobiological s
Publikováno v:
Hippocampus. 27(12)
Glucagon-like peptide-1 (GLP-1) is an endogenous gut hormone and a key regulator in maintaining glucose homeostasis by stimulating insulin secretion. Its natural cleavage product GLP-1 (9-36), used to be considered a "bio-inactive" metabolite mainly