Binge‐Pattern Ethanol Exposure During Adolescence, but Not Adulthood, Causes Persistent Changes in GABAA Receptor‐Mediated Tonic Inhibition in Dentate Granule Cells. (15th February 2013)
- Record Type:
- Journal Article
- Title:
- Binge‐Pattern Ethanol Exposure During Adolescence, but Not Adulthood, Causes Persistent Changes in GABAA Receptor‐Mediated Tonic Inhibition in Dentate Granule Cells. (15th February 2013)
- Main Title:
- Binge‐Pattern Ethanol Exposure During Adolescence, but Not Adulthood, Causes Persistent Changes in GABAA Receptor‐Mediated Tonic Inhibition in Dentate Granule Cells
- Authors:
- Fleming, Rebekah L.
Li, Qiang
Risher, Mary‐Louise
Sexton, Hannah G.
Moore, Scott D.
Wilson, Wilkie A.
Acheson, Shawn K.
Swartzwelder, H. Scott - Abstract:
- <abstract abstract-type="main" xml:lang="en" id="acer12087-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="acer12087-sec-0001" sec-type="section"> <title>Background</title> <p>In recent years, it has become clear that acute ethanol (EtOH) affects various neurobiological and behavioral functions differently in adolescent animals than in adults. However, less is known about the long‐term neural consequences of chronic EtOH exposure during adolescence, and most importantly whether adolescence represents a developmental period of enhanced vulnerability to such effects.</p> </sec> <sec id="acer12087-sec-0002" sec-type="section"> <title>Methods</title> <p>We made whole‐cell recordings of GABA<sub>A</sub> receptor‐mediated tonic inhibitory currents from dentate gyrus granule cells (DGGCs) in hippocampal slices from adult rats that had been treated with chronic intermittent ethanol (CIE) or saline during adolescence, young adulthood, or adulthood.</p> </sec> <sec id="acer12087-sec-0003" sec-type="section"> <title>Results</title> <p>CIE reduced baseline tonic current amplitude in DGGCs from animals pretreated with EtOH during adolescence, but not in GCs from those pretreated with EtOH during young adulthood or adulthood. Similarly, the enhancement of tonic currents by acute EtOH exposure ex vivo was increased in GCs from animals pretreated with EtOH during adolescence, but not in those from animals pretreated during either of the other 2 developmental<abstract abstract-type="main" xml:lang="en" id="acer12087-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="acer12087-sec-0001" sec-type="section"> <title>Background</title> <p>In recent years, it has become clear that acute ethanol (EtOH) affects various neurobiological and behavioral functions differently in adolescent animals than in adults. However, less is known about the long‐term neural consequences of chronic EtOH exposure during adolescence, and most importantly whether adolescence represents a developmental period of enhanced vulnerability to such effects.</p> </sec> <sec id="acer12087-sec-0002" sec-type="section"> <title>Methods</title> <p>We made whole‐cell recordings of GABA<sub>A</sub> receptor‐mediated tonic inhibitory currents from dentate gyrus granule cells (DGGCs) in hippocampal slices from adult rats that had been treated with chronic intermittent ethanol (CIE) or saline during adolescence, young adulthood, or adulthood.</p> </sec> <sec id="acer12087-sec-0003" sec-type="section"> <title>Results</title> <p>CIE reduced baseline tonic current amplitude in DGGCs from animals pretreated with EtOH during adolescence, but not in GCs from those pretreated with EtOH during young adulthood or adulthood. Similarly, the enhancement of tonic currents by acute EtOH exposure ex vivo was increased in GCs from animals pretreated with EtOH during adolescence, but not in those from animals pretreated during either of the other 2 developmental periods.</p> </sec> <sec id="acer12087-sec-0004" sec-type="section"> <title>Conclusions</title> <p>These findings underscore our recent report that CIE during adolescence results in enduring alterations in tonic current and its acute EtOH sensitivity and establish that adolescence is a developmental period during which the hippocampal formation is distinctively vulnerable to long‐term alteration by chronic EtOH exposure.</p> </sec> </abstract> … (more)
- Is Part Of:
- Alcoholism. Volume 37:Number 7(2013:Jul.)
- Journal:
- Alcoholism
- Issue:
- Volume 37:Number 7(2013:Jul.)
- Issue Display:
- Volume 37, Issue 7 (2013)
- Year:
- 2013
- Volume:
- 37
- Issue:
- 7
- Issue Sort Value:
- 2013-0037-0007-0000
- Page Start:
- 1154
- Page End:
- 1160
- Publication Date:
- 2013-02-15
- Subjects:
- Alcoholism -- Periodicals
Alcoholism -- Periodicals
Alcoolisme
Electronic journals
Périodique électronique (Descripteur de forme)
Ressource Internet (Descripteur de forme)
616.861005 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=0145-6008;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1530-0277 ↗
http://www.alcoholism-cer.com/ ↗
http://www.blackwell-synergy.com/loi/acer ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/acer.12087 ↗
- Languages:
- English
- ISSNs:
- 0145-6008
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0786.789300
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3133.xml