Allopregnanolone induces a diurnally dependent hyperphagic effect and alters feeding latency and duration in male Wistar rats. (17th April 2013)
- Record Type:
- Journal Article
- Title:
- Allopregnanolone induces a diurnally dependent hyperphagic effect and alters feeding latency and duration in male Wistar rats. (17th April 2013)
- Main Title:
- Allopregnanolone induces a diurnally dependent hyperphagic effect and alters feeding latency and duration in male Wistar rats
- Authors:
- Holmberg, E.
Bäckström, T.
Johansson, M.
Löfgren, M.
Haage, D. - Abstract:
- <abstract abstract-type="main" xml:lang="en" id="apha12100-abs-0001"> <title>Abstract</title> <sec id="apha12100-sec-0001" sec-type="section"> <title>Aim</title> <p>Gamma‐aminobutyric acid (GABA)‐ergic transmission from the hypothalamus is essential for normal feeding regulation, and hyperphagia can be induced by local application of GABA<sub>A</sub>‐receptor agonists to different feeding‐associated brain areas. The food intake in rats varies diurnally and that may influence the effect of GABA<sub>A</sub>‐receptor active compounds. The progesterone metabolite allopregnanolone is a highly potent endogenous positive modulator of the GABA<sub>A</sub> receptor. Therefore, it is easy to envisage that allopregnanolone would have a hyperphagic effect, but earlier reports in rat have given ambiguous results. However, a contributing factor for the discrepancy may be the time point of the diurnal cycle in which the experiments were performed. The aim of this study was to investigate the effect of allopregnanolone on intake of standard chow in male Wistar rats at different time points of the day.</p> </sec> <sec id="apha12100-sec-0002" sec-type="section"> <title>Methods</title> <p>Chow intake was measured after acute administration of allopregnanolone, and feeding behaviour was analysed to detect meal patterns.</p> </sec> <sec id="apha12100-sec-0003" sec-type="section"> <title>Results</title> <p>We found that allopregnanolone increased chow intake by up to four times in the dark part<abstract abstract-type="main" xml:lang="en" id="apha12100-abs-0001"> <title>Abstract</title> <sec id="apha12100-sec-0001" sec-type="section"> <title>Aim</title> <p>Gamma‐aminobutyric acid (GABA)‐ergic transmission from the hypothalamus is essential for normal feeding regulation, and hyperphagia can be induced by local application of GABA<sub>A</sub>‐receptor agonists to different feeding‐associated brain areas. The food intake in rats varies diurnally and that may influence the effect of GABA<sub>A</sub>‐receptor active compounds. The progesterone metabolite allopregnanolone is a highly potent endogenous positive modulator of the GABA<sub>A</sub> receptor. Therefore, it is easy to envisage that allopregnanolone would have a hyperphagic effect, but earlier reports in rat have given ambiguous results. However, a contributing factor for the discrepancy may be the time point of the diurnal cycle in which the experiments were performed. The aim of this study was to investigate the effect of allopregnanolone on intake of standard chow in male Wistar rats at different time points of the day.</p> </sec> <sec id="apha12100-sec-0002" sec-type="section"> <title>Methods</title> <p>Chow intake was measured after acute administration of allopregnanolone, and feeding behaviour was analysed to detect meal patterns.</p> </sec> <sec id="apha12100-sec-0003" sec-type="section"> <title>Results</title> <p>We found that allopregnanolone increased chow intake by up to four times in the dark part of the 24‐h cycle. The rats ate significantly more, and the effect of allopregnanolone was more prominent in the active (dark) compared with the inactive (light) period. Allopregnanolone also reduced feeding latency and prolonged the meal duration compared with vehicle.</p> </sec> <sec id="apha12100-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Allopregnanolone seems to act at several levels of feeding regulation, that is, to initiate feeding and to prolong the duration of a meal, thereby increasing the meal size, especially in the dark period of the 24‐h cycle.</p> </sec> </abstract> … (more)
- Is Part Of:
- Acta physiologica. Volume 208:Number 4(2013:Aug.)
- Journal:
- Acta physiologica
- Issue:
- Volume 208:Number 4(2013:Aug.)
- Issue Display:
- Volume 208, Issue 4 (2013)
- Year:
- 2013
- Volume:
- 208
- Issue:
- 4
- Issue Sort Value:
- 2013-0208-0004-0000
- Page Start:
- 400
- Page End:
- 409
- Publication Date:
- 2013-04-17
- Subjects:
- Physiology -- Periodicals
Physiology -- Research -- Periodicals
612 - Journal URLs:
- http://www.blackwell-synergy.com/loi/aps ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1748-1716 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/apha.12100 ↗
- Languages:
- English
- ISSNs:
- 1748-1708
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0650.750000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3773.xml