Differences in prefrontal cortex GABA/glutamate ratio after acute restraint stress in rats are associated with specific behavioral and neurobiological patterns. (29th January 2015)
- Record Type:
- Journal Article
- Title:
- Differences in prefrontal cortex GABA/glutamate ratio after acute restraint stress in rats are associated with specific behavioral and neurobiological patterns. (29th January 2015)
- Main Title:
- Differences in prefrontal cortex GABA/glutamate ratio after acute restraint stress in rats are associated with specific behavioral and neurobiological patterns
- Authors:
- Drouet, J.-B.
Fauvelle, F.
Maunoir-Regimbal, S.
Fidier, N.
Maury, R.
Peinnequin, A.
Denis, J.
Buguet, A.
Canini, F. - Abstract:
- Highlights: After 1 h restraint, the rats increased their prefrontal cortex GABA and glutamate contents. The stressed rats can be classified according to GABA/glutamate ratio (High G/g vs. Low G/g). The H-G/g rats presented decreased prefrontal cortex activation and increased HPA axis activation featuring an enhanced stress. The H-G/g rats had a reduced locomotion speed together with neophobia and sustained exploration behavior in open field. The prefrontal G/g ratio might underpin the stress-related inter-individual variability. Abstract: In patients suffering from stress-related pathologies and depression, frontal cortex GABA and glutamate contents are reported to decrease and increase, respectively. This suggests that the GABA and/or glutamate content may participate in pathological phenotype expression. Whether differences in frontal cortex GABA and glutamate contents would be associated with specific behavioral and neurobiological patterns remains unclear, especially in the event of exposure to moderate stress. We hypothesized that an increase in prefrontal cortex GABA/glutamate ratio would be associated with a blunted prefrontal cortex activation, an enhanced hypothalamo-pituitary–adrenocortical (HPA) axis activation and changes in behavior. Rats being restrained for 1-h were then tested in an open-field test in order to assess their behavior while under stress, and were sacrificed immediately afterward. The GABA/glutamate ratio was assessed by 1 H high-resolutionHighlights: After 1 h restraint, the rats increased their prefrontal cortex GABA and glutamate contents. The stressed rats can be classified according to GABA/glutamate ratio (High G/g vs. Low G/g). The H-G/g rats presented decreased prefrontal cortex activation and increased HPA axis activation featuring an enhanced stress. The H-G/g rats had a reduced locomotion speed together with neophobia and sustained exploration behavior in open field. The prefrontal G/g ratio might underpin the stress-related inter-individual variability. Abstract: In patients suffering from stress-related pathologies and depression, frontal cortex GABA and glutamate contents are reported to decrease and increase, respectively. This suggests that the GABA and/or glutamate content may participate in pathological phenotype expression. Whether differences in frontal cortex GABA and glutamate contents would be associated with specific behavioral and neurobiological patterns remains unclear, especially in the event of exposure to moderate stress. We hypothesized that an increase in prefrontal cortex GABA/glutamate ratio would be associated with a blunted prefrontal cortex activation, an enhanced hypothalamo-pituitary–adrenocortical (HPA) axis activation and changes in behavior. Rats being restrained for 1-h were then tested in an open-field test in order to assess their behavior while under stress, and were sacrificed immediately afterward. The GABA/glutamate ratio was assessed by 1 H high-resolution magic angle spinning magnetic resonance spectroscopy ( 1 H-HRMAS-MRS). The neurobiological response was evaluated through prefrontal cortex mRNA expression and plasma corticosterone levels. The stressed rats were distributed into two subgroups according to their high (H-G/g) or low (L-G/g) GABA/glutamate ratio. Compared to the L-G/g rats, the H-G/g rats exhibited a decrease in c-fos, Arc, Npas4, Nr4a2 mRNA expression suggesting blunted prefrontal cortex activation. They also showed a more pronounced stress with an enhanced rise in corticosterone, alanine aminotransferase (ALAT), aspartate aminotransferase (ASAT), creatine kinase (CK) and lactate dehydrogenase (LDH) levels, as well as behavioral disturbances with decreased locomotion speed. These changes were independent from prefrontal cortex energetic status as mammalian target of rapamycin (mTOR) and adenosine monophosphate-activated protein kinase (AMPK) pathway activities were similar in both subpopulations. The differences in GABA/glutamate ratio in the frontal cortex observed in the stressed animals may participate in shaping individual differences in psychophysiological reactions. … (more)
- Is Part Of:
- Neuroscience. Volume 285(2015)
- Journal:
- Neuroscience
- Issue:
- Volume 285(2015)
- Issue Display:
- Volume 285, Issue 2015 (2015)
- Year:
- 2015
- Volume:
- 285
- Issue:
- 2015
- Issue Sort Value:
- 2015-0285-2015-0000
- Page Start:
- 155
- Page End:
- 165
- Publication Date:
- 2015-01-29
- Subjects:
- ALAT alanine aminotransferase -- AMPK adenosine monophosphate-activated protein kinase -- ASAT aspartate aminotransferase -- CK creatine kinase -- CPMG Carr–Purcell–Meiboom–Gill -- ECL enhanced chemiluminescence -- GABA-T GABA transaminase -- GAD glutamate decarboxylases -- 1H-HRMAS-MRS 1H high-resolution magic angle spinning magnetic resonance spectroscopy -- HPA hypothalamo-pituitary–adrenocortical -- LDH lactate dehydrogenase -- mTOR mammalian target of rapamycin -- NAA N-acetylaspartate
GABA -- glutamate -- prefrontal cortex -- locomotion -- glucocorticoids
Neurochemistry -- Periodicals
Neurophysiology -- Periodicals
Neurology -- Periodicals
Neurochimie -- Périodiques
Neurophysiologie -- Périodiques
Neurochemistry
Neurophysiology
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Periodicals
Electronic journals
612.8 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03064522 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/03064522 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/03064522 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuroscience.2014.10.058 ↗
- Languages:
- English
- ISSNs:
- 0306-4522
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