4.5 Article

Forebrain and midbrain distribution of major benzodiazepine-sensitive GABAA receptor subunits in the adult C57 mouse as assessed with in situ hybridization

Journal

NEUROSCIENCE
Volume 150, Issue 2, Pages 370-385

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2007.09.008

Keywords

mice; GABA; inhibition

Categories

Funding

  1. NCRR NIH HHS [P51 RR000165] Funding Source: Medline
  2. NIDA NIH HHS [DA019624, R01 DA019624-02, R01 DA019624, R01 DA019624-01A2] Funding Source: Medline
  3. NIMH NIH HHS [MH069884, F32 MH073389-01, F32 MH073389, F32 MH073389-03, F32 MH073389-02, K01 MH069884] Funding Source: Medline

Ask authors/readers for more resources

In the adult brain, GABA is the major inhibitory neurotransmitter. Understanding of the behavioral and pharmacological functions of GABA has been advanced by recent studies of mouse lines that possess mutations in various GABA receptor subtypes and associated proteins. Genetically altered mice have become important tools for discerning GABAergic function. Thus detailed knowledge of the anatomical distribution of different GABA(A) subtype receptors in mice is a prerequisite for understanding the neural circuitry underlying changes in normal and drug-induced behaviors seen in mutated mice. In the current study, we used in situ hybridization histochemistry with [S-35]UTP-labeled ribo-probes to examine the regional expression pattern of mRNA transcripts for seven major GABA(A) receptor subunits in adjacent coronal brain sections (alpha 1, alpha 2, alpha 3, alpha 5, beta 2, beta 3, and gamma 2). Our results indicate that many of these GABAergic genes are co-expressed in much of the adult brain including the neocortex, hippocampus, amygdala, thalamus and striatum. However, each gene also shows a unique region-specific distribution pattern, indicative of distinct neuronal circuits that may serve specific physiological and pharmacological functions. Published by Elsevier Ltd on behalf of IBRO.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available