Literature DB >> 7700525

Somatostatin neurons are a subpopulation of GABA neurons in the rat dentate gyrus: evidence from colocalization of pre-prosomatostatin and glutamate decarboxylase messenger RNAs.

M Esclapez1, C R Houser.   

Abstract

The distribution and extent of glutamate decarboxylase 65 (GAD65) mRNA-labeled neurons that coexpress pre-prosomatostatin mRNA were studied in the rat dentate gyrus of the dorsal and ventral hippocampal formation. The distribution of each group of neurons was determined initially by nonradioactive in situ hybridization experiments with digoxigenin-labeled riboprobes for GAD65 mRNA and pre-prosomatostatin mRNA. Double labeling experiments were then conducted with digoxigenin-labeled riboprobes for GAD65 mRNA and 35S-labeled riboprobes for pre-prosomatostatin mRNA. In the dorsal and ventral dentate gyrus, GAD65 mRNA-containing neurons were highly concentrated in the hilus and in the innermost part of the granule cell layer whereas only a few labeled neurons were scattered in the molecular layer. Pre-prosomatostatin mRNA-containing neurons were primarily located in the hilus and were virtually absent from the molecular and granule cell layers. The simultaneous detection of GAD65 and pre-prosomatostatin mRNAs in the same sections showed that the vast majority of pre-prosomatostatin mRNA-containing neurons in the hilus of the dentate gyrus were also labeled for GAD65 mRNA. In contrast many GAD65 mRNA-labeled neurons did not contain pre-prosomatostatin mRNA. These included all neurons in the molecular layer, neurons within the inner granule cell layer and neurons interspersed amongst double labeled neurons in the hilus. Quantitative analyses indicated that a very high percentage of hilar pre-prosomatostatin mRNA-containing neurons coexpressed GAD65 mRNA in the dorsal (96%) and ventral (92%) dentate gyrus. In contrast only a part of the total population of hilar GAD65 mRNA-containing neurons were also labeled for pre-prosomatostatin mRNA in the dorsal (43%) and ventral (53%) dentate gyrus. In the CA3c region, the percentages of neurons containing both mRNAs were similar to those observed in the hilus. The findings demonstrate that the vast majority of hilar somatostatin neurons, which have previously been shown to be extremely vulnerable to ischemia and seizure-induced damage, are GABA neurons. However, the total population of GAD65 mRNA-containing neurons in the hilus is substantially larger than the somatostatin-containing subgroup, and these findings reinforce the suggestion that GABA neurons are a major component of the diverse group of neurons in the hilus of the dentate gyrus.

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Year:  1995        PMID: 7700525     DOI: 10.1016/0306-4522(94)00406-u

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  25 in total

1.  Distribution, targeting, and internalization of the sst4 somatostatin receptor in rat brain.

Authors:  M Schreff; S Schulz; M Händel; G Keilhoff; H Braun; G Pereira; M Klutzny; H Schmidt; G Wolf; V Höllt
Journal:  J Neurosci       Date:  2000-05-15       Impact factor: 6.167

2.  Testing the disinhibition hypothesis of epileptogenesis in vivo and during spontaneous seizures.

Authors:  P S Buckmaster; A L Jongen-Rêlo; S B Davari; E H Wong
Journal:  J Neurosci       Date:  2000-08-15       Impact factor: 6.167

3.  Cortistatin is expressed in a distinct subset of cortical interneurons.

Authors:  L de Lecea; J A del Rio; J R Criado; S Alcántara; M Morales; P E Danielson; S J Henriksen; E Soriano; J G Sutcliffe
Journal:  J Neurosci       Date:  1997-08-01       Impact factor: 6.167

4.  Heterogeneity of the supramammillary-hippocampal pathways: evidence for a unique GABAergic neurotransmitter phenotype and regional differences.

Authors:  Rabia Soussi; Nianhui Zhang; Siroun Tahtakran; Carolyn R Houser; Monique Esclapez
Journal:  Eur J Neurosci       Date:  2010-08-16       Impact factor: 3.386

5.  GABA excitation in mouse hilar neuropeptide Y neurons.

Authors:  Li-Ying Fu; Anthony N van den Pol
Journal:  J Physiol       Date:  2007-01-04       Impact factor: 5.182

6.  Selective loss of dentate hilar interneurons contributes to reduced synaptic inhibition of granule cells in an electrical stimulation-based animal model of temporal lobe epilepsy.

Authors:  Chengsan Sun; Zakaria Mtchedlishvili; Edward H Bertram; Alev Erisir; Jaideep Kapur
Journal:  J Comp Neurol       Date:  2007-02-10       Impact factor: 3.215

7.  Involvement of spinal somatostatin receptor SST(2A) in inflammation-induced thermal hyperalgesia: ultrastructural and behavioral studies in rats.

Authors:  Jun Zhao; Jiang-Yuan Hu; Yu-Qiu Zhang; Zhi-Qi Zhao
Journal:  Neurochem Res       Date:  2008-05-02       Impact factor: 3.996

8.  Surviving hilar somatostatin interneurons enlarge, sprout axons, and form new synapses with granule cells in a mouse model of temporal lobe epilepsy.

Authors:  Wei Zhang; Ruth Yamawaki; Xiling Wen; Justin Uhl; Jessica Diaz; David A Prince; Paul S Buckmaster
Journal:  J Neurosci       Date:  2009-11-11       Impact factor: 6.167

9.  Anxiolytic and antidepressant actions of somatostatin: the role of sst2 and sst3 receptors.

Authors:  Elif Engin; Dallas Treit
Journal:  Psychopharmacology (Berl)       Date:  2009-07-17       Impact factor: 4.530

10.  Distally directed dendrotoxicity induced by kainic Acid in hippocampal interneurons of green fluorescent protein-expressing transgenic mice.

Authors:  Anthony A Oliva; Trang T Lam; John W Swann
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

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