Literature DB >> 9802539

Further evidence that the central nucleus of the amygdala is associated with the ethanol-induced locomotor response.

K Demarest1, B Hitzemann, E Mahjubi, J McCaughran, R Hitzemann.   

Abstract

The effect of ethanol on the number of Fos-like immunoreactive (Fos-li) neurons was previously studied in the C57BL/6J (B6) and DBA/2J (D2) inbred mouse strains (Hitzemann and Hitzemann, Alcohol. Clin. Exp. Res. 21:1497-1507, 1997). The data obtained suggested that the locomotor activation response to ethanol found in the D2 but not the B6 strain was associated with an increase in the number of Fos-li neurons (a putative measure of synaptic activity) in the central nucleus of the amygdala (CeA), but not in other brain regions, including the basal ganglia. The current study was performed to obtain data supporting a role for the CeA in the locomotor response. B6D2 F2 intercross animals were phenotyped for their locomotor response to ethanol (1.5 g/kg). The animals from the extreme phenotypes (> 1 SD from the mean) were denoted as very high and very low activity (HH, LL) and differed in their ethanol response by >9,000 cm/15 min (baseline activity was similar in both phenotypes: 5,500 cm/15 min). These extremes especially differed from the parental strains in that the LL group showed a significant ethanol-induced inhibition of activity. After 2 weeks, HH and LL animals were rechallenged with 1.5 g/kg of ethanol or saline and the number of Fos-li neurons determined 1 hr later. In the HH group, ethanol increased the number of Fos-li neurons >600%, whereas in the LL group the increase was 170% (difference: p < 0.001). The increase in the HH group was principally located in the GABA neuron-rich lateral aspect of the CeA and not in the medial posterior-ventral division or the caps division. No significant difference was found between groups in the Fos response for the basolateral or lateral amygdala. Other brain regions were also examined, including the basal ganglia, the hippocampus (CA1, CA3, and dentate gyrus), the bed nucleus of the stria terminalis, and several cortical regions. In some regions (e.g., the bed nucleus), a significant ethanol effect was detected, but it did not differentiate the HH and LL groups. Overall, the data obtained further argue that the CeA has an important role in regulating the acute locomotor response to ethanol.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9802539

Source DB:  PubMed          Journal:  Alcohol Clin Exp Res        ISSN: 0145-6008            Impact factor:   3.455


  9 in total

1.  Behavioral sensitization to ethanol does not result in cross-sensitization to NMDA receptor antagonists.

Authors:  Paul J Meyer; Tamara J Phillips
Journal:  Psychopharmacology (Berl)       Date:  2007-07-26       Impact factor: 4.530

2.  Comparison of ethanol locomotor sensitization in adolescent and adult DBA/2J mice.

Authors:  Rebekah A Stevenson; Joyce Besheer; Clyde W Hodge
Journal:  Psychopharmacology (Berl)       Date:  2007-12-22       Impact factor: 4.530

3.  Identification of an acute ethanol response quantitative trait locus on mouse chromosome 2.

Authors:  K Demarest; J McCaughran; E Mahjubi; L Cipp; R Hitzemann
Journal:  J Neurosci       Date:  1999-01-15       Impact factor: 6.167

4.  Rostroventral caudate putamen involvement in ethanol withdrawal is influenced by a chromosome 4 locus.

Authors:  G Chen; K J Buck
Journal:  Genes Brain Behav       Date:  2010-09-01       Impact factor: 3.449

5.  Involvement of the limbic basal ganglia in ethanol withdrawal convulsivity in mice is influenced by a chromosome 4 locus.

Authors:  Gang Chen; Laura B Kozell; Robert Hitzemann; Kari J Buck
Journal:  J Neurosci       Date:  2008-09-24       Impact factor: 6.167

Review 6.  Ethanol effects on N-methyl-D-aspartate receptors in the bed nucleus of the stria terminalis.

Authors:  Tiffany A Wills; Danny G Winder
Journal:  Cold Spring Harb Perspect Med       Date:  2013-04-01       Impact factor: 6.915

7.  The bed nucleus of the stria terminalis regulates ethanol-seeking behavior in mice.

Authors:  Melanie M Pina; Emily A Young; Andrey E Ryabinin; Christopher L Cunningham
Journal:  Neuropharmacology       Date:  2015-08-21       Impact factor: 5.250

8.  Differential activation of limbic circuitry associated with chronic ethanol withdrawal in DBA/2J and C57BL/6J mice.

Authors:  Gang Chen; Matthew T Reilly; Laura B Kozell; Robert Hitzemann; Kari J Buck
Journal:  Alcohol       Date:  2009-09       Impact factor: 2.405

9.  Oxytocin blocks enhanced motivation for alcohol in alcohol dependence and blocks alcohol effects on GABAergic transmission in the central amygdala.

Authors:  Brendan J Tunstall; Dean Kirson; Lia J Zallar; Sam A McConnell; Janaina C M Vendruscolo; Chelsea P Ho; Christopher S Oleata; Sophia Khom; Maurice Manning; Mary R Lee; Lorenzo Leggio; George F Koob; Marisa Roberto; Leandro F Vendruscolo
Journal:  PLoS Biol       Date:  2019-04-16       Impact factor: 8.029

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.