Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1988 Mar;93(3):483-90.
doi: 10.1111/j.1476-5381.1988.tb10302.x.

Changes in central GABAergic function following acute and repeated stress

Affiliations

Changes in central GABAergic function following acute and repeated stress

M E Otero Losada. Br J Pharmacol. 1988 Mar.

Abstract

1. The function of gamma-aminobutyric acid (GABA)ergic systems in response to acute and repeated stressful manipulations was evaluated in both the corpus striatum and frontal cerebral cortex of the rat. 2. In the corpus striatum the activity of the synthetic enzyme for GABA (glutamic acid decarboxylase, GAD) and the levels of GABA were reduced by acute immobilization stress (1 h). GABA turnover was reduced only by acute cold stress (3 h, 4 degrees C). 3. In the frontal cerebral cortex no changes were observed after acute stressful manipulations, but repeated stress (0.5 h immobilization per day for 14 days) enhanced both GAD activity and GABA turnover, and reduced GABA levels. 4. In conclusion, it would appear that the GABAergic system in the corpus striatum of the rat is most sensitive to acute stress and that the system in the frontal cerebral cortex area is preferentially responsive to chronic stress. It is speculated that the cortical GABAergic system is responsible for adaptive responses to the adverse conditions prevailing during chronic stress.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Life Sci. 1968 Jan 1;7(1):107-12 - PubMed
    1. J Biol Chem. 1959 Apr;234(4):926-8 - PubMed
    1. J Pharmacol Exp Ther. 1968 Nov;164(1):122-34 - PubMed
    1. Life Sci I. 1970 Aug 1;9(15):877-88 - PubMed
    1. Endocrinology. 1973 May;92(5):1367-75 - PubMed

Substances

LinkOut - more resources